Couthouis, Julien: search on Z-Library

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1

LRRK2 modifies α-syn pathology and spread in mouse models and human neurons

Bieri, Gregor, Brahic, Michel, Bousset, Luc, Couthouis, Julien, Kramer, Nicholas J., Ma, Rosanna, Nakayama, Lisa, Monbureau, Marie, Defensor, Erwin, Schüle, Birgitt, Shamloo, Mehrdad, Melki, Ronald, G

Journal:

Acta Neuropathologica

Year:

2019

Language:

english

File:

PDF, 11.75 MB

english, 2019

2

Exome sequencing identifies a DNAJB6 mutation in a family with dominantly-inherited limb-girdle muscular dystrophy

Couthouis, Julien, Raphael, Alya R., Siskind, Carly, Findlay, Andrew R., Buenrostro, Jason D., Greenleaf, William J., Vogel, Hannes, Day, John W., Flanigan, Kevin M., Gitler, Aaron D.

Journal:

Neuromuscular Disorders

Year:

2014

Language:

english

File:

PDF, 1.30 MB

english, 2014

3

PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista Junctions

Tsai, Pei-I, Lin, Chin-Hsien, Hsieh, Chung-Han, Papakyrikos, Amanda M., Kim, Min Joo, Napolioni, Valerio, Schoor, Carmen, Couthouis, Julien, Wu, Ruey-Meei, Wszolek, Zbigniew K., Winter, Dominic, Greic

Journal:

Year:

2018

Language:

english

File:

PDF, 5.85 MB

english, 2018

4

A memory of eS25 loss drives resistance phenotypes

Johnson, Alex G, Flynn, Ryan A, Lapointe, Christopher P, Ooi, Yaw Shin, Zhao, Michael L, Richards, Christopher M, Qiao, Wenjie, Yamada, Shizuka B, Couthouis, Julien, Gitler, Aaron D, Carette, Jan E, P

Journal:

Nucleic Acids Research

Year:

2020

File:

PDF, 5.89 MB

2020

5

Genome-wide synthetic lethal CRISPR screen identifies FIS1 as a genetic interactor of ALS-linked C9ORF72

Chai, Noori, Haney, Michael S., Couthouis, Julien, Morgens, David W., Benjamin, Alyssa, Wu, Kathryn, Ousey, James, Fang, Shirleen, Finer, Sarah, Bassik, Michael C., Gitler, Aaron D.

Journal:

Year:

2019

File:

PDF, 684 KB

2019

6

Knockout of reactive astrocyte activating factors slows disease progression in an ALS mouse model

Guttenplan, Kevin A., Weigel, Maya K., Adler, Drew I., Couthouis, Julien, Liddelow, Shane A., Gitler, Aaron D., Barres, Ben A.

Journal:

Nature Communications

Year:

2020

File:

PDF, 3.99 MB

2020

7

Age-related loss of neural stem cell O-GlcNAc promotes a glial fate switch through STAT3 activation

White, Charles W., Fan, Xuelai, Maynard, Jason C., Wheatley, Elizabeth G., Bieri, Gregor, Couthouis, Julien, Burlingame, Alma L., Villeda, Saul A.

Journal:

Proceedings of the National Academy of Sciences

Year:

2020

File:

PDF, 2.17 MB

2020

8

Congenital muscular dystrophy and generalized epilepsy caused by GMPPB mutations

Raphael, Alya R., Couthouis, Julien, Sakamuri, Sarada, Siskind, Carly, Vogel, Hannes, Day, John W., Gitler, Aaron D.

Journal:

Year:

2014

Language:

english

File:

PDF, 3.87 MB

english, 2014

9

CRISPR–Cas9 screens in human cells and primary neurons identify modifiers of C9ORF72 dipeptide-repeat-protein toxicity

Kramer, Nicholas J., Haney, Michael S., Morgens, David W., Jovičić, Ana, Couthouis, Julien, Li, Amy, Ousey, James, Ma, Rosanna, Bieri, Gregor, Tsui, C. Kimberly, Shi, Yingxiao, Hertz, Nicholas T., Tes

Journal:

Nature Genetics

Year:

2018

Language:

english

File:

PDF, 3.58 MB

english, 2018

10

The toxicity of an “artificial” amyloid is related to how it interacts with membranes

Couthouis, Julien, Marchal, Christelle, D’Angelo, Fabien, Berthelot, Karine, Cullin, Christophe

Journal:

Year:

2010

Language:

english

File:

PDF, 1.69 MB

english, 2010

11

NOVEL MISSENSE VARIANT ON EPHA1 IN A PROTECTED APOE4 FAMILY

Khan, Raiyan R., Altmann, Andre, Kim, Lily H., Couthouis, Julien, Napolioni, Valerio, Gitler, Aaron D., Greicius, Michael D.

Journal:

Alzheimer's & Dementia

Year:

2017

Language:

english

File:

PDF, 458 KB

english, 2017

12

RARE MISSENSE VARIANTS ON ZNF679 AND CTD-3214H19.16 SEGREGATE IN A FAMILY WITH A HISTORY OF SYNUCLEINOPATHY

Kim, Yongha, Khan, Raiyan R., Kim, Lily H., Couthouis, Julien, Gitler, Aaron D., Channappa, Divya, Plowey, Edward D., Napolioni, Valerio, Greicius, Michael D.

Journal:

Alzheimer's & Dementia

Year:

2018

Language:

english

File:

PDF, 289 KB

english, 2018

13

Targeted Exon Capture and Sequencing in Sporadic Amyotrophic Lateral Sclerosis

Couthouis, Julien, Raphael, Alya R., Daneshjou, Roxana, Gitler, Aaron D., Gibson, Greg

Journal:

Year:

2014

Language:

english

File:

PDF, 726 KB

english, 2014

14

These violent repeats have violent extends

Couthouis, Julien, Gitler, Aaron D.

Journal:

Neurology: Genetics

Year:

2018

File:

PDF, 153 KB

2018

15

IDENTIFICATION OF AN ITGA7 VARIANT ASSOCIATED WITH ALZHEIMER’S DISEASE AND MULTIPLE OTHER NEURODEGENERATIVE DISEASES

Khan, Raiyan R., Napolioni, Valerio, Altmann, Andre, Seeley, William W., Montine, Thomas J., Coppola, Giovanni, Chen, Jason A., Plowey, Edward D., Channappa, Divya, Gitler, Aaron D., Couthouis, Julien

Journal:

Alzheimer's & Dementia

Year:

2017

Language:

english

File:

PDF, 720 KB

english, 2017

16

A yeast functional screen predicts new candidate ALS disease genes

Julien Couthouis, Michael P. Hart, James Shorter, Mariely DeJesus-Hernandez, Renske Erion, Rachel Oristano, Annie X. Liu, Daniel Ramos, Niti Jethava, Divya Hosangadi, James Epstein, Ashley Chiang, Zam

Journal:

Proceedings of the National Academy of Sciences

Year:

2011

Language:

english

File:

PDF, 2.84 MB

english, 2011

17

Evolution of a Human-Specific Tandem Repeat Associated with ALS

Course, Meredith M., Gudsnuk, Kathryn, Smukowski, Samuel N., Winston, Kosuke, Desai, Nitin, Ross, Jay P., Sulovari, Arvis, Bourassa, Cynthia V., Spiegelman, Dan, Couthouis, Julien, Yu, Chang-En, Tsuan

Journal:

The American Journal of Human Genetics

Year:

2020

File:

PDF, 2.25 MB

2020

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