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Neuron
|
December 14, 2019
Antibody Therapy Targeting RAN Proteins Rescues C9 ALS/FTD Phenotypes in C9orf72 Mouse Model
Lien Nguyen, Fabio Montrasio, Amrutha Pattamatta, et al.
Neuron
|
December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALS
Janel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Neuron
|
February 7, 2020
Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors
Lin Luo, Mateusz C Ambrozkiewicz, Fritz Benseler, et al.
Human Molecular Genetics
|
February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
Adriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Molecular & Cellular Proteomics : MCP
|
March 15, 2025
Comprehensive proteomics metadata and integrative web portals facilitate sharing and integration of LINCS multiomics data
Dušica Vidović, Behrouz Shamsaei, Stephan C Schürer, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 4, 2013
ALS Untangled No. 20: the Deanna protocol
, Christina Fournier, Bedlack Bedlack, et al.
Molecular & Cellular Proteomics : MCP
|
August 9, 2025
Corrigendum to "Comprehensive Proteomics Metadata and Integrative Web Portals Facilitate Sharing and Integration of LINCS Multiomics Data"
Dušica Vidović, Behrouz Shamsaei, Stephan C Schürer, et al.
Cell Systems
|
December 5, 2017
The Library of Integrated Network-Based Cellular Signatures NIH Program: System-Level Cataloging of Human Cells Response to Perturbations
Alexandra B Keenan, Sherry L Jenkins, Kathleen M Jagodnik, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Neuron
|
December 14, 2019
Antibody Therapy Targeting RAN Proteins Rescues C9 ALS/FTD Phenotypes in C9orf72 Mouse Model
Lien Nguyen, Fabio Montrasio, Amrutha Pattamatta, et al.
Neuron
|
December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALS
Janel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Neuron
|
February 7, 2020
Optimizing Nervous System-Specific Gene Targeting with Cre Driver Lines: Prevalence of Germline Recombination and Influencing Factors
Lin Luo, Mateusz C Ambrozkiewicz, Fritz Benseler, et al.
Human Molecular Genetics
|
February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosis
Adriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Molecular & Cellular Proteomics : MCP
|
March 15, 2025
Comprehensive proteomics metadata and integrative web portals facilitate sharing and integration of LINCS multiomics data
Dušica Vidović, Behrouz Shamsaei, Stephan C Schürer, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
May 4, 2013
ALS Untangled No. 20: the Deanna protocol
, Christina Fournier, Bedlack Bedlack, et al.
Molecular & Cellular Proteomics : MCP
|
August 9, 2025
Corrigendum to "Comprehensive Proteomics Metadata and Integrative Web Portals Facilitate Sharing and Integration of LINCS Multiomics Data"
Dušica Vidović, Behrouz Shamsaei, Stephan C Schürer, et al.
Cell Systems
|
December 5, 2017
The Library of Integrated Network-Based Cellular Signatures NIH Program: System-Level Cataloging of Human Cells Response to Perturbations
Alexandra B Keenan, Sherry L Jenkins, Kathleen M Jagodnik, et al.
Page
of 3