tryptophan and Deficiency of GP 2b 3a Complex

tryptophan has been researched along with Deficiency of GP 2b 3a Complex in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (100.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Djaffar, I; Rosa, JP	1
Basani, RB; Bennett, JS; Brown, DL; Poncz, M; Vilaire, G	1

Other Studies

2 other study(ies) available for tryptophan and Deficiency of GP 2b 3a Complex

Article	Year
A second case of variant of Glanzmann's thrombasthenia due to substitution of platelet GPIIIa (integrin beta 3) Arg214 by Trp. Human molecular genetics, 1993, Volume: 2, Issue:12 Topics: Amino Acid Sequence; Arginine; Base Sequence; Blood Platelets; Chromosome Mapping; Chromosomes, Human, Pair 17; Deoxyribonucleases, Type II Site-Specific; Humans; Integrin beta3; Integrins; Molecular Sequence Data; Point Mutation; Polymorphism, Restriction Fragment Length; RNA; Thrombasthenia; Transcription, Genetic; Tryptophan	1993
A Leu117-->Trp mutation within the RGD-peptide cross-linking region of beta3 results in Glanzmann thrombasthenia by preventing alphaIIb beta3 export to the platelet surface. Blood, 1997, Oct-15, Volume: 90, Issue:8 Topics: Alleles; Amino Acid Sequence; Animals; Blood Platelets; COS Cells; Flow Cytometry; Humans; Infant; Leucine; Molecular Sequence Data; Mutation; Oligopeptides; Platelet Glycoprotein GPIIb-IIIa Complex; Protein Conformation; Surface Properties; Thrombasthenia; Tryptophan	1997

Article

Year

A second case of variant of Glanzmann's thrombasthenia due to substitution of platelet GPIIIa (integrin beta 3) Arg214 by Trp.

Human molecular genetics, 1993, Volume: 2, Issue:12

Topics: Amino Acid Sequence; Arginine; Base Sequence; Blood Platelets; Chromosome Mapping; Chromosomes, Human, Pair 17; Deoxyribonucleases, Type II Site-Specific; Humans; Integrin beta3; Integrins; Molecular Sequence Data; Point Mutation; Polymorphism, Restriction Fragment Length; RNA; Thrombasthenia; Transcription, Genetic; Tryptophan

1993

A Leu117-->Trp mutation within the RGD-peptide cross-linking region of beta3 results in Glanzmann thrombasthenia by preventing alphaIIb beta3 export to the platelet surface.

Blood, 1997, Oct-15, Volume: 90, Issue:8

Topics: Alleles; Amino Acid Sequence; Animals; Blood Platelets; COS Cells; Flow Cytometry; Humans; Infant; Leucine; Molecular Sequence Data; Mutation; Oligopeptides; Platelet Glycoprotein GPIIb-IIIa Complex; Protein Conformation; Surface Properties; Thrombasthenia; Tryptophan

1997