| Year |
Citation |
Score |
| 2022 |
Zhu PP, Hung HF, Batchenkova N, Nixon-Abell J, Henderson J, Zheng P, Renvoisé B, Pang S, Xu CS, Saalfeld S, Funke J, Xie Y, Svara F, Hess HF, Blackstone C. Transverse endoplasmic reticulum expansion in hereditary spastic paraplegia corticospinal axons. Human Molecular Genetics. PMID 35348668 DOI: 10.1093/hmg/ddac072 |
0.304 |
|
| 2022 |
Byrne DJ, Garcia-Pardo ME, Cole NB, Batnasan B, Heneghan S, Sohail A, Blackstone C, O'Sullivan NC. Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia. Acta Neuropathologica Communications. 10: 40. PMID 35346366 DOI: 10.1186/s40478-022-01343-6 |
0.37 |
|
| 2022 |
Chen Z, Chai E, Mou Y, Roda RH, Blackstone C, Li XJ. Inhibiting mitochondrial fission rescues degeneration in hereditary spastic paraplegia neurons. Brain : a Journal of Neurology. PMID 35026838 DOI: 10.1093/brain/awab488 |
0.317 |
|
| 2021 |
Zheng P, Obara CJ, Szczesna E, Nixon-Abell J, Mahalingan KK, Roll-Mecak A, Lippincott-Schwartz J, Blackstone C. ER proteins decipher the tubulin code to regulate organelle distribution. Nature. 601: 132-138. PMID 34912111 DOI: 10.1038/s41586-021-04204-9 |
0.329 |
|
| 2020 |
Fowler PC, Byrne DJ, Blackstone C, O'Sullivan NC. Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a Model of Hereditary Spastic Paraplegia. Brain Sciences. 10. PMID 32957716 DOI: 10.3390/Brainsci10090646 |
0.425 |
|
| 2020 |
Lee S, Park H, Zhu PP, Jung SY, Blackstone C, Chang J. Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion. Science Signaling. 13. PMID 31911435 DOI: 10.1126/Scisignal.Aau7500 |
0.444 |
|
| 2019 |
Lee CA, Blackstone C. ER morphology and endo-lysosomal crosstalk: Functions and disease implications. Biochimica Et Biophysica Acta. Molecular and Cell Biology of Lipids. 158544. PMID 31678515 DOI: 10.1016/J.Bbalip.2019.158544 |
0.385 |
|
| 2019 |
Monel B, Rajah MM, Hafirassou ML, Sid-Ahmed S, Burlaud-Gaillard J, Zhu PP, Nevers Q, Buchrieser J, Porrot F, Meunier C, Amraoui S, Chazal M, Salles A, Jouvenet N, Roingeard P, ... Blackstone C, et al. The Atlastin ER-shaping proteins facilitate Zika virus replication. Journal of Virology. PMID 31534046 DOI: 10.1128/Jvi.01047-19 |
0.388 |
|
| 2018 |
Chen YC, Cheng TH, Lin WL, Chen CL, Yang WY, Blackstone C, Chang CR. Srv2 Is a Pro-fission Factor that Modulates Yeast Mitochondrial Morphology and Respiration by Regulating Actin Assembly. Iscience. 11: 305-317. PMID 30639852 DOI: 10.1016/J.Isci.2018.12.021 |
0.414 |
|
| 2018 |
Zheng P, Chen Q, Tian X, Qian N, Chai P, Liu B, Hu J, Blackstone C, Zhu D, Teng J, Chen J. DNA damage triggers tubular endoplasmic reticulum extension to promote apoptosis by facilitating ER-mitochondria signaling. Cell Research. PMID 30030520 DOI: 10.1038/S41422-018-0065-Z |
0.401 |
|
| 2018 |
Blackstone C. Converging cellular themes for the hereditary spastic paraplegias. Current Opinion in Neurobiology. 51: 139-146. PMID 29753924 DOI: 10.1016/J.Conb.2018.04.025 |
0.356 |
|
| 2018 |
Denton K, Mou Y, Xu CC, Shah D, Chang J, Blackstone C, Li XJ. Impaired Mitochondrial Dynamics Underlie Axonal Defects in Hereditary Spastic Paraplegias. Human Molecular Genetics. PMID 29726929 DOI: 10.1093/Hmg/Ddy156 |
0.408 |
|
| 2017 |
Blackstone C. Protein Targeting: ER Leads the Way to the Inner Nuclear Envelope. Current Biology : Cb. 27: R1284-R1286. PMID 29207273 DOI: 10.1016/J.Cub.2017.10.037 |
0.43 |
|
| 2017 |
Roda RH, Schindler AB, Blackstone C. Multigeneration family with dominant SPG30 hereditary spastic paraplegia. Annals of Clinical and Translational Neurology. 4: 821-824. PMID 29159194 DOI: 10.1002/Acn3.452 |
0.325 |
|
| 2017 |
Byrne DJ, Harmon MJ, Simpson JC, Blackstone C, O'Sullivan NC. Roles for the VCP co-factors Npl4 and Ufd1 in neuronal function in Drosophila melanogaster. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 29037990 DOI: 10.1016/J.Jgg.2017.06.003 |
0.372 |
|
| 2017 |
Roda RH, Schindler AB, Blackstone C. De novo REEP2 missense mutation in pure hereditary spastic paraplegia. Annals of Clinical and Translational Neurology. 4: 347-350. PMID 28491902 DOI: 10.1002/Acn3.404 |
0.373 |
|
| 2017 |
Guinto CO, Diarra S, Diallo S, Cissé L, Coulibaly T, Diallo SH, Taméga A, Chen KL, Schindler AB, Bagayoko K, Simaga A, Blackstone C, Fischbeck KH, Landouré G. A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss. Annals of Clinical and Translational Neurology. 4: 272-275. PMID 28382308 DOI: 10.1002/Acn3.402 |
0.314 |
|
| 2016 |
Nixon-Abell J, Obara CJ, Weigel AV, Li D, Legant WR, Xu CS, Pasolli HA, Harvey K, Hess HF, Betzig E, Blackstone C, Lippincott-Schwartz J. Increased spatiotemporal resolution reveals highly dynamic dense tubular matrices in the peripheral ER. Science (New York, N.Y.). 354. PMID 27789813 DOI: 10.1126/Science.Aaf3928 |
0.367 |
|
| 2016 |
Zhao G, Zhu PP, Renvoisé B, Maldonado-Báez L, Park SH, Blackstone C. Mammalian Knock Out Cells Reveal Prominent Roles for Atlastin GTPases in ER Network Morphology. Experimental Cell Research. PMID 27669642 DOI: 10.1016/J.Yexcr.2016.09.015 |
0.457 |
|
| 2016 |
Renvoisé B, Malone B, Falgairolle M, Munasinghe J, Stadler J, Sibilla C, Park SH, Blackstone C. Reep1 null mice reveal a converging role for hereditary spastic paraplegia proteins in lipid droplet regulation. Human Molecular Genetics. PMID 27638887 DOI: 10.1093/Hmg/Ddw315 |
0.449 |
|
| 2016 |
Blackstone C, Prinz WA. Keeping in shape. Elife. 5. PMID 27619978 DOI: 10.7554/Elife.20468 |
0.33 |
|
| 2016 |
Roda RH, FitzGibbon EJ, Boucekkine H, Schindler AB, Blackstone C. Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site. Annals of Clinical and Translational Neurology. 3: 650-4. PMID 27606346 DOI: 10.1002/Acn3.329 |
0.345 |
|
| 2016 |
Nixon-Abell J, Berwick DC, Grannó S, Spain VA, Blackstone C, Harvey K. Protective LRRK2 R1398H Variant Enhances GTPase and Wnt Signaling Activity. Frontiers in Molecular Neuroscience. 9: 18. PMID 27013965 DOI: 10.3389/Fnmol.2016.00018 |
0.356 |
|
| 2016 |
Blackstone C, Belmont LD. Cell biology and the "real world". Molecular Biology of the Cell. 27: 878-9. PMID 26976931 DOI: 10.1091/Mbc.E15-11-0764 |
0.405 |
|
| 2016 |
Lee S, Chang J, Blackstone C. FAM21 directs SNX27-retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus. Nature Communications. 7: 10939. PMID 26956659 DOI: 10.1038/Ncomms10939 |
0.392 |
|
| 2016 |
Blackstone C. KIF1Bβ and Neuroblastoma: Failure to Divide and Cull. Developmental Cell. 36: 127-8. PMID 26812010 DOI: 10.1016/J.Devcel.2016.01.005 |
0.346 |
|
| 2016 |
Klionsky DJ, Abdelmohsen K, Abe A, Abedin MJ, Abeliovich H, Acevedo Arozena A, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, ... ... Blackstone C, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy. 12: 1-222. PMID 26799652 DOI: 10.1080/15548627.2015.1100356 |
0.329 |
|
| 2015 |
Hirst J, Edgar JR, Esteves T, Darios F, Madeo M, Chang J, Roda RH, Dürr A, Anheim M, Gellera C, Li J, Züchner S, Mariotti C, Stevanin G, Blackstone C, et al. Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease. Human Molecular Genetics. PMID 26085577 DOI: 10.1093/Hmg/Ddv220 |
0.39 |
|
| 2014 |
Zhao G, Blackstone C. ER morphology: sculpting with XendoU. Current Biology : Cb. 24: R1170-2. PMID 25514011 DOI: 10.1016/J.Cub.2014.11.005 |
0.425 |
|
| 2014 |
Goyal U, Renvoisé B, Chang J, Blackstone C. Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development. Plos One. 9: e112428. PMID 25390646 DOI: 10.1371/Journal.Pone.0112428 |
0.412 |
|
| 2014 |
Chang J, Lee S, Blackstone C. Spastic paraplegia proteins spastizin and spatacsin mediate autophagic lysosome reformation. The Journal of Clinical Investigation. 124: 5249-62. PMID 25365221 DOI: 10.1172/Jci77598 |
0.445 |
|
| 2014 |
Renvoisé B, Chang J, Singh R, Yonekawa S, FitzGibbon EJ, Mankodi A, Vanderver A, Schindler A, Toro C, Gahl WA, Mahuran DJ, Blackstone C, Pierson TM. Lysosomal abnormalities in hereditary spastic paraplegia types SPG15 and SPG11. Annals of Clinical and Translational Neurology. 1: 379-389. PMID 24999486 DOI: 10.1002/Acn3.64 |
0.424 |
|
| 2014 |
Zhu PP, Denton KR, Pierson TM, Li XJ, Blackstone C. Pharmacologic rescue of axon growth defects in a human iPSC model of hereditary spastic paraplegia SPG3A. Human Molecular Genetics. 23: 5638-48. PMID 24908668 DOI: 10.1093/Hmg/Ddu280 |
0.393 |
|
| 2014 |
Roda RH, Rinaldi C, Singh R, Schindler AB, Blackstone C. Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 21: 1627-31. PMID 24814856 DOI: 10.1016/J.Jocn.2013.11.048 |
0.366 |
|
| 2014 |
Blackstone C. Huntington's disease: from disease mechanisms to therapies. Drug Discovery Today. 19: 949-50. PMID 24792720 DOI: 10.1016/J.Drudis.2014.04.013 |
0.355 |
|
| 2013 |
Chang J, Lee S, Blackstone C. Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation. Proceedings of the National Academy of Sciences of the United States of America. 110: 14954-9. PMID 23969831 DOI: 10.1073/Pnas.1307391110 |
0.49 |
|
| 2013 |
Landouré G, Zhu PP, Lourenço CM, Johnson JO, Toro C, Bricceno KV, Rinaldi C, Meilleur KG, Sangaré M, Diallo O, Pierson TM, Ishiura H, Tsuji S, Hein N, Fink JK, ... ... Blackstone C, et al. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12. Human Mutation. 34: 1357-60. PMID 23857908 DOI: 10.1002/Humu.22378 |
0.338 |
|
| 2013 |
Klemm RW, Norton JP, Cole RA, Li CS, Park SH, Crane MM, Li L, Jin D, Boye-Doe A, Liu TY, Shibata Y, Lu H, Rapoport TA, Farese RV, Blackstone C, et al. A conserved role for atlastin GTPases in regulating lipid droplet size. Cell Reports. 3: 1465-75. PMID 23684613 DOI: 10.1016/J.Celrep.2013.04.015 |
0.405 |
|
| 2013 |
Anderson CA, Blackstone C. SUMO wrestling with Drp1 at mitochondria. The Embo Journal. 32: 1496-8. PMID 23632859 DOI: 10.1038/Emboj.2013.103 |
0.356 |
|
| 2013 |
Goyal U, Blackstone C. Untangling the web: mechanisms underlying ER network formation. Biochimica Et Biophysica Acta. 1833: 2492-8. PMID 23602970 DOI: 10.1016/J.Bbamcr.2013.04.009 |
0.496 |
|
| 2013 |
Chang J, Blackstone C. Rab10 joins the ER social network. Nature Cell Biology. 15: 135-6. PMID 23377026 DOI: 10.1038/Ncb2682 |
0.361 |
|
| 2013 |
Gray JJ, Zommer AE, Bouchard RJ, Duval N, Blackstone C, Linseman DA. N-terminal cleavage of the mitochondrial fusion GTPase OPA1 occurs via a caspase-independent mechanism in cerebellar granule neurons exposed to oxidative or nitrosative stress. Brain Research. 1494: 28-43. PMID 23220553 DOI: 10.1016/J.Brainres.2012.12.001 |
0.366 |
|
| 2012 |
Lee S, Chang J, Renvoisé B, Tipirneni A, Yang S, Blackstone C. MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis. Molecular Biology of the Cell. 23: 4347-61. PMID 23015756 DOI: 10.1091/Mbc.E12-04-0292 |
0.406 |
|
| 2012 |
Renvoisé B, Stadler J, Singh R, Bakowska JC, Blackstone C. Spg20-/- mice reveal multimodal functions for Troyer syndrome protein spartin in lipid droplet maintenance, cytokinesis and BMP signaling. Human Molecular Genetics. 21: 3604-18. PMID 22619377 DOI: 10.1093/Hmg/Dds191 |
0.373 |
|
| 2012 |
Blackstone C. Cellular pathways of hereditary spastic paraplegia. Annual Review of Neuroscience. 35: 25-47. PMID 22540978 DOI: 10.1146/Annurev-Neuro-062111-150400 |
0.338 |
|
| 2012 |
Blackstone C, Murphy CT. Cell biology of disease and aging: A two-way street Molecular Biology of the Cell. 23: 975. DOI: 10.1091/Mbc.E11-12-0985 |
0.399 |
|
| 2011 |
Pierson TM, Adams D, Bonn F, Martinelli P, Cherukuri PF, Teer JK, Hansen NF, Cruz P, Mullikin JC, Blakesley RW, Golas G, Kwan J, Sandler A, Fajardo K, Markello T, ... ... Blackstone C, et al. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases Plos Genetics. 7. PMID 22022284 DOI: 10.1371/Journal.Pgen.1002325 |
0.44 |
|
| 2011 |
Blackstone C, Chang CR. Mitochondria unite to survive. Nature Cell Biology. 13: 521-2. PMID 21540850 DOI: 10.1038/Ncb0511-521 |
0.34 |
|
| 2011 |
Guelly C, Zhu PP, Leonardis L, Papić L, Zidar J, Schabhüttl M, Strohmaier H, Weis J, Strom TM, Baets J, Willems J, De Jonghe P, Reilly MM, Fröhlich E, Hatz M, ... ... Blackstone C, et al. Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I. American Journal of Human Genetics. 88: 99-105. PMID 21194679 DOI: 10.1016/J.Ajhg.2010.12.003 |
0.378 |
|
| 2011 |
Blackstone C, O'Kane CJ, Reid E. Hereditary spastic paraplegias: membrane traffic and the motor pathway. Nature Reviews. Neuroscience. 12: 31-42. PMID 21139634 DOI: 10.1038/Nrn2946 |
0.33 |
|
| 2011 |
Blackstone C, O'Kane CJ, Reid E. Erratum: Hereditary spastic paraplegias: membrane traffic and the motor pathway Nature Reviews Neuroscience. 12: 118-118. DOI: 10.1038/Nrn2990 |
0.312 |
|
| 2010 |
Renvoisé B, Parker RL, Yang D, Bakowska JC, Hurley JH, Blackstone C. SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesis. Molecular Biology of the Cell. 21: 3293-303. PMID 20719964 DOI: 10.1091/Mbc.E09-10-0879 |
0.459 |
|
| 2010 |
Chang CR, Manlandro CM, Arnoult D, Stadler J, Posey AE, Hill RB, Blackstone C. A lethal de novo mutation in the middle domain of the dynamin-related GTPase Drp1 impairs higher order assembly and mitochondrial division. The Journal of Biological Chemistry. 285: 32494-503. PMID 20696759 DOI: 10.1074/Jbc.M110.142430 |
0.424 |
|
| 2010 |
Renvoisé B, Blackstone C. Emerging themes of ER organization in the development and maintenance of axons. Current Opinion in Neurobiology. 20: 531-7. PMID 20678923 DOI: 10.1016/J.Conb.2010.07.001 |
0.436 |
|
| 2010 |
Chang CR, Blackstone C. Dynamic regulation of mitochondrial fission through modification of the dynamin-related protein Drp1. Annals of the New York Academy of Sciences. 1201: 34-9. PMID 20649536 DOI: 10.1111/J.1749-6632.2010.05629.X |
0.434 |
|
| 2010 |
Park SH, Blackstone C. Further assembly required: construction and dynamics of the endoplasmic reticulum network. Embo Reports. 11: 515-21. PMID 20559323 DOI: 10.1038/Embor.2010.92 |
0.493 |
|
| 2010 |
Park SH, Zhu PP, Parker RL, Blackstone C. Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network. The Journal of Clinical Investigation. 120: 1097-110. PMID 20200447 DOI: 10.1172/Jci40979 |
0.503 |
|
| 2009 |
Hu J, Shibata Y, Zhu PP, Voss C, Rismanchi N, Prinz WA, Rapoport TA, Blackstone C. A class of dynamin-like GTPases involved in the generation of the tubular ER network. Cell. 138: 549-61. PMID 19665976 DOI: 10.1016/J.Cell.2009.05.025 |
0.747 |
|
| 2009 |
Figueroa-Romero C, Iñiguez-Lluhí JA, Stadler J, Chang CR, Arnoult D, Keller PJ, Hong Y, Blackstone C, Feldman EL. SUMOylation of the mitochondrial fission protein Drp1 occurs at multiple nonconsensus sites within the B domain and is linked to its activity cycle. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 23: 3917-27. PMID 19638400 DOI: 10.1096/Fj.09-136630 |
0.448 |
|
| 2009 |
Hanna MC, Blackstone C. Interaction of the SPG21 protein ACP33/maspardin with the aldehyde dehydrogenase ALDH16A1. Neurogenetics. 10: 217-28. PMID 19184135 DOI: 10.1007/S10048-009-0172-6 |
0.459 |
|
| 2009 |
Rismanchi N, Puertollano R, Blackstone C. STAM adaptor proteins interact with COPII complexes and function in ER-to-Golgi trafficking. Traffic (Copenhagen, Denmark). 10: 201-17. PMID 19054391 DOI: 10.1111/J.1600-0854.2008.00856.X |
0.752 |
|
| 2009 |
Loucks FA, Schroeder EK, Zommer AE, Hilger S, Kelsey NA, Bouchard RJ, Blackstone C, Brewster JL, Linseman DA. Caspases indirectly regulate cleavage of the mitochondrial fusion GTPase OPA1 in neurons undergoing apoptosis. Brain Research. 1250: 63-74. PMID 19046944 DOI: 10.1016/J.Brainres.2008.10.081 |
0.363 |
|
| 2008 |
Yang D, Rismanchi N, Renvoisé B, Lippincott-Schwartz J, Blackstone C, Hurley JH. Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B. Nature Structural & Molecular Biology. 15: 1278-86. PMID 18997780 DOI: 10.1038/Nsmb.1512 |
0.731 |
|
| 2008 |
Cereghetti GM, Stangherlin A, Martins de Brito O, Chang CR, Blackstone C, Bernardi P, Scorrano L. Dephosphorylation by calcineurin regulates translocation of Drp1 to mitochondria. Proceedings of the National Academy of Sciences of the United States of America. 105: 15803-8. PMID 18838687 DOI: 10.1073/Pnas.0808249105 |
0.402 |
|
| 2008 |
Bakowska JC, Wang H, Xin B, Sumner CJ, Blackstone C. Lack of spartin protein in Troyer syndrome: a loss-of-function disease mechanism? Archives of Neurology. 65: 520-4. PMID 18413476 DOI: 10.1001/Archneur.65.4.520 |
0.41 |
|
| 2008 |
Rismanchi N, Soderblom C, Stadler J, Zhu PP, Blackstone C. Atlastin GTPases are required for Golgi apparatus and ER morphogenesis. Human Molecular Genetics. 17: 1591-604. PMID 18270207 DOI: 10.1093/Hmg/Ddn046 |
0.755 |
|
| 2008 |
Guillery O, Malka F, Landes T, Guillou E, Blackstone C, Lombès A, Belenguer P, Arnoult D, Rojo M. Metalloprotease-mediated OPA1 processing is modulated by the mitochondrial membrane potential. Biology of the Cell / Under the Auspices of the European Cell Biology Organization. 100: 315-25. PMID 18076378 DOI: 10.1042/Bc20070110 |
0.385 |
|
| 2007 |
Chang CR, Blackstone C. Drp1 phosphorylation and mitochondrial regulation. Embo Reports. 8: 1088-9; author reply. PMID 18059302 DOI: 10.1038/Sj.Embor.7401118 |
0.357 |
|
| 2007 |
Chang CR, Blackstone C. Cyclic AMP-dependent protein kinase phosphorylation of Drp1 regulates its GTPase activity and mitochondrial morphology. The Journal of Biological Chemistry. 282: 21583-7. PMID 17553808 DOI: 10.1074/Jbc.C700083200 |
0.446 |
|
| 2007 |
Bakowska JC, Jupille H, Fatheddin P, Puertollano R, Blackstone C. Troyer syndrome protein spartin is mono-ubiquitinated and functions in EGF receptor trafficking. Molecular Biology of the Cell. 18: 1683-92. PMID 17332501 DOI: 10.1091/Mbc.E06-09-0833 |
0.379 |
|
| 2006 |
Soderblom C, Blackstone C. Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias. Pharmacology & Therapeutics. 109: 42-56. PMID 16005518 DOI: 10.1016/J.Pharmthera.2005.06.001 |
0.386 |
|
| 2005 |
Arnoult D, Rismanchi N, Grodet A, Roberts RG, Seeburg DP, Estaquier J, Sheng M, Blackstone C. Bax/Bak-dependent release of DDP/TIMM8a promotes Drp1-mediated mitochondrial fission and mitoptosis during programmed cell death. Current Biology : Cb. 15: 2112-8. PMID 16332536 DOI: 10.1016/J.Cub.2005.10.041 |
0.721 |
|
| 2005 |
Arnoult D, Grodet A, Lee YJ, Estaquier J, Blackstone C. Release of OPA1 during apoptosis participates in the rapid and complete release of cytochrome c and subsequent mitochondrial fragmentation. The Journal of Biological Chemistry. 280: 35742-50. PMID 16115883 DOI: 10.1074/Jbc.M505970200 |
0.343 |
|
| 2005 |
Bakowska JC, Jenkins R, Pendleton J, Blackstone C. The Troyer syndrome (SPG20) protein spartin interacts with Eps15. Biochemical and Biophysical Research Communications. 334: 1042-8. PMID 16036216 DOI: 10.1016/J.Bbrc.2005.06.201 |
0.439 |
|
| 2004 |
Zhu PP, Patterson A, Stadler J, Seeburg DP, Sheng M, Blackstone C. Intra- and intermolecular domain interactions of the C-terminal GTPase effector domain of the multimeric dynamin-like GTPase Drp1. The Journal of Biological Chemistry. 279: 35967-74. PMID 15208300 DOI: 10.1074/Jbc.M404105200 |
0.4 |
|
| 2003 |
Zhu PP, Patterson A, Lavoie B, Stadler J, Shoeb M, Patel R, Blackstone C. Cellular localization, oligomerization, and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin. The Journal of Biological Chemistry. 278: 49063-71. PMID 14506257 DOI: 10.1074/Jbc.M306702200 |
0.451 |
|
| 2003 |
Miller DW, Ahmad R, Hague S, Baptista MJ, Canet-Aviles R, McLendon C, Carter DM, Zhu PP, Stadler J, Chandran J, Klinefelter GR, Blackstone C, Cookson MR. L166P mutant DJ-1, causative for recessive Parkinson's disease, is degraded through the ubiquitin-proteasome system. The Journal of Biological Chemistry. 278: 36588-95. PMID 12851414 DOI: 10.1074/Jbc.M304272200 |
0.375 |
|
| 2003 |
Blackstone C, Roberts RG, Seeburg DP, Sheng M. Interaction of the deafness-dystonia protein DDP/TIMM8a with the signal transduction adaptor molecule STAM1. Biochemical and Biophysical Research Communications. 305: 345-52. PMID 12745081 DOI: 10.1016/S0006-291X(03)00767-8 |
0.444 |
|
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