| Year |
Citation |
Score |
| 2022 |
DeGeer J, Datwyler AL, Rickenbach C, Ommer A, Gerber D, Fimiani C, Gerber J, Pereira JA, Suter U. Ral GTPases are critical regulators of spinal cord myelination and homeostasis. Cell Reports. 40: 111413. PMID 36170840 DOI: 10.1016/j.celrep.2022.111413 |
0.382 |
|
| 2021 |
Gerber D, Pereira JA, Gerber J, Tan G, Dimitrieva S, Yángüez E, Suter U. Transcriptional profiling of mouse peripheral nerves to the single-cell level to build a sciatic nerve ATlas (SNAT). Elife. 10. PMID 33890853 DOI: 10.7554/eLife.58591 |
0.378 |
|
| 2020 |
Pereira JA, Gerber J, Ghidinelli M, Gerber D, Tortola L, Ommer A, Bachofner S, Santarella F, Tinelli E, Lin S, Rüegg MA, Kopf M, Toyka KV, Suter U. Mice carrying an analogous heterozygous Dynamin 2 K562E mutation that causes neuropathy in humans develop predominant characteristics of a primary myopathy. Human Molecular Genetics. PMID 32129442 DOI: 10.1093/Hmg/Ddaa034 |
0.383 |
|
| 2019 |
Ommer A, Figlia G, Pereira JA, Datwyler AL, Gerber J, DeGeer J, Lalli G, Suter U. Ral GTPases in Schwann cells promote radial axonal sorting in the peripheral nervous system. The Journal of Cell Biology. PMID 31201267 DOI: 10.1083/Jcb.201811150 |
0.509 |
|
| 2019 |
Dimas P, Montani L, Pereira JA, Moreno D, Trötzmüller M, Gerber J, Semenkovich CF, Köfeler HC, Suter U. CNS myelination and remyelination depend on fatty acid synthesis by oligodendrocytes. Elife. 8. PMID 31063129 DOI: 10.7554/Elife.44702 |
0.471 |
|
| 2019 |
Gerber D, Ghidinelli M, Tinelli E, Somandin C, Gerber J, Pereira JA, Ommer A, Figlia G, Miehe M, Nägeli LG, Suter V, Tadini V, Sidiropoulos PN, Wessig C, Toyka KV, ... Suter U, et al. Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function. Elife. 8. PMID 30648534 DOI: 10.7554/Elife.42404 |
0.513 |
|
| 2019 |
Suter U, Nave KA. Transgenic Mouse Models of CMT1A and HNPP. Annals of the New York Academy of Sciences. 883: 247-253. PMID 29086924 DOI: 10.1111/j.1749-6632.1999.tb08586.x |
0.333 |
|
| 2019 |
Dimas P, Montani L, Pereira JA, Moreno D, Trötzmüller M, Gerber J, Semenkovich CF, Köfeler HC, Suter U. Author response: CNS myelination and remyelination depend on fatty acid synthesis by oligodendrocytes Elife. DOI: 10.7554/Elife.44702.030 |
0.389 |
|
| 2018 |
Gökbuget D, Pereira JA, Opitz L, Christe D, Kessler T, Marchais A, Suter U. The miRNA biogenesis pathway prevents inappropriate expression of injury response genes in developing and adult Schwann cells. Glia. PMID 30295958 DOI: 10.1002/Glia.23516 |
0.438 |
|
| 2018 |
Norrmén C, Figlia G, Pfistner P, Pereira JA, Bachofner S, Suter U. mTORC1 is transiently reactivated in injured nerves to promote c-Jun elevation and Schwann cell dedifferentiation. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. PMID 29695414 DOI: 10.1523/Jneurosci.3619-17.2018 |
0.518 |
|
| 2018 |
Montani L, Pereira JA, Norrmén C, Pohl HBF, Tinelli E, Trötzmüller M, Figlia G, Dimas P, von Niederhäusern B, Schwager R, Jessberger S, Semenkovich CF, Köfeler HC, Suter U. De novo fatty acid synthesis by Schwann cells is essential for peripheral nervous system myelination. The Journal of Cell Biology. PMID 29434029 DOI: 10.1083/Jcb.201706010 |
0.491 |
|
| 2018 |
Gerber D, Ghidinelli M, Tinelli E, Somandin C, Gerber J, Pereira JA, Ommer A, Figlia G, Miehe M, Nägeli LG, Suter V, Tadini V, Sidiropoulos PN, Wessig C, Toyka KV, ... Suter U, et al. Author response: Schwann cells, but not Oligodendrocytes, Depend Strictly on Dynamin 2 Function Elife. DOI: 10.7554/Elife.42404.024 |
0.381 |
|
| 2017 |
Figlia G, Gerber D, Suter U. Myelination and mTOR. Glia. PMID 29210103 DOI: 10.1002/Glia.23273 |
0.481 |
|
| 2017 |
Figlia G, Norrmén C, Pereira JA, Gerber D, Suter U. Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system. Elife. 6. PMID 28880149 DOI: 10.7554/Elife.29241 |
0.51 |
|
| 2017 |
Figlia G, Norrmén C, Pereira JA, Gerber D, Suter U. Author response: Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system Elife. DOI: 10.7554/Elife.29241.035 |
0.423 |
|
| 2016 |
Mogha A, Harty BL, Carlin D, Joseph J, Sanchez NE, Suter U, Piao X, Cavalli V, Monk KR. Gpr126/Adgrg6 Has Schwann Cell Autonomous and Nonautonomous Functions in Peripheral Nerve Injury and Repair. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 36: 12351-12367. PMID 27927955 DOI: 10.1523/Jneurosci.3854-15.2016 |
0.501 |
|
| 2016 |
Huber N, Bieniossek C, Wagner KM, Elsässer HP, Suter U, Berger I, Niemann A. Glutathione-conjugating and membrane-remodeling activity of GDAP1 relies on amphipathic C-terminal domain. Scientific Reports. 6: 36930. PMID 27841286 DOI: 10.1038/Srep36930 |
0.369 |
|
| 2016 |
Kaucka M, Ivashkin E, Gyllborg D, Zikmund T, Tesarova M, Kaiser J, Xie M, Petersen J, Pachnis V, Nicolis SK, Yu T, Sharpe P, Arenas E, Brismar H, Blom H, ... ... Suter U, et al. Analysis of neural crest-derived clones reveals novel aspects of facial development. Science Advances. 2: e1600060. PMID 27493992 DOI: 10.1126/Sciadv.1600060 |
0.341 |
|
| 2016 |
Fernando RN, Cotter L, Perrin-Tricaud C, Berthelot J, Bartolami S, Pereira JA, Gonzalez S, Suter U, Tricaud N. Optimal myelin elongation relies on YAP activation by axonal growth and inhibition by Crb3/Hippo pathway. Nature Communications. 7: 12186. PMID 27435623 DOI: 10.1038/Ncomms12186 |
0.513 |
|
| 2016 |
Quintes S, Brinkmann BG, Ebert M, Fröb F, Kungl T, Arlt FA, Tarabykin V, Huylebroeck D, Meijer D, Suter U, Wegner M, Sereda MW, Nave KA. Zeb2 is essential for Schwann cell differentiation, myelination and nerve repair. Nature Neuroscience. PMID 27294512 DOI: 10.1038/Nn.4321 |
0.583 |
|
| 2015 |
Gökbuget D, Pereira JA, Bachofner S, Marchais A, Ciaudo C, Stoffel M, Schulte JH, Suter U. The Lin28/let-7 axis is critical for myelination in the peripheral nervous system. Nature Communications. 6: 8584. PMID 26466203 DOI: 10.1038/Ncomms9584 |
0.409 |
|
| 2015 |
Brügger V, Engler S, Pereira JA, Ruff S, Horn M, Welzl H, Münger E, Vaquié A, Sidiropoulos PN, Egger B, Yotovski P, Filgueira L, Somandin C, Lühmann TC, D'Antonio M, ... ... Suter U, et al. HDAC1/2-Dependent P0 Expression Maintains Paranodal and Nodal Integrity Independently of Myelin Stability through Interactions with Neurofascins. Plos Biology. 13: e1002258. PMID 26406915 DOI: 10.1371/Journal.Pbio.1002258 |
0.535 |
|
| 2015 |
Lebrun-Julien F, Suter U. Combined HDAC1 and HDAC2 Depletion Promotes Retinal Ganglion Cell Survival After Injury Through Reduction of p53 Target Gene Expression. Asn Neuro. 7. PMID 26129908 DOI: 10.1177/1759091415593066 |
0.3 |
|
| 2015 |
Dumas L, Heitz-Marchaland C, Fouquet S, Suter U, Livet J, Moreau-Fauvarque C, Chédotal A. Multicolor analysis of oligodendrocyte morphology, interactions, and development with Brainbow. Glia. 63: 699-717. PMID 25530205 DOI: 10.1002/Glia.22779 |
0.475 |
|
| 2014 |
Norrmén C, Figlia G, Lebrun-Julien F, Pereira JA, Trötzmüller M, Köfeler HC, Rantanen V, Wessig C, van Deijk AL, Smit AB, Verheijen MH, Rüegg MA, Hall MN, Suter U. mTORC1 controls PNS myelination along the mTORC1-RXRγ-SREBP-lipid biosynthesis axis in Schwann cells. Cell Reports. 9: 646-60. PMID 25310982 DOI: 10.1016/J.Celrep.2014.09.001 |
0.51 |
|
| 2014 |
Kaukua N, Shahidi MK, Konstantinidou C, Dyachuk V, Kaucka M, Furlan A, An Z, Wang L, Hultman I, Ahrlund-Richter L, Blom H, Brismar H, Lopes NA, Pachnis V, Suter U, et al. Glial origin of mesenchymal stem cells in a tooth model system. Nature. 513: 551-4. PMID 25079316 DOI: 10.1038/Nature13536 |
0.337 |
|
| 2014 |
Lebrun-Julien F, Bachmann L, Norrmén C, Trötzmüller M, Köfeler H, Rüegg MA, Hall MN, Suter U. Balanced mTORC1 activity in oligodendrocytes is required for accurate CNS myelination. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 8432-48. PMID 24948799 DOI: 10.1523/Jneurosci.1105-14.2014 |
0.463 |
|
| 2014 |
Jacob C, Lötscher P, Engler S, Baggiolini A, Varum Tavares S, Brügger V, John N, Büchmann-Møller S, Snider PL, Conway SJ, Yamaguchi T, Matthias P, Sommer L, Mantei N, Suter U. HDAC1 and HDAC2 control the specification of neural crest cells into peripheral glia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 6112-22. PMID 24760871 DOI: 10.1523/Jneurosci.5212-13.2014 |
0.472 |
|
| 2014 |
Porcheri C, Suter U, Jessberger S. Dissecting integrin-dependent regulation of neural stem cell proliferation in the adult brain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 5222-32. PMID 24719101 DOI: 10.1523/Jneurosci.4928-13.2014 |
0.321 |
|
| 2014 |
Montani L, Buerki-Thurnherr T, de Faria JP, Pereira JA, Dias NG, Fernandes R, Gonçalves AF, Braun A, Benninger Y, Böttcher RT, Costell M, Nave KA, Franklin RJ, Meijer D, Suter U, et al. Profilin 1 is required for peripheral nervous system myelination. Development (Cambridge, England). 141: 1553-61. PMID 24598164 DOI: 10.1242/Dev.101840 |
0.511 |
|
| 2014 |
Niemann A, Huber N, Wagner KM, Somandin C, Horn M, Lebrun-Julien F, Angst B, Pereira JA, Halfter H, Welzl H, Feltri ML, Wrabetz L, Young P, Wessig C, Toyka KV, ... Suter U, et al. The Gdap1 knockout mouse mechanistically links redox control to Charcot-Marie-Tooth disease. Brain : a Journal of Neurology. 137: 668-82. PMID 24480485 DOI: 10.1093/Brain/Awt371 |
0.383 |
|
| 2014 |
Guo J, Wang L, Zhang Y, Wu J, Arpag S, Hu B, Imhof BA, Tian X, Carter BD, Suter U, Li J. Abnormal junctions and permeability of myelin in PMP22-deficient nerves. Annals of Neurology. 75: 255-65. PMID 24339129 DOI: 10.1002/Ana.24086 |
0.547 |
|
| 2013 |
Ribeiro S, Napoli I, White IJ, Parrinello S, Flanagan AM, Suter U, Parada LF, Lloyd AC. Injury signals cooperate with Nf1 loss to relieve the tumor-suppressive environment of adult peripheral nerve. Cell Reports. 5: 126-36. PMID 24075988 DOI: 10.1016/J.Celrep.2013.08.033 |
0.372 |
|
| 2013 |
Norrmén C, Suter U. Akt/mTOR signalling in myelination. Biochemical Society Transactions. 41: 944-50. PMID 23863161 DOI: 10.1042/Bst20130046 |
0.424 |
|
| 2013 |
Tinelli E, Pereira JA, Suter U. Muscle-specific function of the centronuclear myopathy and Charcot-Marie-Tooth neuropathy-associated dynamin 2 is required for proper lipid metabolism, mitochondria, muscle fibers, neuromuscular junctions and peripheral nerves. Human Molecular Genetics. 22: 4417-29. PMID 23813975 DOI: 10.1093/Hmg/Ddt292 |
0.338 |
|
| 2013 |
Huber N, Guimaraes S, Schrader M, Suter U, Niemann A. Charcot-Marie-Tooth disease-associated mutants of GDAP1 dissociate its roles in peroxisomal and mitochondrial fission. Embo Reports. 14: 545-52. PMID 23628762 DOI: 10.1038/Embor.2013.56 |
0.303 |
|
| 2013 |
Vadodaria KC, Brakebusch C, Suter U, Jessberger S. Stage-specific functions of the small Rho GTPases Cdc42 and Rac1 for adult hippocampal neurogenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 1179-89. PMID 23325254 DOI: 10.1523/Jneurosci.2103-12.2013 |
0.304 |
|
| 2013 |
Nave KA, Suter U. Neurological Mouse Mutants: A Molecular-Genetic Analysis of Myelin Proteins Neuroglia. DOI: 10.1093/acprof:oso/9780195152227.003.0043 |
0.313 |
|
| 2012 |
Horn M, Baumann R, Pereira JA, Sidiropoulos PN, Somandin C, Welzl H, Stendel C, Lühmann T, Wessig C, Toyka KV, Relvas JB, Senderek J, Suter U. Myelin is dependent on the Charcot-Marie-Tooth Type 4H disease culprit protein FRABIN/FGD4 in Schwann cells. Brain : a Journal of Neurology. 135: 3567-83. PMID 23171661 DOI: 10.1093/Brain/Aws275 |
0.591 |
|
| 2012 |
Somandin C, Gerber D, Pereira JA, Horn M, Suter U. LITAF (SIMPLE) regulates Wallerian degeneration after injury but is not essential for peripheral nerve development and maintenance: implications for Charcot-Marie-Tooth disease. Glia. 60: 1518-28. PMID 22729949 DOI: 10.1002/Glia.22371 |
0.517 |
|
| 2012 |
Fünfschilling U, Supplie LM, Mahad D, Boretius S, Saab AS, Edgar J, Brinkmann BG, Kassmann CM, Tzvetanova ID, Möbius W, Diaz F, Meijer D, Suter U, Hamprecht B, Sereda MW, et al. Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity. Nature. 485: 517-21. PMID 22622581 DOI: 10.1038/Nature11007 |
0.461 |
|
| 2012 |
Hari L, Miescher I, Shakhova O, Suter U, Chin L, Taketo M, Richardson WD, Kessaris N, Sommer L. Temporal control of neural crest lineage generation by Wnt/β-catenin signaling. Development (Cambridge, England). 139: 2107-17. PMID 22573620 DOI: 10.1242/Dev.073064 |
0.315 |
|
| 2012 |
Sidiropoulos PN, Miehe M, Bock T, Tinelli E, Oertli CI, Kuner R, Meijer D, Wollscheid B, Niemann A, Suter U. Dynamin 2 mutations in Charcot-Marie-Tooth neuropathy highlight the importance of clathrin-mediated endocytosis in myelination. Brain : a Journal of Neurology. 135: 1395-411. PMID 22451505 DOI: 10.1093/Brain/Aws061 |
0.466 |
|
| 2012 |
Pereira JA, Lebrun-Julien F, Suter U. Molecular mechanisms regulating myelination in the peripheral nervous system. Trends in Neurosciences. 35: 123-34. PMID 22192173 DOI: 10.1016/J.Tins.2011.11.006 |
0.518 |
|
| 2012 |
Adameyko I, Lallemend F, Furlan A, Zinin N, Aranda S, Kitambi SS, Blanchart A, Favaro R, Nicolis S, Lübke M, Müller T, Birchmeier C, Suter U, Zaitoun I, Takahashi Y, et al. Sox2 and Mitf cross-regulatory interactions consolidate progenitor and melanocyte lineages in the cranial neural crest. Development (Cambridge, England). 139: 397-410. PMID 22186729 DOI: 10.1242/Dev.065581 |
0.456 |
|
| 2012 |
Mueggler T, Pohl H, Baltes C, Riethmacher D, Suter U, Rudin M. MRI signature in a novel mouse model of genetically induced adult oligodendrocyte cell death. Neuroimage. 59: 1028-36. PMID 21945466 DOI: 10.1016/J.Neuroimage.2011.09.001 |
0.339 |
|
| 2012 |
Guo J, Yan Q, Sosinsky G, Ellisman M, Suter U, Li J. Virtual Demyelination and Tight Junction Defect in PMP22 Deficiency (IN1-1.003) Neurology. 78: IN1-1.003-IN1-1.003. DOI: 10.1212/Wnl.78.1_Meetingabstracts.In1-1.003 |
0.474 |
|
| 2011 |
Jacob C, Lebrun-Julien F, Suter U. How histone deacetylases control myelination. Molecular Neurobiology. 44: 303-12. PMID 21861092 DOI: 10.1007/S12035-011-8198-9 |
0.508 |
|
| 2011 |
Zimoń M, Baets J, Fabrizi GM, Jaakkola E, Kabzińska D, Pilch J, Schindler AB, Cornblath DR, Fischbeck KH, Auer-Grumbach M, Guelly C, Huber N, De Vriendt E, Timmerman V, Suter U, et al. Dominant GDAP1 mutations cause predominantly mild CMT phenotypes. Neurology. 77: 540-8. PMID 21753178 DOI: 10.1212/Wnl.0B013E318228Fc70 |
0.37 |
|
| 2011 |
Saporta MA, Katona I, Zhang X, Roper HP, McClelland L, Macdonald F, Brueton L, Blake J, Suter U, Reilly MM, Shy ME, Li J. Neuropathy in a human without the PMP22 gene. Archives of Neurology. 68: 814-21. PMID 21670407 DOI: 10.1001/Archneurol.2011.110 |
0.461 |
|
| 2011 |
Le LQ, Liu C, Shipman T, Chen Z, Suter U, Parada LF. Susceptible stages in Schwann cells for NF1-associated plexiform neurofibroma development. Cancer Research. 71: 4686-95. PMID 21551250 DOI: 10.1158/0008-5472.Can-10-4577 |
0.414 |
|
| 2011 |
Bremer M, Fröb F, Kichko T, Reeh P, Tamm ER, Suter U, Wegner M. Sox10 is required for Schwann-cell homeostasis and myelin maintenance in the adult peripheral nerve. Glia. 59: 1022-32. PMID 21491499 DOI: 10.1002/Glia.21173 |
0.539 |
|
| 2011 |
Herzog D, Loetscher P, van Hengel J, Knüsel S, Brakebusch C, Taylor V, Suter U, Relvas JB. The small GTPase RhoA is required to maintain spinal cord neuroepithelium organization and the neural stem cell pool. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 5120-30. PMID 21451048 DOI: 10.1523/Jneurosci.4807-10.2011 |
0.361 |
|
| 2011 |
Jacob C, Christen CN, Pereira JA, Somandin C, Baggiolini A, Lötscher P, Ozçelik M, Tricaud N, Meijer D, Yamaguchi T, Matthias P, Suter U. HDAC1 and HDAC2 control the transcriptional program of myelination and the survival of Schwann cells. Nature Neuroscience. 14: 429-36. PMID 21423190 DOI: 10.1038/Nn.2762 |
0.478 |
|
| 2011 |
Kabzińska D, Niemann A, Drac H, Huber N, Potulska-Chromik A, Hausmanowa-Petrusewicz I, Suter U, Kochański A. A new missense GDAP1 mutation disturbing targeting to the mitochondrial membrane causes a severe form of AR-CMT2C disease. Neurogenetics. 12: 145-53. PMID 21365284 DOI: 10.1007/S10048-011-0276-7 |
0.348 |
|
| 2011 |
Pohl HB, Porcheri C, Mueggler T, Bachmann LC, Martino G, Riethmacher D, Franklin RJ, Rudin M, Suter U. Genetically induced adult oligodendrocyte cell death is associated with poor myelin clearance, reduced remyelination, and axonal damage. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 1069-80. PMID 21248132 DOI: 10.1523/Jneurosci.5035-10.2011 |
0.806 |
|
| 2011 |
Berger P, Tersar K, Ballmer-Hofer K, Suter U. The CMT4B disease-causing proteins MTMR2 and MTMR13/SBF2 regulate AKT signalling. Journal of Cellular and Molecular Medicine. 15: 307-15. PMID 19912440 DOI: 10.1111/J.1582-4934.2009.00967.X |
0.353 |
|
| 2010 |
Stendel C, Roos A, Kleine H, Arnaud E, Ozçelik M, Sidiropoulos PN, Zenker J, Schüpfer F, Lehmann U, Sobota RM, Litchfield DW, Lüscher B, Chrast R, Suter U, Senderek J. SH3TC2, a protein mutant in Charcot-Marie-Tooth neuropathy, links peripheral nerve myelination to endosomal recycling. Brain : a Journal of Neurology. 133: 2462-74. PMID 20826437 DOI: 10.1093/Brain/Awq168 |
0.584 |
|
| 2010 |
Goebbels S, Oltrogge JH, Kemper R, Heilmann I, Bormuth I, Wolfer S, Wichert SP, Möbius W, Liu X, Lappe-Siefke C, Rossner MJ, Groszer M, Suter U, Frahm J, Boretius S, et al. Elevated phosphatidylinositol 3,4,5-trisphosphate in glia triggers cell-autonomous membrane wrapping and myelination. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 8953-64. PMID 20592216 DOI: 10.1523/Jneurosci.0219-10.2010 |
0.515 |
|
| 2010 |
Zawadzka M, Rivers LE, Fancy SP, Zhao C, Tripathi R, Jamen F, Young K, Goncharevich A, Pohl H, Rizzi M, Rowitch DH, Kessaris N, Suter U, Richardson WD, Franklin RJ. CNS-resident glial progenitor/stem cells produce Schwann cells as well as oligodendrocytes during repair of CNS demyelination. Cell Stem Cell. 6: 578-90. PMID 20569695 DOI: 10.1016/J.Stem.2010.04.002 |
0.484 |
|
| 2010 |
Pereira JA, Baumann R, Norrmén C, Somandin C, Miehe M, Jacob C, Lühmann T, Hall-Bozic H, Mantei N, Meijer D, Suter U. Dicer in Schwann cells is required for myelination and axonal integrity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 6763-75. PMID 20463238 DOI: 10.1523/Jneurosci.0801-10.2010 |
0.528 |
|
| 2010 |
Cotter L, Ozçelik M, Jacob C, Pereira JA, Locher V, Baumann R, Relvas JB, Suter U, Tricaud N. Dlg1-PTEN interaction regulates myelin thickness to prevent damaging peripheral nerve overmyelination. Science (New York, N.Y.). 328: 1415-8. PMID 20448149 DOI: 10.1126/Science.1187735 |
0.53 |
|
| 2010 |
Ozçelik M, Cotter L, Jacob C, Pereira JA, Relvas JB, Suter U, Tricaud N. Pals1 is a major regulator of the epithelial-like polarization and the extension of the myelin sheath in peripheral nerves. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 4120-31. PMID 20237282 DOI: 10.1523/Jneurosci.5185-09.2010 |
0.518 |
|
| 2010 |
Bai Y, Zhang X, Katona I, Saporta MA, Shy ME, O'Malley HA, Isom LL, Suter U, Li J. Conduction block in PMP22 deficiency. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 600-8. PMID 20071523 DOI: 10.1523/Jneurosci.4264-09.2010 |
0.495 |
|
| 2010 |
Gonçalves AF, Dias NG, Moransard M, Correia R, Pereira JA, Witke W, Suter U, Relvas JB. Gelsolin is required for macrophage recruitment during remyelination of the peripheral nervous system. Glia. 58: 706-15. PMID 20014276 DOI: 10.1002/Glia.20956 |
0.512 |
|
| 2010 |
Arnaud E, Zenker J, Charles ASDP, Stendel C, Roos A, Médard JJ, Tricaud N, Kleine H, Luscher B, Weis J, Suter U, Senderek J, Chrast R. SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system (Proceedings of the National Academy of Sciences of the United States of America (2009) 106, 41, (17528-17533) DOI: 10.1073/pnas.0905523106) Proceedings of the National Academy of Sciences of the United States of America. 107: 15305. DOI: 10.1073/Pnas.1010446107 |
0.381 |
|
| 2010 |
Goncalo-Dias N, Pereira J, Gonçalves AF, Relvas J, Suter U, Fässler R. Role of the IPP complex in myelination and remyelination International Journal of Developmental Neuroscience. 28: 707. DOI: 10.1016/J.Ijdevneu.2010.07.189 |
0.405 |
|
| 2009 |
Adameyko I, Lallemend F, Aquino JB, Pereira JA, Topilko P, Müller T, Fritz N, Beljajeva A, Mochii M, Liste I, Usoskin D, Suter U, Birchmeier C, Ernfors P. Schwann cell precursors from nerve innervation are a cellular origin of melanocytes in skin. Cell. 139: 366-79. PMID 19837037 DOI: 10.1016/J.Cell.2009.07.049 |
0.416 |
|
| 2009 |
Arnaud E, Zenker J, de Preux Charles AS, Stendel C, Roos A, Médard JJ, Tricaud N, Kleine H, Luscher B, Weis J, Suter U, Senderek J, Chrast R. SH3TC2/KIAA1985 protein is required for proper myelination and the integrity of the node of Ranvier in the peripheral nervous system. Proceedings of the National Academy of Sciences of the United States of America. 106: 17528-33. PMID 19805030 DOI: 10.1073/Pnas.0905523106 |
0.563 |
|
| 2009 |
Schildknecht A, Probst HC, McCoy KD, Miescher I, Brenner C, Leone DP, Suter U, Ohashi PS, van den Broek M. Antigens expressed by myelinating glia cells induce peripheral cross-tolerance of endogenous CD8+ T cells. European Journal of Immunology. 39: 1505-15. PMID 19462379 DOI: 10.1002/Eji.200839019 |
0.344 |
|
| 2009 |
Pereira JA, Benninger Y, Baumann R, Gonçalves AF, Ozçelik M, Thurnherr T, Tricaud N, Meijer D, Fässler R, Suter U, Relvas JB. Integrin-linked kinase is required for radial sorting of axons and Schwann cell remyelination in the peripheral nervous system. The Journal of Cell Biology. 185: 147-61. PMID 19349584 DOI: 10.1083/Jcb.200809008 |
0.45 |
|
| 2009 |
Leal A, Huehne K, Bauer F, Sticht H, Berger P, Suter U, Morera B, Del Valle G, Lupski JR, Ekici A, Pasutto F, Endele S, Barrantes R, Berghoff C, Berghoff M, et al. Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data, functional studies of the SH3 recognition motif and correlation between wild-type MED25 and PMP22 RNA levels in CMT1A animal models. Neurogenetics. 10: 275-87. PMID 19290556 DOI: 10.1007/S10048-009-0183-3 |
0.414 |
|
| 2009 |
Fuchs S, Herzog D, Sumara G, Büchmann-Møller S, Civenni G, Wu X, Chrostek-Grashoff A, Suter U, Ricci R, Relvas JB, Brakebusch C, Sommer L. Stage-specific control of neural crest stem cell proliferation by the small rho GTPases Cdc42 and Rac1. Cell Stem Cell. 4: 236-47. PMID 19265663 DOI: 10.1016/J.Stem.2009.01.017 |
0.319 |
|
| 2008 |
Krause S, Stendel C, Senderek J, Relvas JB, Suter U. Small Rho GTPases are key regulators of peripheral nerve biology in health and disease. Journal of the Peripheral Nervous System : Jpns. 13: 188-99. PMID 18844785 DOI: 10.1111/J.1529-8027.2008.00177.X |
0.465 |
|
| 2008 |
Feltri ML, Suter U, Relvas JB. The function of RhoGTPases in axon ensheathment and myelination. Glia. 56: 1508-17. PMID 18803320 DOI: 10.1002/Glia.20752 |
0.502 |
|
| 2008 |
Jacob C, Grabner H, Atanasoski S, Suter U. Expression and localization of Ski determine cell type-specific TGFbeta signaling effects on the cell cycle. The Journal of Cell Biology. 182: 519-30. PMID 18695043 DOI: 10.1083/Jcb.200710161 |
0.428 |
|
| 2008 |
Genoud N, Ott D, Braun N, Prinz M, Schwarz P, Suter U, Trono D, Aguzzi A. Antiprion prophylaxis by gene transfer of a soluble prion antagonist. The American Journal of Pathology. 172: 1287-96. PMID 18372425 DOI: 10.2353/Ajpath.2008.070836 |
0.331 |
|
| 2008 |
Delaunay D, Heydon K, Cumano A, Schwab MH, Thomas JL, Suter U, Nave KA, Zalc B, Spassky N. Early neuronal and glial fate restriction of embryonic neural stem cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 2551-62. PMID 18322099 DOI: 10.1523/Jneurosci.5497-07.2008 |
0.364 |
|
| 2008 |
Atanasoski S, Boentert M, De Ventura L, Pohl H, Baranek C, Beier K, Young P, Barbacid M, Suter U. Postnatal Schwann cell proliferation but not myelination is strictly and uniquely dependent on cyclin-dependent kinase 4 (cdk4). Molecular and Cellular Neurosciences. 37: 519-27. PMID 18191580 DOI: 10.1016/J.Mcn.2007.11.005 |
0.494 |
|
| 2008 |
Maier M, Berger P, Nave KA, Suter U. Promoter analysis of the CMT1A-disease gene PMP22 in vivo Journal of Neurochemistry. 81: 77-77. DOI: 10.1046/J.1471-4159.81.S1.45_2.X |
0.475 |
|
| 2007 |
Suter U. Phosphoinositides and Charcot-Marie-tooth disease: new keys to old questions. Cellular and Molecular Life Sciences : Cmls. 64: 3261-5. PMID 17965826 DOI: 10.1007/s00018-007-7381-7 |
0.375 |
|
| 2007 |
Tersar K, Boentert M, Berger P, Bonneick S, Wessig C, Toyka KV, Young P, Suter U. Mtmr13/Sbf2-deficient mice: an animal model for CMT4B2. Human Molecular Genetics. 16: 2991-3001. PMID 17855448 DOI: 10.1093/Hmg/Ddm257 |
0.489 |
|
| 2007 |
Heredia A, Bui CC, Suter U, Young P, Schäffer TE. AFM combines functional and morphological analysis of peripheral myelinated and demyelinated nerve fibers. Neuroimage. 37: 1218-26. PMID 17689984 DOI: 10.1016/J.Neuroimage.2007.06.007 |
0.492 |
|
| 2007 |
Benninger Y, Thurnherr T, Pereira JA, Krause S, Wu X, Chrostek-Grashoff A, Herzog D, Nave KA, Franklin RJ, Meijer D, Brakebusch C, Suter U, Relvas JB. Essential and distinct roles for cdc42 and rac1 in the regulation of Schwann cell biology during peripheral nervous system development. The Journal of Cell Biology. 177: 1051-61. PMID 17576798 DOI: 10.1083/Jcb.200610108 |
0.495 |
|
| 2007 |
Stendel C, Roos A, Deconinck T, Pereira J, Castagner F, Niemann A, Kirschner J, Korinthenberg R, Ketelsen UP, Battaloglu E, Parman Y, Nicholson G, Ouvrier R, Seeger J, De Jonghe P, ... ... Suter U, et al. Peripheral nerve demyelination caused by a mutant Rho GTPase guanine nucleotide exchange factor, frabin/FGD4. American Journal of Human Genetics. 81: 158-64. PMID 17564972 DOI: 10.1086/518770 |
0.54 |
|
| 2007 |
Lino MM, Atanasoski S, Kvajo M, Fayard B, Moreno E, Brenner HR, Suter U, Monard D. Mice lacking protease nexin-1 show delayed structural and functional recovery after sciatic nerve crush. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 3677-85. PMID 17409231 DOI: 10.1523/Jneurosci.0277-07.2007 |
0.489 |
|
| 2006 |
Wong CE, Paratore C, Dours-Zimmermann MT, Rochat A, Pietri T, Suter U, Zimmermann DR, Dufour S, Thiery JP, Meijer D, Beermann F, Barrandon Y, Sommer L. Neural crest-derived cells with stem cell features can be traced back to multiple lineages in the adult skin. The Journal of Cell Biology. 175: 1005-15. PMID 17158956 DOI: 10.1083/Jcb.200606062 |
0.315 |
|
| 2006 |
Thurnherr T, Benninger Y, Wu X, Chrostek A, Krause SM, Nave KA, Franklin RJ, Brakebusch C, Suter U, Relvas JB. Cdc42 and Rac1 signaling are both required for and act synergistically in the correct formation of myelin sheaths in the CNS. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 10110-9. PMID 17021167 DOI: 10.1523/Jneurosci.2158-06.2006 |
0.505 |
|
| 2006 |
Berger P, Niemann A, Suter U. Schwann cells and the pathogenesis of inherited motor and sensory neuropathies (Charcot-Marie-Tooth disease). Glia. 54: 243-57. PMID 16856148 DOI: 10.1002/Glia.20386 |
0.574 |
|
| 2006 |
Niemann A, Berger P, Suter U. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease. Neuromolecular Medicine. 8: 217-42. PMID 16775378 DOI: 10.1385/Nmm:8:1-2:217 |
0.556 |
|
| 2006 |
Weller M, Krautler N, Mantei N, Suter U, Taylor V. Jagged1 ablation results in cerebellar granule cell migration defects and depletion of Bergmann glia. Developmental Neuroscience. 28: 70-80. PMID 16508305 DOI: 10.1159/000090754 |
0.404 |
|
| 2006 |
Atanasoski S, Scherer SS, Sirkowski E, Leone D, Garratt AN, Birchmeier C, Suter U. ErbB2 signaling in Schwann cells is mostly dispensable for maintenance of myelinated peripheral nerves and proliferation of adult Schwann cells after injury. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 2124-31. PMID 16481445 DOI: 10.1523/Jneurosci.4594-05.2006 |
0.522 |
|
| 2006 |
Berger P, Berger I, Schaffitzel C, Tersar K, Volkmer B, Suter U. Multi-level regulation of myotubularin-related protein-2 phosphatase activity by myotubularin-related protein-13/set-binding factor-2. Human Molecular Genetics. 15: 569-79. PMID 16399794 DOI: 10.1093/Hmg/Ddi473 |
0.412 |
|
| 2006 |
Atanasoski S, Boller D, De Ventura L, Koegel H, Boentert M, Young P, Werner S, Suter U. Cell cycle inhibitors p21 and p16 are required for the regulation of Schwann cell proliferation. Glia. 53: 147-57. PMID 16206162 DOI: 10.1002/Glia.20263 |
0.41 |
|
| 2006 |
Castagner F, Atanasoski S, Balda M, Matter K, Suter U. [P35]: Role of dbpA in neural crest and Schwann cell development International Journal of Developmental Neuroscience. 24: 510-510. DOI: 10.1016/J.Ijdevneu.2006.09.099 |
0.339 |
|
| 2006 |
Jacob C, Grabner H, Atanasoski S, Suter U. [P31]: Involvement of ski in TGFbeta-induced proliferation of Schwann cells International Journal of Developmental Neuroscience. 24: 509-509. DOI: 10.1016/J.Ijdevneu.2006.09.095 |
0.343 |
|
| 2005 |
Bonneick S, Boentert M, Berger P, Atanasoski S, Mantei N, Wessig C, Toyka KV, Young P, Suter U. An animal model for Charcot-Marie-Tooth disease type 4B1. Human Molecular Genetics. 14: 3685-95. PMID 16249189 DOI: 10.1093/Hmg/Ddi400 |
0.524 |
|
| 2005 |
Niemann A, Ruegg M, La Padula V, Schenone A, Suter U. Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease. The Journal of Cell Biology. 170: 1067-78. PMID 16172208 DOI: 10.1083/Jcb.200507087 |
0.371 |
|
| 2005 |
Nyfeler Y, Kirch RD, Mantei N, Leone DP, Radtke F, Suter U, Taylor V. Jagged1 signals in the postnatal subventricular zone are required for neural stem cell self-renewal. The Embo Journal. 24: 3504-15. PMID 16163386 DOI: 10.1038/Sj.Emboj.7600816 |
0.337 |
|
| 2005 |
Leone DP, Relvas JB, Campos LS, Hemmi S, Brakebusch C, Fässler R, Ffrench-Constant C, Suter U. Regulation of neural progenitor proliferation and survival by beta1 integrins. Journal of Cell Science. 118: 2589-99. PMID 15928047 DOI: 10.1242/Jcs.02396 |
0.339 |
|
| 2005 |
Kléber M, Lee HY, Wurdak H, Buchstaller J, Riccomagno MM, Ittner LM, Suter U, Epstein DJ, Sommer L. Neural crest stem cell maintenance by combinatorial Wnt and BMP signaling. The Journal of Cell Biology. 169: 309-20. PMID 15837799 DOI: 10.1083/Jcb.200411095 |
0.332 |
|
| 2005 |
Giambonini-Brugnoli G, Buchstaller J, Sommer L, Suter U, Mantei N. Distinct disease mechanisms in peripheral neuropathies due to altered peripheral myelin protein 22 gene dosage or a Pmp22 point mutation. Neurobiology of Disease. 18: 656-68. PMID 15755691 DOI: 10.1016/J.Nbd.2004.10.023 |
0.478 |
|
| 2005 |
Wurdak H, Ittner LM, Lang KS, Leveen P, Suter U, Fischer JA, Karlsson S, Born W, Sommer L. Inactivation of TGFbeta signaling in neural crest stem cells leads to multiple defects reminiscent of DiGeorge syndrome. Genes & Development. 19: 530-5. PMID 15741317 DOI: 10.1101/Gad.317405 |
0.316 |
|
| 2005 |
Suter U, Martini R. Myelination Peripheral Neuropathy. 1: 411-431. DOI: 10.1016/B978-0-7216-9491-7.50022-3 |
0.337 |
|
| 2004 |
Berger P, Sirkowski EE, Scherer SS, Suter U. Expression analysis of the N-Myc downstream-regulated gene 1 indicates that myelinating Schwann cells are the primary disease target in hereditary motor and sensory neuropathy-Lom. Neurobiology of Disease. 17: 290-9. PMID 15474366 DOI: 10.1016/J.Nbd.2004.07.014 |
0.568 |
|
| 2004 |
Schaeren-Wiemers N, Bonnet A, Erb M, Erne B, Bartsch U, Kern F, Mantei N, Sherman D, Suter U. The raft-associated protein MAL is required for maintenance of proper axon--glia interactions in the central nervous system. The Journal of Cell Biology. 166: 731-42. PMID 15337780 DOI: 10.1083/Jcb.200406092 |
0.507 |
|
| 2004 |
Atanasoski S, Notterpek L, Lee HY, Castagner F, Young P, Ehrengruber MU, Meijer D, Sommer L, Stavnezer E, Colmenares C, Suter U. The protooncogene Ski controls Schwann cell proliferation and myelination. Neuron. 43: 499-511. PMID 15312649 DOI: 10.1016/J.Neuron.2004.08.001 |
0.755 |
|
| 2004 |
Stidworthy MF, Genoud S, Li WW, Leone DP, Mantei N, Suter U, Franklin RJ. Notch1 and Jagged1 are expressed after CNS demyelination, but are not a major rate-determining factor during remyelination. Brain : a Journal of Neurology. 127: 1928-41. PMID 15289265 DOI: 10.1093/Brain/Awh217 |
0.392 |
|
| 2004 |
Campos LS, Leone DP, Relvas JB, Brakebusch C, Fässler R, Suter U, ffrench-Constant C. Beta1 integrins activate a MAPK signalling pathway in neural stem cells that contributes to their maintenance. Development (Cambridge, England). 131: 3433-44. PMID 15226259 DOI: 10.1242/Dev.01199 |
0.314 |
|
| 2004 |
Buchstaller J, Sommer L, Bodmer M, Hoffmann R, Suter U, Mantei N. Efficient isolation and gene expression profiling of small numbers of neural crest stem cells and developing Schwann cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 2357-65. PMID 15014110 DOI: 10.1523/Jneurosci.4083-03.2004 |
0.413 |
|
| 2004 |
Klein AL, Zilian O, Suter U, Taylor V. Murine numb regulates granule cell maturation in the cerebellum. Developmental Biology. 266: 161-77. PMID 14729486 DOI: 10.1016/J.Ydbio.2003.10.017 |
0.39 |
|
| 2004 |
Lee HY, Kléber M, Hari L, Brault V, Suter U, Taketo MM, Kemler R, Sommer L. Instructive role of Wnt/beta-catenin in sensory fate specification in neural crest stem cells. Science (New York, N.Y.). 303: 1020-3. PMID 14716020 DOI: 10.1126/Science.1091611 |
0.301 |
|
| 2004 |
Heredia A, Bui CC, Suter U, Young P, Sch�ffer T. Mechanical properties of myelinated and de-myelinated peripheral axons with the atomic force microscope Gbm Annual Fall Meeting M�Nster 2004. 2004. DOI: 10.1240/SAV_GBM_2004_H_000822 |
0.305 |
|
| 2003 |
Young P, Suter U. The causes of Charcot-Marie-Tooth disease. Cellular and Molecular Life Sciences : Cmls. 60: 2547-60. PMID 14685682 DOI: 10.1007/s00018-003-3133-5 |
0.336 |
|
| 2003 |
Maier M, Castagner F, Berger P, Suter U. Distinct elements of the peripheral myelin protein 22 (PMP22) promoter regulate expression in Schwann cells and sensory neurons. Molecular and Cellular Neurosciences. 24: 803-17. PMID 14664827 DOI: 10.1016/S1044-7431(03)00246-X |
0.529 |
|
| 2003 |
Sereda MW, Meyer zu Hörste G, Suter U, Uzma N, Nave KA. Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A). Nature Medicine. 9: 1533-7. PMID 14608378 DOI: 10.1038/Nm957 |
0.471 |
|
| 2003 |
Berger P, Schaffitzel C, Berger I, Ban N, Suter U. Membrane association of myotubularin-related protein 2 is mediated by a pleckstrin homology-GRAM domain and a coiled-coil dimerization module. Proceedings of the National Academy of Sciences of the United States of America. 100: 12177-82. PMID 14530412 DOI: 10.1073/Pnas.2132732100 |
0.343 |
|
| 2003 |
Suter U, Scherer SS. Disease mechanisms in inherited neuropathies. Nature Reviews. Neuroscience. 4: 714-26. PMID 12951564 DOI: 10.1038/Nrn1196 |
0.454 |
|
| 2003 |
Stidworthy MF, Genoud S, Suter U, Mantei N, Franklin RJ. Quantifying the early stages of remyelination following cuprizone-induced demyelination. Brain Pathology (Zurich, Switzerland). 13: 329-39. PMID 12946022 DOI: 10.1111/J.1750-3639.2003.Tb00032.X |
0.436 |
|
| 2003 |
Leone DP, Genoud S, Atanasoski S, Grausenburger R, Berger P, Metzger D, Macklin WB, Chambon P, Suter U. Tamoxifen-inducible glia-specific Cre mice for somatic mutagenesis in oligodendrocytes and Schwann cells. Molecular and Cellular Neurosciences. 22: 430-40. PMID 12727441 DOI: 10.1016/S1044-7431(03)00029-0 |
0.427 |
|
| 2003 |
Berger P, Bonneick S, Willi S, Wymann M, Suter U. Loss of Phosphatase Activity in Myotubularin‐related Protein 2 is Associated with Charcot‐marie‐tooth Disease Type 4B1 Journal of the Peripheral Nervous System. 8: 128-133. DOI: 10.1046/J.1529-8027.2003.03016_2.X |
0.501 |
|
| 2002 |
Hari L, Brault V, Kléber M, Lee HY, Ille F, Leimeroth R, Paratore C, Suter U, Kemler R, Sommer L. Lineage-specific requirements of beta-catenin in neural crest development. The Journal of Cell Biology. 159: 867-80. PMID 12473692 DOI: 10.1083/Jcb.200209039 |
0.316 |
|
| 2002 |
Paratore C, Eichenberger C, Suter U, Sommer L. Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease. Human Molecular Genetics. 11: 3075-85. PMID 12417529 DOI: 10.1093/Hmg/11.24.3075 |
0.369 |
|
| 2002 |
Schweitzer B, Suter U, Taylor V. Neural membrane protein 35/Lifeguard is localized at postsynaptic sites and in dendrites. Brain Research. Molecular Brain Research. 107: 47-56. PMID 12414123 DOI: 10.1016/S0169-328X(02)00445-X |
0.375 |
|
| 2002 |
Young P, Boussadia O, Berger P, Leone DP, Charnay P, Kemler R, Suter U. E-cadherin is required for the correct formation of autotypic adherens junctions of the outer mesaxon but not for the integrity of myelinated fibers of peripheral nerves. Molecular and Cellular Neurosciences. 21: 341-51. PMID 12401452 DOI: 10.1006/Mcne.2002.1177 |
0.329 |
|
| 2002 |
Pot C, Simonen M, Weinmann O, Schnell L, Christ F, Stoeckle S, Berger P, Rülicke T, Suter U, Schwab ME. Nogo-A expressed in Schwann cells impairs axonal regeneration after peripheral nerve injury. The Journal of Cell Biology. 159: 29-35. PMID 12379801 DOI: 10.1083/Jcb.200206068 |
0.531 |
|
| 2002 |
Paratore C, Brugnoli G, Lee HY, Suter U, Sommer L. The role of the Ets domain transcription factor Erm in modulating differentiation of neural crest stem cells. Developmental Biology. 250: 168-80. PMID 12297104 DOI: 10.1006/Dbio.2002.0795 |
0.391 |
|
| 2002 |
Genoud S, Lappe-Siefke C, Goebbels S, Radtke F, Aguet M, Scherer SS, Suter U, Nave KA, Mantei N. Notch1 control of oligodendrocyte differentiation in the spinal cord. The Journal of Cell Biology. 158: 709-18. PMID 12186854 DOI: 10.1083/Jcb.200202002 |
0.357 |
|
| 2002 |
Stump G, Durrer A, Klein AL, Lütolf S, Suter U, Taylor V. Notch1 and its ligands Delta-like and Jagged are expressed and active in distinct cell populations in the postnatal mouse brain. Mechanisms of Development. 114: 153-9. PMID 12175503 DOI: 10.1016/S0925-4773(02)00043-6 |
0.346 |
|
| 2002 |
Maier M, Berger P, Suter U. Understanding Schwann cell-neurone interactions: the key to Charcot-Marie-Tooth disease? Journal of Anatomy. 200: 357-66. PMID 12090402 DOI: 10.1046/J.1469-7580.2002.00044.X |
0.453 |
|
| 2002 |
Maier M, Berger P, Nave KA, Suter U. Identification of the regulatory region of the peripheral myelin protein 22 (PMP22) gene that directs temporal and spatial expression in development and regeneration of peripheral nerves. Molecular and Cellular Neurosciences. 20: 93-109. PMID 12056842 DOI: 10.1006/mcne.2002.1116 |
0.444 |
|
| 2002 |
Leimeroth R, Lobsiger C, Lüssi A, Taylor V, Suter U, Sommer L. Membrane-bound neuregulin1 type III actively promotes Schwann cell differentiation of multipotent Progenitor cells. Developmental Biology. 246: 245-58. PMID 12051814 DOI: 10.1006/Dbio.2002.0670 |
0.452 |
|
| 2002 |
Berger P, Bonneick S, Willi S, Wymann M, Suter U. Loss of phosphatase activity in myotubularin-related protein 2 is associated with Charcot-Marie-Tooth disease type 4B1. Human Molecular Genetics. 11: 1569-79. PMID 12045210 DOI: 10.1093/Hmg/11.13.1569 |
0.5 |
|
| 2002 |
Berger P, Young P, Suter U. Molecular cell biology of Charcot-Marie-Tooth disease. Neurogenetics. 4: 1-15. PMID 12030326 DOI: 10.1007/s10048-002-0130-z |
0.405 |
|
| 2002 |
Lobsiger CS, Taylor V, Suter U. The early life of a Schwann cell. Biological Chemistry. 383: 245-53. PMID 11934262 DOI: 10.1515/BC.2002.026 |
0.4 |
|
| 2002 |
Paratore C, Hagedorn L, Floris J, Hari L, Kléber M, Suter U, Sommer L. Cell-intrinsic and cell-extrinsic cues regulating lineage decisions in multipotent neural crest-derived progenitor cells. The International Journal of Developmental Biology. 46: 193-200. PMID 11902683 DOI: 10.1387/Ijdb.11902683 |
0.374 |
|
| 2002 |
Atanasoski S, Scherer SS, Nave KA, Suter U. Proliferation of Schwann cells and regulation of cyclin D1 expression in an animal model of Charcot-Marie-Tooth disease type 1A. Journal of Neuroscience Research. 67: 443-9. PMID 11835311 DOI: 10.1002/Jnr.10133 |
0.446 |
|
| 2001 |
Atanasoski S, Shumas S, Dickson C, Scherer SS, Suter U. Differential cyclin D1 requirements of proliferating Schwann cells during development and after injury. Molecular and Cellular Neurosciences. 18: 581-92. PMID 11749035 DOI: 10.1006/Mcne.2001.1055 |
0.42 |
|
| 2001 |
Young P, Suter U. Disease mechanisms and potential therapeutic strategies in Charcot-Marie-Tooth disease. Brain Research. Brain Research Reviews. 36: 213-21. PMID 11690618 DOI: 10.1016/S0165-0173(01)00097-2 |
0.312 |
|
| 2001 |
Sancho S, Young P, Suter U. Regulation of Schwann cell proliferation and apoptosis in PMP22-deficient mice and mouse models of Charcot-Marie-Tooth disease type 1A. Brain : a Journal of Neurology. 124: 2177-87. PMID 11673320 |
0.423 |
|
| 2001 |
Lobsiger CS, Smith PM, Buchstaller J, Schweitzer B, Franklin RJ, Suter U, Taylor V. SpL201: a conditionally immortalized Schwann cell precursor line that generates myelin. Glia. 36: 31-47. PMID 11571782 DOI: 10.1002/Glia.1093 |
0.473 |
|
| 2001 |
Nobbio L, Mancardi G, Grandis M, Levi G, Suter U, Nave KA, Windebank AJ, Abbruzzese M, Schenone A. PMP22 transgenic dorsal root ganglia cultures show myelin abnormalities similar to those of human CMT1A. Annals of Neurology. 50: 47-55. PMID 11456309 DOI: 10.1002/Ana.1034 |
0.547 |
|
| 2001 |
Zilian O, Saner C, Hagedorn L, Lee HY, Säuberli E, Suter U, Sommer L, Aguet M. Multiple roles of mouse Numb in tuning developmental cell fates. Current Biology : Cb. 11: 494-501. PMID 11412999 DOI: 10.1016/S0960-9822(01)00149-X |
0.401 |
|
| 2001 |
Caduff J, Sansano S, Bonnet A, Suter U, Schaeren-Wiemers N. Characterization of GFP-MAL expression and incorporation in rafts. Microscopy Research and Technique. 52: 645-55. PMID 11276117 DOI: 10.1002/Jemt.1049 |
0.469 |
|
| 2000 |
Colby J, Nicholson R, Dickson KM, Orfali W, Naef R, Suter U, Snipes GJ. PMP22 carrying the trembler or trembler-J mutation is intracellularly retained in myelinating Schwann cells. Neurobiology of Disease. 7: 561-73. PMID 11114256 DOI: 10.1006/Nbdi.2000.0323 |
0.549 |
|
| 2000 |
Hagedorn L, Floris J, Suter U, Sommer L. Autonomic neurogenesis and apoptosis are alternative fates of progenitor cell communities induced by TGFbeta. Developmental Biology. 228: 57-72. PMID 11087626 DOI: 10.1006/Dbio.2000.9936 |
0.361 |
|
| 2000 |
Frank M, Atanasoski S, Sancho S, Magyar JP, Rülicke T, Schwab ME, Suter U. Progressive segregation of unmyelinated axons in peripheral nerves, myelin alterations in the CNS, and cyst formation in the kidneys of myelin and lymphocyte protein-overexpressing mice. Journal of Neurochemistry. 75: 1927-39. PMID 11032882 DOI: 10.1046/J.1471-4159.2000.0751927.X |
0.538 |
|
| 2000 |
Taylor V, Zgraggen C, Naef R, Suter U. Membrane topology of peripheral myelin protein 22. Journal of Neuroscience Research. 62: 15-27. PMID 11002284 DOI: 10.1002/1097-4547(20001001)62:1<15::Aid-Jnr3>3.0.Co;2-F |
0.56 |
|
| 2000 |
Niemann S, Sereda MW, Suter U, Griffiths IR, Nave KA. Uncoupling of myelin assembly and schwann cell differentiation by transgenic overexpression of peripheral myelin protein 22. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 4120-8. PMID 10818147 DOI: 10.1111/J.1529-8027.2000.22-36.X |
0.495 |
|
| 2000 |
Zielasek J, Martini R, Suter U, Toyka KV. Neuromyotonia in mice with hereditary myelinopathies. Muscle & Nerve. 23: 696-701. PMID 10797391 DOI: 10.1002/(Sici)1097-4598(200005)23:5<696::Aid-Mus5>3.0.Co;2-W |
0.445 |
|
| 2000 |
Lobsiger CS, Schweitzer B, Taylor V, Suter U. Platelet-derived growth factor-BB supports the survival of cultured rat Schwann cell precursors in synergy with neurotrophin-3. Glia. 30: 290-300. PMID 10756078 DOI: 10.1002/(Sici)1098-1136(200005)30:3<290::Aid-Glia8>3.0.Co;2-6 |
0.451 |
|
| 2000 |
Ritz MF, Lechner-Scott J, Scott RJ, Fuhr P, Malik N, Erne B, Taylor V, Suter U, Schaeren-Wiemers N, Steck AJ. Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies. Journal of Neuroimmunology. 104: 155-63. PMID 10713355 DOI: 10.1016/S0165-5728(99)00250-7 |
0.416 |
|
| 2000 |
Jetten AM, Suter U. The peripheral myelin protein 22 and epithelial membrane protein family. Progress in Nucleic Acid Research and Molecular Biology. 64: 97-129. PMID 10697408 |
0.307 |
|
| 2000 |
Hagedorn L, Paratore C, Brugnoli G, Baert JL, Mercader N, Suter U, Sommer L. The Ets domain transcription factor Erm distinguishes rat satellite glia from Schwann cells and is regulated in satellite cells by neuregulin signaling. Developmental Biology. 219: 44-58. PMID 10677254 DOI: 10.1006/Dbio.1999.9595 |
0.468 |
|
| 1999 |
Niemann S, Sereda MW, Rossner M, Stewart H, Suter U, Meinck HM, Griffiths IR, Nave KA. The "CMT Rat": Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22. Annals of the New York Academy of Sciences. 883: 254-261. PMID 29086932 DOI: 10.1111/J.1749-6632.1999.Tb08587.X |
0.538 |
|
| 1999 |
Neuberg DH, Suter U. Connexin32 in hereditary neuropathies. Advances in Experimental Medicine and Biology. 468: 227-36. PMID 10635032 DOI: 10.1007/978-1-4615-4685-6_18 |
0.309 |
|
| 1999 |
Niemann S, Sereda MW, Rossner M, Stewart H, Suter U, Meinck HM, Griffiths IR, Nave KA. The "CMT rat": peripheral neuropathy and dysmyelination caused by transgenic overexpression of PMP22. Annals of the New York Academy of Sciences. 883: 254-61. PMID 10586250 |
0.448 |
|
| 1999 |
Suter U, Nave KA. Transgenic mouse models of CMT1A and HNPP. Annals of the New York Academy of Sciences. 883: 247-53. PMID 10586249 DOI: 10.1111/J.1749-6632.1999.Tb08586.X |
0.333 |
|
| 1999 |
Neuberg DH, Sancho S, Suter U. Altered molecular architecture of peripheral nerves in mice lacking the peripheral myelin protein 22 or connexin32. Journal of Neuroscience Research. 58: 612-23. PMID 10561689 DOI: 10.1002/(Sici)1097-4547(19991201)58:5<612::Aid-Jnr2>3.0.Co;2-X |
0.527 |
|
| 1999 |
Carenini S, Neuberg D, Schachner M, Suter U, Martini R. Localization and functional roles of PMP22 in peripheral nerves of P0-deficient mice. Glia. 28: 256-64. PMID 10559784 DOI: 10.1002/(Sici)1098-1136(199912)28:3<256::Aid-Glia9>3.0.Co;2-O |
0.533 |
|
| 1999 |
Wulf P, Suter U. Embryonic expression of epithelial membrane protein 1 in early neurons. Brain Research. Developmental Brain Research. 116: 169-80. PMID 10521561 DOI: 10.1016/S0165-3806(99)00092-9 |
0.46 |
|
| 1999 |
Wulf P, Bernhardt RR, Suter U. Characterization of peripheral myelin protein 22 in zebrafish (zPMP22) suggests an early role in the development of the peripheral nervous system. Journal of Neuroscience Research. 57: 467-78. PMID 10440896 DOI: 10.1002/(Sici)1097-4547(19990815)57:4<467::Aid-Jnr6>3.0.Co;2-3 |
0.572 |
|
| 1999 |
Hagedorn L, Suter U, Sommer L. P0 and PMP22 mark a multipotent neural crest-derived cell type that displays community effects in response to TGF-beta family factors. Development (Cambridge, England). 126: 3781-94. PMID 10433908 |
0.329 |
|
| 1999 |
Paratore C, Suter U, Sommer L. Embryonic gene expression resolved at the cellular level by fluorescence in situ hybridization. Histochemistry and Cell Biology. 111: 435-43. PMID 10429965 DOI: 10.1007/S004180050379 |
0.333 |
|
| 1999 |
Naef R, Suter U. Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies. Neurobiology of Disease. 6: 1-14. PMID 10078969 DOI: 10.1006/Nbdi.1998.0227 |
0.438 |
|
| 1999 |
Tobler AR, Notterpek L, Naef R, Taylor V, Suter U, Shooter EM. Transport of Trembler-J mutant peripheral myelin protein 22 is blocked in the intermediate compartment and affects the transport of the wild-type protein by direct interaction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 19: 2027-36. PMID 10066256 DOI: 10.1523/Jneurosci.19-06-02027.1999 |
0.775 |
|
| 1999 |
Guénard V, Schweitzer B, Flechsig E, Hemmi S, Martini R, Suter U, Schachner M. Effective gene transfer of lacZ and P0 into Schwann cells of P0-deficient mice. Glia. 25: 165-78. PMID 9890631 DOI: 10.1002/(Sici)1098-1136(19990115)25:2<165::Aid-Glia7>3.0.Co;2-L |
0.475 |
|
| 1998 |
Désarnaud F, Do Thi AN, Brown AM, Lemke G, Suter U, Baulieu EE, Schumacher M. Progesterone stimulates the activity of the promoters of peripheral myelin protein-22 and protein zero genes in Schwann cells. Journal of Neurochemistry. 71: 1765-8. PMID 9751213 DOI: 10.1046/J.1471-4159.1998.71041765.X |
0.454 |
|
| 1998 |
Neuberg DH, Carenini S, Schachner M, Martini R, Suter U. Accelerated demyelination of peripheral nerves in mice deficient in connexin 32 and protein zero. Journal of Neuroscience Research. 53: 542-50. PMID 9726425 DOI: 10.1002/(Sici)1097-4547(19980901)53:5<542::Aid-Jnr4>3.0.Co;2-9 |
0.477 |
|
| 1998 |
Schweitzer B, Taylor V, Welcher AA, McClelland M, Suter U. Neural membrane protein 35 (NMP35): a novel member of a gene family which is highly expressed in the adult nervous system. Molecular and Cellular Neurosciences. 11: 260-73. PMID 9698393 DOI: 10.1006/Mcne.1998.0697 |
0.698 |
|
| 1998 |
Naef R, Suter U. Many facets of the peripheral myelin protein PMP22 in myelination and disease. Microscopy Research and Technique. 41: 359-71. PMID 9672419 DOI: 10.1002/(Sici)1097-0029(19980601)41:5<359::Aid-Jemt3>3.0.Co;2-L |
0.569 |
|
| 1998 |
Sommer L, Suter U. The glycoprotein P0 in peripheral gliogenesis. Cell and Tissue Research. 292: 11-6. PMID 9506907 DOI: 10.1007/S004410051029 |
0.484 |
|
| 1997 |
Toyka KV, Zielasek J, Ricker K, Adlkofer K, Suter U. Hereditary neuromyotonia: a mouse model associated with deficiency or increased gene dosage of the PMP22 gene. Journal of Neurology, Neurosurgery, and Psychiatry. 63: 812-3. PMID 9416828 DOI: 10.1136/Jnnp.63.6.812 |
0.31 |
|
| 1997 |
Müller HW, Suter U, Van Broeckhoven C, Hanemann CO, Nelis E, Timmerman V, Sancho S, Barrio L, Bolhuis P, Dermietzel R, Frank M, Gabreëls-Festen A, Gillen C, Haites N, Levi G, et al. Advances in Charcot-Marie-Tooth disease research: cellular function of CMT-related proteins, transgenic animal models, and pathomechanisms. The European CMT Consortium. Neurobiology of Disease. 4: 215-20. PMID 9361297 DOI: 10.1006/Nbdi.1997.0148 |
0.354 |
|
| 1997 |
Adlkofer K, Naef R, Suter U. Analysis of compound heterozygous mice reveals that the Trembler mutation can behave as a gain-of-function allele. Journal of Neuroscience Research. 49: 671-80. PMID 9335255 DOI: 10.1002/(Sici)1097-4547(19970915)49:6<671::Aid-Jnr2>3.0.Co;2-4 |
0.447 |
|
| 1997 |
Pareek S, Notterpek L, Snipes GJ, Naef R, Sossin W, Laliberté J, Iacampo S, Suter U, Shooter EM, Murphy RA. Neurons promote the translocation of peripheral myelin protein 22 into myelin. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 7754-62. PMID 9315897 |
0.785 |
|
| 1997 |
Naef R, Adlkofer K, Lescher B, Suter U. Aberrant protein trafficking in Trembler suggests a disease mechanism for hereditary human peripheral neuropathies. Molecular and Cellular Neurosciences. 9: 13-25. PMID 9204477 DOI: 10.1006/Mcne.1997.0604 |
0.527 |
|
| 1997 |
Taylor V, Suter U. Molecular biology of axon-glia interactions in the peripheral nervous system. Progress in Nucleic Acid Research and Molecular Biology. 56: 225-56. PMID 9187055 DOI: 10.1016/S0079-6603(08)61006-5 |
0.399 |
|
| 1997 |
Adlkofer K, Frei R, Neuberg DH, Zielasek J, Toyka KV, Suter U. Heterozygous peripheral myelin protein 22-deficient mice are affected by a progressive demyelinating tomaculous neuropathy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 4662-71. PMID 9169527 DOI: 10.1523/Jneurosci.17-12-04662.1997 |
0.506 |
|
| 1997 |
Anzini P, Neuberg DH, Schachner M, Nelles E, Willecke K, Zielasek J, Toyka KV, Suter U, Martini R. Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 4545-51. PMID 9169515 |
0.484 |
|
| 1997 |
Magyar JP, Ebensperger C, Schaeren-Wiemers N, Suter U. Myelin and lymphocyte protein (MAL/MVP17/VIP17) and plasmolipin are members of an extended gene family. Gene. 189: 269-75. PMID 9168137 DOI: 10.1016/S0378-1119(96)00861-X |
0.516 |
|
| 1997 |
Suter U. Myelin: keeping nerves well wrapped up. Current Biology : Cb. 7: R21-3. PMID 9072163 DOI: 10.1016/S0960-9822(06)00011-X |
0.522 |
|
| 1997 |
Adlkofer K, Frei R, Neuberg DH, Zielasek J, Toyka KV, Suter U. Heterozygous Peripheral Myelin Protein 22-Deficient Mice Are Affected by a Progressive Demyelinating Tomaculous Neuropathy The Journal of Neuroscience. 17: 4662-4671. DOI: 10.1523/JNEUROSCI.17-12-04662.1997 |
0.372 |
|
| 1997 |
Anzini P, Neuberg DH-, Schachner M, Nelles E, Willecke K, Zielasek J, Toyka KV, Suter U, Martini R. Structural Abnormalities and Deficient Maintenance of Peripheral Nerve Myelin in Mice Lacking the Gap Junction Protein Connexin 32 The Journal of Neuroscience. 17: 4545-4551. DOI: 10.1523/Jneurosci.17-12-04545.1997 |
0.568 |
|
| 1996 |
Taylor V, Suter U. Epithelial membrane protein-2 and epithelial membrane protein-3: two novel members of the peripheral myelin protein 22 gene family. Gene. 175: 115-20. PMID 8917086 DOI: 10.1016/0378-1119(96)00134-5 |
0.452 |
|
| 1996 |
Lobsiger CS, Magyar JP, Taylor V, Wulf P, Welcher AA, Program AE, Suter U. Identification and characterization of a cDNA and the structural gene encoding the mouse epithelial membrane protein-1. Genomics. 36: 379-87. PMID 8884260 DOI: 10.1006/Geno.1996.0482 |
0.696 |
|
| 1996 |
Heymach JV, Krüttgen A, Suter U, Shooter EM. The regulated secretion and vectorial targeting of neurotrophins in neuroendocrine and epithelial cells. The Journal of Biological Chemistry. 271: 25430-7. PMID 8810312 DOI: 10.1074/Jbc.271.41.25430 |
0.596 |
|
| 1996 |
Haney C, Snipes GJ, Shooter EM, Suter U, Garcia C, Griffin JW, Trapp BD. Ultrastructural distribution of PMP22 in Charcot-Marie-Tooth disease type 1A. Journal of Neuropathology and Experimental Neurology. 55: 290-9. PMID 8786387 DOI: 10.1097/00005072-199603000-00004 |
0.665 |
|
| 1996 |
Magyar JP, Martini R, Ruelicke T, Aguzzi A, Adlkofer K, Dembic Z, Zielasek J, Toyka KV, Suter U. Impaired differentiation of Schwann cells in transgenic mice with increased PMP22 gene dosage. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 5351-60. PMID 8757248 DOI: 10.1523/Jneurosci.16-17-05351.1996 |
0.547 |
|
| 1996 |
Sereda M, Griffiths I, Pühlhofer A, Stewart H, Rossner MJ, Zimmerman F, Magyar JP, Schneider A, Hund E, Meinck HM, Suter U, Nave KA. A transgenic rat model of Charcot-Marie-Tooth disease. Neuron. 16: 1049-60. PMID 8630243 DOI: 10.1016/S0896-6273(00)80128-2 |
0.446 |
|
| 1995 |
Baechner D, Liehr T, Hameister H, Altenberger H, Grehl H, Suter U, Rautenstrauss B. Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development. Journal of Neuroscience Research. 42: 733-41. PMID 8847735 DOI: 10.1002/Jnr.490420602 |
0.459 |
|
| 1995 |
Snipes GJ, Suter U. Molecular basis of common hereditary motor and sensory neuropathies in humans and in mouse models. Brain Pathology (Zurich, Switzerland). 5: 233-47. PMID 8520723 DOI: 10.1111/J.1750-3639.1995.Tb00600.X |
0.474 |
|
| 1995 |
Suter U, Snipes GJ. Peripheral myelin protein 22: facts and hypotheses. Journal of Neuroscience Research. 40: 145-51. PMID 7745607 DOI: 10.1002/Jnr.490400202 |
0.541 |
|
| 1995 |
Adlkofer K, Martini R, Aguzzi A, Zielasek J, Toyka KV, Suter U. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice. Nature Genetics. 11: 274-80. PMID 7581450 DOI: 10.1038/Ng1195-274 |
0.539 |
|
| 1995 |
Snipes GJ, Suter U, Welcher AA, Shooter EM. The molecular basis of the neuropathies of mouse and human. Progress in Brain Research. 105: 319-25. PMID 7568894 DOI: 10.1016/S0079-6123(08)63310-5 |
0.812 |
|
| 1995 |
Snipes GJ, Suter U. Molecular anatomy and genetics of myelin proteins in the peripheral nervous system. Journal of Anatomy. 186: 483-94. PMID 7559122 |
0.412 |
|
| 1995 |
Taylor V, Welcher AA, Program AE, Suter U. Epithelial membrane protein-1, peripheral myelin protein 22, and lens membrane protein 20 define a novel gene family. The Journal of Biological Chemistry. 270: 28824-33. PMID 7499407 DOI: 10.1074/Jbc.270.48.28824 |
0.743 |
|
| 1994 |
Suter U, Snipes GJ, Schoener-Scott R, Welcher AA, Pareek S, Lupski JR, Murphy RA, Shooter EM, Patel PI. Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters. The Journal of Biological Chemistry. 269: 25795-808. PMID 7929285 |
0.752 |
|
| 1994 |
Snipes GJ, Suter U. Signaling pathways mediating axon--Schwann cell interactions. Trends in Neurosciences. 17: 399-401. PMID 7530875 DOI: 10.1016/0166-2236(94)90011-6 |
0.381 |
|
| 1994 |
Suter U, Patel PI. Genetic basis of inherited peripheral neuropathies. Human Mutation. 3: 95-102. PMID 7515304 DOI: 10.1002/Humu.1380030203 |
0.435 |
|
| 1993 |
Roa BB, Garcia CA, Suter U, Kulpa DA, Wise CA, Mueller J, Welcher AA, Snipes GJ, Shooter EM, Patel PI, Lupski JR. Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene. The New England Journal of Medicine. 329: 96-101. PMID 8510709 DOI: 10.1056/NEJM199307083290205 |
0.725 |
|
| 1993 |
Pareek S, Suter U, Snipes GJ, Welcher AA, Shooter EM, Murphy RA. Detection and processing of peripheral myelin protein PMP22 in cultured Schwann cells. The Journal of Biological Chemistry. 268: 10372-9. PMID 8486695 |
0.752 |
|
| 1993 |
Roa BB, Garcia CA, Pentao L, Killian JM, Trask BJ, Suter U, Snipes GJ, Ortiz-Lopez R, Shooter EM, Patel PI, Lupski JR. Evidence for a recessive PMP22 point mutation in Charcot-Marie-Tooth disease type 1A. Nature Genetics. 5: 189-94. PMID 8252046 DOI: 10.1038/Ng1093-189 |
0.591 |
|
| 1993 |
Drinkwater CC, Barker PA, Suter U, Shooter EM. The carboxyl terminus of nerve growth factor is required for biological activity. The Journal of Biological Chemistry. 268: 23202-7. PMID 8226840 |
0.638 |
|
| 1993 |
Snipes GJ, Suter U, Shooter EM. Human peripheral myelin protein-22 carries the L2/HNK-1 carbohydrate adhesion epitope. Journal of Neurochemistry. 61: 1961-4. PMID 7693873 DOI: 10.1111/J.1471-4159.1993.Tb09840.X |
0.649 |
|
| 1993 |
Suter U, Welcher AA, Snipes GJ. Progress in the molecular understanding of hereditary peripheral neuropathies reveals new insights into the biology of the peripheral nervous system. Trends in Neurosciences. 16: 50-6. PMID 7680499 DOI: 10.1016/0166-2236(93)90015-E |
0.763 |
|
| 1993 |
Snipes GJ, Suter U, Shooter EM. The genetics of myelin. Current Opinion in Neurobiology. 3: 694-702. PMID 7505139 DOI: 10.1016/0959-4388(93)90140-T |
0.654 |
|
| 1992 |
Suter U, Angst C, Tien CL, Drinkwater CC, Lindsay RM, Shooter EM. NGF/BDNF chimeric proteins: analysis of neurotrophin specificity by homolog-scanning mutagenesis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 12: 306-18. PMID 1729439 DOI: 10.1523/Jneurosci.12-01-00306.1992 |
0.565 |
|
| 1992 |
Snipes GJ, Suter U, Welcher AA, Shooter EM. Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13). The Journal of Cell Biology. 117: 225-38. PMID 1556154 DOI: 10.1083/Jcb.117.1.225 |
0.776 |
|
| 1992 |
Suter U, Welcher AA, Ozcelik T, Snipes GJ, Kosaras B, Francke U, Billings-Gagliardi S, Sidman RL, Shooter EM. Trembler mouse carries a point mutation in a myelin gene. Nature. 356: 241-4. PMID 1552943 DOI: 10.1038/356241A0 |
0.793 |
|
| 1992 |
Suter U, Moskow JJ, Welcher AA, Snipes GJ, Kosaras B, Sidman RL, Buchberg AM, Shooter EM. A leucine-to-proline mutation in the putative first transmembrane domain of the 22-kDa peripheral myelin protein in the trembler-J mouse. Proceedings of the National Academy of Sciences of the United States of America. 89: 4382-6. PMID 1374899 DOI: 10.1073/Pnas.89.10.4382 |
0.776 |
|
| 1992 |
Meakin SO, Suter U, Drinkwater CC, Welcher AA, Shooter EM. The rat trk protooncogene product exhibits properties characteristic of the slow nerve growth factor receptor. Proceedings of the National Academy of Sciences of the United States of America. 89: 2374-8. PMID 1312719 DOI: 10.1073/Pnas.89.6.2374 |
0.729 |
|
| 1992 |
Patel PI, Roa BB, Welcher AA, Schoener-Scott R, Trask BJ, Pentao L, Snipes GJ, Garcia CA, Francke U, Shooter EM, Lupski JR, Suter U. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nature Genetics. 1: 159-65. PMID 1303228 DOI: 10.1038/Ng0692-159 |
0.748 |
|
| 1992 |
Welcher AA, De Leon M, Suter U, Snipes GJ, Meakin SO, Shooter EM. Isolation of transcriptionally regulated sequences associated with neuronal and non-neuronal cell interactions. Progress in Brain Research. 94: 163-76. PMID 1287719 DOI: 10.1016/S0079-6123(08)61748-3 |
0.81 |
|
| 1991 |
Suter U, Heymach JV, Shooter EM. Two conserved domains in the NGF propeptide are necessary and sufficient for the biosynthesis of correctly processed and biologically active NGF. The Embo Journal. 10: 2395-400. PMID 1868828 DOI: 10.1002/J.1460-2075.1991.Tb07778.X |
0.564 |
|
| 1991 |
De Leon M, Welcher AA, Suter U, Shooter EM. Identification of transcriptionally regulated genes after sciatic nerve injury. Journal of Neuroscience Research. 29: 437-48. PMID 1724268 DOI: 10.1002/Jnr.490290404 |
0.806 |
|
| 1991 |
Welcher AA, Suter U, De Leon M, Snipes GJ, Shooter EM. A myelin protein is encoded by the homologue of a growth arrest-specific gene. Proceedings of the National Academy of Sciences of the United States of America. 88: 7195-9. PMID 1714591 DOI: 10.1073/Pnas.88.16.7195 |
0.834 |
|
| 1991 |
Drinkwater CC, Suter U, Angst C, Shooter EM. Mutation of tryptophan-21 in mouse nerve growth factor (NGF) affects binding to the fast NGF receptor but not induction of neurites on PC12 cells. Proceedings. Biological Sciences / the Royal Society. 246: 307-13. PMID 1686097 DOI: 10.1098/Rspb.1991.0159 |
0.58 |
|
| 1991 |
Welcher AA, Suter U, De Leon M, Bitler CM, Shooter EM. Molecular approaches to nerve regeneration. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 331: 295-301. PMID 1677474 DOI: 10.1098/Rstb.1991.0020 |
0.802 |
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