Výsledky vyhledávání - Brett J Winborn
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The Deubiquitinating Enzyme Ataxin-3, a Polyglutamine Disease Protein, Edits Lys63 Linkages in Mixed Linkage Ubiquitin Chains Autor Brett J Winborn, Sue M. Travis, Sokol V. Todi, K. Matthew Scaglione, Ping Xu, Aislinn Williams, Robert E. Cohen, Junmin Peng, Henry L. Paulson
Vydáno 2008Artigo -
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Nuclear ULK1 promotes cell death in response to oxidative stress through PARP1 Autor Aashish Joshi, Rekha Iyengar, Joung Hyuck Joo, XiuJie Li-Harms, C. David Wright, Roberta Marino, Brett J Winborn, Aaron H. Phillips, Jamshid Temirov, Sebastiano Sciarretta, Richard W. Kriwacki, Junmin Peng, Anang A. Shelat, Mondira Kundu
Vydáno 2015Artigo -
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VCP Is Essential for Mitochondrial Quality Control by PINK1/Parkin and this Function Is Impaired by VCP Mutations Autor Nam Chul Kim, Emilie Tresse, Regina-Maria Kolaitis, Amandine Molliex, Ruth Thomas, Nael H. Alami, Bo Wang, Aashish Joshi, Rebecca B. Smith, Gillian P. Ritson, Brett J Winborn, Jennifer C. Moore, Joo‐Yong Lee, Tso-Pang Yao, Leo J. Pallanck, Mondira Kundu, J. Paul Taylor
Vydáno 2013Artigo -
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Axonal Transport of TDP-43 mRNA Granules Is Impaired by ALS-Causing Mutations Autor Nael H. Alami, Rebecca B. Smith, Mónica A. Carrasco, Luis A. Williams, Christina S. Winborn, Steve S.W. Han, Evangelos Kiskinis, Brett J Winborn, Brian D. Freibaum, Anderson Kanagaraj, Alison J. Clare, Nisha M. Badders, Bilada Bilican, Edward Chaum, Siddharthan Chandran, Christopher E. Shaw, Kevin Eggan, Tom Maniatis, J. Paul Taylor
Vydáno 2014Artigo -
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Selective modulation of the androgen receptor AF2 domain rescues degeneration in spinal bulbar muscular atrophy Autor Nisha M. Badders, Ané Korff, Helen C. Miranda, Pradeep K. Vuppala, Rebecca B. Smith, Brett J Winborn, Emmanuelle R. J. Quemin, Bryce L. Sopher, Jennifer Dearman, James Messing, Nam Chul Kim, Jennifer C. Moore, Brian D. Freibaum, Anderson Kanagaraj, Baochang Fan, Heather Tillman, Ping-Chung Chen, Yingzhe Wang, Burgess B. Freeman, Yimei Li, Hong Joo Kim, Albert R. La Spada, J. Paul Taylor
Vydáno 2018Artigo -
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Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis Autor Janel O. Johnson, Erik P. Pioro, Ashley Boehringer, Ruth Chia, Howard Feit, Alan E. Renton, Hannah A. Pliner, Yevgeniya Abramzon, Giuseppe Marangi, Brett J Winborn, J. Raphael Gibbs, Michael A. Nalls, Sarah Morgan, Maryam Shoai, John Hardy, Alan Pittman, Richard W. Orrell, Andrea Malaspina, Katie Sidle, Pietro Fratta, Matthew B. Harms, Robert H. Baloh, Alan Pestronk, Conrad C. Weihl, Ekaterina Rogaeva, Lorne Zinman, Vivian E. Drory, Giuseppe Borghero, Gabriele Mora, Andrea Calvo, Jeffrey D. Rothstein, Carsten Drepper, Michael Sendtner, Andrew Singleton, J. Paul Taylor, Mark Cookson, Gabriella Restagno, Mario Sabatelli, Robert Bowser, Adriano Chió, Bryan J. Traynor
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Biology
Cell biology
Gene
Biochemistry
Disease
Genetics
Medicine
Neuroscience
Ubiquitin
Apoptosis
Autophagy
Chemistry
Deubiquitinating enzyme
Motor neuron
Mutant
Mutation
Pathology
Proteasome
AMPK
Amino acid
Amyotrophic lateral sclerosis
Androgen
Androgen receptor
Atrophy
Axoplasmic transport
C-terminus
Cancer
DNA
DNA damage
Dementia