asparagine and Deficiency of GP 2b 3a Complex

asparagine 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	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Einav, Y; Hauschner, H; Koren, A; Mansour, W; Rosenberg, N; Seligsohn, U	1
Amano, T; Fujita, T; Hayashi, T; Nakayama, M; Tanaka, S; Tani, Y; Yoshimura, K	1

Other Studies

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

Article	Year
An αIIb mutation in patients with Glanzmann thrombasthenia located in the N-terminus of blade 1 of the β-propeller (Asn2Asp) disrupts a calcium binding site in blade 6. Journal of thrombosis and haemostasis : JTH, 2011, Volume: 9, Issue:1 Topics: Adolescent; Amino Acid Sequence; Animals; Arabs; Asparagine; Aspartic Acid; Binding Sites; Blood Platelets; Calcium; Cell Line; Child; Child, Preschool; Cricetinae; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamine; Hemostasis; Heredity; Humans; Hydrogen Bonding; Integrin alpha2; Integrin beta3; Israel; Leucine; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Thrombasthenia; Transfection	2011
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. Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:1 Topics: Adult; Animals; Asparagine; Blotting, Western; COS Cells; DNA Primers; DNA, Complementary; Exons; Female; Flow Cytometry; Genetic Vectors; Heterozygote; Histidine; Humans; Immunoprecipitation; Integrin beta3; Isoleucine; Male; Mutation, Missense; Pedigree; Platelet Glycoprotein GPIIb-IIIa Complex; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proline; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Thrombasthenia; Transfection	2005

Article

Year

An αIIb mutation in patients with Glanzmann thrombasthenia located in the N-terminus of blade 1 of the β-propeller (Asn2Asp) disrupts a calcium binding site in blade 6.

Journal of thrombosis and haemostasis : JTH, 2011, Volume: 9, Issue:1

Topics: Adolescent; Amino Acid Sequence; Animals; Arabs; Asparagine; Aspartic Acid; Binding Sites; Blood Platelets; Calcium; Cell Line; Child; Child, Preschool; Cricetinae; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Glutamine; Hemostasis; Heredity; Humans; Hydrogen Bonding; Integrin alpha2; Integrin beta3; Israel; Leucine; Male; Models, Molecular; Molecular Sequence Data; Mutation; Pedigree; Phenotype; Protein Conformation; Protein Structure, Tertiary; Protein Transport; Thrombasthenia; Transfection

2011

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.

Journal of thrombosis and haemostasis : JTH, 2005, Volume: 3, Issue:1

Topics: Adult; Animals; Asparagine; Blotting, Western; COS Cells; DNA Primers; DNA, Complementary; Exons; Female; Flow Cytometry; Genetic Vectors; Heterozygote; Histidine; Humans; Immunoprecipitation; Integrin beta3; Isoleucine; Male; Mutation, Missense; Pedigree; Platelet Glycoprotein GPIIb-IIIa Complex; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Proline; Reverse Transcriptase Polymerase Chain Reaction; Sequence Analysis, DNA; Thrombasthenia; Transfection

2005