BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 32619258)

  • 21. [Identification of compound heterozygous mutations of F11 gene in a pedigree affected with heriditary coagulation factor XI deficiency].
    Liu M; Li X; Zhou X; Jin Y; Yang L; Pan J; Su K; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Apr; 36(4):363-367. PubMed ID: 30950027
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Analysis of a pedigree affected with hereditary coagulation factor XI deficiency due to compound heterozygous variants of F11 gene].
    Yang T; Zhu J; Yang Q; Liu J; Yang L; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2021 Mar; 38(3):242-246. PubMed ID: 33751533
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Factor XII Osaka: abnormal factor XII with partially defective prekallikrein cleavage activity.
    Iijima K; Arakawa Y; Sugahara Y; Matsushita M; Moriguchi Y; Shimohiro H; Nakagawa M
    Thromb Haemost; 2011 Mar; 105(3):473-8. PubMed ID: 21264442
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Analysis of F12 gene variants and molecular mechanisms in patients with coagulation factor Ⅻ deficiency].
    Fang S; Yang J; Zhang X; Yang L; Wang G
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2023 Apr; 40(4):429-434. PubMed ID: 36972937
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Whole-exome sequencing reveals a novel frameshift mutation in a consanguineous family with a hereditary coagulation factor XII deficiency.
    Ren S; Cai D; Xiao L; Shen H; Ren C
    Clin Biochem; 2023 Aug; 118():110602. PubMed ID: 37391120
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Phenotypic and genotypic analysis of a pedigree affected with hereditary protein C deficiency due to heterozygous deletional mutation of PROC gene].
    Liu S; Yu F; Luo S; Li X; Jin Y; Yang L; Zhou X; Zhang H; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Oct; 37(10):1108-1112. PubMed ID: 32924112
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Phenotypic and genetic analysis of a pedigree affected with hereditary FV deficiency due to a novel deletional variant of F5 gene].
    Ding H; Su K; Hu L; Zhang H; Zhu L; Yang L; Jin Y; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Nov; 36(11):1100-1103. PubMed ID: 31703135
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Molecular genetic analysis of Korean patients with coagulation factor XII deficiency.
    Kwon MJ; Kim HJ; Lee KO; Jung CW; Kim SH
    Blood Coagul Fibrinolysis; 2010 Jun; 21(4):308-12. PubMed ID: 20386432
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel mutation in the coagulation factor 12 gene in subjects with hereditary angioedema and normal C1-inhibitor.
    Bork K; Wulff K; Meinke P; Wagner N; Hardt J; Witzke G
    Clin Immunol; 2011 Oct; 141(1):31-5. PubMed ID: 21849258
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Molecular analysis of multiple genetic variants in Spanish FXII-deficient families.
    Mordillo C; Martinez-Marchán E; Fontcuberta J; Soria JM
    Haematologica; 2007 Nov; 92(11):1569-72. PubMed ID: 18024408
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Homozygous missense variant F12 (Gly506Asp) associated with severe factor XII deficiency: a case report.
    Aljabry M; Algazlan A; Alsubaie N; Dher SB; Aljabri HS; Alotaibi GS
    J Med Case Rep; 2023 Dec; 17(1):504. PubMed ID: 38057855
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The prevalence of heterozygous F12 mutations in Chinese population and its relevance to incidents of thrombosis.
    Wu X; Ding Q; Wang X; Dai J; Wu W
    BMC Med Genet; 2018 Mar; 19(1):50. PubMed ID: 29587641
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Identification of novel compound heterozygous variants in a pedigree affected with hereditary coagulation factor XI deficiency].
    Xia H; Li X; Zhu L; Jin Y; Yang L; Pan J; Zhang H; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):501-504. PubMed ID: 32335872
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification and characterization of two novel mutations (Q421 K and R123P) in congenital factor XII deficiency.
    Kanaji T; Kanaji S; Osaki K; Kuroiwa M; Sakaguchi M; Mihara K; Niho Y; Okamura T
    Thromb Haemost; 2001 Dec; 86(6):1409-15. PubMed ID: 11776307
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A common C-->T polymorphism at nt 46 in the promoter region of coagulation factor XII is associated with decreased factor XII activity.
    Endler G; Exner M; Mannhalter C; Meier S; Ruzicka K; Handler S; Panzer S; Wagner O; Quehenberger P
    Thromb Res; 2001 Feb; 101(4):255-60. PubMed ID: 11248286
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Phenotypic and mutational analysis of a pedigree affected with hereditary coagulation factor Ⅴ deficiency].
    Tian M; Xia H; Zhang Z; Jin Y; Su K; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):202-206. PubMed ID: 29652992
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.
    Lombardi AM; Bortoletto E; Scarparo P; Scapin M; Santarossa L; Girolami A
    Blood Coagul Fibrinolysis; 2008 Oct; 19(7):639-43. PubMed ID: 18832903
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A Novel Homozygous Missense Mutation (Ile583Asn) in a Consanguineous Marriage Family with Hereditary Factor XII Deficiency: A Case Report.
    Jiang S; Chen Y; Xie H; Liu M; Zheng X; Wang M
    Hamostaseologie; 2023 Apr; 43(2):142-145. PubMed ID: 36481867
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genetic analysis of a novel missense mutation (Gly542Ser) with factor XII deficiency in a Chinese patient of consanguineous marriage.
    Zou A; Wang M; Jin Y; Cheng X; Su K; Yang L
    Int J Hematol; 2018 Apr; 107(4):436-441. PubMed ID: 29383625
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Genetic analyses and expression studies identified a novel mutation (W486C) as a molecular basis of congenital coagulation factor XII deficiency.
    Ishii K; Oguchi S; Moriki T; Yatabe Y; Takeshita E; Murata M; Ikeda Y; Watanabe K
    Blood Coagul Fibrinolysis; 2004 Jul; 15(5):367-73. PubMed ID: 15205584
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.