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 *

196 related articles for article (PubMed ID: 14575584)

  • 1. [Prothrombin deficiency resulted from a homozygous Glu29 to Gly mutation in the prothrombin gene].
    Wang WB; Wang HL; Huang CY; Fang Y; Fu QH; Zhou RF; Xie S; Ding QL; Wu WM; Wang XF; Hu YQ; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2003 Sep; 24(9):449-51. PubMed ID: 14575584
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Two novel factor V gene mutations associated with congenital coagulation factor V deficiency, study of one pedigree].
    Fu QH; Wang HL; Wang MS; Ding QL; Wu WM; Hu YQ; Wang XF; Wang ZY
    Zhonghua Yi Xue Za Zhi; 2003 Feb; 83(4):312-5. PubMed ID: 12812650
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Inherited coagulation factor X deficiency caused by two novel mutations in factor X gene].
    Wang WB; Wang HL; Wang XF; Fu QH; Zhou RF; Xie S; Hu YQ; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2004 Sep; 25(9):519-22. PubMed ID: 15569527
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Severe hereditary coagulation factor V deficiency caused by two novel heterozygous mutations].
    Zhou RF; Fu QH; Xu XC; Wang WB; Wu WM; Ding QL; Xie S; Zhai ZM; Hu YQ; Wang XF; Wu JS; Wang HL
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):129-32. PubMed ID: 15946520
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Homozygosity for a novel missense mutation in the prothrombin gene causing a severe bleeding disorder.
    Poort SR; Michiels JJ; Reitsma PH; Bertina RM
    Thromb Haemost; 1994 Dec; 72(6):819-24. PubMed ID: 7740448
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The inherited coagulation factor XI deficiency caused by intronic mutation IVS J-4delgttg].
    Xie S; Wang HL; Wang XF; Wu WM; Zhou RF; Wang WB; Hu YQ; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):144-7. PubMed ID: 15946525
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Compound heterozygosity for two novel missense mutations in the prothrombin gene in a patient with a severe bleeding tendency.
    Poort SR; Landolfi R; Bertina RM
    Thromb Haemost; 1997 Apr; 77(4):610-5. PubMed ID: 9134629
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary hemorrhagic telangiectasia resulted from a nonsense mutation Arg479 Stop in the ALK-1 gene].
    Xie BS; Xie S; Chen P; Zhu MY; Zheng JY; Wang XF; Fu QH; Zhou RF; Wang WB; Wu WM; Ding QL; Wang HL; Hu LM
    Zhonghua Xue Ye Xue Za Zhi; 2004 Sep; 25(9):536-9. PubMed ID: 15569532
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Phenotypic and genetic analysis of dysprothrombinemia due to a novel homozygous mutation.
    Su K; Jin Y; Miao Z; Cheng X; Yang L; Wang M
    Hematology; 2017 Jul; 22(6):380-385. PubMed ID: 28196451
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Biochemical activity and gene analysis of inherited protein C and antithrombin deficiency in two Chinese pedigrees.
    Zhou RF; Fu QH; Wang WB; Xie S; Hu YQ; Wang XF; Wang ZY; Wang HL
    Chin Med J (Engl); 2004 Jun; 117(6):813-7. PubMed ID: 15198878
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Analysis of a consanguineous pedigree featuring hereditary coagulation factor Ⅴ deficiency].
    Xie YS; Zhang Y; Zhu LQ; Jin YH; Yang LH; Xie HX; Wang MS; Yang XL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):161-4. PubMed ID: 23568726
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Type I hereditary protein C deficiency due to C5498T mutation in protein C gene].
    Zhou RF; Wang HL; Fu QH; Wang WB; Wu WM; Ding QL; Xie S; Hu YQ; Wang XF; Wang ZY
    Zhonghua Yi Xue Za Zhi; 2003 Oct; 83(19):1694-7. PubMed ID: 14642106
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A novel mutation in antithrombin gene results in hereditary antithrombin deficiency].
    Zhang FH; Ding QL; Wu JS; Zhou RF; Wang XF; Xu XC
    Zhonghua Xue Ye Xue Za Zhi; 2006 Sep; 27(9):598-601. PubMed ID: 17278425
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prothrombin Shanghai: hypoprothrombinaemia caused by substitution of Gla29 by Gly.
    Wang W; Fu Q; Zhou R; Wu W; Ding Q; Hu Y; Wang X; Wang H; Wang Z
    Haemophilia; 2004 Jan; 10(1):94-7. PubMed ID: 14962227
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prophylactic administration of prothrombin complex concentrates for congenital prothrombin deficiency with a novel frameshift mutation, prothrombin saitama.
    Seki M; Koh K; Inoue T; Tomita Y; Kato M; Shimizu M; Morishita E; Hanada R
    Pediatr Blood Cancer; 2013 Mar; 60(3):503-5. PubMed ID: 23152198
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Phenotype and genotype analysis for a consanguineous pedigree with combined coagulation factor VII and X deficiency].
    Jin Y; Wang M; Wang Y; Yang X; Yang L; Xie Y; Xie H; Zhu L; Yu F
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Feb; 31(1):16-20. PubMed ID: 24510554
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification and three-dimensional structural analysis of nine novel mutations in patients with prothrombin deficiency.
    Akhavan S; Mannucci PM; Lak M; Mancuso G; Mazzucconi MG; Rocino A; Jenkins PV; Perkins SJ
    Thromb Haemost; 2000 Dec; 84(6):989-97. PubMed ID: 11154146
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Molecular analysis of two pedigrees with hereditary F VII deficiency].
    Chu H; Wang H; Wang X; Guo X; Qu B; Duan B; Yin J; Kang W; Wang Z
    Zhonghua Xue Ye Xue Za Zhi; 2002 Mar; 23(3):130-3. PubMed ID: 12015065
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Relations of Budd-Chiari syndrome to prothrombin gene mutation.
    Lin GL; Xu PQ; Qi H; Lian JH; Zheng H; Dang XW
    Hepatobiliary Pancreat Dis Int; 2004 May; 3(2):214-8. PubMed ID: 15138112
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.