229 related articles for article (PubMed ID: 9226167)
41. 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]
42. Truncation of the cytoplasmic domain of beta3 in a variant form of Glanzmann thrombasthenia abrogates signaling through the integrin alpha(IIb)beta3 complex.
Wang R; Shattil SJ; Ambruso DR; Newman PJ
J Clin Invest; 1997 Nov; 100(9):2393-403. PubMed ID: 9351872
[TBL] [Abstract][Full Text] [Related]
43. A novel Pro126His beta propeller mutation in integrin alphaIIb causes Glanzmann thrombasthenia by impairing progression of pro-alphaIIbbeta3 from endoplasmic reticulum to Golgi.
Shen WZ; Ding QL; Jin PP; Wang XF; Jiang YZ; Li SM; Wang HL
Blood Cells Mol Dis; 2009; 42(1):44-50. PubMed ID: 18976939
[TBL] [Abstract][Full Text] [Related]
44. 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]
45. 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]
46. A 1063G-->A mutation in exon 12 of glycoprotein (GP)IIb associated with a thrombasthenic phenotype: mutation analysis of [324E]GPIIb.
Tao J; Arias-Salgado EG; González-Manchón C; Iruín G; Butta N; Ayuso MS; Parrilla R
Br J Haematol; 2000 Dec; 111(3):965-73. PubMed ID: 11122161
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. 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]
49. [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]
50. 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]
51. Novel point mutations in the alphaIIb subunit (Phe289-->Ser, Glu324-->Lys and Gln747-->Pro) causing thrombasthenic phenotypes in four Japanese patients.
Ambo H; Kamata T; Handa M; Kawai Y; Oda A; Murata M; Takada Y; Ikeda Y
Br J Haematol; 1998 Aug; 102(3):829-40. PubMed ID: 9722314
[TBL] [Abstract][Full Text] [Related]
52. A new platelet polymorphism Duv(a+), localized within the RGD binding domain of glycoprotein IIIa, is associated with neonatal thrombocytopenia.
Jallu V; Meunier M; Brément M; Kaplan C
Blood; 2002 Jun; 99(12):4449-56. PubMed ID: 12036875
[TBL] [Abstract][Full Text] [Related]
53. AlphaIIbG236E causes Glanzmann thrombasthenia by impairing association with beta3.
Afrasiabi A; Gelain F; Artoni A; Mannucci PM
Platelets; 2008 Aug; 19(5):322-7. PubMed ID: 18791937
[TBL] [Abstract][Full Text] [Related]
54. Molecular characterization of Glanzmann's thrombasthenia in Iran: identification of three novel mutations.
Kazemi A; Abolghasemi H; Kazemzadeh S; Vahidi R; Faranoush M; Farsinejad A; Ala F
Blood Coagul Fibrinolysis; 2017 Dec; 28(8):681-686. PubMed ID: 29084015
[TBL] [Abstract][Full Text] [Related]
55. A novel 196Leu to Pro substitution in the beta3 subunit of the alphaIIbbeta3 integrin in a patient with a variant form of Glanzmann thrombasthenia.
Nurden AT; Ruan J; Pasquet JM; Gauthier B; Combrié R; Kunicki T; Nurden P
Platelets; 2002 Mar; 13(2):101-11. PubMed ID: 11897046
[TBL] [Abstract][Full Text] [Related]
56. [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]
57. 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]
58. 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]
59. Disruption of the long-range GPIIIa Cys(5)-Cys(435) disulfide bond results in the production of constitutively active GPIIb-IIIa (alpha(IIb)beta(3)) integrin complexes.
Sun QH; Liu CY; Wang R; Paddock C; Newman PJ
Blood; 2002 Sep; 100(6):2094-101. PubMed ID: 12200372
[TBL] [Abstract][Full Text] [Related]
60. Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease.
Ghosh K; Kulkarni B; Nair S; Shetty S; Mohanty D
Br J Haematol; 2002 Nov; 119(2):348-53. PubMed ID: 12406067
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
