histidine has been researched along with Amyotrophic Lateral Sclerosis in 27 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (3.70) | 18.7374 |
| 1990's | 3 (11.11) | 18.2507 |
| 2000's | 10 (37.04) | 29.6817 |
| 2010's | 10 (37.04) | 24.3611 |
| 2020's | 3 (11.11) | 2.80 |
| Authors | Studies |
|---|---|
| Lee, JY; Muneeswaran, G | 2 |
| Bonaccorsi, M; Dannatt, HRW; Emsley, L; Felli, IC; Knight, MJ; Le Marchand, T; Pierattelli, R; Pintacuda, G; Salmon, L; Schubeis, T | 1 |
| Chen, Y; Dong, Y; Lu, JH; Sun, YM; Wang, J; Wu, JJ | 1 |
| Chen, T; Gao, L; Huang, B; Huang, C; Shi, X | 1 |
| Gomes, J; Padhi, AK | 1 |
| Connor, JR; Lee, SY; Mitchell, RM; Simmons, Z; Stephens, HE; Su, XW | 1 |
| English, AM; Martins, D | 1 |
| Abdolvahabi, A; Shaw, BF; Shi, Y | 1 |
| Aoki, M; Itoyama, Y; Kobayashi, M; Nagai, M; Sasaki, S | 1 |
| Babu, GN; Bala, L; Kalita, J; Khetrapal, CL; Kumar, A; Misra, UK; Singh, RL | 1 |
| Elliott, JL; Luther, C; Puttaparthi, K; Son, M; Srikanth, U | 1 |
| Borchelt, DR; Brown, HH; Lelie, H; Prudencio, M; Valentine, JS; Whitelegge, JP | 1 |
| Gomes, J; Jayaram, B; Padhi, AK | 1 |
| Borchelt, DR; Coonfield, M; Copeland, NG; Fromholt, D; Gonzales, V; Jenkins, NA; Slunt, H; Wang, J | 1 |
| Fukada, K; Hirata, S; Nagano, S; Nakanishi, T; Okuno, T; Sakoda, S; Sato, T; Shimizu, A; Sugai, F; Yamamoto, Y; Zhou, Z | 1 |
| Kato, S; Nabeshima, K; Ohi, T; Takechi, S; Yazawa, S | 1 |
| Antonyuk, S; Doucette, PA; Elam, JS; Hart, PJ; Hasnain, SS; Hayward, LJ; Hough, MA; Rodriguez, JA; Strange, RW; Valentine, JS | 1 |
| Gaggelli, E; Kozlowski, H; Valensin, D; Valensin, G | 1 |
| Andersen, PM; Collinge, J; Fisher, EM; Hardiman, O; Highley, R; Ince, PG; Morrison, KE; Pall, HS; Parkinson, N; Shaw, PJ; Skibinski, G; Smith, MO | 1 |
| Njajou, OT; Sinke, RJ; Sutedja, NA; Van den Berg, LH; Van der Linden, MW; Van der Schouw, YT; Van Duijn, CM; Van Vught, PW; Veldink, JH; Wokke, JH | 1 |
| Bjørgo, K; Holmøy, T; Roos, PM | 1 |
| Corbett, AJ; Griggs, RC; Moxley, RT | 1 |
| Ono, S; Yamauchi, M | 2 |
| Borchelt, DR; Cleveland, DW; Corson, LB; Culotta, VC; Ratovitski, T; Strain, J; Wong, P | 1 |
| Ai, J; Eggers, DK; Faull, KF; Goto, JJ; Gralla, EB; Liu, H; Nersissian, AM; Sanders-Loehr, J; Valentine, JS; Zhu, H | 1 |
1 review(s) available for histidine and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Copper homeostasis and neurodegenerative disorders (Alzheimer's, prion, and Parkinson's diseases and amyotrophic lateral sclerosis).
Topics: Adenosine Triphosphatases; Alzheimer Disease; Amyloid beta-Peptides; Amyotrophic Lateral Sclerosis; Animals; Copper; Histidine; Homeostasis; Humans; Mice; Models, Chemical; Models, Molecular; Molecular Conformation; Molecular Structure; Neurodegenerative Diseases; Oxidative Stress; Parkinson Disease; Prion Diseases; Protein Binding | 2006 |
26 other study(ies) available for histidine and Amyotrophic Lateral Sclerosis
| Article | Year |
|---|---|
Histidine tautomerism dependent conformational transitions driven aggregation of profilin-1: Implications in amyotrophic lateral sclerosis.
Topics: Amyotrophic Lateral Sclerosis; Histidine; Humans; Mutation; Neurodegenerative Diseases; Profilins; Protein Aggregates; Protein Conformation | 2022 |
Mechanistic insights into the conformational switch in profilin-1 subject to collective effects of mutation and histidine tautomerism.
Topics: Amyotrophic Lateral Sclerosis; Histidine; Humans; Molecular Conformation; Mutation; Profilins | 2023 |
Multimodal Response to Copper Binding in Superoxide Dismutase Dynamics.
Topics: Amyotrophic Lateral Sclerosis; Binding Sites; Copper; Crystallization; Histidine; Humans; Kinetics; Magnetic Fields; Magnetic Resonance Spectroscopy; Metalloproteins; Models, Molecular; Protein Conformation; Protein Multimerization; Superoxide Dismutase; Zinc | 2020 |
A novel mutation of VAPB in one Chinese familial amyotrophic lateral sclerosis pedigree and its clinical characteristics.
Topics: Amyotrophic Lateral Sclerosis; Asian People; C9orf72 Protein; Electromyography; Family Health; Female; Genetic Testing; Histidine; Humans; Male; Middle Aged; Models, Molecular; Mutation; Proline; Vesicular Transport Proteins | 2017 |
Mutant UBQLN2
Topics: Administration, Oral; Amyotrophic Lateral Sclerosis; Animals; Autophagy; Choline O-Acetyltransferase; Disease Models, Animal; DNA-Binding Proteins; Doxycycline; Gene Expression Regulation; Histidine; Lysosomal-Associated Membrane Protein 2; Motor Disorders; Motor Neurons; Muscle, Skeletal; Mutation; Proline; Psychomotor Performance; Rats; Rats, Transgenic; Spinal Cord; Ubiquitins | 2018 |
A molecular dynamics based investigation reveals the role of rare Ribonuclease 4 variants in amyotrophic lateral sclerosis susceptibility.
Topics: Amino Acid Sequence; Amyotrophic Lateral Sclerosis; Catalysis; Cell Nucleus; Crystallography, X-Ray; Genetic Predisposition to Disease; Histidine; Humans; Molecular Dynamics Simulation; Mutation, Missense; Protein Conformation; Protein Transport; Ribonucleases; Sequence Homology, Amino Acid | 2019 |
H63D HFE polymorphisms are associated with increased disease duration and decreased muscle superoxide dismutase-1 expression in amyotrophic lateral sclerosis patients.
Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Female; Gene Expression Regulation; Genetic Association Studies; Genotype; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Middle Aged; Muscle, Skeletal; Phenylalanine; Polymorphism, Single Nucleotide; Superoxide Dismutase; Superoxide Dismutase-1 | 2013 |
SOD1 oxidation and formation of soluble aggregates in yeast: relevance to sporadic ALS development.
Topics: Amyotrophic Lateral Sclerosis; Chromatography, High Pressure Liquid; Cysteine; Green Fluorescent Proteins; Histidine; Humans; Mutation; Oxidation-Reduction; Protein Folding; Protein Processing, Post-Translational; Protein Stability; Recombinant Fusion Proteins; Recombinant Proteins; Saccharomyces cerevisiae; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Superoxide Dismutase; Superoxide Dismutase-1 | 2014 |
Protein charge ladders reveal that the net charge of ALS-linked superoxide dismutase can be different in sign and magnitude from predicted values.
Topics: Acetylation; Amyotrophic Lateral Sclerosis; Catalytic Domain; Deuterium Exchange Measurement; Electrophoresis, Capillary; Histidine; Humans; Hydrogen-Ion Concentration; Mutation, Missense; Protein Folding; Protein Stability; Superoxide Dismutase; Superoxide Dismutase-1; Zinc | 2014 |
Mitochondrial alterations in transgenic mice with an H46R mutant Cu/Zn superoxide dismutase gene.
Topics: Age Factors; Amyotrophic Lateral Sclerosis; Animals; Arginine; Disease Models, Animal; Histidine; Mice; Mice, Transgenic; Microscopy, Immunoelectron; Mitochondria; Mutation; Spinal Cord; Superoxide Dismutase | 2009 |
Metabolomic analysis of serum by (1) H NMR spectroscopy in amyotrophic lateral sclerosis.
Topics: 3-Hydroxybutyric Acid; Acetates; Acetone; Adult; Amyotrophic Lateral Sclerosis; Female; Formates; Glutamic Acid; Glutamine; Histidine; Humans; Magnetic Resonance Spectroscopy; Male; Protons; Sensitivity and Specificity | 2010 |
Biochemical properties and in vivo effects of the SOD1 zinc-binding site mutant (H80G).
Topics: Age Factors; Amyotrophic Lateral Sclerosis; Animals; Color Therapy; Disease Models, Animal; Endopeptidase K; Glutamine; Histidine; Humans; Hydrophobic and Hydrophilic Interactions; Mice; Mice, Transgenic; Mutation; Oxidation-Reduction; Protein Binding; Spinal Cord; Superoxide Dismutase; Superoxide Dismutase-1; Zinc | 2011 |
A novel variant of human superoxide dismutase 1 harboring amyotrophic lateral sclerosis-associated and experimental mutations in metal-binding residues and free cysteines lacks toxicity in vivo.
Topics: Amyotrophic Lateral Sclerosis; Animals; Binding Sites; Blotting, Northern; Cells, Cultured; Copper; Cysteine; HEK293 Cells; Histidine; Humans; Immunohistochemistry; Metals; Mice; Mice, Transgenic; Mutation; Polymerase Chain Reaction; RNA, Messenger; Spinal Cord; Superoxide Dismutase; Superoxide Dismutase-1; Transfection; Zinc | 2012 |
Prediction of functional loss of human angiogenin mutants associated with ALS by molecular dynamics simulations.
Topics: Amyotrophic Lateral Sclerosis; Histidine; Humans; Hydrogen Bonding; Molecular Dynamics Simulation; Mutation; Mutation, Missense; Nuclear Localization Signals; Protein Conformation; Ribonuclease, Pancreatic | 2013 |
Copper-binding-site-null SOD1 causes ALS in transgenic mice: aggregates of non-native SOD1 delineate a common feature.
Topics: alpha-Crystallin B Chain; Amyotrophic Lateral Sclerosis; Animals; Axons; Binding Sites; Cells, Cultured; Copper; Histidine; Humans; Intermediate Filament Proteins; Intracellular Signaling Peptides and Proteins; Mice; Mice, Transgenic; Motor Neurons; Mutation; Nerve Tissue Proteins; Protein Kinases; Protein Serine-Threonine Kinases; Spinal Cord; Superoxide Dismutase; Superoxide Dismutase-1 | 2003 |
Identification of two novel mutations in the Cu/Zn superoxide dismutase gene with familial amyotrophic lateral sclerosis: mass spectrometric and genomic analyses.
Topics: Age of Onset; Amyotrophic Lateral Sclerosis; Aspartic Acid; Chromatography, Liquid; DNA Mutational Analysis; Erythrocytes; Exons; Family Health; Female; Glutamic Acid; Glycine; Histidine; Humans; Male; Molecular Biology; Molecular Sequence Data; Mutation; Precipitin Tests; Spectrometry, Mass, Electrospray Ionization; Superoxide Dismutase | 2004 |
Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions.
Topics: Adult; Age of Onset; Amyotrophic Lateral Sclerosis; Antigens, CD; Antigens, Differentiation, Myelomonocytic; Arginine; Astrocytes; Autopsy; Family Health; Female; Histidine; Humans; Hyalin; Immunohistochemistry; Lewy Bodies; Male; Middle Aged; Mutation; Pyramidal Tracts; Spinal Cord; Staining and Labeling; Superoxide Dismutase; Superoxide Dismutase-1 | 2004 |
Structural consequences of the familial amyotrophic lateral sclerosis SOD1 mutant His46Arg.
Topics: Amyotrophic Lateral Sclerosis; Arginine; Histidine; Humans; Models, Molecular; Point Mutation; Protein Conformation; Superoxide Dismutase; Superoxide Dismutase-1; Zinc | 2005 |
ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B).
Topics: Adaptor Proteins, Signal Transducing; Aged; alpha-Synuclein; Amyotrophic Lateral Sclerosis; Brain; DNA Mutational Analysis; Endosomal Sorting Complexes Required for Transport; Glial Fibrillary Acidic Protein; Glutamine; Histidine; Humans; Immunohistochemistry; Isoleucine; Male; Mutation; Nerve Tissue Proteins; Neurofilament Proteins; Phenotype; Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Sequestosome-1 Protein; Spinal Cord; tau Proteins; Ubiquitin; Valine | 2006 |
The association between H63D mutations in HFE and amyotrophic lateral sclerosis in a Dutch population.
Topics: Adult; Aged; Aged, 80 and over; Amyotrophic Lateral Sclerosis; Asparagine; Confidence Intervals; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Genotype; Hemochromatosis Protein; Histidine; Histocompatibility Antigens Class I; Humans; Male; Membrane Proteins; Middle Aged; Mutation; Netherlands; Odds Ratio; Retrospective Studies | 2007 |
Slowly progressing amyotrophic lateral sclerosis caused by H46R SOD1 mutation.
Topics: Amyotrophic Lateral Sclerosis; Arginine; Disease Progression; DNA Mutational Analysis; Family Health; Histidine; Humans; Male; Middle Aged; Mutation; Superoxide Dismutase; Superoxide Dismutase-1 | 2007 |
Skeletal muscle catabolism in amyotrophic lateral sclerosis and chronic spinal muscular atrophy.
Topics: Adult; Aged; Amyotrophic Lateral Sclerosis; Chronic Disease; Creatinine; Female; Histidine; Humans; Male; Methylhistidines; Middle Aged; Muscle Proteins; Muscular Atrophy | 1982 |
Collagen fibril diameter and its relation to cross-linking of collagen in the skin of patients with amyotrophic lateral sclerosis.
Topics: Aged; Amyotrophic Lateral Sclerosis; Collagen; Cross-Linking Reagents; Dipeptides; Female; Histidine; Humans; Male; Microscopy, Electron; Middle Aged; Skin | 1993 |
Variation in the biochemical/biophysical properties of mutant superoxide dismutase 1 enzymes and the rate of disease progression in familial amyotrophic lateral sclerosis kindreds.
Topics: Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Animals; Centrifugation; Copper; COS Cells; Disease Progression; Endopeptidase K; Family Health; Genetic Variation; Glycine; Histidine; Humans; Mice; Mice, Transgenic; Mutation; Protein Binding; Solubility; Superoxide Dismutase; Superoxide Dismutase-1; Time Factors; Tumor Cells, Cultured | 1999 |
Copper(2+) binding to the surface residue cysteine 111 of His46Arg human copper-zinc superoxide dismutase, a familial amyotrophic lateral sclerosis mutant.
Topics: Amyotrophic Lateral Sclerosis; Arginine; Binding, Competitive; Cobalt; Copper; Cysteine; Histidine; Humans; Models, Molecular; Mutation; Protein Processing, Post-Translational; Saccharomyces cerevisiae; Silver; Spectrum Analysis, Raman; Superoxide Dismutase; Titrimetry | 2000 |
Collagen cross-linking of skin in patients with amyotrophic lateral sclerosis.
Topics: Aged; Aging; Amyotrophic Lateral Sclerosis; Arm; Borohydrides; Collagen; Desmosine; Dipeptides; Female; Histidine; Humans; Male; Middle Aged; Muscular Diseases; Nervous System Diseases; Oxidation-Reduction; Skin | 1992 |