| Year |
Citation |
Score |
| 2019 |
Kim MJ, Bible KL, Regnier M, Adams ME, Froehner SC, Whitehead NP. Simvastatin provides long-term improvement of left ventricular function and prevents cardiac fibrosis in muscular dystrophy. Physiological Reports. 7: e14018. PMID 30912308 DOI: 10.14814/Phy2.14018 |
0.325 |
|
| 2018 |
Kim MJ, Whitehead NP, Bible KL, Adams ME, Froehner SC. Mice lacking α-,β1- and β2-syntrophins exhibit diminished function and reduced dystrophin expression in both cardiac and skeletal muscle. Human Molecular Genetics. PMID 30256963 DOI: 10.1093/hmg/ddy341 |
0.416 |
|
| 2018 |
Adams ME, Odom GL, Kim MJ, Chamberlain JS, Froehner SC. Syntrophin binds directly to multiple spectrin-like repeats in dystrophin and mediates binding of nNOS to repeats 16-17. Human Molecular Genetics. PMID 29790927 DOI: 10.1093/hmg/ddy197 |
0.34 |
|
| 2016 |
Whitehead NP, Bible KL, Kim MJ, Odom GL, Adams ME, Froehner SC. Validation of ultrasonography for non-invasive assessment of diaphragm function in muscular dystrophy. The Journal of Physiology. PMID 27570057 DOI: 10.1113/JP272707 |
0.378 |
|
| 2016 |
Nanou E, Yan J, Whitehead NP, Kim MJ, Froehner SC, Scheuer T, Catterall WA. Altered short-term synaptic plasticity and reduced muscle strength in mice with impaired regulation of presynaptic CaV2.1 Ca2+ channels. Proceedings of the National Academy of Sciences of the United States of America. PMID 26755585 DOI: 10.1073/Pnas.1524650113 |
0.366 |
|
| 2016 |
Allen DG, Whitehead NP, Froehner SC. Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy. Physiological Reviews. 96: 253-305. PMID 26676145 DOI: 10.1152/physrev.00007.2015 |
0.422 |
|
| 2015 |
Rebolledo DL, Kim MJ, Whitehead NP, Adams ME, Froehner SC. Sarcolemmal targeting of nNOSμ improves contractile function of mdx muscle. Human Molecular Genetics. PMID 26604149 DOI: 10.1093/hmg/ddv466 |
0.426 |
|
| 2015 |
Whitehead NP, Kim MJ, Bible KL, Adams ME, Froehner SC. A new therapeutic effect of simvastatin revealed by functional improvement in muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. PMID 26417069 DOI: 10.1073/pnas.1509536112 |
0.404 |
|
| 2015 |
Eisinger K, Froehner SC, Adams ME, Krautbauer S, Buechler C. Evaluation of the specificity of four commercially available antibodies to alpha-syntrophin. Analytical Biochemistry. 484: 99-101. PMID 26079703 DOI: 10.1016/j.ab.2015.06.012 |
0.309 |
|
| 2015 |
Hebel T, Eisinger K, Neumeier M, Rein-Fischboeck L, Pohl R, Meier EM, Boettcher A, Froehner SC, Adams ME, Liebisch G, Krautbauer S, Buechler C. Lipid abnormalities in alpha/beta2-syntrophin null mice are independent from ABCA1. Biochimica Et Biophysica Acta. 1851: 527-36. PMID 25625330 DOI: 10.1016/j.bbalip.2015.01.012 |
0.313 |
|
| 2015 |
Froehner SC, Reed SM, Anderson KN, Huang PL, Percival JM. Loss of nNOS inhibits compensatory muscle hypertrophy and exacerbates inflammation and eccentric contraction-induced damage in mdx mice. Human Molecular Genetics. 24: 492-505. PMID 25214536 DOI: 10.1093/Hmg/Ddu469 |
0.43 |
|
| 2015 |
Odom GL, Banks GB, Adams ME, Bible KL, Froehner SC, Chamberlain JS. 611. Alpha-Dystrobrevin-3 Prevents Myopathy and Restores Diaphragm Function in the Alpha-Dystrobrevin Null Mouse Molecular Therapy. 23: S242-S243. DOI: 10.1016/S1525-0016(16)34220-4 |
0.394 |
|
| 2015 |
Whitehead N, Kim M, Bible K, Adams M, Froehner S. Simvastatin improves physiological function and protects against muscle degeneration in mdx mice: A novel therapeutic approach for Duchenne muscular dystrophy Neuromuscular Disorders. 25: S315. DOI: 10.1016/j.nmd.2015.06.457 |
0.4 |
|
| 2015 |
Kim M, Rebolledo D, Whitehead N, Adams M, Froehner S. Sarcolemmal nNOSµ targeting in mdx mice improves muscle function and restores dystrophin complex proteins via α-syntrophin Neuromuscular Disorders. 25: S290-S291. DOI: 10.1016/j.nmd.2015.06.374 |
0.425 |
|
| 2014 |
Froehner S, Reed S, Anderson K, Huang P, Percival J. Defective skeletal muscle nNOS-cGMP signaling as a therapeutic target in Duchenne muscular dystrophy Nitric Oxide. 42: 114. DOI: 10.1016/J.Niox.2014.09.047 |
0.371 |
|
| 2013 |
Neumeier M, Krautbauer S, Schmidhofer S, Hader Y, Eisinger K, Eggenhofer E, Froehner SC, Adams ME, Mages W, Buechler C. Adiponectin receptor 1 C-terminus interacts with PDZ-domain proteins such as syntrophins. Experimental and Molecular Pathology. 95: 180-6. PMID 23860432 DOI: 10.1016/j.yexmp.2013.07.002 |
0.361 |
|
| 2013 |
Cruz NF, Ball KK, Froehner SC, Adams ME, Dienel GA. Regional registration of [6-(14)C]glucose metabolism during brain activation of α-syntrophin knockout mice. Journal of Neurochemistry. 125: 247-59. PMID 23346911 DOI: 10.1111/jnc.12166 |
0.324 |
|
| 2013 |
Rybalkin SD, Shimizu M, Rybalkina IG, Patrucco E, Bible K, Minami E, O'Brien J, Wennogle LP, Hofmann F, Beavo JA, Froehner SC. Differential effects of PDE5 inhibitors on cardiac dysfunction in the MDX ouse model of Duchenne muscular dystrophy Bmc Pharmacology and Toxicology. 14. DOI: 10.1186/2050-6511-14-S1-O38 |
0.317 |
|
| 2012 |
Fuhrmann-Stroissnigg H, Noiges R, Descovich L, Fischer I, Albrecht DE, Nothias F, Froehner SC, Propst F. The light chains of microtubule-associated proteins MAP1A and MAP1B interact with α1-syntrophin in the central and peripheral nervous system. Plos One. 7: e49722. PMID 23152929 DOI: 10.1371/journal.pone.0049722 |
0.333 |
|
| 2012 |
Johnson EK, Zhang L, Adams ME, Phillips A, Freitas MA, Froehner SC, Green-Church KB, Montanaro F. Proteomic analysis reveals new cardiac-specific dystrophin-associated proteins. Plos One. 7: e43515. PMID 22937058 DOI: 10.1371/Journal.Pone.0043515 |
0.387 |
|
| 2012 |
Percival JM, Whitehead NP, Adams ME, Adamo CM, Beavo JA, Froehner SC. Sildenafil reduces respiratory muscle weakness and fibrosis in the mdx mouse model of Duchenne muscular dystrophy. The Journal of Pathology. 228: 77-87. PMID 22653783 DOI: 10.1002/Path.4054 |
0.401 |
|
| 2012 |
Eilert-Olsen M, Haj-Yasein NN, Vindedal GF, Enger R, Gundersen GA, Hoddevik EH, Petersen PH, Haug FM, Skare Ø, Adams ME, Froehner SC, Burkhardt JM, Thoren AE, Nagelhus EA. Deletion of aquaporin-4 changes the perivascular glial protein scaffold without disrupting the brain endothelial barrier. Glia. 60: 432-40. PMID 22131281 DOI: 10.1002/Glia.22277 |
0.343 |
|
| 2012 |
Percival J, Whitehead N, Adams M, Adamo C, Beavo J, Froehner S. T.P.5 Sildenafil (Viagra®) improves cardiac and diaphragm muscle function in the dystrophic mouse Neuromuscular Disorders. 22: 848. DOI: 10.1016/J.Nmd.2012.06.151 |
0.391 |
|
| 2011 |
Martinez-Pena y Valenzuela I, Mouslim C, Pires-Oliveira M, Adams ME, Froehner SC, Akaaboune M. Nicotinic acetylcholine receptor stability at the NMJ deficient in α-syntrophin in vivo. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 15586-96. PMID 22031904 DOI: 10.1523/Jneurosci.4038-11.2011 |
0.426 |
|
| 2011 |
Kim MJ, Froehner SC, Adams ME, Kim HS. α-Syntrophin is required for the hepatocyte growth factor-induced migration of cultured myoblasts. Experimental Cell Research. 317: 2914-24. PMID 22001117 DOI: 10.1016/j.yexcr.2011.09.017 |
0.346 |
|
| 2011 |
Percival JM, Adamo CM, Beavo JA, Froehner SC. Evaluation of the therapeutic utility of phosphodiesterase 5A inhibition in the mdx mouse model of duchenne muscular dystrophy. Handbook of Experimental Pharmacology. 323-44. PMID 21695647 DOI: 10.1007/978-3-642-17969-3_14 |
0.408 |
|
| 2010 |
Whitehead NP, Yeung EW, Froehner SC, Allen DG. Skeletal muscle NADPH oxidase is increased and triggers stretch-induced damage in the mdx mouse. Plos One. 5: e15354. PMID 21187957 DOI: 10.1371/journal.pone.0015354 |
0.414 |
|
| 2010 |
Kim MJ, Hwang SH, Lim JA, Froehner SC, Adams ME, Kim HS. Α-syntrophin modulates myogenin expression in differentiating myoblasts. Plos One. 5: e15355. PMID 21179410 DOI: 10.1371/journal.pone.0015355 |
0.416 |
|
| 2010 |
Adamo CM, Dai DF, Percival JM, Minami E, Willis MS, Patrucco E, Froehner SC, Beavo JA. Sildenafil reverses cardiac dysfunction in the mdx mouse model of Duchenne muscular dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 107: 19079-83. PMID 20956307 DOI: 10.1073/Pnas.1013077107 |
0.349 |
|
| 2010 |
Adams ME, Anderson KN, Froehner SC. The alpha-syntrophin PH and PDZ domains scaffold acetylcholine receptors, utrophin, and neuronal nitric oxide synthase at the neuromuscular junction. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 11004-10. PMID 20720107 DOI: 10.1523/JNEUROSCI.1930-10.2010 |
0.409 |
|
| 2010 |
Bragg AD, Das SS, Froehner SC. Dystrophin-associated protein scaffolding in brain requires alpha-dystrobrevin. Neuroreport. 21: 695-9. PMID 20508543 DOI: 10.1097/WNR.0b013e32833b0a3b |
0.366 |
|
| 2010 |
Migliati ER, Amiry-Moghaddam M, Froehner SC, Adams ME, Ottersen OP, Bhardwaj A. Na(+)-K (+)-2Cl (-) cotransport inhibitor attenuates cerebral edema following experimental stroke via the perivascular pool of aquaporin-4. Neurocritical Care. 13: 123-31. PMID 20458553 DOI: 10.1007/s12028-010-9376-8 |
0.328 |
|
| 2010 |
Percival JM, Anderson KN, Huang P, Adams ME, Froehner SC. Golgi and sarcolemmal neuronal NOS differentially regulate contraction-induced fatigue and vasoconstriction in exercising mouse skeletal muscle. The Journal of Clinical Investigation. 120: 816-26. PMID 20124730 DOI: 10.1172/Jci40736 |
0.4 |
|
| 2009 |
Banks GB, Chamberlain JS, Froehner SC. Truncated dystrophins can influence neuromuscular synapse structure. Molecular and Cellular Neurosciences. 40: 433-41. PMID 19171194 DOI: 10.1016/j.mcn.2008.12.011 |
0.426 |
|
| 2009 |
Steen MS, Adams ME, Tesch Y, Froehner SC. Amelioration of muscular dystrophy by transgenic expression of Niemann-Pick C1. Molecular Biology of the Cell. 20: 146-52. PMID 18946078 DOI: 10.1091/Mbc.E08-08-0811 |
0.749 |
|
| 2008 |
Compton AG, Albrecht DE, Seto JT, Cooper ST, Ilkovski B, Jones KJ, Challis D, Mowat D, Ranscht B, Bahlo M, Froehner SC, North KN. Mutations in contactin-1, a neural adhesion and neuromuscular junction protein, cause a familial form of lethal congenital myopathy. American Journal of Human Genetics. 83: 714-24. PMID 19026398 DOI: 10.1016/J.Ajhg.2008.10.022 |
0.417 |
|
| 2008 |
Percival JM, Anderson KN, Gregorevic P, Chamberlain JS, Froehner SC. Functional deficits in nNOSmu-deficient skeletal muscle: myopathy in nNOS knockout mice. Plos One. 3: e3387. PMID 18852886 DOI: 10.1371/journal.pone.0003387 |
0.425 |
|
| 2008 |
Zeynalov E, Chen CH, Froehner SC, Adams ME, Ottersen OP, Amiry-Moghaddam M, Bhardwaj A. The perivascular pool of aquaporin-4 mediates the effect of osmotherapy in postischemic cerebral edema. Critical Care Medicine. 36: 2634-40. PMID 18679106 DOI: 10.1097/CCM.0b013e3181847853 |
0.341 |
|
| 2008 |
Liu X, Zhang W, Alkayed NJ, Froehner SC, Adams ME, Amiry-Moghaddam M, Ottersen OP, Hurn PD, Bhardwaj A. Lack of sex-linked differences in cerebral edema and aquaporin-4 expression after experimental stroke. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 28: 1898-906. PMID 18648381 DOI: 10.1038/jcbfm.2008.83 |
0.301 |
|
| 2008 |
Albrecht DE, Sherman DL, Brophy PJ, Froehner SC. The ABCA1 cholesterol transporter associates with one of two distinct dystrophin-based scaffolds in Schwann cells. Glia. 56: 611-8. PMID 18286648 DOI: 10.1002/glia.20636 |
0.336 |
|
| 2008 |
Adams ME, Tesch Y, Percival JM, Albrecht DE, Conhaim JI, Anderson K, Froehner SC. Differential targeting of nNOS and AQP4 to dystrophin-deficient sarcolemma by membrane-directed alpha-dystrobrevin. Journal of Cell Science. 121: 48-54. PMID 18057022 DOI: 10.1242/jcs.020701 |
0.377 |
|
| 2007 |
Wang D, Kelly BB, Albrecht DE, Adams ME, Froehner SC, Feng G. Complete deletion of all alpha-dystrobrevin isoforms does not reveal new neuromuscular junction phenotype. Gene Expression. 14: 47-57. PMID 17933218 DOI: 10.3727/000000007783991745 |
0.42 |
|
| 2007 |
Percival JM, Gregorevic P, Odom GL, Banks GB, Chamberlain JS, Froehner SC. rAAV6-microdystrophin rescues aberrant Golgi complex organization in mdx skeletal muscles. Traffic (Copenhagen, Denmark). 8: 1424-39. PMID 17714427 DOI: 10.1111/j.1600-0854.2007.00622.x |
0.431 |
|
| 2007 |
Percival JM, Froehner SC. Golgi complex organization in skeletal muscle: a role for Golgi-mediated glycosylation in muscular dystrophies? Traffic (Copenhagen, Denmark). 8: 184-94. PMID 17319799 DOI: 10.1111/j.1600-0854.2006.00523.x |
0.431 |
|
| 2007 |
Steen M, Tesch Y, Adams M, Froehner S. G.P.6.01 NPC1 overexpression attenuates muscular dystrophy in mdx and α-dystrobrevin-null mice Neuromuscular Disorders. 17: 801. DOI: 10.1016/J.Nmd.2007.06.136 |
0.711 |
|
| 2006 |
Alessi A, Bragg AD, Percival JM, Yoo J, Albrecht DE, Froehner SC, Adams ME. gamma-Syntrophin scaffolding is spatially and functionally distinct from that of the alpha/beta syntrophins. Experimental Cell Research. 312: 3084-95. PMID 16857187 DOI: 10.1016/j.yexcr.2006.06.019 |
0.398 |
|
| 2006 |
Gregorevic P, Allen JM, Minami E, Blankinship MJ, Haraguchi M, Meuse L, Finn E, Adams ME, Froehner SC, Murry CE, Chamberlain JS. rAAV6-microdystrophin preserves muscle function and extends lifespan in severely dystrophic mice. Nature Medicine. 12: 787-9. PMID 16819550 DOI: 10.1038/Nm1439 |
0.404 |
|
| 2006 |
Mercado ML, Amenta AR, Hagiwara H, Rafii MS, Lechner BE, Owens RT, McQuillan DJ, Froehner SC, Fallon JR. Biglycan regulates the expression and sarcolemmal localization of dystrobrevin, syntrophin, and nNOS. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 20: 1724-6. PMID 16807372 DOI: 10.1096/Fj.05-5124Fje |
0.446 |
|
| 2006 |
Bragg AD, Amiry-Moghaddam M, Ottersen OP, Adams ME, Froehner SC. Assembly of a perivascular astrocyte protein scaffold at the mammalian blood-brain barrier is dependent on alpha-syntrophin. Glia. 53: 879-90. PMID 16609960 DOI: 10.1002/glia.20347 |
0.342 |
|
| 2006 |
Puwarawuttipanit W, Bragg AD, Frydenlund DS, Mylonakou MN, Nagelhus EA, Peters MF, Kotchabhakdi N, Adams ME, Froehner SC, Haug FM, Ottersen OP, Amiry-Moghaddam M. Differential effect of alpha-syntrophin knockout on aquaporin-4 and Kir4.1 expression in retinal macroglial cells in mice. Neuroscience. 137: 165-75. PMID 16257493 DOI: 10.1016/j.neuroscience.2005.08.051 |
0.401 |
|
| 2005 |
Luo S, Chen Y, Lai KO, Arévalo JC, Froehner SC, Adams ME, Chao MV, Ip NY. {alpha}-Syntrophin regulates ARMS localization at the neuromuscular junction and enhances EphA4 signaling in an ARMS-dependent manner. The Journal of Cell Biology. 169: 813-24. PMID 15939763 DOI: 10.1083/Jcb.200412008 |
0.446 |
|
| 2005 |
Compton AG, Cooper ST, Hill PM, Yang N, Froehner SC, North KN. The syntrophin-dystrobrevin subcomplex in human neuromuscular disorders. Journal of Neuropathology and Experimental Neurology. 64: 350-61. PMID 15835271 DOI: 10.1093/Jnen/64.4.350 |
0.466 |
|
| 2004 |
Adams ME, Kramarcy N, Fukuda T, Engel AG, Sealock R, Froehner SC. Structural abnormalities at neuromuscular synapses lacking multiple syntrophin isoforms. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 10302-9. PMID 15548643 DOI: 10.1523/JNEUROSCI.3408-04.2004 |
0.396 |
|
| 2004 |
Shiao T, Fond A, Deng B, Wehling-Henricks M, Adams ME, Froehner SC, Tidball JG. Defects in neuromuscular junction structure in dystrophic muscle are corrected by expression of a NOS transgene in dystrophin-deficient muscles, but not in muscles lacking alpha- and beta1-syntrophins. Human Molecular Genetics. 13: 1873-84. PMID 15238508 DOI: 10.1093/Hmg/Ddh204 |
0.468 |
|
| 2004 |
Connors NC, Adams ME, Froehner SC, Kofuji P. The potassium channel Kir4.1 associates with the dystrophin-glycoprotein complex via alpha-syntrophin in glia. The Journal of Biological Chemistry. 279: 28387-92. PMID 15102837 DOI: 10.1074/Jbc.M402604200 |
0.345 |
|
| 2004 |
Leonoudakis D, Conti LR, Anderson S, Radeke CM, McGuire LM, Adams ME, Froehner SC, Yates JR, Vandenberg CA. Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins. The Journal of Biological Chemistry. 279: 22331-46. PMID 15024025 DOI: 10.1074/Jbc.M400285200 |
0.366 |
|
| 2004 |
Albrecht DE, Froehner SC. DAMAGE, a novel alpha-dystrobrevin-associated MAGE protein in dystrophin complexes. The Journal of Biological Chemistry. 279: 7014-23. PMID 14623885 DOI: 10.1074/jbc.M312205200 |
0.422 |
|
| 2003 |
Banks GB, Fuhrer C, Adams ME, Froehner SC. The postsynaptic submembrane machinery at the neuromuscular junction: requirement for rapsyn and the utrophin/dystrophin-associated complex. Journal of Neurocytology. 32: 709-26. PMID 15034263 DOI: 10.1023/B:NEUR.0000020619.24681.2b |
0.443 |
|
| 2003 |
Amiry-Moghaddam M, Williamson A, Palomba M, Eid T, de Lanerolle NC, Nagelhus EA, Adams ME, Froehner SC, Agre P, Ottersen OP. Delayed K+ clearance associated with aquaporin-4 mislocalization: phenotypic defects in brains of alpha-syntrophin-null mice. Proceedings of the National Academy of Sciences of the United States of America. 100: 13615-20. PMID 14597704 DOI: 10.1073/Pnas.2336064100 |
0.352 |
|
| 2003 |
Jones KJ, Compton AG, Yang N, Mills MA, Peters MF, Mowat D, Kunkel LM, Froehner SC, North KN. Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy. Neuromuscular Disorders : Nmd. 13: 456-67. PMID 12899872 DOI: 10.1016/S0960-8966(03)00066-X |
0.391 |
|
| 2003 |
Steen MS, Froehner SC. PerleCan fix your muscle AChEs. Trends in Neurosciences. 26: 241-2. PMID 12744839 DOI: 10.1016/S0166-2236(03)00077-8 |
0.73 |
|
| 2003 |
Thomas GD, Shaul PW, Yuhanna IS, Froehner SC, Adams ME. Vasomodulation by skeletal muscle-derived nitric oxide requires alpha-syntrophin-mediated sarcolemmal localization of neuronal Nitric oxide synthase. Circulation Research. 92: 554-60. PMID 12600881 DOI: 10.1161/01.RES.0000061570.83105.52 |
0.472 |
|
| 2003 |
Amiry-Moghaddam M, Otsuka T, Hurn PD, Traystman RJ, Haug FM, Froehner SC, Adams ME, Neely JD, Agre P, Ottersen OP, Bhardwaj A. An alpha-syntrophin-dependent pool of AQP4 in astroglial end-feet confers bidirectional water flow between blood and brain. Proceedings of the National Academy of Sciences of the United States of America. 100: 2106-11. PMID 12578959 DOI: 10.1073/Pnas.0437946100 |
0.363 |
|
| 2002 |
Albrecht DE, Froehner SC. Syntrophins and dystrobrevins: defining the dystrophin scaffold at synapses. Neuro-Signals. 11: 123-9. PMID 12138249 DOI: 10.1159/000065053 |
0.408 |
|
| 2002 |
Froehner SC. Just say NO to muscle degeneration? Trends in Molecular Medicine. 8: 51-3. PMID 11815264 DOI: 10.1016/S1471-4914(02)02275-X |
0.426 |
|
| 2001 |
Neely JD, Amiry-Moghaddam M, Ottersen OP, Froehner SC, Agre P, Adams ME. Syntrophin-dependent expression and localization of Aquaporin-4 water channel protein. Proceedings of the National Academy of Sciences of the United States of America. 98: 14108-13. PMID 11717465 DOI: 10.1073/Pnas.241508198 |
0.435 |
|
| 2001 |
Adams ME, Mueller HA, Froehner SC. In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4. The Journal of Cell Biology. 155: 113-22. PMID 11571312 DOI: 10.1083/jcb.200106158 |
0.407 |
|
| 2000 |
Ort T, Maksimova E, Dirkx R, Kachinsky AM, Berghs S, Froehner SC, Solimena M. The receptor tyrosine phosphatase-like protein ICA512 binds the PDZ domains of beta2-syntrophin and nNOS in pancreatic beta-cells. European Journal of Cell Biology. 79: 621-30. PMID 11043403 DOI: 10.1078/0171-9335-00095 |
0.322 |
|
| 2000 |
Crawford GE, Faulkner JA, Crosbie RH, Campbell KP, Froehner SC, Chamberlain JS. Assembly of the dystrophin-associated protein complex does not require the dystrophin COOH-terminal domain. The Journal of Cell Biology. 150: 1399-410. PMID 10995444 DOI: 10.1083/Jcb.150.6.1399 |
0.399 |
|
| 2000 |
Adams ME, Kramarcy N, Krall SP, Rossi SG, Rotundo RL, Sealock R, Froehner SC. Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin. The Journal of Cell Biology. 150: 1385-98. PMID 10995443 DOI: 10.1083/jcb.150.6.1385 |
0.426 |
|
| 1999 |
Won S, Si J, Colledge M, Ravichandran KS, Froehner SC, Mei L. Neuregulin-increased expression of acetylcholine receptor epsilon-subunit gene requires ErbB interaction with Shc. Journal of Neurochemistry. 73: 2358-68. PMID 10582594 DOI: 10.1046/j.1471-4159.1999.0732358.x |
0.371 |
|
| 1999 |
Kachinsky AM, Froehner SC, Milgram SL. A PDZ-containing scaffold related to the dystrophin complex at the basolateral membrane of epithelial cells. The Journal of Cell Biology. 145: 391-402. PMID 10209032 DOI: 10.1083/jcb.145.2.391 |
0.392 |
|
| 1998 |
Froehner SC. Gathering glycine receptors at synapses. Science (New York, N.Y.). 282: 1277-9. PMID 9867632 DOI: 10.1126/Science.282.5392.1277 |
0.309 |
|
| 1998 |
Peters MF, Sadoulet-Puccio HM, Grady MR, Kramarcy NR, Kunkel LM, Sanes JR, Sealock R, Froehner SC. Differential membrane localization and intermolecular associations of alpha-dystrobrevin isoforms in skeletal muscle. The Journal of Cell Biology. 142: 1269-78. PMID 9732287 DOI: 10.1083/jcb.142.5.1269 |
0.421 |
|
| 1998 |
Colledge M, Froehner SC. Signals mediating ion channel clustering at the neuromuscular junction. Current Opinion in Neurobiology. 8: 357-63. PMID 9687350 DOI: 10.1016/S0959-4388(98)80061-5 |
0.338 |
|
| 1998 |
Colledge M, Froehner SC. To muster a cluster: anchoring neurotransmitter receptors at synapses. Proceedings of the National Academy of Sciences of the United States of America. 95: 3341-3. PMID 9520364 DOI: 10.1073/pnas.95.7.3341 |
0.328 |
|
| 1998 |
Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC. Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 128-37. PMID 9412493 DOI: 10.1523/Jneurosci.18-01-00128.1998 |
0.416 |
|
| 1998 |
Montanaro F, Gee SH, Jacobson C, Lindenbaum MH, Froehner SC, Carbonetto S. Laminin and α-Dystroglycan Mediate Acetylcholine Receptor Aggregation via a MuSK-Independent Pathway The Journal of Neuroscience. 18: 1250-1260. DOI: 10.1523/Jneurosci.18-04-01250.1998 |
0.331 |
|
| 1997 |
Peters MF, O'Brien KF, Sadoulet-Puccio HM, Kunkel LM, Adams ME, Froehner SC. beta-dystrobrevin, a new member of the dystrophin family. Identification, cloning, and protein associations. The Journal of Biological Chemistry. 272: 31561-9. PMID 9395493 DOI: 10.1074/jbc.272.50.31561 |
0.369 |
|
| 1997 |
Peters MF, Adams ME, Froehner SC. Differential association of syntrophin pairs with the dystrophin complex. The Journal of Cell Biology. 138: 81-93. PMID 9214383 DOI: 10.1083/jcb.138.1.81 |
0.38 |
|
| 1997 |
Colledge M, Froehner SC. Tyrosine phosphorylation of nicotinic acetylcholine receptor mediates Grb2 binding. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 5038-45. PMID 9185541 DOI: 10.1523/Jneurosci.17-13-05038.1997 |
0.348 |
|
| 1996 |
Chao DS, Gorospe JR, Brenman JE, Rafael JA, Peters MF, Froehner SC, Hoffman EP, Chamberlain JS, Bredt DS. Selective loss of sarcolemmal nitric oxide synthase in Becker muscular dystrophy. The Journal of Experimental Medicine. 184: 609-18. PMID 8760814 DOI: 10.1084/Jem.184.2.609 |
0.451 |
|
| 1996 |
Dai Z, Scotland PB, Froehner SC, Peng HB. Association of phosphotyrosine with rapsyn expression in Xenopus embryonic cells. Neuroreport. 7: 657-61. PMID 8730851 DOI: 10.1097/00001756-199601310-00066 |
0.337 |
|
| 1996 |
Blake DJ, Nawrotzki R, Peters MF, Froehner SC, Davies KE. Isoform diversity of dystrobrevin, the murine 87-kDa postsynaptic protein. The Journal of Biological Chemistry. 271: 7802-10. PMID 8631824 DOI: 10.1074/jbc.271.13.7802 |
0.431 |
|
| 1996 |
Brenman JE, Chao DS, Gee SH, McGee AW, Craven SE, Santillano DR, Wu Z, Huang F, Xia H, Peters MF, Froehner SC, Bredt DS. Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha1-syntrophin mediated by PDZ domains. Cell. 84: 757-67. PMID 8625413 DOI: 10.1016/S0092-8674(00)81053-3 |
0.437 |
|
| 1995 |
Adams ME, Dwyer TM, Dowler LL, White RA, Froehner SC. Mouse alpha 1- and beta 2-syntrophin gene structure, chromosome localization, and homology with a discs large domain. The Journal of Biological Chemistry. 270: 25859-65. PMID 7592771 DOI: 10.1074/jbc.270.43.25859 |
0.32 |
|
| 1995 |
Dwyer TM, Froehner SC. Direct binding of Torpedo syntrophin to dystrophin and the 87 kDa dystrophin homologue. Febs Letters. 375: 91-4. PMID 7498489 DOI: 10.1016/0014-5793(95)01176-F |
0.316 |
|
| 1995 |
Barry EL, Gesek FA, Froehner SC, Friedman PA. Multiple calcium channel transcripts in rat osteosarcoma cells: selective activation of alpha 1D isoform by parathyroid hormone. Proceedings of the National Academy of Sciences of the United States of America. 92: 10914-8. PMID 7479909 DOI: 10.1073/Pnas.92.24.10914 |
0.313 |
|
| 1994 |
Sealock R, Froehner SC. Dystrophin-associated proteins and synapse formation: is alpha-dystroglycan the agrin receptor? Cell. 77: 617-9. PMID 8205610 DOI: 10.1016/0092-8674(94)90045-0 |
0.387 |
|
| 1994 |
Bloch RJ, Sealock R, Pumplin DW, Luther PW, Froehner SC. Association of acetylcholine receptors with peripheral membrane proteins: evidence from antibody-induced coaggregation. The Journal of Membrane Biology. 138: 13-28. PMID 8189428 DOI: 10.1007/Bf00211065 |
0.378 |
|
| 1994 |
Morton ME, Cassidy TN, Froehner SC, Gilmour BP, Laurens RL. Alpha 1 and alpha 2 Ca2+ channel subunit expression in human neuronal and small cell carcinoma cells. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 8: 884-8. PMID 8070639 DOI: 10.1096/fasebj.8.11.8070639 |
0.348 |
|
| 1994 |
Ousley AH, Froehner SC. An anti-peptide antibody specific for the class A calcium channel alpha 1 subunit labels mammalian neuromuscular junction. Proceedings of the National Academy of Sciences of the United States of America. 91: 12263-7. PMID 7991616 DOI: 10.1073/Pnas.91.25.12263 |
0.307 |
|
| 1994 |
Peters MF, Kramarcy NR, Sealock R, Froehner SC. beta 2-Syntrophin: localization at the neuromuscular junction in skeletal muscle. Neuroreport. 5: 1577-80. PMID 7819523 |
0.35 |
|
| 1994 |
Peters MF, Kramarcy NR, Sealock R, Froehner SC. β2–syntrophin: Localization at the neuromuscular junction in skeletal muscle Neuroreport. 5: 1577-1580. DOI: 10.1097/00001756-199408150-00009 |
0.461 |
|
| 1993 |
Scotland PB, Colledge M, Melnikova I, Dai Z, Froehner SC. Clustering of the acetylcholine receptor by the 43-kD protein: involvement of the zinc finger domain. The Journal of Cell Biology. 123: 719-28. PMID 8227134 DOI: 10.1083/Jcb.123.3.719 |
0.38 |
|
| 1993 |
Adams ME, Butler MH, Dwyer TM, Peters MF, Murnane AA, Froehner SC. Two forms of mouse syntrophin, a 58 kd dystrophin-associated protein, differ in primary structure and tissue distribution. Neuron. 11: 531-40. PMID 7691103 DOI: 10.1016/0896-6273(93)90157-M |
0.419 |
|
| 1993 |
Froehner SC. Regulation of ion channel distribution at synapses. Annual Review of Neuroscience. 16: 347-68. PMID 7681636 DOI: 10.1146/annurev.ne.16.030193.002023 |
0.384 |
|
| 1992 |
Brennan C, Scotland PB, Froehner SC, Henderson LP. Functional properties of acetylcholine receptors coexpressed with the 43K protein in heterologous cell systems. Developmental Biology. 149: 100-11. PMID 1370223 DOI: 10.1016/0012-1606(92)90267-K |
0.394 |
|
| 1991 |
Sealock R, Butler MH, Kramarcy NR, Gao KX, Murnane AA, Douville K, Froehner SC. Localization of dystrophin relative to acetylcholine receptor domains in electric tissue and adult and cultured skeletal muscle. The Journal of Cell Biology. 113: 1133-44. PMID 2040646 DOI: 10.1083/Jcb.113.5.1133 |
0.421 |
|
| 1990 |
LaRochelle WJ, Witzemann V, Fiedler W, Froehner SC. Developmental expression of the 43K and 58K postsynaptic membrane proteins and nicotinic acetylcholine receptors in Torpedo electrocytes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 10: 3460-7. PMID 2213148 DOI: 10.1523/Jneurosci.10-10-03460.1990 |
0.334 |
|
| 1990 |
Flucher BE, Morton ME, Froehner SC, Daniels MP. Localization of the alpha 1 and alpha 2 subunits of the dihydropyridine receptor and ankyrin in skeletal muscle triads. Neuron. 5: 339-51. PMID 2169270 DOI: 10.1016/0896-6273(90)90170-K |
0.411 |
|
| 1990 |
Froehner SC, Luetje CW, Scotland PB, Patrick J. The postsynaptic 43K protein clusters muscle nicotinic acetylcholine receptors in Xenopus oocytes. Neuron. 5: 403-10. PMID 1698395 DOI: 10.1016/0896-6273(90)90079-U |
0.395 |
|
| 1989 |
Sealock R, Murnane AA, Paulin D, Froehner SC. Immunochemical identification of desmin in Torpedo postsynaptic membranes and at the rat neuromuscular junction. Synapse (New York, N.Y.). 3: 315-24. PMID 2740991 DOI: 10.1002/syn.890030404 |
0.367 |
|
| 1989 |
Froehner SC. Expression of RNA transcripts for the postsynaptic 43 kDa protein in innervated and denervated rat skeletal muscle. Febs Letters. 249: 229-33. PMID 2737281 DOI: 10.1016/0014-5793(89)80629-5 |
0.454 |
|
| 1989 |
LaRochelle WJ, Ralston E, Forsayeth JR, Froehner SC, Hall ZW. Clusters of 43-kDa protein are absent from genetic variants of C2 muscle cells with reduced acetylcholine receptor expression. Developmental Biology. 132: 130-8. PMID 2645181 DOI: 10.1016/0012-1606(89)90211-X |
0.407 |
|
| 1989 |
Morton ME, Froehner SC. The alpha 1 and alpha 2 polypeptides of the dihydropyridine-sensitive calcium channel differ in developmental expression and tissue distribution. Neuron. 2: 1499-506. PMID 2560646 DOI: 10.1016/0896-6273(89)90196-7 |
0.391 |
|
| 1987 |
LaRochelle WJ, Froehner SC. Comparison of the postsynaptic 43-kDa protein from muscle cells that differ in acetylcholine receptor clustering activity. The Journal of Biological Chemistry. 262: 8190-5. PMID 3597369 |
0.344 |
|
| 1987 |
Bloch RJ, Froehner SC. The relationship of the postsynaptic 43K protein to acetylcholine receptors in receptor clusters isolated from cultured rat myotubes. The Journal of Cell Biology. 104: 645-54. PMID 3546336 DOI: 10.1083/Jcb.104.3.645 |
0.346 |
|
| 1987 |
Froehner SC, Murnane AA, Tobler M, Peng HB, Sealock R. A postsynaptic Mr 58,000 (58K) protein concentrated at acetylcholine receptor-rich sites in Torpedo electroplaques and skeletal muscle. The Journal of Cell Biology. 104: 1633-46. PMID 3294859 DOI: 10.1083/Jcb.104.6.1633 |
0.433 |
|
| 1986 |
Froehner SC. The role of the postsynaptic cytoskeleton in AChR organization Trends in Neurosciences. 9: 37-41. DOI: 10.1016/0166-2236(86)90013-5 |
0.398 |
|
| 1985 |
LaRochelle WJ, Wray BE, Sealock R, Froehner SC. Immunochemical demonstration that amino acids 360-377 of the acetylcholine receptor gamma-subunit are cytoplasmic. The Journal of Cell Biology. 100: 684-91. PMID 3972889 DOI: 10.1083/Jcb.100.3.684 |
0.341 |
|
| 1984 |
Sealock R, Wray BE, Froehner SC. Ultrastructural localization of the Mr 43,000 protein and the acetylcholine receptor in Torpedo postsynaptic membranes using monoclonal antibodies. The Journal of Cell Biology. 98: 2239-44. PMID 6725413 DOI: 10.1083/Jcb.98.6.2239 |
0.349 |
|
| 1981 |
Froehner SC, Gulbrandsen V, Hyman C, Jeng AY, Neubig RR, Cohen JB. Immunofluorescence localization at the mammalian neuromuscular junction of the Mr 43,000 protein of Torpedo postsynaptic membranes. Proceedings of the National Academy of Sciences of the United States of America. 78: 5230-4. PMID 7029531 DOI: 10.1073/Pnas.78.8.5230 |
0.428 |
|
| Show low-probability matches. |