BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

229 related articles for article (PubMed ID: 9226167)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Double heterozygosity for a novel missense mutation of Ile304 to Asn in addition to the missense mutation His280 to Pro in the integrin beta3 gene as a cause of the absence of platelet alphaIIbbeta3 in Glanzmann's thrombasthenia.
    Tanaka S; Hayashi T; Yoshimura K; Nakayama M; Fujita T; Amano T; Tani Y
    J Thromb Haemost; 2005 Jan; 3(1):68-73. PubMed ID: 15634267
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Serine 752 in the cytoplasmic domain of the beta 3 integrin subunit is not required for alpha v beta 3 postreceptor signaling events.
    Kieffer N; Melchior C; Guinet JM; Michels S; Gouon V; Bron N
    Cell Adhes Commun; 1996 Jul; 4(1):25-39. PubMed ID: 8870971
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Glanzmann's thrombasthenia caused by homozygosity for a splice defect that leads to deletion of the first coding exon of the glycoprotein IIIa mRNA.
    Simsek S; Heyboer H; de Bruijne-Admiraal LG; Goldschmeding R; Cuijpers HT; von dem Borne AE
    Blood; 1993 Apr; 81(8):2044-9. PubMed ID: 8471765
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Leu262Pro mutation in the integrin beta(3) subunit results in an alpha(IIb)-beta(3) complex that binds fibrin but not fibrinogen.
    Ward CM; Kestin AS; Newman PJ
    Blood; 2000 Jul; 96(1):161-9. PubMed ID: 10891446
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 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. 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]  

  • 14. A naturally occurring point mutation in the beta3 integrin MIDAS-like domain affects differently alphavbeta3 and alphaIIIbbeta3 receptor function.
    Morel-Kopp MC; Melchior C; Chen P; Ammerlaan W; Lecompte T; Kaplan C; Kieffer N
    Thromb Haemost; 2001 Dec; 86(6):1425-34. PubMed ID: 11776310
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Nonsense mutation in exon-19 of GPIIb associated with thrombasthenic phenotype. Failure of GPIIb(delta597-1008) to form stable complexes with GPIIIa.
    Arias-Salgado EG; Tao J; González-Manchón C; Butta N; Vicente V; Ayuso MS; Parrilla R
    Thromb Haemost; 2002 Apr; 87(4):684-91. PubMed ID: 12008952
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A Leu55 to Pro substitution in the integrin alphaIIb is responsible for a case of Glanzmann's thrombasthenia.
    Tanaka S; Hayashi T; Hori Y; Terada C; Han KS; Ahn HS; Bourre F; Tani Y
    Br J Haematol; 2002 Sep; 118(3):833-5. PubMed ID: 12181054
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Probing conformational changes in the I-like domain and the cysteine-rich repeat of human beta 3 integrins following disulfide bond disruption by cysteine mutations: identification of cysteine 598 involved in alphaIIbbeta3 activation.
    Chen P; Melchior C; Brons NH; Schlegel N; Caen J; Kieffer N
    J Biol Chem; 2001 Oct; 276(42):38628-35. PubMed ID: 11507099
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.
    Tokgoz H; Torun Ozkan D; Caliskan U; Akar N
    Platelets; 2015; 26(8):779-82. PubMed ID: 25734216
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 12.