Resultats de la cerca - Ryan T. Libby
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Sporadic ALS has compartment-specific aberrant exon splicing and altered cell–matrix adhesion biology per Stuart J. Rabin, Jae Mun Kim, Michael W. Baughn, Ryan T. Libby, Young Joo Kim, Yuxin Fan, Randell T. Libby, Albert La Spada, Brad Stone, John Ravits
Publicat 2009Artigo -
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Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis per Matthew B. Harms, Janet Cady, Craig M. Zaidman, Paul Cooper, Taha Bali, Peggy Allred, Carlos Cruchaga, Michael W. Baughn, Ryan T. Libby, Alan Pestronk, Alison Goate, John Ravits, Robert H. Baloh
Publicat 2013Artigo -
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Dysregulated mi <scp>RNA</scp> biogenesis downstream of cellular stress and <scp>ALS</scp> ‐causing mutations: a new mechanism for <scp>ALS</scp> per Anna Emde, Chen Eitan, Lee‐Loung Liou, Ryan T. Libby, Natali Rivkin, Iddo Magen, Irit Reichenstein, Hagar Oppenheim, Raya Eilam, Aurelio Silvestroni, Betty Alajajian, Iddo Z. Ben‐Dov, Julianne Aebischer, Alon Savidor, Yishai Levin, Robert Sons, Scott M. Hammond, John Ravits, Thomas Möller, Eran Hornstein
Publicat 2015Artigo -
4
Transcriptome–pathology correlation identifies interplay between TDP-43 and the expression of its kinase CK1E in sporadic ALS per Florian Krach, Ranjan Batra, Emily C. Wheeler, Anthony Q. Vu, Ruth Wang, Kasey R. Hutt, Stuart J. Rabin, Michael W. Baughn, Ryan T. Libby, Sandra Díaz-García, Jennifer E. Stauffer, Elaine Pirie, Shahram Saberi, Maria José Gómez-Rodríguez, Assael A. Madrigal, Zacharias Kohl, Beate Winner, G Yeo, John Ravits
Publicat 2018Artigo
Eines de cerca:
Matèries relacionades
Biology
Gene
Genetics
Amyotrophic lateral sclerosis
Cell biology
Disease
Gene expression
Laser capture microdissection
Medicine
Molecular biology
Neurodegeneration
RNA
RNA splicing
Allele
Alternative splicing
C9orf72
Cajal body
Cell
Cell adhesion
Coding region
Computer science
Dementia
Exon
Frontotemporal dementia
Gain of function
Gene expression profiling
Internal medicine
Library science
Loss function
Mutation