| 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 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2015 |
Rinaldi C, Schmidt T, Situ AJ, Johnson JO, Lee PR, Chen KL, Bott LC, Fadó R, Harmison GH, Parodi S, Grunseich C, Renvoisé B, Biesecker LG, De Michele G, Santorelli FM, ... ... Blackstone C, et al. Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia. Jama Neurology. 72: 561-70. PMID 25751282 DOI: 10.1001/Jamaneurol.2014.4769 |
0.298 |
|
| 2016 |
Hirst J, Madeo M, Smets K, Edgar JR, Schols L, Li J, Yarrow A, Deconinck T, Baets J, Van Aken E, De Bleecker J, Datiles MB, Roda RH, Liepert J, Züchner S, ... ... Blackstone C, et al. Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48). Neurology. Genetics. 2: e98. PMID 27606357 DOI: 10.1212/Nxg.0000000000000098 |
0.297 |
|
| 1994 |
Blackstone C, Murphy TH, Moss SJ, Baraban JM, Huganir RL. Cyclic AMP and synaptic activity-dependent phosphorylation of AMPA-preferring glutamate receptors. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 14: 7585-93. PMID 7527845 DOI: 10.1523/Jneurosci.14-12-07585.1994 |
0.296 |
|
| 2012 |
Pierson TM, Simeonov DR, Sincan M, Adams DA, Markello T, Golas G, Fuentes-Fajardo K, Hansen NF, Cherukuri PF, Cruz P, Mullikin JC, Blackstone C, Tifft C, Boerkoel CF, Gahl WA, et al. Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration. European Journal of Human Genetics : Ejhg. 20: 476-9. PMID 22146942 DOI: 10.1038/Ejhg.2011.222 |
0.289 |
|
| 2014 |
Roda RH, Schindler AB, Blackstone C, Mammen AL, Corse AM, Lloyd TE. Laing distal myopathy pathologically resembling inclusion body myositis. Annals of Clinical and Translational Neurology. 1: 1053-8. PMID 25574480 DOI: 10.1002/Acn3.140 |
0.279 |
|
| 2007 |
Meijer IA, Dion P, Laurent S, Dupré N, Brais B, Levert A, Puymirat J, Rioux MF, Sylvain M, Zhu PP, Soderblom C, Stadler J, Blackstone C, Rouleau GA. Characterization of a novel SPG3A deletion in a French-Canadian family. Annals of Neurology. 61: 599-603. PMID 17427918 DOI: 10.1002/Ana.21114 |
0.277 |
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| 2011 |
Blackstone C. Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist. The Lancet. Neurology. 10: 24-5. PMID 21112252 DOI: 10.1016/S1474-4422(10)70280-5 |
0.275 |
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| 2002 |
Blackstone C, Sheng M. Postsynaptic calcium signaling microdomains in neurons. Frontiers in Bioscience : a Journal and Virtual Library. 7: d872-85. PMID 11897549 DOI: 10.2741/Blacksto |
0.27 |
|
| 2007 |
Papapetropoulos S, Friedman J, Blackstone C, Kleiner GI, Bowen BC, Singer C. A progressive, fatal dystonia-Parkinsonism syndrome in a patient with primary immunodeficiency receiving chronic IVIG therapy. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 1664-6. PMID 17588239 DOI: 10.1002/Mds.21631 |
0.27 |
|
| 1994 |
Krishek BJ, Xie X, Blackstone C, Huganir RL, Moss SJ, Smart TG. Regulation of GABAA receptor function by protein kinase C phosphorylation. Neuron. 12: 1081-95. PMID 8185945 DOI: 10.1016/0896-6273(94)90316-6 |
0.263 |
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| 2022 |
Feng X, Cheng XT, Zheng P, Li Y, Hakim J, Zhang SQ, Anderson SM, Linask K, Zou J, Sheng ZH, Blackstone C. Ligand-free mitochondria-localized mutant AR-induced cytotoxicity in spinal bulbar muscular atrophy. Brain : a Journal of Neurology. PMID 35867854 DOI: 10.1093/brain/awac269 |
0.259 |
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| 2010 |
Meilleur KG, Traoré M, Sangaré M, Britton A, Landouré G, Coulibaly S, Niaré B, Mochel F, La Pean A, Rafferty I, Watts C, Shriner D, Littleton-Kearney MT, Blackstone C, Singleton A, et al. Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19. Neurogenetics. 11: 313-8. PMID 20039086 DOI: 10.1007/S10048-009-0230-0 |
0.257 |
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| 2024 |
Obara CJ, Nixon-Abell J, Moore AS, Riccio F, Hoffman DP, Shtengel G, Xu CS, Schaefer K, Pasolli HA, Masson JB, Hess HF, Calderon CP, Blackstone C, Lippincott-Schwartz J. Motion of VAPB molecules reveals ER-mitochondria contact site subdomains. Nature. PMID 38267577 DOI: 10.1038/s41586-023-06956-y |
0.256 |
|
| 1993 |
Martin LJ, Blackstone CD, Levey AI, Huganir RL, Price DL. Cellular localizations of AMPA glutamate receptors within the basal forebrain magnocellular complex of rat and monkey. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 13: 2249-63. PMID 8386757 DOI: 10.1523/Jneurosci.13-05-02249.1993 |
0.254 |
|
| 2003 |
Blackstone C. The Neuron: Cell and Molecular Biology Archives of Neurology. 60: 901. DOI: 10.1001/Archneur.60.6.901 |
0.254 |
|
| 2018 |
Trummer B, Haubenberger D, Blackstone C. Clinical Trial Designs and Measures in Hereditary Spastic Paraplegias. Frontiers in Neurology. 9: 1017. PMID 30627115 DOI: 10.3389/Fneur.2018.01017 |
0.254 |
|
| 2009 |
Blackstone C. Infantile parkinsonism-dystonia: a dopamine "transportopathy". The Journal of Clinical Investigation. 119: 1455-8. PMID 19504720 DOI: 10.1172/Jci39632 |
0.253 |
|
| 2014 |
Pierson TM, Renvoisé B, Chang J, Toro C, Blackstone C. Hereditary spastic paraplegias types 15 and 11 are associated with lysosomal abnormalities Molecular Genetics and Metabolism. 111: S86. DOI: 10.1016/J.Ymgme.2013.12.208 |
0.249 |
|
| 2022 |
Yang H, Sibilla C, Liu R, Yun J, Hay BA, Blackstone C, Chan DC, Harvey RJ, Guo M. Clueless/CLUH regulates mitochondrial fission by promoting recruitment of Drp1 to mitochondria. Nature Communications. 13: 1582. PMID 35332133 DOI: 10.1038/s41467-022-29071-4 |
0.245 |
|
| 2015 |
Dworzak J, Renvoisé B, Habchi J, Yates EV, Combadière C, Knowles TP, Dobson CM, Blackstone C, Paulsen O, Murphy PM. Neuronal Cx3cr1 Deficiency Protects against Amyloid β-Induced Neurotoxicity. Plos One. 10: e0127730. PMID 26038823 DOI: 10.1371/Journal.Pone.0127730 |
0.244 |
|
| 2020 |
Blackstone C. Early-onset hereditary spastic paraplegia: the possibility of a genetic diagnosis. Developmental Medicine and Child Neurology. PMID 32420616 DOI: 10.1111/Dmcn.14564 |
0.237 |
|
| 2006 |
Zhu PP, Soderblom C, Tao-Cheng JH, Stadler J, Blackstone C. SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development. Human Molecular Genetics. 15: 1343-53. PMID 16537571 DOI: 10.1093/Hmg/Ddl054 |
0.224 |
|
| 2022 |
Zheng P, Obara CJ, Szczesna E, Nixon-Abell J, Mahalingan KK, Roll-Mecak A, Lippincott-Schwartz J, Blackstone C. Publisher Correction: ER proteins decipher the tubulin code to regulate organelle distribution. Nature. PMID 35322235 DOI: 10.1038/s41586-022-04656-7 |
0.223 |
|
| 2013 |
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, Fuentes Fajardo K, Markello T, ... ... Blackstone C, et al. Correction: Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases Plos Genetics. 9. DOI: 10.1371/annotation/273d7d98-3a1b-494b-839e-de31a0f33d28 |
0.211 |
|
| 2019 |
Johnson TP, Larman HB, Lee MH, Whitehead SS, Kowalak J, Toro C, Lau CC, Kim J, Johnson KR, Reoma LB, Faustin A, Pardo C, Kottapalli S, Howard J, Monaco D, ... ... Blackstone C, et al. Chronic dengue virus encephalitis in a patient with progressive dementia with extrapyramidal features. Annals of Neurology. PMID 31461177 DOI: 10.1002/Ana.25588 |
0.207 |
|
| 2019 |
Chang CL, Weigel AV, Ioannou MS, Pasolli HA, Xu CS, Peale DR, Shtengel G, Freeman M, Hess HF, Blackstone C, Lippincott-Schwartz J. Spastin tethers lipid droplets to peroxisomes and directs fatty acid trafficking through ESCRT-III. The Journal of Cell Biology. PMID 31227594 DOI: 10.1083/jcb.201902061 |
0.202 |
|
| 2016 |
Klionsky DJ, Abdelmohsen K, Abe A, Abedin J, Abeliovich H, Arozena AA, Adachi H, Adams CM, Adams PD, Adeli K, Adhihetty PJ, Adler SG, Agam G, Agarwal R, Aghi MK, ... ... Blackstone C, et al. Erratum to: Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) (Autophagy, 12, 1, 1-222, 10.1080/15548627.2015.1100356 Autophagy. 12: 443-443. PMID 26902590 DOI: 10.1080/15548627.2016.1147886 |
0.192 |
|
| 2017 |
Roda RH, Schindler AB, Blackstone C. SCA8 should not be tested in isolation for ataxia. Neurology. Genetics. 3: e150. PMID 28451643 DOI: 10.1212/Nxg.0000000000000150 |
0.19 |
|
| 2010 |
Soderblom C, Stadler J, Jupille H, Blackstone C, Shupliakov O, Hanna MC. Targeted disruption of the Mast syndrome gene SPG21 in mice impairs hind limb function and alters axon branching in cultured cortical neurons. Neurogenetics. 11: 369-78. PMID 20661613 DOI: 10.1007/S10048-010-0252-7 |
0.188 |
|
| 2022 |
Alecu JE, Saffari A, Jordan C, Srivastava S, Blackstone C, Ebrahimi-Fakhari D. De novo variants cause complex symptoms in HSP-ATL1 (SPG3A) and uncover genotype-phenotype correlations. Human Molecular Genetics. PMID 35925862 DOI: 10.1093/hmg/ddac182 |
0.186 |
|
| 2017 |
Blackstone C. A Larger BAT Improves Metabolism but Whiffs on Safety. Ebiomedicine. PMID 28988595 DOI: 10.1016/J.Ebiom.2017.09.036 |
0.183 |
|
| 2014 |
Denton KR, Lei L, Grenier J, Rodionov V, Blackstone C, Li XJ. Loss of spastin function results in disease-specific axonal defects in human pluripotent stem cell-based models of hereditary spastic paraplegia. Stem Cells (Dayton, Ohio). 32: 414-23. PMID 24123785 DOI: 10.1002/Stem.1569 |
0.182 |
|
| 2022 |
Saffari A, Kellner M, Jordan C, Rosengarten H, Mo A, Zhang B, Strelko O, Neuser S, Davis MY, Yoshikura N, Futamura N, Takeuchi T, Nabatame S, Ishiura H, Tsuji S, ... ... Blackstone C, et al. The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15. Brain : a Journal of Neurology. PMID 36315648 DOI: 10.1093/brain/awac391 |
0.182 |
|
| 2022 |
Mo A, Saffari A, Kellner M, Döbler-Neumann M, Jordan C, Srivastava S, Zhang B, Sahin M, Fink JK, Smith L, Posey JE, Alter KE, Toro C, Blackstone C, Soldatos AG, et al. Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 36103453 DOI: 10.1002/mds.29225 |
0.181 |
|
| 2020 |
Mou Y, Dong Y, Chen Z, Denton KR, Duff MO, Blackstone C, Zhang SC, Li XJ. Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia. Acta Neuropathologica Communications. 8: 214. PMID 33287888 DOI: 10.1186/s40478-020-01088-0 |
0.169 |
|
| 2023 |
Liu J, He Y, Lwin C, Han M, Guan B, Naik A, Bender C, Moore N, Huryn LA, Sergeev Y, Qian H, Zeng Y, Dong L, Liu P, Lei J, ... ... Blackstone C, et al. Neuropathy target esterase activity predicts retinopathy among disorders. Biorxiv : the Preprint Server For Biology. PMID 37333224 DOI: 10.1101/2023.06.09.544373 |
0.166 |
|
| 2018 |
Blackstone C. Hereditary spastic paraplegia. Handbook of Clinical Neurology. 148: 633-652. PMID 29478605 DOI: 10.1016/B978-0-444-64076-5.00041-7 |
0.164 |
|
| 2013 |
Donkervoort S, Dastgir J, Hu Y, Zein WM, Marks H, Blackstone C, Bönnemann CG. Phenotypic variability of a likely FA2H founder mutation in a family with complicated hereditary spastic paraplegia. Clinical Genetics. 85: 393-5. PMID 23745665 DOI: 10.1111/cge.12185 |
0.161 |
|
| 2016 |
Fraidakis MJ, Brunetti M, Blackstone C, Filippi M, Chiò A. Novel Compound Heterozygous Spatacsin Mutations in a Greek Kindred with Hereditary Spastic Paraplegia SPG11 and Dementia. Neuro-Degenerative Diseases. 16: 373-381. PMID 27318863 DOI: 10.1159/000444715 |
0.161 |
|
| 2021 |
Blackstone C, Elwood F, Plun-Favreau H, Lewis PA. Vesicle trafficking and pathways to neurodegeneration. Molecular Neurodegeneration. 16: 56. PMID 34419119 DOI: 10.1186/s13024-021-00480-1 |
0.154 |
|
| 2023 |
Mou Y, Nandi G, Mukte S, Chai E, Chen Z, Nielsen JE, Nielsen TT, Criscuolo C, Blackstone C, Fraidakis MJ, Li XJ. Chenodeoxycholic acid rescues axonal degeneration in induced pluripotent stem cell-derived neurons from spastic paraplegia type 5 and cerebrotendinous xanthomatosis patients. Orphanet Journal of Rare Diseases. 18: 72. PMID 37024986 DOI: 10.1186/s13023-023-02666-w |
0.15 |
|
| 2022 |
Johnson B, Kokkinis A, Gai N, Shamim EA, Blackstone C, Fischbeck KH, Grunseich C. Nonalcoholic Fatty Liver Disease in Patients with Inherited and Sporadic Motor Neuron Degeneration. Genes. 13. PMID 35741698 DOI: 10.3390/genes13060936 |
0.11 |
|
| 2021 |
Breza M, Hirst J, Chelban V, Banneau G, Tissier L, Kol B, Bourinaris T, Said SA, Péréon Y, Heinzmann A, Debs R, Juntas-Morales R, Martinez VG, Camdessanche JP, Scherer-Gagou C, ... ... Blackstone C, et al. Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare Disease. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 33543803 DOI: 10.1002/mds.28487 |
0.099 |
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| 2022 |
Vander Stichele G, Durr A, Yoon G, Schüle R, Blackstone C, Esposito G, Buffel C, Oliveira I, Freitag C, van Rooijen S, Hoffmann S, Thielemans L, Cowling BS. An integrated modelling methodology for estimating global incidence and prevalence of hereditary spastic paraplegia subtypes SPG4, SPG7, SPG11, and SPG15. Bmc Neurology. 22: 115. PMID 35331153 DOI: 10.1186/s12883-022-02595-4 |
0.096 |
|
| 2024 |
Goodheart AE, Blackstone C. Getting to the heart of Lewy body disease. The Journal of Clinical Investigation. 134. PMID 38165040 DOI: 10.1172/JCI175798 |
0.089 |
|
| 2022 |
Blackstone C. Importance of genetic testing for childhood-onset hereditary spastic paraplegia. Developmental Medicine and Child Neurology. PMID 36168202 DOI: 10.1111/dmcn.15416 |
0.085 |
|
| 2015 |
Dworzak J, Renvoisé B, Habchi J, Yates EV, Combadière C, Knowles TP, Dobson CM, Blackstone C, Paulsen O, Murphy PM. Neuronal Cx3cr1 deficiency protects against amyloid β-induced neurotoxicity Plos One. 10. DOI: 10.1371/journal.pone.0127730 |
0.084 |
|
| 2021 |
Martinuzzi A, Blackstone C, O'Kane CJ, Stevanin G. Editorial: Hereditary Spastic Paraplegias: At the Crossroads of Molecular Pathways and Clinical Options. Frontiers in Neuroscience. 15: 708642. PMID 34239414 DOI: 10.3389/fnins.2021.708642 |
0.082 |
|
| 1996 |
Blackstone C. It Has Been Said Perspectives in Biology and Medicine. 39: 308-310. DOI: 10.1353/pbm.1996.0019 |
0.01 |
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