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 *

143 related articles for article (PubMed ID: 1687449)

  • 1. [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]  

  • 2. Application of GPIIIa gene Taq I polymorphism to determination of carrier status in Glanzmann's thrombasthenia families of Chinese origin.
    Ruan C; Gu J; Wang X; Chu X; Pan J
    Thromb Haemost; 1993 Jan; 69(1):64-9. PubMed ID: 8095357
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. [Molecular pathology of inherited Glanzmann's thrombasthenia. Report of 11 cases].
    Ruan CG; Gu JM; Li JY
    Zhonghua Nei Ke Za Zhi; 1992 Oct; 31(10):639-41, 659. PubMed ID: 1306460
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Role of RFLP using TspRI for carrier detection in Glanzmann's thrombasthenia: a report on two families.
    Kannan M; Yadav BK; Ahmad F; Saxena R
    Int J Lab Hematol; 2010 Feb; 32(1 Pt 1):e158-62. PubMed ID: 19170775
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel homozygous mutation (c.175delG) in platelet glycoprotein ITGA2B gene as cause of Glanzmann's thrombasthenia type I.
    Vannier C; Behnisch W; Bartsch I; Sandrock K; Ertle F; Schmidt K; Busse A; Superti-Furga A; Kulozik A; Santoso S; Zieger B
    Klin Padiatr; 2010 May; 222(3):150-3. PubMed ID: 20514618
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Different biochemical expression pattern of platelet surface glycoproteins suggests molecular diversity of Glanzmann's thrombasthenia in Iran.
    Farsinejad A; Farajollahi MM; Kazemi A; Saemi N; Faranoush M
    Blood Coagul Fibrinolysis; 2013 Sep; 24(6):613-8. PubMed ID: 23912132
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. 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]  

  • 13. Glanzmann's thrombasthenia: updated.
    Nair S; Ghosh K; Kulkarni B; Shetty S; Mohanty D
    Platelets; 2002 Nov; 13(7):387-93. PubMed ID: 12487785
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Homozygous Cys542-->Arg substitution in GPIIIa in a Swiss patient with type I Glanzmann's thrombasthenia.
    Ruan J; Schmugge M; Clemetson KJ; Cazes E; Combrie R; Bourre F; Nurden AT
    Br J Haematol; 1999 May; 105(2):523-31. PubMed ID: 10233432
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Classification of Iranian patients with Glanzmann's Thrombasthenia using a flow cytometric method.
    Farsinejad A; Abolghasemi H; Kazemi A; Aghaiipour M; Hadjati E; Faranoush M; Jazebi M; Ala F
    Platelets; 2011; 22(5):321-7. PubMed ID: 21526886
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. Diagnosis of Glanzmann's thrombasthenia and carrier detection using monoclonal antibodies to platelet glycoprotein IIb and IIIa in immunoblotting.
    Perutelli P; Marchese P; Mori PG
    Haemostasis; 1992; 22(6):330-3. PubMed ID: 1478543
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Double heterozygosity of the GPIIb gene in a Swiss patient with Glanzmann's thrombasthenia.
    Ruan J; Peyruchaud O; Alberio L; Valles G; Clemetson K; Bourre F; Nurden AT
    Br J Haematol; 1998 Sep; 102(4):918-25. PubMed ID: 9734640
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Immunological study of platelet glycoproteins and alloantigens in families of patients with Glanzmann's thrombasthenia.
    Boizard-Boval B; Wautier JL; Gruel Y; Caen JP
    Nouv Rev Fr Hematol (1978); 1992; 34(1):93-8. PubMed ID: 1523103
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.