cysteine has been researched along with Charcot-Marie-Tooth Disease in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (14.29) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 4 (57.14) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hadziselimovic, A; Hampton, CM; Ke, Z; Law, CL; Li, J; Marinko, JT; Mittendorf, KF; Ohi, MD; Sanders, CR; Schlebach, JP; Wright, ER | 1 |
Bombardi, R; Briani, C; Fabrizi, GM; Lucchetta, M; Taioli, F | 1 |
Avila, RL; Bachi, A; D'Antonio, M; Feltri, ML; Inouye, H; Kirschner, DA; Wrabetz, L | 1 |
Bai, Y; Dillon, LM; Feltri, ML; Kamholz, J; Katona, I; Kirschner, D; Patzkó, A; Saporta, MA; Sarkar, FH; Shy, ME; Vizzuso, D; Wang, S; Wrabetz, L; Wu, X | 1 |
Ammar, N; Amouri, R; Barisić, N; Ceuterick, C; De Jonghe, P; Hentati, F; Martin, JJ; Merlini, L; Nelis, E; Timmerman, V | 1 |
Abe, KT; Brotto, MW; Hirata, MT; Lino, AM; Marchiori, PE; Pavanello, RC; Zatz, M | 1 |
Barinaga, M | 1 |
7 other study(ies) available for cysteine and Charcot-Marie-Tooth Disease
Article | Year |
---|---|
Peripheral myelin protein 22 alters membrane architecture.
Topics: Cell Membrane; Charcot-Marie-Tooth Disease; Cysteine; Humans; Lipid Bilayers; Lipids; Liposomes; Mutation; Myelin Proteins; Recombinant Proteins | 2017 |
Adult onset Charcot-Marie-Tooth disease type 1D with an Arg381Cys mutation of EGR2.
Topics: Adult; Amino Acid Substitution; Arginine; Charcot-Marie-Tooth Disease; Codon; Cysteine; Early Growth Response Protein 2; Female; Humans | 2010 |
P0 (protein zero) mutation S34C underlies instability of internodal myelin in S63C mice.
Topics: Animals; Charcot-Marie-Tooth Disease; Cysteine; Disease Models, Animal; Disulfides; Gene Expression Regulation; Genotype; Hereditary Sensory and Motor Neuropathy; Mice; Mice, Transgenic; Mutation; Myelin P0 Protein; Myelin Sheath; Phosphines; Protein Structure, Tertiary; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization | 2010 |
Curcumin derivatives promote Schwann cell differentiation and improve neuropathy in R98C CMT1B mice.
Topics: Action Potentials; Age Factors; Analysis of Variance; Animals; Animals, Newborn; Anti-Inflammatory Agents, Non-Steroidal; Arginine; Cell Differentiation; Cells, Cultured; Charcot-Marie-Tooth Disease; Chlorocebus aethiops; COS Cells; Curcumin; Cysteine; Disease Models, Animal; DNA-Binding Proteins; Early Growth Response Protein 2; Electric Stimulation; Gene Expression Regulation; Green Fluorescent Proteins; Humans; Mice; Mice, Transgenic; Motor Activity; Muscle Strength; Mutation; Myelin P0 Protein; Neuromuscular Junction; Octamer Transcription Factor-6; Protein Folding; Proto-Oncogene Proteins c-jun; Regulatory Factor X Transcription Factors; Rotarod Performance Test; Schwann Cells; Transcription Factors; Transfection; X-Box Binding Protein 1 | 2012 |
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
Topics: Alleles; Arginine; Charcot-Marie-Tooth Disease; Cysteine; Demyelinating Diseases; DNA Mutational Analysis; Electrophysiology; Family Health; Female; Genetic Predisposition to Disease; Glycine; Histidine; Humans; Male; Microscopy, Electron; Mutation; Nerve Tissue Proteins; Neural Conduction; Pedigree; Peripheral Nerves; Sequence Analysis, DNA; Tryptophan | 2003 |
A novel stop codon mutation in the PMP22 gene associated with a variable phenotype.
Topics: Adolescent; Adult; Aged; Axons; Biopsy; Charcot-Marie-Tooth Disease; Codon, Terminator; Cysteine; DNA Mutational Analysis; Family Health; Female; Humans; Male; Microscopy, Electron; Middle Aged; Mutation; Myelin Proteins; Neurologic Examination; Pedigree; Phenotype; Polymerase Chain Reaction; Polymorphism, Single-Stranded Conformational; Sural Nerve | 2004 |
Glimpsing myelin's protein glue.
Topics: Cell Membrane; Charcot-Marie-Tooth Disease; Crystallization; Crystallography, X-Ray; Cysteine; Hereditary Sensory and Motor Neuropathy; Humans; Mutation; Myelin P0 Protein; Myelin Sheath; Schwann Cells | 1996 |