BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 30808881)

  • 1. Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes.
    Burillo-Sanz S; Montes-Cano MA; García-Lozano JR; Olivas-Martínez I; Ortego-Centeno N; García-Hernández FJ; Espinosa G; Graña-Gil G; Sánchez-Bursón J; Juliá MR; 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; 2019 Feb; 9(1):2777. PubMed ID: 30808881
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. MEFV, TNFRSF1A and CARD15 mutation analysis in Behçet's disease.
    Baruch Y; Dagan E; Rosner I; Fiorilli M; Gershoni-Baruch R; Rozenbaum M
    Clin Exp Rheumatol; 2011; 29(4 Suppl 67):S24-7. PubMed ID: 21385537
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of NLRP3, MVK and TNFRSF1A variants in adult Greek patients with autoinflammatory symptoms.
    Karagianni P; Nezos A; Ioakeim F; Tzioufas AG; Moutsopoulos HM
    Clin Exp Rheumatol; 2018; 36(6 Suppl 115):86-89. PubMed ID: 30418111
    [TBL] [Abstract][Full Text] [Related]  

  • 5. In vitro analysis of the functional effects of an NLRP3 G809S variant with the co-existence of MEFV haplotype variants in atypical autoinflammatory syndrome.
    Kubota K; Ohnishi H; Teramoto T; Matsui E; Murase K; Kanoh H; Kato Z; Kaneko H; Seishima M; Kondo N
    J Clin Immunol; 2013 Feb; 33(2):325-34. PubMed ID: 23015306
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
    Karacan İ; Balamir A; Uğurlu S; Aydın AK; Everest E; Zor S; Önen MÖ; Daşdemir S; Özkaya O; Sözeri B; Tufan A; Yıldırım DG; Yüksel S; Ayaz NA; Ömeroğlu RE; Öztürk K; Çakan M; Söylemezoğlu O; Şahin S; Barut K; Adroviç A; Seyahi E; Özdoğan H; Kasapçopur Ö; Turanlı ET
    Rheumatol Int; 2019 May; 39(5):911-919. PubMed ID: 30783801
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Autoinflammatory gene mutations in Behçet's disease.
    Koné-Paut I; Sanchez E; Le Quellec A; Manna R; Touitou I
    Ann Rheum Dis; 2007 Jun; 66(6):832-4. PubMed ID: 17213252
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A comprehensive overview on the genetics of Behçet's disease.
    Mahmoudi M; Aslani S; Meguro A; Akhtari M; Fatahi Y; Mizuki N; Shahram F
    Int Rev Immunol; 2022; 41(2):84-106. PubMed ID: 33258398
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.
    Sighart R; Rech J; Hueber A; Blank N; Löhr S; Reis A; Sticht H; Hüffmeier U
    Rheumatol Int; 2018 Jan; 38(1):111-120. PubMed ID: 29159471
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Behçet's disease from the aspect of autoinflammatory disease].
    Ishigatsubo Y; Samukawa S
    Nihon Rinsho Meneki Gakkai Kaishi; 2011; 34(5):408-19. PubMed ID: 22041429
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.
    De Pieri C; Vuch J; De Martino E; Bianco AM; Ronfani L; Athanasakis E; Bortot B; Crovella S; Taddio A; Severini GM; Tommasini A
    Pediatr Rheumatol Online J; 2015; 13():11. PubMed ID: 25866490
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CARD15 polymorphisms in Behçet's disease.
    Ahmad T; Zhang L; Gogus F; Verity D; Wallace G; Madanat W; Fayyad F; James T; Neville M; Kanawati C; Fortune F; Celik A; Stanford M; Jewell DP; Marshall SE
    Scand J Rheumatol; 2005; 34(3):233-7. PubMed ID: 16134731
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes.
    Ozyilmaz B; Kirbiyik O; Koc A; Ozdemir TR; Kaya Ozer O; Kutbay YB; Erdogan KM; Saka Guvenc M; Ozturk C
    Int J Immunogenet; 2019 Aug; 46(4):232-240. PubMed ID: 31135083
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. ISSAID/EMQN Best Practice Guidelines for the Genetic Diagnosis of Monogenic Autoinflammatory Diseases in the Next-Generation Sequencing Era.
    Shinar Y; Ceccherini I; Rowczenio D; Aksentijevich I; Arostegui J; Ben-Chétrit E; Boursier G; Gattorno M; Hayrapetyan H; Ida H; Kanazawa N; Lachmann HJ; Mensa-Vilaro A; Nishikomori R; Oberkanins C; Obici L; Ohara O; Ozen S; Sarkisian T; Sheils K; Wolstenholme N; Zonneveld-Huijssoon E; van Gijn ME; Touitou I
    Clin Chem; 2020 Apr; 66(4):525-536. PubMed ID: 32176780
    [TBL] [Abstract][Full Text] [Related]  

  • 16. HLA and non-HLA genes in Behçet's disease: a multicentric study in the Spanish population.
    Montes-Cano MA; Conde-Jaldón M; García-Lozano JR; Ortiz-Fernández L; Ortego-Centeno N; Castillo-Palma MJ; Espinosa G; Graña-Gil G; González-Gay MA; Barnosi-Marín AC; Solans R; Fanlo P; Camps T; Castañeda S; Sánchez-Bursón J; Núñez-Roldán A; Martín J; González-Escribano MF
    Arthritis Res Ther; 2013 Oct; 15(5):R145. PubMed ID: 24286189
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hereditary autoinflammatory syndromes: a Brazilian multicenter study.
    Jesus AA; Fujihira E; Watase M; Terreri MT; Hilario MO; Carneiro-Sampaio M; Len CA; Oliveira SK; Rodrigues MC; Pereira RM; Bica B; Silva NA; Cavalcanti A; Marini R; Sztajnbok F; Quintero MV; Ferriani VP; Moraes-Vasconcelos D; Silva CA; Oliveira JB
    J Clin Immunol; 2012 Oct; 32(5):922-32. PubMed ID: 22566169
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Hereditary systemic autoinflammatory diseases].
    Aróstegui JI
    Reumatol Clin; 2011; 7(1):45-50. PubMed ID: 21794778
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The prevalence of Behçet's syndrome, familial Mediterranean fever, HLA-B51 and MEFV gene mutations among ethnic Armenians living in Istanbul, Turkey.
    Seyahi E; Tahir Turanli E; Mangan MS; Celikyapi G; Oktay V; Cevirgen D; Kuzuoglu D; Ozoglu S; Yazici H
    Clin Exp Rheumatol; 2010; 28(4 Suppl 60):S67-75. PubMed ID: 20868574
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Behçet's disease and hereditary periodic fever syndromes: casual association or causal relationship?
    Espinosa G; Arostegui JI; Plaza S; Rius J; Cervera R; Yagüe J; Font J
    Clin Exp Rheumatol; 2005; 23(4 Suppl 38):S64-6. PubMed ID: 16273767
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.