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 *

169 related articles for article (PubMed ID: 11722423)

  • 1. A Val193Met mutation in GPIIIa results in a GPIIb/IIIa receptor with a constitutively high affinity for a small ligand.
    Fullard J; Murphy R; O'Neill S; Moran N; Ottridge B; Fitzgerald DJ
    Br J Haematol; 2001 Oct; 115(1):131-9. PubMed ID: 11722423
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (alphaIIbbeta3) integrin receptor locked in a high-affinity state and a Glanzmann thrombasthenia-like phenotype.
    Ruiz C; Liu CY; Sun QH; Sigaud-Fiks M; Fressinaud E; Muller JY; Nurden P; Nurden AT; Newman PJ; Valentin N
    Blood; 2001 Oct; 98(8):2432-41. PubMed ID: 11588040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A Cys374Tyr homozygous mutation of platelet glycoprotein IIIa (beta 3) in a Chinese patient with Glanzmann's thrombasthenia.
    Grimaldi CM; Chen F; Scudder LE; Coller BS; French DL
    Blood; 1996 Sep; 88(5):1666-75. PubMed ID: 8781422
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Glycoprotein IIb Leu214Pro mutation produces glanzmann thrombasthenia with both quantitative and qualitative abnormalities in GPIIb/IIIa.
    Grimaldi CM; Chen F; Wu C; Weiss HJ; Coller BS; French DL
    Blood; 1998 Mar; 91(5):1562-71. PubMed ID: 9473221
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A new variant of Glanzmann's thrombasthenia (Strasbourg I). Platelets with functionally defective glycoprotein IIb-IIIa complexes and a glycoprotein IIIa 214Arg----214Trp mutation.
    Lanza F; Stierlé A; Fournier D; Morales M; André G; Nurden AT; Cazenave JP
    J Clin Invest; 1992 Jun; 89(6):1995-2004. PubMed ID: 1602006
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Molecular genetic analysis of a compound heterozygote for the glycoprotein (GP) IIb gene associated with Glanzmann's thrombasthenia: disruption of the 674-687 disulfide bridge in GPIIb prevents surface exposure of GPIIb-IIIa complexes.
    González-Manchón C; Fernández-Pinel M; Arias-Salgado EG; Ferrer M; Alvarez MV; García-Muñoz S; Ayuso MS; Parrilla R
    Blood; 1999 Feb; 93(3):866-75. PubMed ID: 9920835
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel (288delC) mutation in exon 2 of GPIIb associated with type I Glanzmann's thrombasthenia.
    Tao J; Arias-Salgado EG; González-Manchón C; Díaz-Cremades J; Ayuso MS; Parrilla R
    Br J Haematol; 2000 Oct; 111(1):96-103. PubMed ID: 11091187
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Abnormal processing of the glycoprotein IIb transcript due to a nonsense mutation in exon 17 associated with Glanzmann's thrombasthenia.
    Tomiyama Y; Kashiwagi H; Kosugi S; Shiraga M; Kanayama Y; Kurata Y; Matsuzawa Y
    Thromb Haemost; 1995 May; 73(5):756-62. PubMed ID: 7482399
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Aggregation of chymotrypsin-treated thrombasthenic platelets is mediated by fibrinogen binding to glycoproteins IIb and IIIa.
    Niewiarowski S; Kornecki E; Hershock D; Tuszynski GP; Bennett JS; Soria C; Soria J; Dunn F; Pidard D; Kieffer N
    J Lab Clin Med; 1985 Dec; 106(6):651-60. PubMed ID: 2999274
    [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. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Platelet integrin alpha IIb beta 3 (GPIIb-IIIa) is not implicated in the binding of LDL to intact resting platelets.
    Pedreño J; Fernández R; Cullaré C; Barceló A; Elorza MA; de Castellarnau C
    Arterioscler Thromb Vasc Biol; 1997 Jan; 17(1):156-63. PubMed ID: 9012651
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [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]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.