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pro vyhledávání: '"Haley S. Smith"'
Autor:
Juan A. Ortega, Christopher J. Donnelly, Marisa Samani, Haley S. Smith, Elizabeth L. Daley, Evangelos Kiskinis, Sukhleen Kour, Elizabeth A. H. Hall, Jeffrey N. Savas, Yung Hsu Tsai, Teepu Siddique, Tania F. Gendron, Udai Bhan Pandey, Y. Taylan Esengul, Liana Tellez
SUMMARYThe most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) is a hexanucleotide repeat expansion in C9orf72 (C9-HRE). While RNA and dipeptide repeats produced by the C9-HRE disrupt nucleocytoplasmic t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e944948dbf3037afb7b2ef895da761e
https://doi.org/10.1101/677419
https://doi.org/10.1101/677419
Autor:
Tania F. Gendron, Liana Tellez, Elizabeth L. Daley, Elizabeth A. H. Hall, Jeffrey N. Savas, Sukhleen Kour, Udai Bhan Pandey, Y. Taylan Esengul, Marisa Samani, Yung Hsu Tsai, Evangelos Kiskinis, Haley S. Smith, Christopher J. Donnelly, Teepu Siddique, Juan A. Ortega
Publikováno v:
Neuron. 106:90-107.e13
Summary The most common genetic cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) is a hexanucleotide repeat expansion in C9orf72 (C9-HRE). While RNA and dipeptide repeats produced by C9-HRE disrupt nucleocytoplasmic tran