These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

212 related articles for article (PubMed ID: 31235738)

  • 21. Genetic contribution and functional impairment of inflammasome in sickle cell disease.
    de Freitas Dutra V; Leal VNC; Fernandes FP; Souza CRL; Figueiredo MS; Pontillo A
    Cytokine; 2022 Jan; 149():155717. PubMed ID: 34627079
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutational profile of rare variants in inflammasome-related genes in Behçet disease: A Next Generation Sequencing approach.
    Burillo-Sanz S; Montes-Cano MA; García-Lozano JR; Ortiz-Fernández L; Ortego-Centeno N; García-Hernández FJ; Espinosa G; Graña-Gil G; Sánchez-Bursón J; Rosa Juliá M; Solans R; Blanco R; Barnosi-Marín AC; Gómez De la Torre R; Fanlo P; Rodríguez-Carballeira M; Rodríguez-Rodríguez L; Camps T; Castañeda S; Alegre-Sancho JJ; Martín J; González-Escribano MF
    Sci Rep; 2017 Aug; 7(1):8453. PubMed ID: 28814775
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Contribution of inflammasome genetics in Plasmodium vivax malaria.
    Santos MLS; Reis EC; Bricher PN; Sousa TN; Brito CFA; Lacerda MVG; Fontes CJF; Carvalho LH; Pontillo A
    Infect Genet Evol; 2016 Jun; 40():162-166. PubMed ID: 26946405
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Monosodium Urate Crystals Activate the Inflammasome in Primary Progressive Multiple Sclerosis.
    Piancone F; Saresella M; Marventano I; La Rosa F; Santangelo MA; Caputo D; Mendozzi L; Rovaris M; Clerici M
    Front Immunol; 2018; 9():983. PubMed ID: 29780394
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Variants of genes encoding TNF receptors and ligands and proteins regulating TNF activation in familial multiple sclerosis.
    Torre-Fuentes L; Matías-Guiu JA; Pytel V; Montero-Escribano P; Maietta P; Álvarez S; Gómez-Pinedo U; Matías-Guiu J
    CNS Neurosci Ther; 2020 Nov; 26(11):1178-1184. PubMed ID: 32951330
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment.
    Mathews RJ; Robinson JI; Battellino M; Wong C; Taylor JC; ; Eyre S; Churchman SM; Wilson AG; Isaacs JD; Hyrich K; Barton A; Plant D; Savic S; Cook GP; Sarzi-Puttini P; Emery P; Barrett JH; Morgan AW; McDermott MF
    Ann Rheum Dis; 2014 Jun; 73(6):1202-10. PubMed ID: 23687262
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Familial Mediterranean fever mutations are hypermorphic mutations that specifically decrease the activation threshold of the Pyrin inflammasome.
    Jamilloux Y; Lefeuvre L; Magnotti F; Martin A; Benezech S; Allatif O; Penel-Page M; Hentgen V; Sève P; Gerfaud-Valentin M; Duquesne A; Desjonquères M; Laurent A; Rémy-Piccolo V; Cimaz R; Cantarini L; Bourdonnay E; Walzer T; Py BF; Belot A; Henry T
    Rheumatology (Oxford); 2018 Jan; 57(1):100-111. PubMed ID: 29040788
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Gain-of-function variants in NLRP1 protect against the development of diabetic kidney disease: NLRP1 inflammasome role in metabolic stress sensing?
    Soares JLS; Fernandes FP; Patente TA; Monteiro MB; Parisi MC; Giannella-Neto D; Corrêa-Giannella ML; Pontillo A
    Clin Immunol; 2018 Feb; 187():46-49. PubMed ID: 29031829
    [TBL] [Abstract][Full Text] [Related]  

  • 30. NLRP3 inflammasome is associated with the response to IFN-β in patients with multiple sclerosis.
    Malhotra S; Río J; Urcelay E; Nurtdinov R; Bustamante MF; Fernández O; Oliver B; Zettl U; Brassat D; Killestein J; Lechner-Scott J; Drulovic J; Chan A; Martinelli-Boneschi F; García-Merino A; Montalban X; Comabella M
    Brain; 2015 Mar; 138(Pt 3):644-52. PubMed ID: 25586466
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis.
    Al-Kafaji G; Bakheit HF; AlAli F; Fattah M; Alhajeri S; Alharbi MA; Daif A; Alsabbagh MM; Alwehaidah MS; Bakhiet M
    PLoS One; 2022; 17(2):e0263606. PubMed ID: 35130313
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course.
    Gil-Varea E; Urcelay E; Vilariño-Güell C; Costa C; Midaglia L; Matesanz F; Rodríguez-Antigüedad A; Oksenberg J; Espino-Paisan L; Dessa Sadovnick A; Saiz A; Villar LM; García-Merino JA; Ramió-Torrentà L; Triviño JC; Quintana E; Robles R; Sánchez-López A; Arroyo R; Alvarez-Cermeño JC; Vidal-Jordana A; Malhotra S; Fissolo N; Montalban X; Comabella M
    J Neuroinflammation; 2018 Sep; 15(1):265. PubMed ID: 30217166
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients.
    Sadovnick AD; Traboulsee AL; Bernales CQ; Ross JP; Forwell AL; Yee IM; Guillot-Noel L; Fontaine B; Cournu-Rebeix I; Alcina A; Fedetz M; Izquierdo G; Matesanz F; Hilven K; Dubois B; Goris A; Astobiza I; Alloza I; Antigüedad A; Vandenbroeck K; Akkad DA; Aktas O; Blaschke P; Buttmann M; Chan A; Epplen JT; Gerdes LA; Kroner A; Kubisch C; Kümpfel T; Lohse P; Rieckmann P; Zettl UK; Zipp F; Bertram L; Lill CM; Fernandez O; Urbaneja P; Leyva L; Alvarez-Cermeño JC; Arroyo R; Garagorri AM; García-Martínez A; Villar LM; Urcelay E; Malhotra S; Montalban X; Comabella M; Berger T; Fazekas F; Reindl M; Schmied MC; Zimprich A; Vilariño-Güell C
    G3 (Bethesda); 2016 Jul; 6(7):2073-9. PubMed ID: 27194806
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genes.
    Gil-Varea E; Spataro N; Villar LM; Tejeda-Velarde A; Midaglia L; Matesanz F; Malhotra S; Eixarch H; Patsopoulos N; Fernández Ó; Oliver-Martos B; Saiz A; Llufriu S; Ramió-Torrentà L; Quintana E; Izquierdo G; Alcina A; Bosch E; Navarro A; Montalban X; Comabella M
    Hum Mutat; 2020 Jul; 41(7):1308-1320. PubMed ID: 32196808
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Genetic variation in inflammasome genes is associated with outcome in bacterial meningitis.
    Geldhoff M; Mook-Kanamori BB; Brouwer MC; Valls Seron M; Baas F; van der Ende A; van de Beek D
    Immunogenetics; 2013 Jan; 65(1):9-16. PubMed ID: 23053059
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rare coding variants in genes encoding GABA
    May P; Girard S; Harrer M; Bobbili DR; Schubert J; Wolking S; Becker F; Lachance-Touchette P; Meloche C; Gravel M; Niturad CE; Knaus J; De Kovel C; Toliat M; Polvi A; Iacomino M; Guerrero-López R; Baulac S; Marini C; Thiele H; Altmüller J; Jabbari K; Ruppert AK; Jurkowski W; Lal D; Rusconi R; Cestèle S; Terragni B; Coombs ID; Reid CA; Striano P; Caglayan H; Siren A; Everett K; Møller RS; Hjalgrim H; Muhle H; Helbig I; Kunz WS; Weber YG; Weckhuysen S; Jonghe P; Sisodiya SM; Nabbout R; Franceschetti S; Coppola A; Vari MS; Kasteleijn-Nolst Trenité D; Baykan B; Ozbek U; Bebek N; Klein KM; Rosenow F; Nguyen DK; Dubeau F; Carmant L; Lortie A; Desbiens R; Clément JF; Cieuta-Walti C; Sills GJ; Auce P; Francis B; Johnson MR; Marson AG; Berghuis B; Sander JW; Avbersek A; McCormack M; Cavalleri GL; Delanty N; Depondt C; Krenn M; Zimprich F; Peter S; Nikanorova M; Kraaij R; van Rooij J; Balling R; Ikram MA; Uitterlinden AG; Avanzini G; Schorge S; Petrou S; Mantegazza M; Sander T; LeGuern E; Serratosa JM; Koeleman BPC; Palotie A; Lehesjoki AE; Nothnagel M; Nürnberg P; Maljevic S; Zara F; Cossette P; Krause R; Lerche H; ; ;
    Lancet Neurol; 2018 Aug; 17(8):699-708. PubMed ID: 30033060
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Differential expression of the inflammasome complex genes in systemic lupus erythematosus.
    da Cruz HLA; Cavalcanti CAJ; de Azêvedo Silva J; de Lima CAD; Fragoso TS; Barbosa AD; Dantas AT; de Ataíde Mariz H; Duarte ALBP; Pontillo A; Crovella S; Sandrin-Garcia P
    Immunogenetics; 2020 May; 72(4):217-224. PubMed ID: 32020248
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Inflammasome polymorphisms in juvenile systemic lupus erythematosus.
    Pontillo A; Reis EC; Liphaus BL; Silva CA; Carneiro-Sampaio M
    Autoimmunity; 2015; 48(7):434-7. PubMed ID: 26182076
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Burden of rare variants in causative genes for amyotrophic lateral sclerosis (ALS) accelerates age at onset of ALS.
    Naruse H; Ishiura H; Mitsui J; Takahashi Y; Matsukawa T; Tanaka M; Doi K; Yoshimura J; Morishita S; Goto J; Toda T; Tsuji S
    J Neurol Neurosurg Psychiatry; 2019 May; 90(5):537-542. PubMed ID: 30355605
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Exome sequencing reveals novel rare variants in Iranian familial multiple sclerosis: The importance of POLD2 in the disease pathogenesis.
    Salehi Z; Keramatipour M; Talebi S; Arab SS; Naser Moghadasi A; Sahraian MA; Izad M
    Genomics; 2021 Jul; 113(4):2645-2655. PubMed ID: 34116171
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.