BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

182 related articles for article (PubMed ID: 31803180)

  • 21. Case Report: A child with NFKB1 haploinsufficiency explaining the linkage between immunodeficiency and short stature.
    Ricci S; Abu-Rumeileh S; Campagna N; Barbati F; Stagi S; Canessa C; Lodi L; Palterer B; Maggi L; Matucci A; Vultaggio A; Annunziato F; Azzari C
    Front Immunol; 2023; 14():1224603. PubMed ID: 37600787
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
    Li J; Lei WT; Zhang P; Rapaport F; Seeleuthner Y; Lyu B; Asano T; Rosain J; Hammadi B; Zhang Y; Pelham SJ; Spaan AN; Migaud M; Hum D; Bigio B; Chrabieh M; Béziat V; Bustamante J; Zhang SY; Jouanguy E; Boisson-Dupuis S; El Baghdadi J; Aimanianda V; Thoma K; Fliegauf M; Grimbacher B; Korganow AS; Saunders C; Rao VK; Uzel G; Freeman AF; Holland SM; Su HC; Cunningham-Rundles C; Fieschi C; Abel L; Puel A; Cobat A; Casanova JL; Zhang Q; Boisson B
    J Exp Med; 2021 Nov; 218(11):. PubMed ID: 34473196
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Th1-skewed profile and excessive production of proinflammatory cytokines in a NFKB1-deficient patient with CVID and severe gastrointestinal manifestations.
    Dieli-Crimi R; Martínez-Gallo M; Franco-Jarava C; Antolin M; Blasco L; Paramonov I; Semidey ME; Álvarez Fernández A; Molero X; Velásquez J; Martín-Nalda A; Pujol-Borrell R; Colobran R
    Clin Immunol; 2018 Oct; 195():49-58. PubMed ID: 30063981
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders.
    Ameratunga R; Ahn Y; Jordan A; Lehnert K; Brothers S; Woon ST
    Expert Rev Clin Immunol; 2018 Jul; 14(7):549-556. PubMed ID: 29806948
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Mutant DD genotype of NFKB1 gene is associated with the susceptibility and severity of coronary artery disease.
    Luo JY; Li XM; Zhou Y; Zhao Q; Chen BD; Liu F; Chen XC; Zheng H; Ma YT; Gao XM; Yang YN
    J Mol Cell Cardiol; 2017 Feb; 103():56-64. PubMed ID: 28088561
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Identification of novel NFKB1 and ICOS frameshift variants in patients with CVID.
    Liu A; Liu Q; Leng S; Zhang X; Feng Q; Peng J; Feng G
    Clin Exp Immunol; 2023 Mar; 211(1):68-77. PubMed ID: 36571238
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Association of NFKB1, which encodes a subunit of the transcription factor NF-kappaB, with alcohol dependence.
    Edenberg HJ; Xuei X; Wetherill LF; Bierut L; Bucholz K; Dick DM; Hesselbrock V; Kuperman S; Porjesz B; Schuckit MA; Tischfield JA; Almasy LA; Nurnberger JI; Foroud T
    Hum Mol Genet; 2008 Apr; 17(7):963-70. PubMed ID: 18079108
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A functional haplotype of NFKB1 influence susceptibility to oral cancer: a population-based and in vitro study.
    Chen F; Liu F; Yan L; Lin L; Qiu Y; Wang J; Wu J; Bao X; Hu Z; Cai L; He B
    Cancer Med; 2018 May; 7(5):2211-2218. PubMed ID: 29635862
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Co-stimulatory CD28 and transcription factor NFKB1 gene variants affect idiopathic recurrent miscarriages.
    Misra MK; Singh B; Mishra A; Agrawal S
    J Hum Genet; 2016 Dec; 61(12):1035-1041. PubMed ID: 27488439
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Lack of association of a functional -94ins/delATTG NFKB1 promoter polymorphism with susceptibility and clinical expression of biopsy-proven giant cell arteritis in northwest Spain.
    Martin J; Perez-Armengol C; Miranda-Filloy JA; Vilchez JR; Lopez-Nevot MA; Garcia-Porrua C; Gonzalez-Gay MA
    J Rheumatol; 2006 Feb; 33(2):285-8. PubMed ID: 16465659
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Common Variable Immunodeficiency with Genetic Defects Identified by Whole Exome Sequencing.
    Li R; Zheng Y; Li Y; Zhang R; Wang F; Yang D; Ma Y; Mu X; Cao Z; Gao Z
    Biomed Res Int; 2018; 2018():3724630. PubMed ID: 30363934
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Association of NFKB1 -94ins/del ATTG promoter polymorphism with susceptibility to and phenotype of Graves' disease.
    Kurylowicz A; Hiromatsu Y; Jurecka-Lubieniecka B; Kula D; Kowalska M; Ichimura M; Koga H; Kaku H; Bar-Andziak E; Nauman J; Jarzab B; Ploski R; Bednarczuk T
    Genes Immun; 2007 Oct; 8(7):532-8. PubMed ID: 17690684
    [TBL] [Abstract][Full Text] [Related]  

  • 33. A functional promoter polymorphism in NFKB1 increases susceptibility to endometriosis.
    Zhou B; Rao L; Peng Y; Wang Y; Qie M; Zhang Z; Song Y; Zhang L
    DNA Cell Biol; 2010 May; 29(5):235-9. PubMed ID: 20218898
    [TBL] [Abstract][Full Text] [Related]  

  • 34. TCF3 haploinsufficiency defined by immune, clinical, gene-dosage, and murine studies.
    Boast B; Goel S; González-Granado LI; Niemela J; Stoddard J; Edwards ESJ; Seneviratne S; Spensberger D; Quesada-Espinosa JF; Allende LM; McDonnell J; Haseley A; Lesmana H; Walkiewicz MA; Muhammad E; Bosco JJ; Fleisher TA; Cohen S; Holland SM; van Zelm MC; Enders A; Kuehn HS; Rosenzweig SD
    J Allergy Clin Immunol; 2023 Sep; 152(3):736-747. PubMed ID: 37277074
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Evaluating the role of the genetic variations of PTPN22, NFKB1, and FcGRIIIA genes in inflammatory bowel disease: a meta-analysis.
    Latiano A; Palmieri O; Valvano MR; Bossa F; Latiano T; Corritore G; DeSanto E; Andriulli A; Annese V
    Inflamm Bowel Dis; 2007 Oct; 13(10):1212-9. PubMed ID: 17600378
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies.
    Coopmans EC; Chunharojrith P; Neggers SJCMM; van der Ent MW; Swagemakers SMA; Hollink IH; Barendregt BH; van der Spek PJ; van der Lely AJ; van Hagen PM; Dalm VASH
    Front Immunol; 2019; 10():2079. PubMed ID: 31543881
    [No Abstract]   [Full Text] [Related]  

  • 37. Case Report: A Novel Synonymous ARPC1B Gene Mutation Causes a Syndrome of Combined Immunodeficiency, Asthma, and Allergy With Significant Intrafamilial Clinical Heterogeneity.
    Papadatou I; Marinakis N; Botsa E; Tzanoudaki M; Kanariou M; Orfanou I; Kanaka-Gantenbein C; Traeger-Synodinos J; Spoulou V
    Front Immunol; 2021; 12():634313. PubMed ID: 33679784
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder.
    Keller MD; Pandey R; Li D; Glessner J; Tian L; Henrickson SE; Chinn IK; Monaco-Shawver L; Heimall J; Hou C; Otieno FG; Jyonouchi S; Calabrese L; van Montfrans J; Orange JS; Hakonarson H
    J Allergy Clin Immunol; 2016 Aug; 138(2):544-550.e4. PubMed ID: 27016798
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Functional annotation of a novel NFKB1 promoter polymorphism that increases risk for ulcerative colitis.
    Karban AS; Okazaki T; Panhuysen CI; Gallegos T; Potter JJ; Bailey-Wilson JE; Silverberg MS; Duerr RH; Cho JH; Gregersen PK; Wu Y; Achkar JP; Dassopoulos T; Mezey E; Bayless TM; Nouvet FJ; Brant SR
    Hum Mol Genet; 2004 Jan; 13(1):35-45. PubMed ID: 14613970
    [TBL] [Abstract][Full Text] [Related]  

  • 40. NFKB1 promoter polymorphism: A new predictive marker of cytomegalovirus infection after kidney transplantation.
    Leone F; Gigliotti P; La Russa A; Lofaro D; Perri A; Vizza D; Lupinacci S; Toteda G; Bonofiglio M; Presta P; Talarico R; Aquino B; Bonofiglio R
    Transpl Infect Dis; 2019 Feb; 21(1):e13027. PubMed ID: 30431214
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.