histidine 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 |
|---|---|
| Busse, E; Deeg, N; Halimeh, S; Kappert, G; Sandrock, K; Sauer, K; Wiegering, V; Zieger, B | 1 |
| Amano, T; Fujita, T; Hayashi, T; Nakayama, M; Tanaka, S; Tani, Y; Yoshimura, K | 1 |
2 other study(ies) available for histidine and Deficiency of GP 2b 3a Complex
| Article | Year |
|---|---|
Homozygous point mutations in platelet glycoprotein ITGA2B gene as cause of Glanzmann thrombasthenia in 2 families.
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 |
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 |