asparagine has been researched along with Deficiency of GP 2b 3a Complex in 2 studies
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 | 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 |
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.
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.
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 |