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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 14, 2024. (Total: 234362Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Sclerosis and EPHA4[original query]
Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genes.
Multiple sclerosis (Houndmills, Basingstoke, England) 2011 Dec .
Varadé J, Comabella M, Ortiz MA, Arroyo R, Fernández O, Pinto-Medel MJ, Fedetz M, Izquierdo G, Lucas M, López Gómez C, Catalá Rabasa A, Alcina A, Matesanz F, Alloza I, Antigüedad A, García-Barcina M, Otaegui D, Olascoaga J, Saiz A, Blanco Y, Montalbán X, Vandenbroeck K, Urcelay E
Genome-wide copy number variation in sporadic amyotrophic lateral sclerosis in the Turkish population: deletion of EPHA3 is a possible protective factor.
PloS one 2013 8 (8): e72381.
Uyan Özgün, Ömür Özgür, A??m Zeynep Sena, Özo?uz Asl?han, Li Hong, Parman Ye?im, Deymeer Feza, Oflazer Piraye, Koç Filiz, Tan Ersin, Özçelik Hilmi, Ba?ak A Naz
Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis & frontotemporal degeneration 2016 Sep 1-7.
Gaastra Benjamin, Shatunov Aleksey, Pulit Sara, Jones Ashley R, Sproviero William, Gillett Alexandra, Chen Zhongbo, Kirby Janine, Fogh Isabella, Powell John F, Leigh P Nigel, Morrison Karen E, Shaw Pamela J, Shaw Christopher E, van den Berg Leonard H, Veldink Jan H, Lewis Cathryn M, Al-Chalabi Amm
Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosis.
Cellular and molecular life sciences : CMLS 2024 7 81 (1): 316.
Maria Guarnaccia, Giovanna Morello, Valentina La Cognata, Vincenzo La Bella, Francesca Luisa Conforti, Sebastiano Cavalla
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