BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

58 related articles for article (PubMed ID: 9290264)

  • 1. G-->A transition at nucleotide 2110 in the human platelet glycoprotein (GP) IX gene resulting in Ala139(ACC)-->Thr(GCC) substitution.
    Hayashi T; Suzuki K; Akiba J; Yahagi A; Tajima K; Satoh S; Sasaki H
    Jpn J Hum Genet; 1997 Jun; 42(2):369-71. PubMed ID: 9290264
    [No Abstract]   [Full Text] [Related]  

  • 2. Establishment and characterization of transgenic mice expressing human platelet glycoprotein Ib alpha.
    Kitaguchi T; Murata M; Kuramochi T; Kobayashi K; Ito M; Ueyama Y; Nomura T; Hikichi K; Miyakawa Y; Handa M; Hiraoka Y; Aiso S; Ikeda Y
    Biochem Biophys Res Commun; 1996 Mar; 220(2):418-24. PubMed ID: 8645320
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Molecular biological study of glycoprotein IX gene defect in Bernard-Soulier syndrome].
    Zhao XJ; Wang ZY; Duan WM; Fu JX; Lu ME; Wang JM; Bai X; Ruan CG
    Zhonghua Xue Ye Xue Za Zhi; 2003 Sep; 24(9):480-3. PubMed ID: 14575593
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [A novel point mutation in the transmembrane domain of platelet glycoprotein IX gene identified in a Bernard-Soulier syndrome patient].
    Wang Z; Shi J; Han Y
    Zhonghua Xue Ye Xue Za Zhi; 2001 Sep; 22(9):464-6. PubMed ID: 11758225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Corrected DNA sequence of the platelet glycoprotein IX gene.
    Hayashi T; Suzuki K; Yahagi A; Akiba J; Tajima K; Satoh S; Sasaki H
    Thromb Haemost; 1997 May; 77(5):1034-5. PubMed ID: 9184424
    [No Abstract]   [Full Text] [Related]  

  • 6. Association between platelet glycoprotein Ib-alpha and myocardial infarction: results of a pilot study performed in male and female patients from Sicily.
    Candore G; Piazza G; Crivello A; Grimaldi MP; Orlando V; Caruso M; Caimi G; Hoffmann E; Incalcaterra E; Lio D; Caruso C
    Ann N Y Acad Sci; 2006 Nov; 1089():502-8. PubMed ID: 17261793
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Correlation between the polymorphism of platelet glycoprotein GPIb α Kozak gene and transient ischemic attack].
    Song YQ; Zou HL; Zhang C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Oct; 23(5):561-4. PubMed ID: 17029210
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Bernard-Soulier syndrome with severe bleeding: absent platelet glycoprotein Ib alpha due to a homozygous one-base deletion.
    Li C; Pasquale DN; Roth GJ
    Thromb Haemost; 1996 Nov; 76(5):670-4. PubMed ID: 8950770
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Platelet glycoprotein Ia C807T, Ib C3550T, and IIIa Pl(A1/A2) polymorphisms and ischemic stroke in young Taiwanese.
    Chen CH; Lo YK; Ke D; Liu CK; Liou CW; Wu HL; Lai ML;
    J Neurol Sci; 2004 Dec; 227(1):1-5. PubMed ID: 15546585
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Low prevalence of a polymorphism of platelet membrane glycoprotein Ib beta associated with neonatal alloimmune thrombocytopenic purpura in Asian populations.
    Ishida F; Ito T; Santoso S; Kodaira H; Kitano K; Kiyosawa K
    Int J Hematol; 1999 Jan; 69(1):54-6. PubMed ID: 10641444
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Stroke and platelet glycoprotein Ibalpha polymorphisms.
    Sonoda A; Murata M; Ikeda Y; Fukuuchi Y; Watanabe K
    Thromb Haemost; 2001 Mar; 85(3):573-4. PubMed ID: 11307841
    [No Abstract]   [Full Text] [Related]  

  • 12. A novel missense mutation shows that GPIbbeta has a dual role in controlling the processing and stability of the platelet GPIb-IX adhesion receptor.
    Strassel C; Pasquet JM; Alessi MC; Juhan-Vague I; Chambost H; Combrié R; Nurden P; Bas MJ; De La Salle C; Cazenave JP; Lanza F; Nurden AT
    Biochemistry; 2003 Apr; 42(15):4452-62. PubMed ID: 12693941
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic analysis of a variant Bernard-Soulier syndrome due to compound heterozygosity for two novel glycoprotein Ibbeta mutations.
    Kunishima S; Sako M; Yamazaki T; Hamaguchi M; Saito H
    Eur J Haematol; 2006 Dec; 77(6):501-12. PubMed ID: 16978236
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Myocardial infarction: absence of association with VNTR polymorphism of GP Ibalpha.
    Mercier B; Munier S; Bertault V; Mansourati J; Blanc JJ; Férec C
    Thromb Haemost; 2000 Nov; 84(5):921-2. PubMed ID: 11127880
    [No Abstract]   [Full Text] [Related]  

  • 15. Polymorphisms of platelet membrane glycoprotein Ib alpha and plasma von Willebrand factor antigen in coronary artery disease.
    Ito T; Ishida F; Shimodaira S; Kitano K
    Int J Hematol; 1999 Jul; 70(1):47-51. PubMed ID: 10446495
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of a homozygous single base pair deletion in the gene coding for the human platelet glycoprotein Ib alpha causing Bernard-Soulier syndrome.
    Simsek S; Admiraal LG; Modderman PW; van der Schoot CE; von dem Borne AE
    Thromb Haemost; 1994 Sep; 72(3):444-9. PubMed ID: 7855797
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygous loss of platelet glycoprotein (GP) Ib-V-IX variably affects platelet function in velocardiofacial syndrome (VCFS) patients.
    Liang HP; Morel-Kopp MC; Curtin J; Wilson M; Hewson J; Chen W; Ward CM
    Thromb Haemost; 2007 Dec; 98(6):1298-308. PubMed ID: 18064328
    [TBL] [Abstract][Full Text] [Related]  

  • 18. NH2-terminal globular domain of human platelet glycoprotein Ib alpha has a methionine 145/threonine145 amino acid polymorphism, which is associated with the HPA-2 (Ko) alloantigens.
    Kuijpers RW; Faber NM; Cuypers HT; Ouwehand WH; von dem Borne AE
    J Clin Invest; 1992 Feb; 89(2):381-4. PubMed ID: 1346615
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A point mutation in glycoprotein IX coding sequence (Cys73 (TGT) to Tyr(TAT)) causes impaired surface expression of GPIb/IX/V complex in two families with Bernard-Soulier syndrome.
    Noda M; Fujimura K; Takafuta T; Shimomura T; Fujii T; Katsutani S; Fujimoto T; Kuramoto A; Yamazaki T; Mochizuki T; Matsuzaki M; Sano M
    Thromb Haemost; 1996 Dec; 76(6):874-8. PubMed ID: 8972003
    [TBL] [Abstract][Full Text] [Related]  

  • 20. von Willebrand factor but not alpha-thrombin binding to platelet glycoprotein Ibalpha is influenced by the HPA-2 polymorphism.
    Ulrichts H; Vanhoorelbeke K; Cauwenberghs S; Vauterin S; Kroll H; Santoso S; Deckmyn H
    Arterioscler Thromb Vasc Biol; 2003 Jul; 23(7):1302-7. PubMed ID: 12775575
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.