histidine has been researched along with Abnormalities, Sex Chromosome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Erbe, RW; Wang, JC | 1 |
| Saruta, F; Tatsuzawa, O; Tsunawaki, S; Yoshida, LS; Yoshikawa, K | 1 |
| Aldred, MJ; Crawford, PJ; Hart, PS; Hart, TC; Wright, JT; Wright, NJ | 1 |
3 other study(ies) available for histidine and Abnormalities, Sex Chromosome
| Article | Year |
|---|---|
Folate metabolism in humans.
Topics: Amino Acids; Cells, Cultured; Chemical Phenomena; Chemistry; Culture Media; Folic Acid; Folic Acid Deficiency; Fragile X Syndrome; Histidine; Homocysteine; Humans; Intellectual Disability; Lymphocytes; Sex Chromosome Aberrations; Tetrahydrofolates | 1984 |
Mutation at histidine 338 of gp91(phox) depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase.
Topics: Amino Acid Sequence; Binding Sites; Biological Transport; Child, Preschool; Cytochrome b Group; Cytosol; Ferredoxin-NADP Reductase; Flavin-Adenine Dinucleotide; Genetic Linkage; Granulomatous Disease, Chronic; Heme; Histidine; Humans; Male; Membrane Glycoproteins; Membrane Transport Proteins; Molecular Sequence Data; Mutation; NADPH Dehydrogenase; NADPH Oxidase 2; NADPH Oxidases; Neutrophils; Phosphoproteins; Sequence Homology, Amino Acid; Sex Chromosome Aberrations; Superoxides; X Chromosome | 1998 |
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations.
Topics: Amelogenesis Imperfecta; Amelogenin; Amino Acid Sequence; Amino Acid Substitution; Codon, Nonsense; Dental Enamel Proteins; DNA Mutational Analysis; Female; Frameshift Mutation; Genetic Linkage; Genotype; Histidine; Humans; Leucine; Male; Mutation, Missense; Pedigree; Phenotype; Protein Structure, Tertiary; Sex Chromosome Aberrations; X Chromosome | 2002 |