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histidine and Autosomal Chromosome Disorders

histidine has been researched along with Autosomal Chromosome Disorders in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19904 (66.67)18.7374
1990's2 (33.33)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Baffa, R; Cotticelli, MG; Croce, CM; De Gregorio, L; Huebner, K; Inoue, H; Negrini, M; Ohta, M; Pastorino, U; Pierotti, MA; Pilotti, S; Sozzi, G; Tornielli, S; Veronese, ML1
Harper, PS1
Bardet, J; de Blois, MC; Kamoun, P; Lejeune, J; Parvy, P; Peeters, M; Rabier, D; Rethoré, MO1
Bulfield, G; Kacser, H1
Berry, HK; Bruckman, C; Dasenbrock, RJ1
Beatty, AV; Beatty, JW1

Reviews

1 review(s) available for histidine and Autosomal Chromosome Disorders

ArticleYear
Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.
    Journal of medical genetics, 1977, Volume: 14, Issue:6

    Topics: Alzheimer Disease; Animals; Chromosome Aberrations; Chromosome Disorders; Creutzfeldt-Jakob Syndrome; Erythroblastosis, Fetal; Female; Genes, Dominant; Genetic Diseases, Inborn; Haplorhini; Hepatitis B; Hepatitis B Surface Antigens; Histidine; Humans; Huntington Disease; Infant, Newborn; Kuru; Liver Diseases; Male; Maternal-Fetal Exchange; Mice; Myotonia Congenita; Nephritis, Hereditary; Optic Atrophy; Phenylketonurias; Pregnancy; Scrapie; Sheep; Slow Virus Diseases

1977

Other Studies

5 other study(ies) available for histidine and Autosomal Chromosome Disorders

ArticleYear
The FHIT gene 3p14.2 is abnormal in lung cancer.
    Cell, 1996, Apr-05, Volume: 85, Issue:1

    Topics: Amino Acid Sequence; Base Sequence; Blotting, Southern; Carcinoma, Non-Small-Cell Lung; Carcinoma, Small Cell; Chromosome Aberrations; Chromosome Disorders; Chromosome Fragile Sites; Chromosome Fragility; Chromosomes, Human, Pair 3; DNA, Complementary; DNA, Satellite; Gene Deletion; Gene Expression Regulation, Neoplastic; Heterozygote; Histidine; Humans; Lung Neoplasms; Molecular Sequence Data; Polymerase Chain Reaction; Sequence Analysis, DNA

1996
[Cri-du-chat disease: plasma and urinary amino acids].
    Annales de genetique, 1990, Volume: 33, Issue:1

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Amino Acids; Asparagine; Aspartic Acid; Child; Child, Preschool; Chromosome Aberrations; Chromosome Deletion; Chromosome Disorders; Chromosome Mapping; Chromosomes, Human, Pair 5; Cri-du-Chat Syndrome; Female; Histidine; Humans; Intellectual Disability; Male; Models, Biological; Purine-Pyrimidine Metabolism, Inborn Errors

1990
Histidinaemia in mouse and man.
    Archives of disease in childhood, 1974, Volume: 49, Issue:7

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Brain Chemistry; Chromosome Aberrations; Chromosome Disorders; Congenital Abnormalities; Disease Models, Animal; Female; Genes, Recessive; Histidine; Histidine Ammonia-Lyase; Homozygote; Humans; Intellectual Disability; Liver; Male; Mice; Movement Disorders; Mutation; Postural Balance; Vestibule, Labyrinth

1974
Histidinemia in two successive generations.
    American journal of diseases of children (1960), 1970, Volume: 119, Issue:3

    Topics: Adolescent; Adult; Audiometry; Child; Chromatography, Paper; Chromosome Aberrations; Chromosome Disorders; FIGLU Test; Histidine; Humans; Intelligence Tests; Male; Metabolism, Inborn Errors; Pedigree; Physical Examination; Psychometrics; Skin

1970
Reduction of radiation damage to Tradescantia chromosomes by adenosine triphosphate, proline, and histidine.
    Genetics, 1966, Volume: 53, Issue:1

    Topics: Adenosine Triphosphate; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Histidine; In Vitro Techniques; Plant Cells; Proline; Radiation Genetics

1966