Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: TAF15[original query] |
---|
Mutational analysis reveals the FUS homolog TAF15 as a candidate gene for familial amyotrophic lateral sclerosis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Apr 156B (3): 285-90. Ticozzi N, Vance C, Leclerc A L, Keagle P, Glass J D, McKenna-Yasek D, Sapp P C, Silani V, Bosco D A, Shaw C E, Brown R H, Landers J |
Distinct and shared functions of ALS-associated proteins TDP-43, FUS and TAF15 revealed by multisystem analyses. Nature communications 2016 7 12143. Kapeli Katannya, Pratt Gabriel A, Vu Anthony Q, Hutt Kasey R, Martinez Fernando J, Sundararaman Balaji, Batra Ranjan, Freese Peter, Lambert Nicole J, Huelga Stephanie C, Chun Seung J, Liang Tiffany Y, Chang Jeremy, Donohue John P, Shiue Lily, Zhang Jiayu, Zhu Haining, Cambi Franca, Kasarskis Edward, Hoon Shawn, Ares Manuel, Burge Christopher B, Ravits John, Rigo Frank, Yeo Gene |
Analysis of known amyotrophic lateral sclerosis and frontotemporal dementia genes reveals a substantial genetic burden in patients manifesting both diseases not carrying the C9orf72 expansion mutation. Journal of neurology, neurosurgery, and psychiatry 2017 9 89 (2): 162-168. Dols-Icardo Oriol, García-Redondo Alberto, Rojas-García Ricardo, Borrego-Hernández Daniel, Illán-Gala Ignacio, Muñoz-Blanco José Luís, Rábano Alberto, Cervera-Carles Laura, Juárez-Rufián Alexandra, Spataro Nino, De Luna Noemí, Galán Lucía, Cortes-Vicente Elena, Fortea Juan, Blesa Rafael, Grau-Rivera Oriol, Lleó Alberto, Esteban-Pérez Jesús, Gelpi Ellen, Clarimón Jor |
Interactome analyses revealed that the U1 snRNP machinery overlaps extensively with the RNAP II machinery and contains multiple ALS/SMA-causative proteins. Scientific reports 2018 6 8 (1): 8755. Chi Binkai, O'Connell Jeremy D, Yamazaki Tomohiro, Gangopadhyay Jaya, Gygi Steven P, Reed Rob |
Genetic Spectrum and Variability in Chinese Patients with Amyotrophic Lateral Sclerosis. Aging and disease 2019 Dec 10 (6): 1199-1206. Liu Zhi-Jun, Lin Hui-Xia, Wei Qiao, Zhang Qi-Jie, Chen Cong-Xin, Tao Qing-Qing, Liu Gong-Lu, Ni Wang, Gitler Aaron D, Li Hong-Fu, Wu Zhi-Yi |
Mixed model-based eQTL analysis reveals lncRNAs associated with regulation of genes involved in sex determination and spermatogenesis: The key to understanding human gender imbalance. Computational biology and chemistry 2022 6 99 107713. An Yeeun, Lee Chaeyou |
Genotype-phenotype characterisation of long survivors with motor neuron disease in Scotland. Journal of neurology 2022 12 . Leighton Danielle J, Ansari Morad, Newton Judith, Parry David, Cleary Elaine, Colville Shuna, Stephenson Laura, Larraz Juan, Johnson Micheala, Beswick Emily, Wong Michael, Gregory Jenna, Carod Artal Javier, Davenport Richard, Duncan Callum, Morrison Ian, Smith Colin, Swingler Robert, Deary Ian J, Porteous Mary, Aitman Timothy J, Chandran Siddharthan, Gorrie George H, Pal Suvankar, , |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: