histidine has been researched along with Cerebral Pseudosclerosis in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (33.33) | 18.7374 |
| 1990's | 2 (16.67) | 18.2507 |
| 2000's | 5 (41.67) | 29.6817 |
| 2010's | 1 (8.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bahde, R; Bhargava, KK; Gupta, S; Kapoor, S; Palestro, CJ; Schilsky, ML | 1 |
| Efremov, RG; Lutsenko, S; Tsivkovskii, R | 1 |
| Aoyama, Y; Morifuji, M; Sakakibara, S; Salamatulla, Q; Xu, H | 1 |
| Abonyi, M; Folhoffer, A; Lakatos, PL | 1 |
| Cherninkova, S; Jelev, H; Kremensky, I; Mihaylova, V; Raycheva, M; Savov, A; Todorov, T; Tournev, I | 1 |
| Neumann, PZ; Silverberg, M | 2 |
| Andrews, NC; Lin, W; Trenor, C | 1 |
| Czlonkowska, A; Gajda, J; Houwen, RH; Juyn, J; Ploos van Amstel, HK; Rodo, M | 1 |
| Cauza, E; Ferenci, P; Gangl, A; Polli, C; Ulrich-Pur, H | 1 |
| Katsuki, Y | 1 |
| Carson, NA; Martin, VA | 1 |
1 review(s) available for histidine and Cerebral Pseudosclerosis
| Article | Year |
|---|---|
[Wilson disease].
Topics: Adenosine Triphosphatases; Cation Transport Proteins; Copper; Copper-Transporting ATPases; Glutamine; Hepatolenticular Degeneration; Histidine; Humans; Mutation | 2004 |
11 other study(ies) available for histidine and Cerebral Pseudosclerosis
| Article | Year |
|---|---|
PET with 64Cu-histidine for noninvasive diagnosis of biliary copper excretion in Long-Evans cinnamon rat model of Wilson disease.
Topics: Animals; Bile; Copper; Copper Radioisotopes; Disease Models, Animal; Hepatocytes; Hepatolenticular Degeneration; Histidine; Liver Diseases; Metabolic Clearance Rate; Positron-Emission Tomography; Rats; Rats, Inbred F344; Rats, Inbred LEC | 2012 |
The role of the invariant His-1069 in folding and function of the Wilson's disease protein, the human copper-transporting ATPase ATP7B.
Topics: Adenosine Triphosphatases; Adenosine Triphosphate; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Binding Sites; Cation Transport Proteins; Cell Membrane; Copper-Transporting ATPases; DNA Primers; Hepatolenticular Degeneration; Histidine; Humans; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Protein Folding; Protein Structure, Secondary; Recombinant Proteins; Sequence Alignment; Sequence Homology, Amino Acid | 2003 |
Excess dietary histidine decreases the liver copper level and serum alanine aminotransferase activity in Long-Evans Cinnamon rats.
Topics: Alanine Transaminase; Animals; Catalase; Copper; Diet; Glutathione Peroxidase; Hepatolenticular Degeneration; Histidine; Lipids; Liver; Male; Organ Size; Rats; Rats, Inbred F344; Rats, Inbred LEC; Species Specificity; Superoxide Dismutase; Weight Gain; Zinc | 2003 |
Wilson's disease in two consecutive generations in a Bulgarian Roma family.
Topics: Adult; Aspartate Aminotransferases; Bulgaria; Child; Family Health; Female; Glutamine; Hepatolenticular Degeneration; Histidine; Humans; Male; Mutation | 2007 |
Metabolic pathways of red blood cell copper in normal humans and in Wilson's disease.
Topics: Amino Acids; Biological Transport; Carbon Isotopes; Cell Membrane Permeability; Child; Copper; Erythrocytes; Hepatolenticular Degeneration; Histidine; Humans; In Vitro Techniques; Kinetics; Male; Models, Theoretical; Radioisotopes | 1967 |
Novel bacterial P-type ATPases with histidine-rich heavy-metal-associated sequences.
Topics: Adenosine Triphosphatases; Amino Acid Sequence; Bacteria; Base Sequence; Cloning, Molecular; DNA Probes; DNA, Complementary; Escherichia coli; Gene Library; Hepatolenticular Degeneration; Histidine; Humans; Menkes Kinky Hair Syndrome; Metals; Molecular Sequence Data; Sequence Homology, Amino Acid; Species Specificity | 1994 |
Very high frequency of the His1069Gln mutation in Polish Wilson disease patients.
Topics: Adolescent; Adult; Amino Acid Substitution; Hepatolenticular Degeneration; Histidine; Humans; Point Mutation; Poland | 1997 |
Distribution of patients with Wilson disease carrying the H1069Q mutation in Austria.
Topics: Amino Acid Substitution; Austria; Emigration and Immigration; Europe, Eastern; Exons; Female; Hepatolenticular Degeneration; Histidine; Humans; Male; Mutation; Population Surveillance; Prevalence; Surveys and Questionnaires | 2000 |
[Urinary excretion of methylhistidine in children. 2. Methylhistidine metabolism in children].
Topics: Child; Child, Preschool; Diet; Dipeptides; Hepatolenticular Degeneration; Histidine; Humans; Infant; Lipidoses; Muscles; Neurofibromatosis 1; Peptides | 1969 |
Inborn metabolic disorders with associated ocular lesions in Northern Ireland.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Cataract; Child; Child, Preschool; Cornea; Eye Diseases; Female; Galactosemias; Hepatolenticular Degeneration; Histidine; Homocystinuria; Humans; Infant; Lens, Crystalline; Male; Myopia; Northern Ireland; Pigmentation Disorders; Renal Aminoacidurias | 1967 |
Active copper transport in mammalian tissues--a possible role in Wilson's disease.
Topics: Animals; Asparagine; Carcinoma, Ehrlich Tumor; Copper; Glutamine; Hepatolenticular Degeneration; Histidine; In Vitro Techniques; Kidney; Liver; Radioisotopes; Rats; Threonine | 1966 |