cysteine has been researched along with Dementia Multi-Infarct in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 6 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Joutel, A; Tournier-Lasserve, E | 1 |
Arboleda-Velasquez, JF; Arcos-Burgos, M; Betensky, RA; Frosch, MP; Gutierrez, JE; Kosik, KS; Lebo, RV; Lopera, F; Lopez, E; Martinez De Arrieta, C; Medina, M; Restrepo, JC; Rivera, D; Sepulveda-Falla, D; Slaugenhaupt, SA; Vargas, S; Villegas, A | 1 |
Curtain, R; Griffiths, L; Grigg, R; Lea, R; MacMillian, J; Sullivan, AA | 1 |
Fryxell, KJ; Jordan, TV; Soderlund, M | 1 |
Dichgans, M; Gasser, T; Herzog, J | 1 |
Abe, K; Hayashi, T; Iwatsuki, K; Manabe, Y; Matsubara, E; Murakami, T; Nagano, I; Sato, K; Shoji, M | 1 |
1 review(s) available for cysteine and Dementia Multi-Infarct
Article | Year |
---|---|
[Molecular basis and physiopathogenic mechanisms of CADASIL: a model of small vessel diseases of the brain].
Topics: Cell Membrane; Cerebral Arteries; Cysteine; Dementia, Multi-Infarct; Humans; Muscle, Smooth, Vascular; Mutation; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch | 2002 |
5 other study(ies) available for cysteine and Dementia Multi-Infarct
Article | Year |
---|---|
C455R notch3 mutation in a Colombian CADASIL kindred with early onset of stroke.
Topics: Adult; Age of Onset; Aged; Arginine; Colombia; Cysteine; Dementia, Multi-Infarct; DNA Mutational Analysis; Female; Heterozygote; Humans; Male; Middle Aged; Mutation; Stroke | 2002 |
Identification of a novel mutation C144F in the Notch3 gene in an Australian CADASIL pedigree.
Topics: Adult; Amino Acid Substitution; Australia; Cysteine; Dementia, Multi-Infarct; Humans; Leukoencephalopathy, Progressive Multifocal; Mutation, Missense; Pedigree; Phenylalanine; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch | 2000 |
An animal model for the molecular genetics of CADASIL. (Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy).
Topics: Animals; Anura; Arteries; Arterioles; Cell Differentiation; Cell Division; Collagen; Cysteine; Dementia, Multi-Infarct; Disease Models, Animal; Drosophila melanogaster; Epidermal Growth Factor; Genes, Dominant; Genes, Lethal; Genetic Linkage; Humans; Mice; Muscle, Smooth, Vascular; Mutation; Myosins; Nerve Fibers, Myelinated; Organ Specificity; Phenotype; Protein Structure, Tertiary; Proto-Oncogene Proteins; Receptor, Notch3; Receptor, Notch4; Receptors, Cell Surface; Receptors, Notch; Signal Transduction | 2001 |
NOTCH3 mutation involving three cysteine residues in a family with typical CADASIL.
Topics: Adult; Aged; Amino Acid Sequence; Base Sequence; Cysteine; Dementia, Multi-Infarct; DNA Mutational Analysis; Family Health; Female; Humans; Male; Middle Aged; Molecular Sequence Data; Pedigree; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch; Repetitive Sequences, Nucleic Acid | 2001 |
Two Japanese CADASIL families with a R141C mutation in the Notch3 gene.
Topics: Agenesis of Corpus Callosum; Arginine; Cysteine; Dementia, Multi-Infarct; DNA Mutational Analysis; Female; Humans; Middle Aged; Mutation, Missense; Pedigree; Point Mutation; Polymerase Chain Reaction; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch | 2001 |