BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

94 related articles for article (PubMed ID: 34399789)

  • 1. Comment on: homozygous variant p. Arg90His in NCF1 is associated with early-onset interferonopathy: a case report.
    Goulielmos GN; Zervou MI; Eliopoulos E
    Pediatr Rheumatol Online J; 2021 Aug; 19(1):125. PubMed ID: 34399789
    [No Abstract]   [Full Text] [Related]  

  • 2. Homozygous variant p. Arg90His in NCF1 is associated with early-onset Interferonopathy: a case report.
    Schnappauf O; Heale L; Dissanayake D; Tsai WL; Gadina M; Leto TL; Kastner DL; Malech HL; Kuhns DB; Aksentijevich I; Laxer RM
    Pediatr Rheumatol Online J; 2021 Apr; 19(1):54. PubMed ID: 33892719
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Variant type Glanzmann thrombasthenia caused by homozygous p.724R>X mutation in beta3 integrin.
    Bagoly Z; Fazakas F; Marosi A; Török O; Bereczky Z; Haramura G; Tóth J; Kappelmayer J; Muszbek L
    Thromb Res; 2010 May; 125(5):427-31. PubMed ID: 20106508
    [No Abstract]   [Full Text] [Related]  

  • 4. A common variant on chromosome 9p21 affects the risk of myocardial infarction.
    Helgadottir A; Thorleifsson G; Manolescu A; Gretarsdottir S; Blondal T; Jonasdottir A; Jonasdottir A; Sigurdsson A; Baker A; Palsson A; Masson G; Gudbjartsson DF; Magnusson KP; Andersen K; Levey AI; Backman VM; Matthiasdottir S; Jonsdottir T; Palsson S; Einarsdottir H; Gunnarsdottir S; Gylfason A; Vaccarino V; Hooper WC; Reilly MP; Granger CB; Austin H; Rader DJ; Shah SH; Quyyumi AA; Gulcher JR; Thorgeirsson G; Thorsteinsdottir U; Kong A; Stefansson K
    Science; 2007 Jun; 316(5830):1491-3. PubMed ID: 17478679
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) influences age at onset of obsessive-compulsive disorder.
    Lennertz L; Franke PE; Grabe HJ; Rampacher F; Schulze-Rauschenbach S; Guttenthaler V; Ruhrmann S; Pukrop R; Klosterkötter J; Falkai P; Maier W; Wagner M; Mössner R
    Int J Neuropsychopharmacol; 2013 Oct; 16(9):1951-8. PubMed ID: 23680103
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comment: studies of the Pro12Ala polymorphism of the PPAR-gamma gene in the Danish MONICA cohort: homozygosity of the Ala allele confers a decreased risk of the insulin resistance syndrome.
    Frederiksen L; Brødbaek K; Fenger M; Jørgensen T; Borch-Johnsen K; Madsbad S; Urhammer SA
    J Clin Endocrinol Metab; 2002 Aug; 87(8):3989-92. PubMed ID: 12161548
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Low copy numbers of complement C4 and homozygous deficiency of C4A may predispose to severe disease and earlier disease onset in patients with systemic lupus erythematosus.
    Jüptner M; Flachsbart F; Caliebe A; Lieb W; Schreiber S; Zeuner R; Franke A; Schröder JO
    Lupus; 2018 Apr; 27(4):600-609. PubMed ID: 29050534
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence of increased risk for major depressive disorder in individuals homozygous for the high-expressing 5-HTTLPR/rs25531 (L(A)) allele of the serotonin transporter promoter.
    Stacey D; Cohen-Woods S; Toben C; Arolt V; Dannlowski U; Baune BT
    Psychiatr Genet; 2013 Oct; 23(5):222-3. PubMed ID: 23969989
    [No Abstract]   [Full Text] [Related]  

  • 9. Single nucleotide polymorphisms in multiple novel thrombospondin genes may be associated with familial premature myocardial infarction.
    Topol EJ; McCarthy J; Gabriel S; Moliterno DJ; Rogers WJ; Newby LK; Freedman M; Metivier J; Cannata R; O'Donnell CJ; Kottke-Marchant K; Murugesan G; Plow EF; Stenina O; Daley GQ
    Circulation; 2001 Nov; 104(22):2641-4. PubMed ID: 11723011
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Homozygous
    Alesi V; Dentici ML; Genovese S; Loddo S; Bellacchio E; Orlando V; Di Tommaso S; Catino G; Calacci C; Calvieri G; Pompili D; Ubertini G; Dallapiccola B; Capolino R; Novelli A
    Int J Mol Sci; 2021 Jan; 22(2):. PubMed ID: 33451138
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Importance of RNF213 polymorphism on clinical features and long-term outcome in moyamoya disease.
    Kim EH; Yum MS; Ra YS; Park JB; Ahn JS; Kim GH; Goo HW; Ko TS; Yoo HW
    J Neurosurg; 2016 May; 124(5):1221-7. PubMed ID: 26430847
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Association of echocardiographic left ventricular structure and -344C/T aldosterone synthase gene variant: A meta-analysis.
    Wang L; Zhou J; Zhang B; Wang H; Li M; Niu Q; Chen Y; Chen R; Wen S
    J Renin Angiotensin Aldosterone Syst; 2015 Dec; 16(4):858-71. PubMed ID: 25208931
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Aurora kinases A and B and familial breast cancer risk.
    Tchatchou S; Wirtenberger M; Hemminki K; Sutter C; Meindl A; Wappenschmidt B; Kiechle M; Bugert P; Schmutzler RK; Bartram CR; Burwinkel B
    Cancer Lett; 2007 Mar; 247(2):266-72. PubMed ID: 16762494
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Sibling cases of moyamoya disease having homozygous and heterozygous c.14576G>A variant in RNF213 showed varying clinical course and severity.
    Miyatake S; Touho H; Miyake N; Ohba C; Doi H; Saitsu H; Taguri M; Morita S; Matsumoto N
    J Hum Genet; 2012 Dec; 57(12):804-6. PubMed ID: 22931863
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a homozygous mutation of SLC24A5 (OCA6) in two patients with oculocutaneous albinism from French Guiana.
    Bertolotti A; Lasseaux E; Plaisant C; Trimouille A; Morice-Picard F; Rooryck C; Lacombe D; Couppie P; Arveiler B
    Pigment Cell Melanoma Res; 2016 Jan; 29(1):104-6. PubMed ID: 26491832
    [No Abstract]   [Full Text] [Related]  

  • 16. Inconsistent susceptibility to autoimmunity in inbred LEW rats is due to genetic crossbreeding involving segregation of the arthritis-regulating gene Ncf1.
    Olofsson P; Johansson A; Wedekind D; Klöting I; Klinga-Levan K; Lu S; Holmdahl R
    Genomics; 2004 May; 83(5):765-71. PubMed ID: 15081107
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian population.
    Newman WG; Zhang Q; Liu X; Walker E; Ternan H; Owen J; Johnson B; Greer W; Mosher DP; Maksymowych WP; Bykerk VP; Keystone EC; Amos CI; Siminovitch KA
    Arthritis Rheum; 2006 Dec; 54(12):3820-7. PubMed ID: 17133579
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Association of the luteinizing hormone/choriogonadotropin receptor gene polymorphism with polycystic ovary syndrome.
    Bassiouny YA; Rabie WA; Hassan AA; Darwish RK
    Gynecol Endocrinol; 2014 Jun; 30(6):428-30. PubMed ID: 24592983
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cenani-Lenz syndactyly in siblings with a novel homozygous LRP4 mutation and recurrent hypoglycaemia.
    Steel E; Hurst JA; Cullup T; Calder A; Sivakumar B; Shah P; Wilson LC
    Clin Dysmorphol; 2020 Apr; 29(2):73-80. PubMed ID: 31895055
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association between MMP-9 -1562 C/T polymorphism and susceptibility to digestive cancers: A meta-analysis.
    Hu C; Weng F; Li L; Dai W; Yan J; Peng L; Zhou R
    Gene; 2018 Oct; 673():88-94. PubMed ID: 29890308
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.