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.
178 related articles for article (PubMed ID: 31490209)
1. Plasma phenotypes of protein S Lys196Glu and protein C Lys193del variants prevalent among young Japanese women. Noguchi K; Nakazono E; Tsuda T; Jin X; Sata S; Miya M; Nakano S; Tsuda H Blood Coagul Fibrinolysis; 2019 Dec; 30(8):393-400. PubMed ID: 31490209 [TBL] [Abstract][Full Text] [Related]
2. Racial differences in protein S Tokushima and two protein C variants as genetic risk factors for venous thromboembolism. Tsuda H; Noguchi K; Oh D; Bereczky Z; Lee LH; Kang D; Dusse LMS; das G Carvalho M; Morishita E; Res Pract Thromb Haemost; 2020 Nov; 4(8):1295-1300. PubMed ID: 33313468 [TBL] [Abstract][Full Text] [Related]
3. Activated protein C anticoagulant system dysfunction and thrombophilia in Asia. Hamasaki N; Kuma H; Tsuda H Ann Lab Med; 2013 Jan; 33(1):8-13. PubMed ID: 23301217 [TBL] [Abstract][Full Text] [Related]
4. Genotyping analysis of protein S-Tokushima (K196E) and the involvement of protein S antigen and activity in patients with recurrent pregnancy loss. Matsukawa Y; Asano E; Tsuda T; Kuma H; Kitaori T; Katano K; Ozaki Y; Sugiura-Ogasawara M Eur J Obstet Gynecol Reprod Biol; 2017 Apr; 211():90-97. PubMed ID: 28214760 [TBL] [Abstract][Full Text] [Related]
5. Prevalence of genetic mutations in protein S, protein C and antithrombin genes in Japanese patients with deep vein thrombosis. Miyata T; Sato Y; Ishikawa J; Okada H; Takeshita S; Sakata T; Kokame K; Kimura R; Honda S; Kawasaki T; Suehisa E; Tsuji H; Madoiwa S; Sakata Y; Kojima T; Murata M; Ikeda Y Thromb Res; 2009 May; 124(1):14-8. PubMed ID: 18954896 [TBL] [Abstract][Full Text] [Related]
6. Effects of low-dose combined oral contraceptives and protein S K196E mutation on anticoagulation factors: a prospective observational study. Miyoshi T; Oku H; Asahara S; Okamoto A; Kokame K; Nakai M; Nishimura K; Otsuka F; Higashiyama A; Yoshimatsu J; Miyata T Int J Hematol; 2019 Jun; 109(6):641-649. PubMed ID: 30891674 [TBL] [Abstract][Full Text] [Related]
7. Protein C/S ratio, an accurate and simple tool to identify carriers of a protein C gene mutation. Libourel EJ; Meinardi JR; de Kam PJ; Veenstra R; van der Schaaf W; Ruiters MH; van der Meer J Br J Haematol; 2002 Aug; 118(2):615-8. PubMed ID: 12139756 [TBL] [Abstract][Full Text] [Related]
8. Dysfunction of protein C anticoagulant system, main genetic risk factor for venous thromboembolism in northeast Asians. Yin T; Miyata T J Thromb Thrombolysis; 2014 Jan; 37(1):56-65. PubMed ID: 24233386 [TBL] [Abstract][Full Text] [Related]
9. Protein S and protein C gene mutations in Japanese deep vein thrombosis patients. Kinoshita S; Iida H; Inoue S; Watanabe K; Kurihara M; Wada Y; Tsuda H; Kang D; Hamasaki N Clin Biochem; 2005 Oct; 38(10):908-15. PubMed ID: 15978566 [TBL] [Abstract][Full Text] [Related]
10. Analysis of PROC and PROS1 single nucleotide polymorphisms in a thrombophilia family. Wu D; Zhong Z; Chen Y; Ding H; Yang M; Lian N; Huang Z; Zhang Q; Zhao J; Deng C Clin Respir J; 2019 Aug; 13(8):530-537. PubMed ID: 31295762 [TBL] [Abstract][Full Text] [Related]
11. Genetic risk factors for thrombophilia in Japanese. Miyata T; Okada H; Kawasaki T; Tsuji H; Madoiwa S; Sakata Y; Kojima T; Murata M; Ikeda Y Rinsho Ketsueki; 2009 May; 50(5):381-8. PubMed ID: 19483398 [No Abstract] [Full Text] [Related]
12. Hereditary thrombophilia in a family with three independent protein S and C mutations. A cause of adverse perinatal outcome. Schild RL; Lobb MO; Voke JM Eur J Obstet Gynecol Reprod Biol; 1998 Oct; 80(2):283-5. PubMed ID: 9846686 [TBL] [Abstract][Full Text] [Related]
13. [Study of thrombophilia in Japan achieved by the Department of Clinical Chemistry and Laboratory Medicine, Kyushu University]. Hamasaki N Fukuoka Igaku Zasshi; 2006 Jan; 97(1):1-7. PubMed ID: 16613213 [No Abstract] [Full Text] [Related]
14. Association of protein S p.Pro667Pro dimorphism with plasma protein S levels in normal individuals and patients with inherited protein S deficiency. Castaman G; Biguzzi E; Razzari C; Tosetto A; Fontana G; Asti D; Brancaccio V; Castori D; Lane DA; Faioni EM; Thromb Res; 2007; 120(3):421-6. PubMed ID: 17157360 [TBL] [Abstract][Full Text] [Related]
15. Genetic background analysis of protein C deficiency demonstrates a recurrent mutation associated with venous thrombosis in Chinese population. Tang L; Guo T; Yang R; Mei H; Wang H; Lu X; Yu J; Wang Q; Hu Y PLoS One; 2012; 7(4):e35773. PubMed ID: 22545135 [TBL] [Abstract][Full Text] [Related]
16. Hereditary protein C-deficiency: laboratory values in transmitters and guidelines for the diagnostic procedure. Report on a study of the SSC Subcommittee on Protein C and Protein S. Protein C Transmitter Study Group. Pabinger I; Allaart CF; Hermans J; Briët E; Bertina RM Thromb Haemost; 1992 Oct; 68(4):470-4. PubMed ID: 1448781 [TBL] [Abstract][Full Text] [Related]
17. [Genetic background of Japanese thrombophilia]. Hamasaki N; Kinoshita S; Abe Y Rinsho Byori; 2002 Nov; Suppl 123():104-11. PubMed ID: 12652797 [TBL] [Abstract][Full Text] [Related]
18. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations. Boinot C; Borgel D; Kitzis A; Guicheteau M; Aiach M; Alhenc-Gelas M Blood Coagul Fibrinolysis; 2003 Feb; 14(2):191-6. PubMed ID: 12632031 [TBL] [Abstract][Full Text] [Related]
19. Multicentre evaluation of combined prothrombotic defects associated with thrombophilia in childhood. Childhood Thrombophilia Study Group. Ehrenforth S; Junker R; Koch HG; Kreuz W; Münchow N; Scharrer I; Nowak-Göttl U Eur J Pediatr; 1999 Dec; 158 Suppl 3():S97-104. PubMed ID: 10650845 [TBL] [Abstract][Full Text] [Related]