BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

123 related articles for article (PubMed ID: 34799507)

  • 21. [Phenotype and Genotype Analysis in Two Pedigrees with Hereditary Coagulation Factor Ⅺ Deficiency].
    Weng MS; Lin F; Zhang JC; Wu JR; Yu XM; Yang LY
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2020 Mar; 51(2):252-256. PubMed ID: 32220196
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A focus on dominant negative variants in a series of 170 heterozygous FXI-deficient patients.
    de Mazancourt P; Quélin F; Flaujac C; de Raucourt E; Guillet B; Bauduer F; Ernest V; Beurrier P; Avril A; d'Oiron R; Biron-Andréani C; Meunier S; Dargaud Y
    Haemophilia; 2023 Jul; 29(4):1113-1120. PubMed ID: 37252892
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.
    de la Morena-Barrio B; Palomo Á; Padilla J; Martín-Fernández L; Rojo-Carrillo JJ; Cifuentes R; Bravo-Pérez C; Garrido-Rodríguez P; Miñano A; Rubio AM; Pagán J; Llamas M; Vicente V; Vidal F; Lozano ML; Corral J; de la Morena-Barrio ME
    J Thromb Haemost; 2023 Jul; 21(7):1779-1788. PubMed ID: 36940803
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Clinical manifestations and mutation spectrum of 57 subjects with congenital factor XI deficiency in China.
    Shao Y; Cao Y; Lu Y; Dai J; Ding Q; Wang X; Xi X; Wang H
    Blood Cells Mol Dis; 2016 May; 58():29-34. PubMed ID: 27067486
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Factor 11 single-nucleotide variants in women with heavy menstrual bleeding.
    Wiewel-Verschueren S; Mulder AB; Meijer K; Mulder R
    J Obstet Gynaecol; 2017 Oct; 37(7):912-918. PubMed ID: 28609141
    [TBL] [Abstract][Full Text] [Related]  

  • 26. High incidence of FXI deficiency in a Spanish town caused by 11 different mutations and the first duplication of F11: Results from the Yecla study.
    Esteban J; de la Morena-Barrio ME; Salloum-Asfar S; Padilla J; Miñano A; Roldán V; Soria JM; Vidal F; Corral J; Vicente V
    Haemophilia; 2017 Nov; 23(6):e488-e496. PubMed ID: 28960694
    [TBL] [Abstract][Full Text] [Related]  

  • 27. A case of a severe factor XI deficiency in a Chinese woman with heavy menorrhagia.
    Wang Y; Wang Q; Zhang Y; Ma P; Ding H
    Blood Coagul Fibrinolysis; 2019 Mar; 30(2):75-79. PubMed ID: 30720488
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel F11 mutation in a Chinese paediatric patient with severe factor XI deficiency.
    Leung PY; Li CK; Cheng CK; Ng MHL; Chan NCN
    Thromb Res; 2020 Jun; 190():89-90. PubMed ID: 32335422
    [No Abstract]   [Full Text] [Related]  

  • 29. Genetic analysis of a pedigree with combined factor XII and factor XI deficiency.
    Ye X; Feng Y; Ding Q; Dai J; Wang X
    Blood Coagul Fibrinolysis; 2011 Mar; 22(2):118-22. PubMed ID: 21192253
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A novel heterozygous missense mutation (His127Arg) in a family with inherited cross-reacting material positive factor XI deficiency.
    Castaman G; Giacomelli SH; Tagliaferri A; Rodeghiero F
    Blood Coagul Fibrinolysis; 2013 Sep; 24(6):670-2. PubMed ID: 23571684
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Molecular mechanism analysis of a family with hereditary coagulation F Ⅺ deficiency caused by compound heterozygous mutations].
    Chen Y; Qin LY; Lin SR; Yang LL; Zhang K; Ye LY; Jin YH; Wang MS
    Zhonghua Xue Ye Xue Za Zhi; 2024 Mar; 45(3):294-298. PubMed ID: 38716603
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Identification of two novel factor XI non-sense mutation Trp228stop and Trp383stop in a Chinese pedigree of congenital factor XI deficiency].
    Wu WM; Wang HL; Wang XF; Chu HY; Fu QH; Ding QL; Hu YQ; Shen ZX; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2003 Mar; 24(3):126-8. PubMed ID: 12697122
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Two cases of coagulation factor Ⅺ deficiency caused by compound heterozygous mutations].
    Li Q; Zhou M; Xu Y; Zeng H; Xu Y; Xu P; Chen B; Zhou R
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2022 Jun; 39(6):597-601. PubMed ID: 35773762
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Cys482Trp missense mutation in the coagulation factor XI gene (F11) in a Korean patient with factor XI deficiency.
    Choi SJ; Kim J; Lee KA; Choi JR; Yoo J
    Ann Lab Med; 2014 Jul; 34(4):332-5. PubMed ID: 24982842
    [No Abstract]   [Full Text] [Related]  

  • 35. [Analysis of three Chinese pedigrees affected with Hereditary factor Ⅶ deficiency due to compound heterozygous variants of F7 gene].
    Ye L; Chen H; Su Z; Zhang K; Yang L; Jin Y; Wen M; Wang M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Apr; 41(4):393-398. PubMed ID: 38565502
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [FXI gene mutations in two pedigrees of congenital clotting factor XI deficiency].
    Wu WM; Ding QL; Wang XF; Fu QH; Wang WB; Dai J; Fang Y; Zhou RF; Xie S; Hu YQ; Sheng ZX; Wang HL; Wang ZY
    Zhonghua Xue Ye Xue Za Zhi; 2004 Mar; 25(3):132-5. PubMed ID: 15182578
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetic analysis in Factor XI deficient patients from central China: identification of one novel and seven recurrent mutations.
    Liu H; Wang HF; Tang L; Yang Y; Wang QY; Zeng W; Wu YY; Cheng ZP; Hu B; Guo T; Hu Y
    Gene; 2015 Apr; 561(1):101-6. PubMed ID: 25681615
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A case of factor XI deficiency caused by compound heterozygous F11 gene mutation.
    Wang J; Wang X; Dai J; Ding Q; Fu Q; Wang H; Shen L; Li D
    Haemophilia; 2009 Mar; 15(2):603-6. PubMed ID: 19347998
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Gene variants in four pedigrees with hereditary coagulation factor XI deficiency and one novel mutation identification.
    Lin F; Weng MS; Wu JR; Fang SH; Yang LY
    Blood Coagul Fibrinolysis; 2020 Mar; 31(2):160-164. PubMed ID: 31815744
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defect.
    Guella I; Soldà G; Spena S; Asselta R; Ghiotto R; Tenchini ML; Castaman G; Duga S
    Thromb Haemost; 2008 Mar; 99(3):523-30. PubMed ID: 18327400
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.