cysteine has been researched along with Diabetes Insipidus, Neurogenic in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Castino, R; Isidoro, C; Murphy, D | 1 |
Beaucourt, S; Castino, R; Davies, J; Isidoro, C; Murphy, D | 1 |
Abbes, AP; Bruggeman, EJ; de Groot, MR; Engel, H; Franken, AA; van den Akker, EL | 1 |
Browning, JE; DiMeglio, LA; Gagliardi, PC; Quigley, CA; Repaske, DR | 1 |
4 other study(ies) available for cysteine and Diabetes Insipidus, Neurogenic
Article | Year |
---|---|
Autophagy-dependent cell survival and cell death in an autosomal dominant familial neurohypophyseal diabetes insipidus in vitro model.
Topics: Adenoviridae; Animals; Autophagy; Cadaverine; Caspases; Cell Death; Cell Line, Tumor; Cell Survival; Codon, Terminator; Cysteine; Diabetes Insipidus, Neurogenic; Disease Models, Animal; Dopamine; Fluorescent Dyes; Gene Expression; Genetic Vectors; Mice; Mutation; Neuroblastoma; Phagosomes; Transfection; Transgenes; Vacuoles; Vasopressins | 2005 |
Autophagy is a prosurvival mechanism in cells expressing an autosomal dominant familial neurohypophyseal diabetes insipidus mutant vasopressin transgene.
Topics: Acridine Orange; Adenoviridae; Animals; Animals, Genetically Modified; Autophagy; Blotting, Western; Cadaverine; Cathepsin D; Cell Line, Tumor; Codon, Terminator; Cysteine; Diabetes Insipidus, Neurogenic; Fluorescent Antibody Technique; Fluorescent Dyes; Gene Expression; Genetic Vectors; Hydrogen-Ion Concentration; Lysosomes; Mutation; Neurites; Neuroblastoma; Neurons; Organelles; Rats; Recombinant Proteins; Transfection; Transgenes; Vacuoles; Vasopressins | 2005 |
[Identification of a new mutation (CysII6Gly) in a family with neurogenic diabetes insipidus].
Topics: Adult; Child, Preschool; Cysteine; Diabetes Insipidus, Neurogenic; Genetic Carrier Screening; Glycine; Guanine; Humans; Male; Mutation; Neurophysins; Pedigree; Polymerase Chain Reaction; Restriction Mapping; Thymine | 2000 |
A missense mutation encoding cys(67) --> gly in neurophysin ii is associated with early onset autosomal dominant neurohypophyseal diabetes insipidus.
Topics: Amino Acids; Child; Child, Preschool; Cysteine; Diabetes Insipidus, Neurogenic; Disulfides; DNA Restriction Enzymes; Exons; Family Health; Female; Genes, Dominant; Glycine; Humans; Hypothalamus; Infant; Infant, Newborn; Magnetic Resonance Imaging; Male; Models, Genetic; Mutation; Mutation, Missense; Neurophysins; Pedigree; Pituitary Gland; Sequence Analysis, DNA | 2001 |