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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

136 related items for PubMed ID: 20880255

  • 1. Protein S inherited qualitative deficiency: novel mutations and phenotypic influence.
    Alhenc-Gelas M, Canonico M, Morange PE, Emmerich J, Geht Genetic Thrombophilia Group.
    J Thromb Haemost; 2010 Dec; 8(12):2718-26. PubMed ID: 20880255
    [Abstract] [Full Text] [Related]

  • 2. Compound heterozygous mutations identified in severe type I protein S deficiency impaired the secretion of protein S.
    Zhou J, Shen W, Gu Y, Li M, Shen W.
    J Clin Pathol; 2020 Jan; 73(1):7-13. PubMed ID: 31422373
    [Abstract] [Full Text] [Related]

  • 3. Clinical Manifestation and Mutation Spectrum of 53 Unrelated Pedigrees with Protein S Deficiency in China.
    Li L, Wu X, Wu W, Ding Q, Cai X, Wang X.
    Thromb Haemost; 2019 Mar; 119(3):449-460. PubMed ID: 30669159
    [Abstract] [Full Text] [Related]

  • 4. PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency.
    Alhenc-Gelas M, Plu-Bureau G, Horellou MH, Rauch A, Suchon P, GEHT genetic thrombophilia group.
    Thromb Haemost; 2016 Mar; 115(3):570-9. PubMed ID: 26466767
    [Abstract] [Full Text] [Related]

  • 5. PROS1 analysis in 87 pedigrees with hereditary protein S deficiency demonstrates striking genotype-phenotype associations.
    Ten Kate MK, Platteel M, Mulder R, Terpstra P, Nicolaes GA, Reitsma PH, van der Steege G, van der Meer J.
    Hum Mutat; 2008 Jul; 29(7):939-47. PubMed ID: 18435454
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. A rare splicing mutation in the PROS1 gene of a Korean patient with type I hereditary protein S deficiency.
    Choi J, Kim HJ, Chang MH, Choi JR, Yoo JH.
    Ann Clin Lab Sci; 2011 Jul; 41(4):397-400. PubMed ID: 22166512
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Analysis of PROS1 mutations and clinical characteristics in three Chinese families with hereditary protein S deficiency.
    Xu F, Zhou X, Jin Y, Yang L, Pan J, Wang M, Chen X.
    Ann Hematol; 2024 Feb; 103(2):653-662. PubMed ID: 38175252
    [Abstract] [Full Text] [Related]

  • 12. Low cut-off values increase diagnostic performance of protein S assays.
    Mulder R, Ten Kate MK, Kluin-Nelemans HC, Mulder AB.
    Thromb Haemost; 2010 Sep; 104(3):618-25. PubMed ID: 20539904
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. A novel nonsense mutation Tyr301* of PROS1 causing protein S deficiency.
    Jang MA, Kim SH, Kim DK, Kim HJ.
    Blood Coagul Fibrinolysis; 2015 Mar; 26(2):223-4. PubMed ID: 25255242
    [Abstract] [Full Text] [Related]

  • 16. Gene analysis of six cases of congenital protein S deficiency and functional analysis of protein S mutations (A139V, C449F, R451Q, C475F, A525V and D599TfsTer13).
    Taniguchi F, Morishita E, Sekiya A, Nomoto H, Katsu S, Kaneko S, Asakura H, Ohtake S.
    Thromb Res; 2017 Mar; 151():8-16. PubMed ID: 28088608
    [Abstract] [Full Text] [Related]

  • 17. Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.
    ten Kate MK, Mulder R, Platteel M, Brouwer JL, van der Steege G, van der Meer J.
    Haematologica; 2006 Aug; 91(8):1151-2. PubMed ID: 16885060
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Molecular basis of protein S deficiency in China.
    Tang L, Jian XR, Hamasaki N, Guo T, Wang HF, Lu X, Wang QY, Hu Y.
    Am J Hematol; 2013 Oct; 88(10):899-905. PubMed ID: 23813890
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.