Harvard Catalyst Profiles

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Craig David Blackstone, Ph.D., M.D.

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Research
The research activities and funding listed below are automatically derived from NIH ExPORTER and other sources, which might result in incorrect or missing items. Faculty can login to make corrections and additions.
  1. K08NS002045 (BLACKSTONE, CRAIG D) Jul 1, 1998 - Sep 20, 2001
    NIH
    Function of the DRPLA Gene Product Atrophin
    Role: Principal Investigator
  2. Z01NS002992 (BLACKSTONE, CRAIG D)
    NIH
    Molecular Pathogenesis Of Hereditary Spastic Paraplegias
    Role: Principal Investigator

Bibliographic
Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
  1. Chen Z, Chai E, Mou Y, Roda RH, Blackstone C, Li XJ. Inhibiting mitochondrial fission rescues degeneration in hereditary spastic paraplegia neurons. Brain. 2022 Nov 21; 145(11):4016-4031. PMID: 35026838.
    Citations: 1     Fields:    
  2. 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, Aldeen HS, Cali E, Rocca C, Houlden H, Efthymiou S, Assmann B, Yoon G, Trombetta BA, Kivisäkk P, Eichler F, Nan H, Takiyama Y, Tessa A, Santorelli FM, Sahin M, Blackstone C, Yang E, Schüle R, Ebrahimi-Fakhari D. The clinical and molecular spectrum of ZFYVE26-associated hereditary spastic paraplegia: SPG15. Brain. 2022 Oct 31. PMID: 36315648.
    Citations:    Fields:    
  3. Blackstone C. Importance of genetic testing for childhood-onset hereditary spastic paraplegia. Dev Med Child Neurol. 2022 Sep 27. PMID: 36168202.
    Citations:    Fields:    
  4. 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, Christie M, Schüle R, Ebrahimi-Fakhari D. Early-Onset and Severe Complex Hereditary Spastic Paraplegia Caused by De Novo Variants in SPAST. Mov Disord. 2022 Sep 14. PMID: 36103453.
    Citations:    Fields:    
  5. 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. Hum Mol Genet. 2022 08 23; 31(16):2779-2795. PMID: 35348668; PMCID: PMC9402237.
    Citations:    Fields:    Translation:HumansAnimalsCells
  6. 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. Hum Mol Genet. 2022 Aug 04. PMID: 35925862.
    Citations:    Fields:    
  7. 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. 2022 Jul 22. PMID: 35867854.
    Citations:    Fields:    
  8. 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. 2022 Apr; 604(7904):E11. PMID: 35322235; PMCID: PMC8986530.
    Citations:    Fields:    
  9. 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 Neuropathol Commun. 2022 03 28; 10(1):40. PMID: 35346366; PMCID: PMC8961908.
    Citations: 1     Fields:    Translation:HumansAnimalsCells
  10. 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 Neurol. 2022 Mar 24; 22(1):115. PMID: 35331153; PMCID: PMC8944001.
    Citations:    Fields:    Translation:Humans
  11. 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. Nat Commun. 2022 03 24; 13(1):1582. PMID: 35332133; PMCID: PMC8948191.
    Citations: 1     Fields:    Translation:AnimalsCells
  12. 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. 2022 01; 601(7891):132-138. PMID: 34912111; PMCID: PMC8732269.
    Citations: 10     Fields:    Translation:HumansAnimalsCells
  13. Blackstone C, Elwood F, Plun-Favreau H, Lewis PA. Vesicle trafficking and pathways to neurodegeneration. Mol Neurodegener. 2021 08 21; 16(1):56. PMID: 34419119; PMCID: PMC8379594.
    Citations:    Fields:    Translation:AnimalsCells
  14. Martinuzzi A, Blackstone C, O'Kane CJ, Stevanin G. Editorial: Hereditary Spastic Paraplegias: At the Crossroads of Molecular Pathways and Clinical Options. Front Neurosci. 2021; 15:708642. PMID: 34239414; PMCID: PMC8258316.
    Citations:    
  15. 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, Zola JM, Athanasiou-Fragkouli A, Efthymiou S, Vavougios G, Velonakis G, Stamelou M, Tzartos J, Potagas C, Zambelis T, Mariotti C, Blackstone C, Vandrovcova J, Mavridis T, Kartanou C, Stefanis L, Wood N, Karadima G, LeGuern E, Koutsis G, Houlden H, Stevanin G. Expanding the Spectrum of AP5Z1-Related Hereditary Spastic Paraplegia (HSP-SPG48): A Multicenter Study on a Rare Disease. Mov Disord. 2021 04; 36(4):1034-1038. PMID: 33543803.
    Citations: 5     Fields:    Translation:Humans
  16. 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 Neuropathol Commun. 2020 12 07; 8(1):214. PMID: 33287888; PMCID: PMC7720406.
    Citations: 9     Fields:    Translation:HumansCells
  17. Fowler PC, Byrne DJ, Blackstone C, O'Sullivan NC. Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a Drosophila Model of Hereditary Spastic Paraplegia. Brain Sci. 2020 Sep 17; 10(9). PMID: 32957716; PMCID: PMC7564485.
    Citations: 3     
  18. Blackstone C. Early-onset hereditary spastic paraplegia: the possibility of a genetic diagnosis. Dev Med Child Neurol. 2020 09; 62(9):1011. PMID: 32420616.
    Citations: 1     Fields:    Translation:Humans
  19. Lee S, Park H, Zhu PP, Jung SY, Blackstone C, Chang J. Hereditary spastic paraplegia SPG8 mutations impair CAV1-dependent, integrin-mediated cell adhesion. Sci Signal. 2020 01 07; 13(613). PMID: 31911435; PMCID: PMC7231525.
    Citations: 8     Fields:    Translation:HumansAnimalsCells
  20. 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, Amara A, Schwartz O. Atlastin Endoplasmic Reticulum-Shaping Proteins Facilitate Zika Virus Replication. J Virol. 2019 12 01; 93(23). PMID: 31534046; PMCID: PMC6854498.
    Citations: 19     Fields:    Translation:HumansCells
  21. Lee CA, Blackstone C. ER morphology and endo-lysosomal crosstalk: Functions and disease implications. Biochim Biophys Acta Mol Cell Biol Lipids. 2020 01; 1865(1):158544. PMID: 31678515; PMCID: PMC6904894.
    Citations: 15     Fields:    Translation:HumansAnimalsCells
  22. Johnson TP, Larman HB, Lee MH, Whitehead SS, Kowalak J, Toro C, Lau CC, Kim J, Johnson KR, Reoma LB, Faustin A, Pardo CA, Kottapalli S, Howard J, Monaco D, Weisfeld-Adams J, Blackstone C, Galetta S, Snuderl M, Gahl WA, Kister I, Nath A. Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features. Ann Neurol. 2019 11; 86(5):695-703. PMID: 31461177.
    Citations: 7     Fields:    Translation:HumansCells
  23. 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. J Cell Biol. 2019 08 05; 218(8):2583-2599. PMID: 31227594; PMCID: PMC6683741.
    Citations: 68     Fields:    Translation:HumansCells
  24. Trummer B, Haubenberger D, Blackstone C. Clinical Trial Designs and Measures in Hereditary Spastic Paraplegias. Front Neurol. 2018; 9:1017. PMID: 30627115; PMCID: PMC6309810.
    Citations: 4     
  25. 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 Res. 2018 08; 28(8):833-854. PMID: 30030520; PMCID: PMC6063967.
    Citations: 37     Fields:    Translation:HumansAnimalsCells
  26. Denton K, Mou Y, Xu CC, Shah D, Chang J, Blackstone C, Li XJ. Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias. Hum Mol Genet. 2018 07 15; 27(14):2517-2530. PMID: 29726929; PMCID: PMC6031053.
    Citations: 20     Fields:    Translation:HumansCells
  27. Blackstone C. Hereditary spastic paraplegia. Handb Clin Neurol. 2018; 148:633-652. PMID: 29478605.
    Citations: 47     Fields:    Translation:Humans
  28. Blackstone C. Protein Targeting: ER Leads the Way to the Inner Nuclear Envelope. Curr Biol. 2017 12 04; 27(23):R1284-R1286. PMID: 29207273.
    Citations:    Fields:    Translation:Cells
  29. Roda RH, Schindler AB, Blackstone C. Multigeneration family with dominant SPG30 hereditary spastic paraplegia. Ann Clin Transl Neurol. 2017 11; 4(11):821-824. PMID: 29159194; PMCID: PMC5682118.
    Citations: 8     Fields:    
  30. Roda RH, Schindler AB, Blackstone C. SCA8 should not be tested in isolation for ataxia. Neurol Genet. 2017 Jun; 3(3):e150. PMID: 28451643; PMCID: PMC5400807.
    Citations: 1     
  31. Roda RH, Schindler AB, Blackstone C. De novo REEP2 missense mutation in pure hereditary spastic paraplegia. Ann Clin Transl Neurol. 2017 05; 4(5):347-350. PMID: 28491902; PMCID: PMC5420804.
    Citations: 5     Fields:    
  32. 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. Ann Clin Transl Neurol. 2017 04; 4(4):272-275. PMID: 28382308; PMCID: PMC5376762.
    Citations: 10     Fields:    
  33. 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. Hum Mol Genet. 2016 12 01; 25(23):5111-5125. PMID: 27638887; PMCID: PMC6078631.
    Citations: 46     Fields:    Translation:HumansAnimalsCells
  34. 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. 2016 10 28; 354(6311). PMID: 27789813; PMCID: PMC6528812.
    Citations: 150     Fields:    Translation:HumansAnimalsCells
  35. 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. Exp Cell Res. 2016 Nov 15; 349(1):32-44. PMID: 27669642.
    Citations: 22     Fields:    Translation:HumansAnimalsCells
  36. Blackstone C, Prinz WA. Keeping in shape. Elife. 2016 09 13; 5. PMID: 27619978; PMCID: PMC5021519.
    Citations:    Fields:    Translation:AnimalsCells
  37. 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, Mariotti C, De Jonghe P, Blackstone C, Kruer MC. Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48). Neurol Genet. 2016 Oct; 2(5):e98. PMID: 27606357; PMCID: PMC5001803.
    Citations: 15     
  38. Roda RH, FitzGibbon EJ, Boucekkine H, Schindler AB, Blackstone C. Neurologic syndrome associated with homozygous mutation at MAG sialic acid binding site. Ann Clin Transl Neurol. 2016 08; 3(8):650-4. PMID: 27606346; PMCID: PMC4999596.
    Citations: 6     Fields:    
  39. 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. Neurodegener Dis. 2016; 16(5-6):373-81. PMID: 27318863.
    Citations: 6     Fields:    Translation:Humans
  40. Lee S, Chang J, Blackstone C. FAM21 directs SNX27-retromer cargoes to the plasma membrane by preventing transport to the Golgi apparatus. Nat Commun. 2016 Mar 09; 7:10939. PMID: 26956659; PMCID: PMC4786876.
    Citations: 36     Fields:    Translation:HumansCells
  41. 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, Agnello M, Agostinis P, Aguilar PV, Aguirre-Ghiso J, Airoldi EM, Ait-Si-Ali S, Akematsu T, Akporiaye ET, Al-Rubeai M, Albaiceta GM, Albanese C, Albani D, Albert ML, Aldudo J, Algül H, Alirezaei M, Alloza I, Almasan A, Almonte-Beceril M, Alnemri ES, Alonso C, Altan-Bonnet N, Altieri DC, Alvarez S, Alvarez-Erviti L, Alves S, Amadoro G, Amano A, Amantini C, Ambrosio S, Amelio I, Amer AO, Amessou M, Amon A, An Z, Anania FA, Andersen SU, Andley UP, Andreadi CK, Andrieu-Abadie N, Anel A, Ann DK, Anoopkumar-Dukie S, Antonioli M, Aoki H, Apostolova N, Aquila S, Aquilano K, Araki K, Arama E, Aranda A, Araya J, Arcaro A, Arias E, Arimoto H, Ariosa AR, Armstrong JL, Arnould T, Arsov I, Asanuma K, Askanas V, Asselin E, Atarashi R, Atherton SS, Atkin JD, Attardi LD, Auberger P, Auburger G, Aurelian L, Autelli R, Avagliano L, Avantaggiati ML, Avrahami L, Awale S, Azad N, Bachetti T, Backer JM, Bae DH, Bae JS, Bae ON, Bae SH, Baehrecke EH, Baek SH, Baghdiguian S, Bagniewska-Zadworna A, Bai H, Bai J, Bai XY, Bailly Y, Balaji KN, Balduini W, Ballabio A, Balzan R, Banerjee R, Bánhegyi G, Bao H, Barbeau B, Barrachina MD, Barreiro E, Bartel B, Bartolomé A, Bassham DC, Bassi MT, Bast RC, Basu A, Batista MT, Batoko H, Battino M, Bauckman K, Baumgarner BL, Bayer KU, Beale R, Beaulieu JF, Beck GR, Becker C, Beckham JD, Bédard PA, Bednarski PJ, Begley TJ, Behl C, Behrends C, Behrens GM, Behrns KE, Bejarano E, Belaid A, Belleudi F, Bénard G, Berchem G, Bergamaschi D, Bergami M, Berkhout B, Berliocchi L, Bernard A, Bernard M, Bernassola F, Bertolotti A, Bess AS, Besteiro S, Bettuzzi S, Bhalla S, Bhattacharyya S, Bhutia SK, Biagosch C, Bianchi MW, Biard-Piechaczyk M, Billes V, Bincoletto C, Bingol B, Bird SW, Bitoun M, Bjedov I, Blackstone C, Blanc L, Blanco GA, Blomhoff HK, Boada-Romero E, Böckler S, Boes M, Boesze-Battaglia K, Boise LH, Bolino A, Boman A, Bonaldo P, Bordi M, Bosch J, Botana LM, Botti J, Bou G, Bouché M, Bouchecareilh M, Boucher MJ, Boulton ME, Bouret SG, Boya P, Boyer-Guittaut M, Bozhkov PV, Brady N, Braga VM, Brancolini C, Braus GH, Bravo-San Pedro JM, Brennan LA, Bresnick EH, Brest P, Bridges D, Bringer MA, Brini M, Brito GC, Brodin B, Brookes PS, Brown EJ, Brown K, Broxmeyer HE, Bruhat A, Brum PC, Brumell JH, Brunetti-Pierri N, Bryson-Richardson RJ, Buch S, Buchan AM, Budak H, Bulavin DV, Bultman SJ, Bultynck G, Bumbasirevic V, Burelle Y, Burke RE, Burmeister M, Bütikofer P, Caberlotto L, Cadwell K, Cahova M, Cai D, Cai J, Cai Q, Calatayud S, Camougrand N, Campanella M, Campbell GR, Campbell M, Campello S, Candau R, Caniggia I, Cantoni L, Cao L, Caplan AB, Caraglia M, Cardinali C, Cardoso SM, Carew JS, Carleton LA, Carlin CR, Carloni S, Carlsson SR, Carmona-Gutierrez D, Carneiro LA, Carnevali O, Carra S, Carrier A, Carroll B, Casas C, Casas J, Cassinelli G, Castets P, Castro-Obregon S, Cavallini G, Ceccherini I, Cecconi F, Cederbaum AI, Ceña V, Cenci S, Cerella C, Cervia D, Cetrullo S, Chaachouay H, Chae HJ, Chagin AS, Chai CY, Chakrabarti G, Chamilos G, Chan EY, Chan MT, Chandra D, Chandra P, Chang CP, Chang RC, Chang TY, Chatham JC, Chatterjee S, Chauhan S, Che Y, Cheetham ME, Cheluvappa R, Chen CJ, Chen G, Chen GC, Chen G, Chen H, Chen JW, Chen JK, Chen M, Chen M, Chen P, Chen Q, Chen Q, Chen SD, Chen S, Chen SS, Chen W, Chen WJ, Chen WQ, Chen W, Chen X, Chen YH, Chen YG, Chen Y, Chen Y, Chen Y, Chen YJ, Chen YQ, Chen Y, Chen Z, Chen Z, Cheng A, Cheng CH, Cheng H, Cheong H, Cherry S, Chesney J, Cheung CH, Chevet E, Chi HC, Chi SG, Chiacchiera F, Chiang HL, Chiarelli R, Chiariello M, Chieppa M, Chin LS, Chiong M, Chiu GN, Cho DH, Cho SG, Cho WC, Cho YY, Cho YS, Choi AM, Choi EJ, Choi EK, Choi J, Choi ME, Choi SI, Chou TF, Chouaib S, Choubey D, Choubey V, Chow KC, et al. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy. 2016; 12(1):1-222. PMID: 26799652; PMCID: PMC4835977.
    Citations: 2567     Fields:    Translation:HumansAnimals
  42. 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, Kruer MC, Robinson MS. Loss of AP-5 results in accumulation of aberrant endolysosomes: defining a new type of lysosomal storage disease. Hum Mol Genet. 2015 Sep 01; 24(17):4984-96. PMID: 26085577; PMCID: PMC4527494.
    Citations: 35     Fields:    Translation:HumansCells
  43. 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, Filla A, Stevanin G, Dürr A, Brice A, Casals N, Traynor BJ, Blackstone C, Ulmer TS, Fischbeck KH. Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia. JAMA Neurol. 2015 May; 72(5):561-70. PMID: 25751282; PMCID: PMC5612424.
    Citations: 29     Fields:    Translation:HumansAnimals
  44. Goyal U, Renvoisé B, Chang J, Blackstone C. Spastin-interacting protein NA14/SSNA1 functions in cytokinesis and axon development. PLoS One. 2014; 9(11):e112428. PMID: 25390646; PMCID: PMC4229207.
    Citations: 12     Fields:    Translation:HumansAnimalsCells
  45. Chang J, Lee S, Blackstone C. Spastic paraplegia proteins spastizin and spatacsin mediate autophagic lysosome reformation. J Clin Invest. 2014 Dec; 124(12):5249-62. PMID: 25365221; PMCID: PMC4348974.
    Citations: 88     Fields:    Translation:HumansCells
  46. 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. Hum Mol Genet. 2014 Nov 01; 23(21):5638-48. PMID: 24908668; PMCID: PMC4189900.
    Citations: 36     Fields:    Translation:HumansAnimalsCells
  47. 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. Ann Clin Transl Neurol. 2014 Jun 01; 1(6):379-389. PMID: 24999486; PMCID: PMC4078876.
    Citations: 53     Fields:    
  48. 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. 2014 Feb; 32(2):414-23. PMID: 24123785; PMCID: PMC3947148.
    Citations: 68     Fields:    Translation:HumansAnimalsCells
  49. Chang J, Lee S, Blackstone C. Protrudin binds atlastins and endoplasmic reticulum-shaping proteins and regulates network formation. Proc Natl Acad Sci U S A. 2013 Sep 10; 110(37):14954-9. PMID: 23969831; PMCID: PMC3773775.
    Citations: 32     Fields:    Translation:HumansCells
  50. 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, Stoll M, Nicholson G, Gonzalez MA, Speziani F, Dürr A, Stevanin G, Biesecker LG, Accardi J, Landis DM, Gahl WA, Traynor BJ, Marques W, Züchner S, Blackstone C, Fischbeck KH, Burnett BG. Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12. Hum Mutat. 2013 Oct; 34(10):1357-60. PMID: 23857908; PMCID: PMC3819934.
    Citations: 37     Fields:    Translation:HumansCells
  51. 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, Guo Y, Mak HY. A conserved role for atlastin GTPases in regulating lipid droplet size. Cell Rep. 2013 May 30; 3(5):1465-75. PMID: 23684613.
    Citations: 63     Fields:    Translation:HumansAnimalsCells
  52. Anderson CA, Blackstone C. SUMO wrestling with Drp1 at mitochondria. EMBO J. 2013 May 29; 32(11):1496-8. PMID: 23632859; PMCID: PMC3671251.
    Citations: 14     Fields:    Translation:HumansAnimalsCells
  53. 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 Res. 2013 Feb 04; 1494:28-43. PMID: 23220553; PMCID: PMC3575199.
    Citations: 11     Fields:    Translation:AnimalsCells
  54. Lee S, Chang J, Renvoisé B, Tipirneni A, Yang S, Blackstone C. MITD1 is recruited to midbodies by ESCRT-III and participates in cytokinesis. Mol Biol Cell. 2012 Nov; 23(22):4347-61. PMID: 23015756; PMCID: PMC3496609.
    Citations: 19     Fields:    Translation:HumansCells
  55. 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. Hum Mol Genet. 2012 Aug 15; 21(16):3604-18. PMID: 22619377; PMCID: PMC3406757.
    Citations: 31     Fields:    Translation:HumansAnimalsCells
  56. Blackstone C. Cellular pathways of hereditary spastic paraplegia. Annu Rev Neurosci. 2012; 35:25-47. PMID: 22540978; PMCID: PMC5584684.
    Citations: 145     Fields:    Translation:HumansAnimalsCells
  57. Pierson TM, Adams D, Bonn F, Martinelli P, Cherukuri PF, Teer JK, Hansen NF, Cruz P, Mullikin For The Nisc Comparative Sequencing Program JC, Blakesley RW, Golas G, Kwan J, Sandler A, Fuentes Fajardo K, Markello T, Tifft C, Blackstone C, Rugarli EI, Langer T, Gahl WA, Toro C. Whole-exome sequencing identifies homozygous AFG3L2 mutations in a spastic ataxia-neuropathy syndrome linked to mitochondrial m-AAA proteases. PLoS Genet. 2011 Oct; 7(10):e1002325. PMID: 22022284; PMCID: PMC3192828.
    Citations: 96     Fields:    Translation:HumansAnimalsCells
  58. Blackstone C, Chang CR. Mitochondria unite to survive. Nat Cell Biol. 2011 May; 13(5):521-2. PMID: 21540850.
    Citations: 25     Fields:    Translation:HumansAnimalsCells
  59. Guelly C, Zhu PP, Leonardis L, Papic L, Zidar J, Schabhüttl M, Strohmaier H, Weis J, Strom TM, Baets J, Willems J, De Jonghe P, Reilly MM, Fröhlich E, Hatz M, Trajanoski S, Pieber TR, Janecke AR, Blackstone C, Auer-Grumbach M. Targeted high-throughput sequencing identifies mutations in atlastin-1 as a cause of hereditary sensory neuropathy type I. Am J Hum Genet. 2011 Jan 07; 88(1):99-105. PMID: 21194679; PMCID: PMC3014370.
    Citations: 58     Fields:    Translation:HumansAnimalsCells
  60. 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. J Biol Chem. 2010 Oct 15; 285(42):32494-503. PMID: 20696759; PMCID: PMC2952251.
    Citations: 92     Fields:    Translation:HumansAnimalsCells
  61. 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. 2010 Oct; 11(4):369-78. PMID: 20661613; PMCID: PMC5667354.
    Citations: 12     Fields:    Translation:AnimalsCells
  62. Chang CR, Blackstone C. Dynamic regulation of mitochondrial fission through modification of the dynamin-related protein Drp1. Ann N Y Acad Sci. 2010 Jul; 1201:34-9. PMID: 20649536; PMCID: PMC5585781.
    Citations: 263     Fields:    Translation:AnimalsCells
  63. Park SH, Blackstone C. Further assembly required: construction and dynamics of the endoplasmic reticulum network. EMBO Rep. 2010 Jul; 11(7):515-21. PMID: 20559323; PMCID: PMC2897125.
    Citations: 71     Fields:    Translation:HumansAnimalsCells
  64. 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. J Clin Invest. 2010 Apr; 120(4):1097-110. PMID: 20200447; PMCID: PMC2846052.
    Citations: 184     Fields:    Translation:HumansAnimalsCells
  65. 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. 2009 Aug 07; 138(3):549-61. PMID: 19665976; PMCID: PMC2746359.
    Citations: 265     Fields:    Translation:AnimalsCells
  66. 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 J. 2009 Nov; 23(11):3917-27. PMID: 19638400; PMCID: PMC2775011.
    Citations: 101     Fields:    Translation:HumansCells
  67. Blackstone C. Infantile parkinsonism-dystonia: a dopamine "transportopathy". J Clin Invest. 2009 Jun; 119(6):1455-8. PMID: 19504720; PMCID: PMC2689103.
    Citations: 9     Fields:    Translation:HumansAnimals
  68. Rismanchi N, Puertollano R, Blackstone C. STAM adaptor proteins interact with COPII complexes and function in ER-to-Golgi trafficking. Traffic. 2009 Feb; 10(2):201-17. PMID: 19054391; PMCID: PMC2694054.
    Citations: 6     Fields:    Translation:HumansCells
  69. 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 Res. 2009 Jan 23; 1250:63-74. PMID: 19046944; PMCID: PMC2771186.
    Citations: 13     Fields:    Translation:HumansAnimalsCells
  70. 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. Nat Struct Mol Biol. 2008 Dec; 15(12):1278-86. PMID: 18997780; PMCID: PMC2593743.
    Citations: 115     Fields:    Translation:HumansCells
  71. 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. Biol Cell. 2008 May; 100(5):315-25. PMID: 18076378.
    Citations: 65     Fields:    Translation:HumansCells
  72. Rismanchi N, Soderblom C, Stadler J, Zhu PP, Blackstone C. Atlastin GTPases are required for Golgi apparatus and ER morphogenesis. Hum Mol Genet. 2008 Jun 01; 17(11):1591-604. PMID: 18270207; PMCID: PMC2902292.
    Citations: 101     Fields:    Translation:HumansAnimalsCells
  73. Chang CR, Blackstone C. Drp1 phosphorylation and mitochondrial regulation. EMBO Rep. 2007 Dec; 8(12):1088-9; author reply 1089-90. PMID: 18059302; PMCID: PMC2267246.
    Citations: 44     Fields:    Translation:HumansAnimalsCells
  74. 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. Mov Disord. 2007 Aug 15; 22(11):1664-6. PMID: 17588239.
    Citations: 3     Fields:    Translation:Humans
  75. Chang CR, Blackstone C. Cyclic AMP-dependent protein kinase phosphorylation of Drp1 regulates its GTPase activity and mitochondrial morphology. J Biol Chem. 2007 Jul 27; 282(30):21583-7. PMID: 17553808.
    Citations: 371     Fields:    Translation:HumansCells
  76. 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. Ann Neurol. 2007 Jun; 61(6):599-603. PMID: 17427918.
    Citations: 8     Fields:    Translation:HumansCells
  77. Bakowska JC, Jupille H, Fatheddin P, Puertollano R, Blackstone C. Troyer syndrome protein spartin is mono-ubiquitinated and functions in EGF receptor trafficking. Mol Biol Cell. 2007 May; 18(5):1683-92. PMID: 17332501; PMCID: PMC1855030.
    Citations: 53     Fields:    Translation:HumansCells
  78. 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. Hum Mol Genet. 2006 Apr 15; 15(8):1343-53. PMID: 16537571.
    Citations: 58     Fields:    Translation:AnimalsCells
  79. 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. Curr Biol. 2005 Dec 06; 15(23):2112-8. PMID: 16332536.
    Citations: 93     Fields:    Translation:HumansAnimalsCells
  80. 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. J Biol Chem. 2005 Oct 21; 280(42):35742-50. PMID: 16115883.
    Citations: 98     Fields:    Translation:HumansCells
  81. Soderblom C, Blackstone C. Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias. Pharmacol Ther. 2006 Jan; 109(1-2):42-56. PMID: 16005518.
    Citations: 35     Fields:    Translation:HumansAnimalsCells
  82. 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. J Biol Chem. 2004 Aug 20; 279(34):35967-74. PMID: 15208300.
    Citations: 98     Fields:    Translation:HumansCells
  83. 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. J Biol Chem. 2003 Dec 05; 278(49):49063-71. PMID: 14506257.
    Citations: 78     Fields:    Translation:HumansAnimalsCells
  84. 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. J Biol Chem. 2003 Sep 19; 278(38):36588-95. PMID: 12851414.
    Citations: 75     Fields:    Translation:HumansAnimalsCells
  85. Blackstone C, Roberts RG, Seeburg DP, Sheng M. Interaction of the deafness-dystonia protein DDP/TIMM8a with the signal transduction adaptor molecule STAM1. Biochem Biophys Res Commun. 2003 May 30; 305(2):345-52. PMID: 12745081.
    Citations: 5     Fields:    Translation:AnimalsCells
  86. Blackstone C, Sheng M. Postsynaptic calcium signaling microdomains in neurons. Front Biosci. 2002 Apr 01; 7:d872-85. PMID: 11897549.
    Citations: 10     Fields:    Translation:AnimalsCells
  87. Martin LJ, Furuta A, Blackstone CD. AMPA receptor protein in developing rat brain: glutamate receptor-1 expression and localization change at regional, cellular, and subcellular levels with maturation. Neuroscience. 1998 Apr; 83(3):917-28. PMID: 9483574.
    Citations: 28     Fields:    Translation:AnimalsCells
  88. Wright DD, Blackstone CD, Huganir RL, Ryugo DK. Immunocytochemical localization of the mGluR1 alpha metabotropic glutamate receptor in the dorsal cochlear nucleus. J Comp Neurol. 1996 Jan 22; 364(4):729-45. PMID: 8821458.
    Citations: 13     Fields:    Translation:AnimalsCells
  89. Peng YW, Blackstone CD, Huganir RL, Yau KW. Distribution of glutamate receptor subtypes in the vertebrate retina. Neuroscience. 1995 May; 66(2):483-97. PMID: 7477889.
    Citations: 39     Fields:    Translation:Animals
  90. Ginsberg SD, Price DL, Blackstone CD, Huganir RL, Martin LJ. Non-NMDA glutamate receptors are present throughout the primate hypothalamus. J Comp Neurol. 1995 Mar 20; 353(4):539-52. PMID: 7759614.
    Citations: 3     Fields:    Translation:AnimalsCells
  91. Ginsberg SD, Price DL, Blackstone CD, Huganir RL, Martin LJ. The AMPA glutamate receptor GluR3 is enriched in oxytocinergic magnocellular neurons and is localized at synapses. Neuroscience. 1995 Mar; 65(2):563-75. PMID: 7777169.
    Citations: 8     Fields:    Translation:AnimalsCells
  92. Prince HK, Conn PJ, Blackstone CD, Huganir RL, Levey AI. Down-regulation of AMPA receptor subunit GluR2 in amygdaloid kindling. J Neurochem. 1995 Jan; 64(1):462-5. PMID: 7798948.
    Citations: 18     Fields:    Translation:AnimalsCells
  93. Craig AM, Blackstone CD, Huganir RL, Banker G. Selective clustering of glutamate and gamma-aminobutyric acid receptors opposite terminals releasing the corresponding neurotransmitters. Proc Natl Acad Sci U S A. 1994 Dec 20; 91(26):12373-7. PMID: 7809044; PMCID: PMC45440.
    Citations: 79     Fields:    Translation:AnimalsCells
  94. Paschen W, Blackstone CD, Huganir RL, Ross CA. Human GluR6 kainate receptor (GRIK2): molecular cloning, expression, polymorphism, and chromosomal assignment. Genomics. 1994 Apr; 20(3):435-40. PMID: 8034316.
    Citations: 18     Fields:    Translation:HumansAnimalsCells
  95. Hyman BT, Penney JB, Blackstone CD, Young AB. Localization of non-N-methyl-D-aspartate glutamate receptors in normal and Alzheimer hippocampal formation. Ann Neurol. 1994 Jan; 35(1):31-7. PMID: 8285589.
    Citations: 4     Fields:    Translation:Humans
  96. Raymond LA, Tingley WG, Blackstone CD, Roche KW, Huganir RL. Glutamate receptor modulation by protein phosphorylation. J Physiol Paris. 1994; 88(3):181-92. PMID: 7530547.
    Citations: 25     Fields:    Translation:HumansAnimalsCells
  97. Craig AM, Blackstone CD, Huganir RL, Banker G. The distribution of glutamate receptors in cultured rat hippocampal neurons: postsynaptic clustering of AMPA-selective subunits. Neuron. 1993 Jun; 10(6):1055-68. PMID: 7686378.
    Citations: 94     Fields:    Translation:AnimalsCells
  98. 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. J Neurosci. 1993 May; 13(5):2249-63. PMID: 8386757; PMCID: PMC6576585.
    Citations: 11     Fields:    Translation:AnimalsCells
  99. Raymond LA, Blackstone CD, Huganir RL. Phosphorylation of amino acid neurotransmitter receptors in synaptic plasticity. Trends Neurosci. 1993 Apr; 16(4):147-53. PMID: 7682348.
    Citations: 41     Fields:    Translation:HumansAnimalsCells
  100. Martin LJ, Blackstone CD, Levey AI, Huganir RL, Price DL. AMPA glutamate receptor subunits are differentially distributed in rat brain. Neuroscience. 1993 Mar; 53(2):327-58. PMID: 8388083.
    Citations: 104     Fields:    Translation:AnimalsCells
  101. Raymond LA, Blackstone CD, Huganir RL. Phosphorylation and modulation of recombinant GluR6 glutamate receptors by cAMP-dependent protein kinase. Nature. 1993 Feb 18; 361(6413):637-41. PMID: 8094892.
    Citations: 54     Fields:    Translation:HumansAnimalsCells
  102. Martin LJ, Blackstone CD, Huganir RL, Price DL. The striatal mosaic in primates: striosomes and matrix are differentially enriched in ionotropic glutamate receptor subunits. J Neurosci. 1993 Feb; 13(2):782-92. PMID: 7678861; PMCID: PMC6576641.
    Citations: 17     Fields:    Translation:AnimalsCells
  103. Moss SJ, Blackstone CD, Huganir RL. Phosphorylation of recombinant non-NMDA glutamate receptors on serine and tyrosine residues. Neurochem Res. 1993 Jan; 18(1):105-10. PMID: 7681938.
    Citations: 8     Fields:    Translation:HumansCells
  104. Milani D, Candeo P, Favaron M, Blackstone CD, Manev H. A subpopulation of cerebellar granule neurons in culture expresses a functional mGluR1 metabotropic glutamate receptor: effect of depolarizing growing conditions. Recept Channels. 1993; 1(3):243-50. PMID: 7922022.
    Citations: 1     Fields:    Translation:AnimalsCells
  105. Martin LJ, Blackstone CD, Huganir RL, Price DL. Cellular localization of a metabotropic glutamate receptor in rat brain. Neuron. 1992 Aug; 9(2):259-70. PMID: 1323311.
    Citations: 106     Fields:    Translation:AnimalsCells
  106. Moss SJ, Smart TG, Blackstone CD, Huganir RL. Functional modulation of GABAA receptors by cAMP-dependent protein phosphorylation. Science. 1992 Jul 31; 257(5070):661-5. PMID: 1323140.
    Citations: 64     Fields:    Translation:AnimalsCells
  107. Blackstone CD, Levey AI, Martin LJ, Price DL, Huganir RL. Immunological detection of glutamate receptor subtypes in human central nervous system. Ann Neurol. 1992 Jun; 31(6):680-3. PMID: 1325139.
    Citations: 9     Fields:    Translation:HumansAnimalsCells
  108. Swope SL, Moss SJ, Blackstone CD, Huganir RL. Phosphorylation of ligand-gated ion channels: a possible mode of synaptic plasticity. FASEB J. 1992 May; 6(8):2514-23. PMID: 1375568.
    Citations: 45     Fields:    Translation:AnimalsCells
  109. Blackstone CD, Moss SJ, Martin LJ, Levey AI, Price DL, Huganir RL. Biochemical characterization and localization of a non-N-methyl-D-aspartate glutamate receptor in rat brain. J Neurochem. 1992 Mar; 58(3):1118-26. PMID: 1371146.
    Citations: 61     Fields:    Translation:Animals
  110. Blackstone CD, Supattapone S, Snyder SH. Inositolphospholipid-linked glutamate receptors mediate cerebellar parallel-fiber-Purkinje-cell synaptic transmission. Proc Natl Acad Sci U S A. 1989 Jun; 86(11):4316-20. PMID: 2542969; PMCID: PMC287443.
    Citations: 18     Fields:    Translation:AnimalsCells
  111. Seino S, Blackstone CD, Chan SJ, Whittaker J, Bell GI, Steiner DF. Appalachian spring: variations on ancient gastro-entero-pancreatic themes in New World mammals. Horm Metab Res. 1988 Jul; 20(7):430-5. PMID: 2459041.
    Citations: 5     Fields:    Translation:AnimalsCells
  112. Blackstone CD, Seino S, Takeuchi T, Yamada T, Steiner DF. Novel organization and processing of the guinea pig pancreatic polypeptide precursor. J Biol Chem. 1988 Feb 25; 263(6):2911-6. PMID: 2830269.
    Citations: 1     Fields:    Translation:HumansAnimalsCells
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.