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 *

302 related articles for article (PubMed ID: 35269902)

  • 1. The Molecular Basis of FIX Deficiency in Hemophilia B.
    Shen G; Gao M; Cao Q; Li W
    Int J Mol Sci; 2022 Mar; 23(5):. PubMed ID: 35269902
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Apparent synonymous mutation F9 c.87A>G causes secretion failure by in-frame mutation with aberrant splicing.
    Odaira K; Tamura S; Suzuki N; Kakihara M; Hattori Y; Tokoro M; Suzuki S; Takagi A; Katsumi A; Hayakawa F; Okamoto S; Suzuki A; Kanematsu T; Matsushita T; Kojima T
    Thromb Res; 2019 Jul; 179():95-103. PubMed ID: 31102861
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Assessment of the F9 genotype-specific FIX inhibitor risks and characterisation of 10 novel severe F9 defects in the first molecular series of Argentinian patients with haemophilia B.
    Radic CP; Rossetti LC; Abelleyro MM; Candela M; Pérez Bianco R; de Tezanos Pinto M; Larripa IB; Goodeve A; De Brasi C
    Thromb Haemost; 2013 Jan; 109(1):24-33. PubMed ID: 23093250
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characterization of missense mutations in the signal peptide and propeptide of FIX in hemophilia B by a cell-based assay.
    Gao W; Xu Y; Liu H; Gao M; Cao Q; Wang Y; Cui L; Huang R; Shen Y; Li S; Yang H; Chen Y; Li C; Yu H; Li W; Shen G
    Blood Adv; 2020 Aug; 4(15):3659-3667. PubMed ID: 32766856
    [TBL] [Abstract][Full Text] [Related]  

  • 5. An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B.
    Rallapalli PM; Kemball-Cook G; Tuddenham EG; Gomez K; Perkins SJ
    J Thromb Haemost; 2013 Jul; 11(7):1329-40. PubMed ID: 23617593
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hemophilia B: molecular pathogenesis and mutation analysis.
    Goodeve AC
    J Thromb Haemost; 2015 Jul; 13(7):1184-95. PubMed ID: 25851415
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel missense mutation in F9 gene causes hemophilia B in a family with clinical variability.
    Yi S; Yang Q; Zuo Y; Li M; Luo J; Qin Z; Zhang Q; Li M; Huang L; Lu Y; Feng S; Fan X
    Blood Coagul Fibrinolysis; 2020 Mar; 31(2):121-126. PubMed ID: 31904612
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Single synonymous mutation in factor IX alters protein properties and underlies haemophilia B.
    Simhadri VL; Hamasaki-Katagiri N; Lin BC; Hunt R; Jha S; Tseng SC; Wu A; Bentley AA; Zichel R; Lu Q; Zhu L; Freedberg DI; Monroe DM; Sauna ZE; Peters R; Komar AA; Kimchi-Sarfaty C
    J Med Genet; 2017 May; 54(5):338-345. PubMed ID: 28007939
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation Spectrum and Genotype-Phenotype Analyses in a Pakistani Cohort With Hemophilia B.
    Khan MTM; Naz A; Ahmed J; Shamsi T; Ahmed S; Ahmed N; Imran A; Farooq N; Khan MTH; Taj AS
    Clin Appl Thromb Hemost; 2018 Jul; 24(5):741-748. PubMed ID: 28752769
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A codon 338 nonsense mutation in the factor IX gene in unrelated hemophilia B patients: factor IX338 New York.
    Driscoll MC; Bouhassira E; Aledort LM
    Blood; 1989 Aug; 74(2):737-42. PubMed ID: 2752145
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Double mutation, a 2-bp deletion and Val211Ile, in the blood coagulation factor IX gene of a patient with severe hemophilia B].
    Seita I; Shinozawa K; Otaki M; Fujita S; Suzuki T; Amano K; Inaba H; Fukutake K
    Rinsho Byori; 2009 May; 57(5):417-24. PubMed ID: 19522246
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular pathogenesis of a novel Met394Thr variant causing hemophilia B.
    Lu L; Wang L; Shen W; Fang S; Zhao L; Hu X; Yang L; Wang G
    Mol Genet Genomic Med; 2023 May; 11(5):e2147. PubMed ID: 36795372
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Generation of an mESC model with a human hemophilia B nonsense mutation via CRISPR/Cas9 technology.
    Ma Y; Sun W; Zhao L; Yao M; Wu C; Su P; Yang L; Wang G
    Stem Cell Res Ther; 2022 Jul; 13(1):353. PubMed ID: 35883203
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Six novel and three recurrent mutations in nine Austrian patients with hemophilia B.
    Walter J; Pabinger-Fasching I; Watzke HH
    Thromb Haemost; 1994 Jul; 72(1):74-7. PubMed ID: 7974379
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expression and Characterization of Gly-317 Variants of Factor IX Causing Variable Bleeding in Hemophilia B Patients.
    Lu Q; Yang L; Manithody C; Wang X; Rezaie AR
    Biochemistry; 2015 Jun; 54(24):3814-21. PubMed ID: 26023895
    [TBL] [Abstract][Full Text] [Related]  

  • 16. F9 mRNA splicing aberration due to a deep Intronic structural variation in a patient with moderate hemophilia B.
    Odaira K; Kawashima F; Tamura S; Suzuki N; Tokoro M; Hayakawa Y; Suzuki A; Kanematsu T; Okamoto S; Takagi A; Katsumi A; Matsushita T; Shima M; Nogami K; Kojima T; Hayakawa F
    Thromb Res; 2022 May; 213():91-96. PubMed ID: 35313235
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An updated interactive database for 1692 genetic variants in coagulation factor IX provides detailed insights into hemophilia B.
    Xu Z; Spencer HJ; Harris VA; Perkins SJ
    J Thromb Haemost; 2023 May; 21(5):1164-1176. PubMed ID: 36787808
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations.
    Huang L; Li L; Lin S; Chen J; Li K; Fan D; Jin W; Li Y; Yang X; Xiong Y; Li F; Yang X; Li M; Li Q
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1482. PubMed ID: 32875744
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations.
    Guo ZP; Yang LH; Qin XY; Liu XE; Chen JF; Zhang YF
    Haemophilia; 2014 Nov; 20(6):859-65. PubMed ID: 25251685
    [TBL] [Abstract][Full Text] [Related]  

  • 20. First case report of hemophilia B Leyden in Japan.
    Yamashita A; Nagae C; Mori M; Ashikaga T; Kojima T; Taki M
    Int J Hematol; 2017 Jul; 106(1):135-137. PubMed ID: 28168417
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.