108 related articles for article (PubMed ID: 24740369)
1. Exome sequencing in single cells from the cerebrospinal fluid in multiple sclerosis.
Kemppinen AK; Baker A; Liao W; Fiddes B; Jones J; Compston A; Ban M; Sawcer S
Mult Scler; 2014 Oct; 20(12):1564-8. PubMed ID: 24740369
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene.
Dyment DA; Cader MZ; Chao MJ; Lincoln MR; Morrison KM; Disanto G; Morahan JM; De Luca GC; Sadovnick AD; Lepage P; Montpetit A; Ebers GC; Ramagopalan SV
Neurology; 2012 Jul; 79(5):406-11. PubMed ID: 22744673
[TBL] [Abstract][Full Text] [Related]
3. The CD6 multiple sclerosis susceptibility allele is associated with alterations in CD4+ T cell proliferation.
Kofler DM; Severson CA; Mousissian N; De Jager PL; Hafler DA
J Immunol; 2011 Sep; 187(6):3286-91. PubMed ID: 21849685
[TBL] [Abstract][Full Text] [Related]
4. Intrathecal somatic hypermutation of IgM in multiple sclerosis and neuroinflammation.
Beltrán E; Obermeier B; Moser M; Coret F; Simó-Castelló M; Boscá I; Pérez-Miralles F; Villar LM; Senel M; Tumani H; Hohlfeld R; Casanova B; Dornmair K
Brain; 2014 Oct; 137(Pt 10):2703-14. PubMed ID: 25060097
[TBL] [Abstract][Full Text] [Related]
5. Successful Replication of GWAS Hits for Multiple Sclerosis in 10,000 Germans Using the Exome Array.
Dankowski T; Buck D; Andlauer TF; Antony G; Bayas A; Bechmann L; Berthele A; Bettecken T; Chan A; Franke A; Gold R; Graetz C; Haas J; Hecker M; Herms S; Infante-Duarte C; Jöckel KH; Kieseier BC; Knier B; Knop M; Kümpfel T; Lichtner P; Lieb W; Lill CM; Limmroth V; Linker RA; Loleit V; Meuth SG; Moebus S; Müller-Myhsok B; Nischwitz S; Nöthen MM; Paul F; Pütz M; Ruck T; Salmen A; Stangel M; Stellmann JP; Strauch K; Stürner KH; Tackenberg B; Then Bergh F; Tumani H; Waldenberger M; Weber F; Wiendl H; Wildemann B; Zettl UK; Ziemann U; Zipp F; Hemmer B; Ziegler A;
Genet Epidemiol; 2015 Dec; 39(8):601-8. PubMed ID: 26497834
[TBL] [Abstract][Full Text] [Related]
6. Rare variants in the CYP27B1 gene are associated with multiple sclerosis.
Ramagopalan SV; Dyment DA; Cader MZ; Morrison KM; Disanto G; Morahan JM; Berlanga-Taylor AJ; Handel A; De Luca GC; Sadovnick AD; Lepage P; Montpetit A; Ebers GC
Ann Neurol; 2011 Dec; 70(6):881-6. PubMed ID: 22190362
[TBL] [Abstract][Full Text] [Related]
7. Exome-Sequence Analyses of Four Multi-Incident Multiple Sclerosis Families.
Zrzavy T; Leutmezer F; Kristoferitsch W; Kornek B; Schneider C; Rommer P; Berger T; Zimprich A
Genes (Basel); 2020 Aug; 11(9):. PubMed ID: 32854198
[TBL] [Abstract][Full Text] [Related]
8. Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer.
Liu Y; Kheradmand F; Davis CF; Scheurer ME; Wheeler D; Tsavachidis S; Armstrong G; Simpson C; Mandal D; Kupert E; Anderson M; You M; Xiong D; Pikielny C; Schwartz AG; Bailey-Wilson J; Gaba C; De Andrade M; Yang P; Pinney SM; ; Amos CI; Spitz MR
J Thorac Oncol; 2016 Jan; 11(1):52-61. PubMed ID: 26762739
[TBL] [Abstract][Full Text] [Related]
9. Decrease of suppressor inducer (CD4+2H4+) T cells in multiple sclerosis cerebrospinal fluid.
Chofflon M; Weiner HL; Morimoto C; Hafler DA
Ann Neurol; 1989 May; 25(5):494-9. PubMed ID: 2528316
[TBL] [Abstract][Full Text] [Related]
10. Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells.
Leikfoss IS; Keshari PK; Gustavsen MW; Bjølgerud A; Brorson IS; Celius EG; Spurkland A; Bos SD; Harbo HF; Berge T
PLoS One; 2015; 10(7):e0132957. PubMed ID: 26203907
[TBL] [Abstract][Full Text] [Related]
11. Phenotypical and functional characterization of T helper 17 cells in multiple sclerosis.
Brucklacher-Waldert V; Stuerner K; Kolster M; Wolthausen J; Tolosa E
Brain; 2009 Dec; 132(Pt 12):3329-41. PubMed ID: 19933767
[TBL] [Abstract][Full Text] [Related]
12. Common T-cell receptor V beta usage in oligoclonal T lymphocytes derived from cerebrospinal fluid and blood of patients with multiple sclerosis.
Lee SJ; Wucherpfennig KW; Brod SA; Benjamin D; Weiner HL; Hafler DA
Ann Neurol; 1991 Jan; 29(1):33-40. PubMed ID: 1847614
[TBL] [Abstract][Full Text] [Related]
13. TCR repertoire diversity in Multiple Sclerosis: High-dimensional bioinformatics analysis of sequences from brain, cerebrospinal fluid and peripheral blood.
Amoriello R; Chernigovskaya M; Greiff V; Carnasciali A; Massacesi L; Barilaro A; Repice AM; Biagioli T; Aldinucci A; Muraro PA; Laplaud DA; Lossius A; Ballerini C
EBioMedicine; 2021 Jun; 68():103429. PubMed ID: 34127432
[TBL] [Abstract][Full Text] [Related]
14. Oligoclonal expansion of memory CD8+ T cells in cerebrospinal fluid from multiple sclerosis patients.
Jacobsen M; Cepok S; Quak E; Happel M; Gaber R; Ziegler A; Schock S; Oertel WH; Sommer N; Hemmer B
Brain; 2002 Mar; 125(Pt 3):538-50. PubMed ID: 11872611
[TBL] [Abstract][Full Text] [Related]
15. Exome-wide Sequencing Shows Low Mutation Rates and Identifies Novel Mutated Genes in Seminomas.
Cutcutache I; Suzuki Y; Tan IB; Ramgopal S; Zhang S; Ramnarayanan K; Gan A; Lee HH; Tay ST; Ooi A; Ong CK; Bolthouse JT; Lane BR; Anema JG; Kahnoski RJ; Tan P; Teh BT; Rozen SG
Eur Urol; 2015 Jul; 68(1):77-83. PubMed ID: 25597018
[TBL] [Abstract][Full Text] [Related]
16. Dynamic Response Genes in CD4+ T Cells Reveal a Network of Interactive Proteins that Classifies Disease Activity in Multiple Sclerosis.
Hellberg S; Eklund D; Gawel DR; Köpsén M; Zhang H; Nestor CE; Kockum I; Olsson T; Skogh T; Kastbom A; Sjöwall C; Vrethem M; Håkansson I; Benson M; Jenmalm MC; Gustafsson M; Ernerudh J
Cell Rep; 2016 Sep; 16(11):2928-2939. PubMed ID: 27626663
[TBL] [Abstract][Full Text] [Related]
17. Genome-wide linkage, exome sequencing and functional analyses identify ABCB6 as the pathogenic gene of dyschromatosis universalis hereditaria.
Liu H; Li Y; Hung KK; Wang N; Wang C; Chen X; Sheng D; Fu X; See K; Foo JN; Low H; Liany H; Irwan ID; Liu J; Yang B; Chen M; Yu Y; Yu G; Niu G; You J; Zhou Y; Ma S; Wang T; Yan X; Goh BK; Common JE; Lane BE; Sun Y; Zhou G; Lu X; Wang Z; Tian H; Cao Y; Chen S; Liu Q; Liu J; Zhang F
PLoS One; 2014; 9(2):e87250. PubMed ID: 24498303
[TBL] [Abstract][Full Text] [Related]
18. Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing.
Pytel V; Matías-Guiu JA; Torre-Fuentes L; Montero-Escribano P; Maietta P; Botet J; Álvarez S; Gómez-Pinedo U; Matías-Guiu J
Brain Behav; 2019 Apr; 9(4):e01272. PubMed ID: 30900415
[TBL] [Abstract][Full Text] [Related]
19. CSF T-cell subsets in multiple sclerosis: relationship to cerebrospinal fluid myelin basic protein and clinical activity.
Salmaggi A; LaMantia L; Milanese C; Bianchi G; Eoli M; Campi A; Nespolo A
J Neurol; 1989 Sep; 236(6):336-9. PubMed ID: 2477508
[TBL] [Abstract][Full Text] [Related]
20. Cerebrospinal-fluid-derived immunoglobulin G of different multiple sclerosis patients shares mutated sequences in complementarity determining regions.
Singh V; Stoop MP; Stingl C; Luitwieler RL; Dekker LJ; van Duijn MM; Kreft KL; Luider TM; Hintzen RQ
Mol Cell Proteomics; 2013 Dec; 12(12):3924-34. PubMed ID: 23970564
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
