224 related articles for article (PubMed ID: 31235738)
1. Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes.
Vidmar L; Maver A; Drulović J; Sepčić J; Novaković I; Ristič S; Šega S; Peterlin B
Sci Rep; 2019 Jun; 9(1):9171. PubMed ID: 31235738
[TBL] [Abstract][Full Text] [Related]
2. Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.
Maver A; Lavtar P; Ristić S; Stopinšek S; Simčič S; Hočevar K; Sepčić J; Drulović J; Pekmezović T; Novaković I; Alenka H; Rudolf G; Šega S; Starčević-Čizmarević N; Palandačić A; Zamolo G; Kapović M; Likar T; Peterlin B
Sci Rep; 2017 Jun; 7(1):3715. PubMed ID: 28623311
[TBL] [Abstract][Full Text] [Related]
3. Variants in NLRP3 and NLRC4 inflammasome associate with susceptibility and severity of multiple sclerosis.
Soares JL; Oliveira EM; Pontillo A
Mult Scler Relat Disord; 2019 Apr; 29():26-34. PubMed ID: 30658261
[TBL] [Abstract][Full Text] [Related]
4. Genetic analysis of nucleotide-binding leucine-rich repeat (NLR) receptors in multiple sclerosis.
Popplewell LF; Encarnacion M; Bernales CQ; Sadovnick AD; Traboulsee AL; Quandt JA; Vilariño-Güell C
Immunogenetics; 2020 Sep; 72(6-7):381-385. PubMed ID: 32529290
[TBL] [Abstract][Full Text] [Related]
5. Analysis of NOD-like receptor NLRP1 in multiple sclerosis families.
Bernales CQ; Encarnacion M; Criscuoli MG; Yee IM; Traboulsee AL; Sadovnick AD; Vilariño-Güell C
Immunogenetics; 2018 Mar; 70(3):205-207. PubMed ID: 28988323
[TBL] [Abstract][Full Text] [Related]
6. Burden of rare coding variants in an Italian cohort of familial multiple sclerosis.
Mascia E; Clarelli F; Zauli A; Guaschino C; Sorosina M; Barizzone N; Basagni C; Santoro S; Ferrè L; Bonfiglio S; Biancolini D; Pozzato M; Guerini FR; Protti A; Liguori M; Moiola L; Vecchio D; Bresolin N; Comi G; Filippi M; Esposito F; D'Alfonso S; Martinelli-Boneschi F
J Neuroimmunol; 2022 Jan; 362():577760. PubMed ID: 34922125
[TBL] [Abstract][Full Text] [Related]
7. Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis.
Min BJ; Kang YK; Chung YG; Seo ME; Chang KB; Joo MW
Clin Orthop Relat Res; 2020 Nov; 478(11):2442-2450. PubMed ID: 32281771
[TBL] [Abstract][Full Text] [Related]
8. Neurological phenotypes in patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants.
Mulazzani E; Wagner D; Havla J; Schlüter M; Meinl I; Gerdes LA; Kümpfel T
J Neuroinflammation; 2020 Jun; 17(1):196. PubMed ID: 32563262
[TBL] [Abstract][Full Text] [Related]
9. An Investigation of the Role of Common and Rare Variants in a Large Italian Multiplex Family of Multiple Sclerosis Patients.
Barizzone N; Cagliani R; Basagni C; Clarelli F; Mendozzi L; Agliardi C; Forni D; Tosi M; Mascia E; Favero F; Corà D; Corrado L; Sorosina M; Esposito F; Zuccalà M; Vecchio D; Liguori M; Comi C; Comi G; Martinelli V; Filippi M; Leone M; Martinelli-Boneschi F; Caputo D; Sironi M; Guerini FR; D'Alfonso S
Genes (Basel); 2021 Oct; 12(10):. PubMed ID: 34681001
[TBL] [Abstract][Full Text] [Related]
10. Rare MEFV variants are not associated with risk to develop multiple sclerosis and severity of disease.
Pauwels I; Cosemans L; Boonen S; Dubois B; Goris A
Mult Scler; 2013 Aug; 19(9):1132-6. PubMed ID: 23325590
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Homozygosity Haplotype and Whole-Exome Sequencing Analysis to Identify Potentially Functional Rare Variants Involved in Multiple Sclerosis among Sardinian Families.
Fazia T; Marzanati D; Carotenuto AL; Beecham A; Hadjixenofontos A; McCauley JL; Saddi V; Piras M; Bernardinelli L; Gentilini D
Curr Issues Mol Biol; 2021 Oct; 43(3):1778-1793. PubMed ID: 34889895
[TBL] [Abstract][Full Text] [Related]
14. Germline NLRP1 Mutations Cause Skin Inflammatory and Cancer Susceptibility Syndromes via Inflammasome Activation.
Zhong FL; Mamaï O; Sborgi L; Boussofara L; Hopkins R; Robinson K; Szeverényi I; Takeichi T; Balaji R; Lau A; Tye H; Roy K; Bonnard C; Ahl PJ; Jones LA; Baker PJ; Lacina L; Otsuka A; Fournie PR; Malecaze F; Lane EB; Akiyama M; Kabashima K; Connolly JE; Masters SL; Soler VJ; Omar SS; McGrath JA; Nedelcu R; Gribaa M; Denguezli M; Saad A; Hiller S; Reversade B
Cell; 2016 Sep; 167(1):187-202.e17. PubMed ID: 27662089
[TBL] [Abstract][Full Text] [Related]
15. Linkage analysis and whole exome sequencing identify a novel candidate gene in a Dutch multiple sclerosis family.
Mescheriakova JY; Verkerk AJ; Amin N; Uitterlinden AG; van Duijn CM; Hintzen RQ
Mult Scler; 2019 Jun; 25(7):909-917. PubMed ID: 29873607
[TBL] [Abstract][Full Text] [Related]
16. Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.
Vilariño-Güell C; Zimprich A; Martinelli-Boneschi F; Herculano B; Wang Z; Matesanz F; Urcelay E; Vandenbroeck K; Leyva L; Gris D; Massaad C; Quandt JA; Traboulsee AL; Encarnacion M; Bernales CQ; Follett J; Yee IM; Criscuoli MG; Deutschländer A; Reinthaler EM; Zrzavy T; Mascia E; Zauli A; Esposito F; Alcina A; Izquierdo G; Espino-Paisán L; Mena J; Antigüedad A; Urbaneja-Romero P; Ortega-Pinazo J; Song W; Sadovnick AD
PLoS Genet; 2019 Jun; 15(6):e1008180. PubMed ID: 31170158
[TBL] [Abstract][Full Text] [Related]
17. Whole Exome Sequencing in Multi-Incident Families Identifies Novel Candidate Genes for Multiple Sclerosis.
Horjus J; van Mourik-Banda T; Heerings MAP; Hakobjan M; De Witte W; Heersema DJ; Jansen AJ; Strijbis EMM; de Jong BA; Slettenaar AEJ; Zeinstra EMPE; Hoogervorst ELJ; Franke B; Kruijer W; Jongen PJ; Visser LJ; Poelmans G
Int J Mol Sci; 2022 Sep; 23(19):. PubMed ID: 36232761
[TBL] [Abstract][Full Text] [Related]
18. Increased inflammasome related gene expression profile in PBMC may facilitate T helper 17 cell induction in multiple sclerosis.
Peelen E; Damoiseaux J; Muris AH; Knippenberg S; Smolders J; Hupperts R; Thewissen M
Mol Immunol; 2015 Feb; 63(2):521-9. PubMed ID: 25458313
[TBL] [Abstract][Full Text] [Related]
19. Investigating the role of common and rare variants in multiplex multiple sclerosis families reveals an increased burden of common risk variation.
Everest E; Ahangari M; Uygunoglu U; Tutuncu M; Bulbul A; Saip S; Duman T; Sezerman U; Reich DS; Riley BP; Siva A; Tahir Turanli E
Sci Rep; 2022 Oct; 12(1):16984. PubMed ID: 36216875
[TBL] [Abstract][Full Text] [Related]
20. Polimorphisms in inflammasome genes are involved in the predisposition to systemic lupus erythematosus.
Pontillo A; Girardelli M; Kamada AJ; Pancotto JA; Donadi EA; Crovella S; Sandrin-Garcia P
Autoimmunity; 2012 Jun; 45(4):271-8. PubMed ID: 22235789
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]