E-LIB Suche - Ergebnisse für: Eitan, Chen

1

Whole-genome sequencing reveals that variants in the Interl..:

Eitan, Chen ; Siany, Aviad ; Barkan, Elad...
Nature Neuroscience. 25 (2022) 4 - p. 433-445 , 2022

Link: https://doi.org/10.1038/..

2

Genome-wide identification of the genetic basis of amyotrop..:

Zhang, Sai ; Cooper-Knock, Johnathan ; Weimer, Annika K....
Neuron. 110 (2022) 6 - p. 992-1008.e11 , 2022

Link: https://doi.org/10.1016/..

3

Rare variant burden analysis within enhancers identifies CA..:

Cooper-Knock, Johnathan ; Zhang, Sai ; Kenna, Kevin P....
Cell Reports. 34 (2021) 5 - p. 108730 , 2021

Link: https://doi.org/10.1016/..

4

Rare Variant Burden Analysis within Enhancers Identifies CA..:

Cooper-Knock, Johnathan ; Zhang, Sai ; Kenna, Kevin P....
Cell Reports. 33 (2020) 9 - p. 108456 , 2020

Link: https://doi.org/10.1016/..

5

Vulnerability of microRNA biogenesis in FTD–ALS:

Eitan, Chen ; Hornstein, Eran
Brain Research. 1647 (2016) - p. 105-111 , 2016

Link: https://doi.org/10.1016/..

6

Dysregulated miRNAbiogenesis downstream of cellular stress ..:

Emde, Anna ; Eitan, Chen ; Liou, Lee‐Loung...
The EMBO Journal. 34 (2015) 21 - p. 2633-2651 , 2015

Link: https://doi.org/10.15252..

7

Astro‐logics with microRNAs:

Eitan, Chen ; Hornstein, Eran
The EMBO Journal. 34 (2015) 9 - p. 1143-1144 , 2015

Link: https://doi.org/10.15252..

8

MicroRNA-19b Associates with Ago2 in the Amygdala Following..:

Volk, Naama ; Paul, Evan D. ; Haramati, Sharon...
The Journal of Neuroscience. 34 (2014) 45 - p. 15070-15082 , 2014

Link: https://doi.org/10.1523/..

9

Whole-genome sequencing reveals that variants in the Interl..:

Eitan, Chen ; Siany, Aviad ; Barkan, Elad...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7614916/. , 2022

Link: http://www.ncbi.nlm.nih...

10

Genome-wide Identification of the Genetic Basis of Amyotrop..:

Zhang, Sai ; Cooper-Knock, Johnathan ; Weimer, Annika K...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9017397/. , 2022

Link: http://www.ncbi.nlm.nih...

11

Genome-wide identification of the genetic basis of amyotrop..:

Zhang, Sai ; Cooper-Knock, Johnathan ; Weimer, Annika K...
Zhang, S., Cooper-Knock, J., Weimer, A. K., Shi, M., Moll, T., Marshall, J. N., . & Snyder, M. P. (2022). Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. Neuron, 110(6), 992-1008.. , 2022

Link: https://www.um.edu.mt/li..

12

Rare Variant Burden Analysis within Enhancers Identifies CA..:

Cooper-Knock, Johnathan ; Zhang, Sai ; Kenna, Kevin P...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7710676/. , 2020

Link: http://www.ncbi.nlm.nih...

13

Rare variant burden analysis within enhancers identifies CA..:

Cooper-Knock, Johnathan ; Zhang, Sai ; Kenna, Kevin P...
Cooper-Knock, J., Zhang, S., Kenna, K. P., Moll, T., Franklin, J. P., Allen, S.,.Shaw, P. J. (2020). Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene. Cell reports, 33(9), 108456.. , 2020

Link: https://www.um.edu.mt/li..

14

Spatiotemporal Proteomic Analysis of Stress Granule Disasse..:

Marmor-Kollet, Hagai ; Siany, Aviad ; Kedersha, Nancy...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7816607/. , 2020

Link: http://www.ncbi.nlm.nih...

15

Human genetics and neuropathology suggest a link between mi..:

Reichenstein, Irit ; Eitan, Chen ; Diaz-Garcia, Sandra...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7057809/. , 2019

Link: http://www.ncbi.nlm.nih...