Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Sclerosis and CXCR5[original query] |
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| MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain : a journal of neurology 2013 Jun 136 (Pt 6): 1778-82. , Lill Christina M, Schjeide Brit-Maren M, Graetz Christine, Ban Maria, Alcina Antonio, Ortiz Miguel A, Pérez Jennifer, Damotte Vincent, Booth David, Lopez de Lapuente Aitzkoa, Broer Linda, Schilling Marcel, Akkad Denis A, Aktas Orhan, Alloza Iraide, Antigüedad Alfredo, Arroyo Rafa, Blaschke Paul, Buttmann Mathias, Chan Andrew, Compston Alastair, Cournu-Rebeix Isabelle, Dörner Thomas, Epplen Joerg T, Fernández Óscar, Gerdes Lisa-Ann, Guillot-Noël Léna, Hartung Hans-Peter, Hoffjan Sabine, Izquierdo Guillermo, Kemppinen Anu, Kroner Antje, Kubisch Christian, Kümpfel Tania, Li Shu-Chen, Lindenberger Ulman, Lohse Peter, Lubetzki Catherine, Luessi Felix, Malhotra Sunny, Mescheriakova Julia, Montalban Xavier, Papeix Caroline, Paredes Lidia F, Rieckmann Peter, Steinhagen-Thiessen Elisabeth, Winkelmann Alexander, Zettl Uwe K, Hintzen Rogier, Vandenbroeck Koen, Stewart Graeme, Fontaine Bertrand, Comabella Manuel, Urcelay Elena, Matesanz Fuencisla, Sawcer Stephen, Bertram Lars, Zipp Frau |
| A survey of endogenous retrovirus (ERV) sequences in the vicinity of multiple sclerosis (MS)-associated single nucleotide polymorphisms (SNPs). Molecular biology reports 2016 May . Brütting Christine, Emmer Alexander, Kornhuber Malte, Staege Martin |
| A genetic link between CXCR5 and IL2RA gene polymorphisms and susceptibility to multiple sclerosis. Neurological research 2018 Dec 40 (12): 1040-1047. Xia Zong-Li, Qin Qing-Mei, Zhao Qing-Yi |
| 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 |
| A common genetic variant rs2821557 in KCNA3 is linked to the severity of multiple sclerosis. Journal of neuroscience research 2020 Feb . Lioudyno Victoria, Abdurasulova Irina, Negoreeva Irina, Stoliarov Igor, Kudriavtsev Igor, Serebryakova Maria, Klimenko Victor, Lioudyno Mar |
| Several genetic variants associated with systemic sclerosis in a Chinese Han population. Clinical rheumatology 2022 10 42 (3): 773-781. Liu Chenxi, Yan Songxin, Chen Haizhen, Wu Ziyan, Li Liubing, Li Yongz |
| Functional genomics in primary T cells and monocytes identifies mechanisms by which genetic susceptibility loci influence systemic sclerosis risk. Arthritis & rheumatology (Hoboken, N.J.) 2022 10 . González-Serna David, Shi Chenfu, Kerick Martin, Hankinson Jenny, Ding James, McGovern Amanda, Tutino Mauro, Villanueva Martin Gonzalo, Ortego-Centeno Norberto, Callejas José Luis, Martin Javier, Orozco Gise |
- Page last reviewed:Feb 1, 2024
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