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Julien Couthouis

Showing results (1-10 of 34) with videos related to

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Neurology. Genetics|August 16, 2018
These violent repeats have violent extendsJulien Couthouis, Aaron D Gitler
Plos Genetics|October 10, 2014
Targeted exon capture and sequencing in sporadic amyotrophic lateral sclerosisJulien Couthouis, Alya R Raphael, Roxana Daneshjou, et al.
Prion|November 9, 2010
The toxicity of an "artificial" amyloid is related to how it interacts with membranesJulien Couthouis, Christelle Marchal, Fabien D'Angelo, et al.
Plos One|March 6, 2009
Screening for toxic amyloid in yeast exemplifies the role of alternative pathway responsible for cytotoxicityJulien Couthouis, Karine Rébora, Françoise Immel, et al.
Brain Research|May 1, 2014
Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutationsAlya R Raphael, Julien Couthouis, Sarada Sakamuri, et al.
Nature Communications|July 29, 2020
Knockout of reactive astrocyte activating factors slows disease progression in an ALS mouse modelKevin A Guttenplan, Maya K Weigel, Drew I Adler, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 28, 2020
Age-related loss of neural stem cell O-GlcNAc promotes a glial fate switch through STAT3 activationCharles W White, Xuelai Fan, Jason C Maynard, et al.
Brain Research|December 18, 2019
Genome-wide synthetic lethal CRISPR screen identifies FIS1 as a genetic interactor of ALS-linked C9ORF72Noori Chai, Michael S Haney, Julien Couthouis, et al.
Cell Reports|October 26, 2022
Genome-wide CRISPR screen reveals v-ATPase as a drug target to lower levels of ALS protein ataxin-2Garam Kim, Lisa Nakayama, Jacob A Blum, et al.
Neuromuscular Disorders : NMD|March 6, 2014
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophyJulien Couthouis, Alya R Raphael, Carly Siskind, et al.
Pageof 4

Showing results (1-10 of 34) with videos related to

Sort By:
Pageof 4
Neurology. Genetics|August 16, 2018
These violent repeats have violent extendsJulien Couthouis, Aaron D Gitler
Plos Genetics|October 10, 2014
Targeted exon capture and sequencing in sporadic amyotrophic lateral sclerosisJulien Couthouis, Alya R Raphael, Roxana Daneshjou, et al.
Prion|November 9, 2010
The toxicity of an "artificial" amyloid is related to how it interacts with membranesJulien Couthouis, Christelle Marchal, Fabien D'Angelo, et al.
Plos One|March 6, 2009
Screening for toxic amyloid in yeast exemplifies the role of alternative pathway responsible for cytotoxicityJulien Couthouis, Karine Rébora, Françoise Immel, et al.
Brain Research|May 1, 2014
Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutationsAlya R Raphael, Julien Couthouis, Sarada Sakamuri, et al.
Nature Communications|July 29, 2020
Knockout of reactive astrocyte activating factors slows disease progression in an ALS mouse modelKevin A Guttenplan, Maya K Weigel, Drew I Adler, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 28, 2020
Age-related loss of neural stem cell O-GlcNAc promotes a glial fate switch through STAT3 activationCharles W White, Xuelai Fan, Jason C Maynard, et al.
Brain Research|December 18, 2019
Genome-wide synthetic lethal CRISPR screen identifies FIS1 as a genetic interactor of ALS-linked C9ORF72Noori Chai, Michael S Haney, Julien Couthouis, et al.
Cell Reports|October 26, 2022
Genome-wide CRISPR screen reveals v-ATPase as a drug target to lower levels of ALS protein ataxin-2Garam Kim, Lisa Nakayama, Jacob A Blum, et al.
Neuromuscular Disorders : NMD|March 6, 2014
Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophyJulien Couthouis, Alya R Raphael, Carly Siskind, et al.
Pageof 4