Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Sclerosis and TSFM[original query] |
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Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genes. Human mutation 2020 Mar . Gil-Varea Elia, Spataro Nino, Villar Luisa María, Tejeda-Velarde Amalia, Midaglia Luciana, Matesanz Fuencisla, Malhotra Sunny, Eixarch Herena, Patsopoulos Nikolaos, Fernández Óscar, Oliver-Martos Begoña, Saiz Albert, Llufriu Sara, Ramió-Torrentà Lluís, Quintana Ester, Izquierdo Guillermo, Alcina Antonio, Bosch Elena, Navarro Arcadi, Montalban Xavier, Comabella Manu |
A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells. Journal of clinical medicine 2020 Feb 9 (3): . Gil-Varea Elia, Fedetz Maria, Eixarch Herena, Spataro Nino, Villar Luisa María, Urcelay Elena, Saiz Albert, Fernández Óscar, Leyva Laura, Ramió-Torrentà Lluís, Vandenbroeck Koen, Otaegui David, Castillo-Triviño Tamara, Izquierdo Guillermo, Malhotra Sunny, Bosch Elena, Navarro Arcadi, Alcina Antonio, Montalban Xavier, Matesanz Fuencisla, Comabella Manu |
Genetic risk variants for multiple sclerosis are linked to differences in alternative pre-mRNA splicing. Frontiers in immunology 2022 11 13 931831. Putscher Elena, Hecker Michael, Fitzner Brit, Boxberger Nina, Schwartz Margit, Koczan Dirk, Lorenz Peter, Zettl Uwe Kla |
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