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 *

154 related articles for article (PubMed ID: 8317479)

  • 1. Homologous recombination among three intragene Alu sequences causes an inversion-deletion resulting in the hereditary bleeding disorder Glanzmann thrombasthenia.
    Li L; Bray PF
    Am J Hum Genet; 1993 Jul; 53(1):140-9. PubMed ID: 8317479
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Identification of an abnormal gene for the GPIIIa subunit of the platelet fibrinogen receptor resulting in Glanzmann's thrombasthenia.
    Bray PF; Shuman MA
    Blood; 1990 Feb; 75(4):881-8. PubMed ID: 1967954
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A deletion in the gene for glycoprotein IIb associated with Glanzmann's thrombasthenia.
    Burk CD; Newman PJ; Lyman S; Gill J; Coller BS; Poncz M
    J Clin Invest; 1991 Jan; 87(1):270-6. PubMed ID: 1702098
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Glanzmann's thrombasthenia associated with deletion-insertion and alternative splicing in the glycoprotein IIb gene.
    Peretz H; Rosenberg N; Usher S; Graff E; Newman PJ; Coller BS; Seligsohn U
    Blood; 1995 Jan; 85(2):414-20. PubMed ID: 7529063
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The molecular genetic basis of Glanzmann thrombasthenia in the Iraqi-Jewish and Arab populations in Israel.
    Newman PJ; Seligsohn U; Lyman S; Coller BS
    Proc Natl Acad Sci U S A; 1991 Apr; 88(8):3160-4. PubMed ID: 2014236
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Structural integrity of the glycoprotein IIb and IIIa genes in Glanzmann thrombasthenia patients from Israel.
    Russell ME; Seligsohn U; Coller BS; Ginsberg MH; Skoglund P; Quertermous T
    Blood; 1988 Nov; 72(5):1833-6. PubMed ID: 3179450
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Glanzmann thrombasthenia caused by an 11.2-kb deletion in the glycoprotein IIIa (beta3) is a second mutation in Iraqi Jews that stemmed from a distinct founder.
    Rosenberg N; Yatuv R; Orion Y; Zivelin A; Dardik R; Peretz H; Seligsohn U
    Blood; 1997 May; 89(10):3654-62. PubMed ID: 9160670
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A three amino acid deletion in glycoprotein IIIa is responsible for type I Glanzmann's thrombasthenia: importance of residues Ile325Pro326Gly327 for beta3 integrin subunit association.
    Morel-Kopp MC; Kaplan C; Proulle V; Jallu V; Melchior C; Peyruchaud O; Aurousseau MH; Kieffer N
    Blood; 1997 Jul; 90(2):669-77. PubMed ID: 9226167
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Carrier detection of Glanzmann's thrombasthenia by Taq I restriction fragment length polymorphism of GPIIIa gene].
    Gu J
    Zhonghua Yi Xue Za Zhi; 1991 Dec; 71(12):680-2, 46. PubMed ID: 1687449
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Truncation of glycoprotein (GP) IIIa (616-762) prevents complex formation with GPIIb: novel mutation in exon 11 of GPIIIa associated with thrombasthenia.
    Ferrer M; Tao J; Iruín G; Sánchez-Ayuso M; González-Rodríguez J; Parrilla R; González-Manchón C
    Blood; 1998 Dec; 92(12):4712-20. PubMed ID: 9845537
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel homozygous mutation (1619delC) in GPIIb gene associated with Glanzmann thrombasthenia, the decay of GPIIb-mRNA and the synthesis of a truncated GPIIb unable to form complex with GPIIIa.
    Losonczy G; Rosenberg N; Kiss C; Kappelmayer J; Vereb G; Kerényi A; Balogh I; Muszbek L
    Thromb Haemost; 2005 May; 93(5):904-9. PubMed ID: 15886807
    [TBL] [Abstract][Full Text] [Related]  

  • 12. An exon 28 mutation resulting in alternative splicing of the glycoprotein IIb transcript and Glanzmann's thrombasthenia.
    Iwamoto S; Nishiumi E; Kajii E; Ikemoto S
    Blood; 1994 Feb; 83(4):1017-23. PubMed ID: 8111043
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular basis for Glanzmann's thrombasthenia (GT) in a compound heterozygote with glycoprotein IIb gene: a proposal for the classification of GT based on the biosynthetic pathway of glycoprotein IIb-IIIa complex.
    Kato A; Yamamoto K; Miyazaki S; Jung SM; Moroi M; Aoki N
    Blood; 1992 Jun; 79(12):3212-8. PubMed ID: 1317725
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a nonsense mutation at amino acid 584-arginine of platelet glycoprotein IIb in patients with type I Glanzmann thrombasthenia.
    Gu JM; Xu WF; Wang XD; Wu QY; Chi CW; Ruan CG
    Br J Haematol; 1993 Mar; 83(3):442-9. PubMed ID: 8485050
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Analysis of the GPIIb and GPIIIa genes in patients with Glanzmann's thrombasthenia].
    Yasunaga M; Ryo R; Adachi M; Sugano W; Yoshida A; Nakayama K; Saigo K; Yasunaga K; Yamaguchi N
    Rinsho Ketsueki; 1992 Feb; 33(2):133-8. PubMed ID: 1635160
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutations in the alphaIIb and beta3 genes that cause Glanzmann thrombasthenia can be distinguished by a simple procedure using transformed B-lymphocytes.
    Rosenberg N; Dardik R; Rosenthal E; Zivelin A; Seligsohn U
    Thromb Haemost; 1998 Feb; 79(2):244-8. PubMed ID: 9493569
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a region in glycoprotein IIIa involved in subunit association with glycoprotein IIb: further lessons from Iraqi-Jewish Glanzmann thrombasthenia.
    Yatuv R; Rosenberg N; Zivelin A; Peretz H; Dardik R; Trakhtenbrot L; Seligsohn U
    Blood; 2001 Aug; 98(4):1063-9. PubMed ID: 11493452
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Glanzmann's thrombasthenia: a rare example of an integrin deficit].
    Perutelli P; Mori PG
    Recenti Prog Med; 1992 Oct; 83(10):577-81. PubMed ID: 1462042
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Glanzmann thrombasthenia secondary to a Gly273-->Asp mutation adjacent to the first calcium-binding domain of platelet glycoprotein IIb.
    Poncz M; Rifat S; Coller BS; Newman PJ; Shattil SJ; Parrella T; Fortina P; Bennett JS
    J Clin Invest; 1994 Jan; 93(1):172-9. PubMed ID: 8282784
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Biochemical and molecular basis of Glanzmann's thrombasthenia.
    Perutelli P; Mori PG
    Haematologica; 1992; 77(5):421-6. PubMed ID: 1483593
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.