glutamine and Deficiency of GP 2b 3a Complex

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

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Einav, Y; Hauschner, H; Koren, A; Mansour, W; Rosenberg, N; Seligsohn, U1
Busse, E; Deeg, N; Halimeh, S; Kappert, G; Sandrock, K; Sauer, K; Wiegering, V; Zieger, B1

Other Studies

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

ArticleYear
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
Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.
    Klinische Padiatrie, 2012, Volume: 224, Issue:3

    Topics: Adolescent; Alleles; Amino Acid Substitution; Child; Child, Preschool; Chromosome Aberrations; Consanguinity; DNA Mutational Analysis; Exons; Female; Flow Cytometry; Genes, Recessive; Genetic Carrier Screening; Glutamine; Histidine; Homozygote; Humans; Integrin alpha2; Male; Mutation, Missense; Platelet Aggregation; Point Mutation; RNA Splicing; RNA, Messenger; Thrombasthenia

2012