BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 19466456)

  • 1. Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.
    Pintao MC; Garcia AA; Borgel D; Alhenc-Gelas M; Spek CA; de Visser MC; Gandrille S; Reitsma PH
    Hum Genet; 2009 Sep; 126(3):449-56. PubMed ID: 19466456
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Small and large PROS1 deletions but no other types of rearrangements detected in patients with protein S deficiency.
    Lind-Halldén C; Dahlen A; Hillarp A; Zöller B; Dahlbäck B; Halldén C
    Thromb Haemost; 2012 Jul; 108(1):94-100. PubMed ID: 22627709
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Large deletions of the PROS1 gene in a large fraction of mutation-negative patients with protein S deficiency.
    Johansson AM; Hillarp A; Säll T; Zöller B; Dahlbäck B; Halldén C
    Thromb Haemost; 2005 Nov; 94(5):951-7. PubMed ID: 16363235
    [TBL] [Abstract][Full Text] [Related]  

  • 5. One novel and one recurrent mutation in the PROS1 gene cause type I protein S deficiency in patients with pulmonary embolism associated with deep vein thrombosis.
    Mizukami K; Nakabayashi T; Naitoh S; Takeda M; Tarumi T; Mizoguchi I; Ieko M; Koike T
    Am J Hematol; 2006 Oct; 81(10):787-97. PubMed ID: 16868938
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variants.
    Espinosa-Parrilla Y; Morell M; Borrell M; Souto JC; Fontcuberta J; Estivill X; Sala N
    Hum Mutat; 2000; 15(5):463-73. PubMed ID: 10790208
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotype and laboratory and clinical phenotypes of protein s deficiency.
    Duebgen S; Kauke T; Marschall C; Giebl A; Lison S; Hart C; Dick A; Spannagl M
    Am J Clin Pathol; 2012 Feb; 137(2):178-84. PubMed ID: 22261441
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A large deletion of the PROS1 gene in a deep vein thrombosis patient with protein S deficiency.
    Yin T; Takeshita S; Sato Y; Sakata T; Shin Y; Honda S; Kawasaki T; Tsuji H; Kojima T; Madoiwa S; Sakata Y; Murata M; Ikeda Y; Miyata T
    Thromb Haemost; 2007 Oct; 98(4):783-9. PubMed ID: 17938802
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel rare c.-39C>T mutation in the PROS1 5'UTR causing PS deficiency by creating a new upstream translation initiation codon.
    Labrouche-Colomer S; Soukarieh O; Proust C; Mouton C; Huguenin Y; Roux M; Besse C; Boland A; Olaso R; Constans J; Deleuze JF; Morange PE; Jaspard-Vinassa B; Trégouët DA;
    Clin Sci (Lond); 2020 May; 134(10):1181-1190. PubMed ID: 32426810
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency.
    Espinosa-Parrilla Y; Morell M; Souto JC; Tirado I; Fontcuberta J; Estivill X; Sala N
    Hum Mutat; 1999; 14(1):30-9. PubMed ID: 10447256
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 41(4):397-400. PubMed ID: 22166512
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.
    Wypasek E; Karpinski M; Alhenc-Gelas M; Undas A
    J Genet; 2017 Dec; 96(6):1047-1051. PubMed ID: 29321366
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary protein S deficiency from a novel large deletion mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification (MLPA).
    Yoo JH; Kim HJ; Maeng HY; Kim YA; Sun YK; Song JW; Choi JR; Kim SH; Lee KA
    Thromb Res; 2009 Mar; 123(5):793-5. PubMed ID: 19168201
    [No Abstract]   [Full Text] [Related]  

  • 16. Characterization of a large chromosomal deletion in the PROS1 gene of a patient with protein S deficiency type I using long PCR.
    Holmes ZR; Bertina RM; Reitsma PH
    Br J Haematol; 1996 Mar; 92(4):986-91. PubMed ID: 8616098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Inherited protein S deficiency as a result of a large duplication mutation of the PROS1 gene detected by multiplex ligation-dependent probe amplification.
    Choung HS; Kim HJ; Gwak GY; Kim SH; Kim DK
    J Thromb Haemost; 2008 Aug; 6(8):1430-2. PubMed ID: 18489710
    [No Abstract]   [Full Text] [Related]  

  • 18. The genomic architecture of the PROS1 gene underlying large tandem duplication mutation that causes thrombophilia from hereditary protein S deficiency.
    Seo JY; Lee KO; Kim SH; Oh D; Kim DK; Kim HJ
    Gene; 2014 Sep; 547(2):295-9. PubMed ID: 24992033
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Severe protein S deficiency resulting from two novel mutations in PROS1 presenting with a relatively mild clinical phenotype.
    Carter IS; Hewitt J; Pu CH; Wu JK; Carter CJ; Macgillivray RT
    J Thromb Haemost; 2008 Jul; 6(7):1237-9. PubMed ID: 18485091
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 10.