Page last updated: 2024-08-17

methionine and Dementias, Transmissible

methionine has been researched along with Dementias, Transmissible in 21 studies

Research

Studies (21)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	3 (14.29)	18.2507
2000's	9 (42.86)	29.6817
2010's	5 (23.81)	24.3611
2020's	4 (19.05)	2.80

Authors

Authors	Studies
Appleby, BS; Brennecke, N; Cali, I; Cohen, ML; Collins, SJ; Cracco, L; Hosszu, LLP; Mead, S; Mok, TH; Prior, TW; Puoti, G; Speedy, H; Stehmann, C	1
Ae, R; Hamaguchi, T; Kitamoto, T; Kosami, K; Mizusawa, H; Nakamura, Y; Sanjo, N; Tsukamoto, T; Yamada, M	1
Brett, F; Calero, M; Calero, O; Catania, M; Collins, SJ; Ferrer, I; Heffernan, J; Hermann, P; Klotz, S; Kovacs, GG; Ladogana, A; Llorens, F; Moda, F; O'Regan, C; Pocchiari, M; Poleggi, A; Sarros, S; Schmitz, M; Stehmann, C; Villar-Piqué, A; Zerr, I	1
Bettinger, J; Ghaemmaghami, S	1
Barria, MA; Green, AJ; Head, MW; Knight, R; Lee, A	1
Beekes, M; Ebert, E; Lüllmann, K; Mitrova, E; Oikonomou, P; Schlomm, M; Schmitz, M; Wohlhage, M; Zafar, S; Zerr, I	1
Coste, J; Lehmann, S; Segarra, C	1
Cabello, G; Colombo, G; Gabizon, R; Gasset, M; Lisa, S; Meli, M	1
Arteagoitia, JM; Atarés, B; Bilbao, MJ; de Pancorbo, MM; Ferrer, I; Garrido, JM; Juste, RA; Rodríguez-Martínez, AB; Zarranz, JJ	1
Colombo, G; Gasset, M; Meli, M	1
Elliott, CL; Tabrizi, SJ; Weissmann, C	1
Domínguez, A; Graus, F; Nos, C; Saiz, A; Sanchez-Valle, R; Yagüe, J	1
Bradbury, J	1
Ghetti, B; Harris, DA; Piccardo, P; Stewart, RS	1
Concepcion, GP; Padlan, EA	1
Jones, EM; Surewicz, K; Surewicz, WK	1
Caughey, B; James, W; Sim, VL; Tahiri-Alaoui, A	1
Bellayou, H; Gazzaz, B; Hachimi, KM; Laplanche, JL; Nadifi, S; Raddaoui, K; Slassi, I	1
Kitamoto, T; Komai, K; Masaharu, T	1
Inaba, A; Itoh, Y; Kamata, T; Kayano, T; Kitamoto, T; Matsushita, M; Mizusawa, H; Okeda, R; Otomo, E; Satoh, S; Suematsu, N; Takashima, M; Wada, Y; Yamada, M	1
Caughey, B; Demaimay, R; Horiuchi, M; Raymond, GJ	1

Reviews

3 review(s) available for methionine and Dementias, Transmissible

Article	Year
Methionine oxidation within the prion protein. Prion, 2020, Volume: 14, Issue:1 Topics: Amino Acid Sequence; Animals; Humans; Methionine; Oxidation-Reduction; Oxidative Stress; Prion Diseases; Prion Proteins; PrPSc Proteins	2020
Ethical issues in human prion diseases. British medical bulletin, 2003, Volume: 66 Topics: Adolescent; Adult; Aged; Amyloid; Anonymous Testing; Appendix; Child; Diet; Ethics, Clinical; Female; Genetic Diseases, Inborn; Genetic Testing; Homozygote; Human Experimentation; Humans; Legislation, Medical; Male; Methionine; Middle Aged; Palatine Tonsil; Polymorphism, Genetic; Pregnancy; Preimplantation Diagnosis; Prion Diseases; Prion Proteins; Prions; Protein Precursors; PrPSc Proteins; Randomized Controlled Trials as Topic; Risk Assessment; United Kingdom	2003
An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity. Neurology, 1999, Jul-13, Volume: 53, Issue:1 Topics: Amino Acid Substitution; Brain; Codon; Female; Humans; Leucine; Male; Methionine; Middle Aged; Mutation, Missense; Nuclear Family; Pedigree; Polymorphism, Genetic; Prion Diseases; Prions; Proline; Valine	1999

Other Studies

18 other study(ies) available for methionine and Dementias, Transmissible

Article	Year
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion. Viruses, 2021, 09-08, Volume: 13, Issue:9 Topics: Aged; Aged, 80 and over; Alleles; Brain; Creutzfeldt-Jakob Syndrome; Female; Humans; Male; Methionine; Middle Aged; Mutagenesis, Insertional; Oligopeptides; Prion Diseases; Prion Proteins; Prions	2021
Methionine homozygosity for PRNP polymorphism and susceptibility to human prion diseases. Journal of neurology, neurosurgery, and psychiatry, 2022, Volume: 93, Issue:7 Topics: Animals; Case-Control Studies; Cattle; Codon; Creutzfeldt-Jakob Syndrome; Encephalopathy, Bovine Spongiform; Humans; Methionine; Prion Diseases; Prion Proteins; Prions	2022
Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease. Biomolecules, 2020, 02-12, Volume: 10, Issue:2 Topics: Adult; Aged; Biomarkers; Corneal Transplantation; Creutzfeldt-Jakob Syndrome; Dura Mater; Electroencephalography; Encephalopathy, Bovine Spongiform; Female; Homozygote; Human Growth Hormone; Humans; Iatrogenic Disease; Kaplan-Meier Estimate; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Neuroimaging; Phenotype; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Registries; Reproducibility of Results; Sex Factors; Time Factors	2020
Rapid amplification of prions from variant Creutzfeldt-Jakob disease cerebrospinal fluid. The journal of pathology. Clinical research, 2018, Volume: 4, Issue:2 Topics: Animals; Brain; Cattle; Codon; Creutzfeldt-Jakob Syndrome; Encephalopathy, Bovine Spongiform; Homozygote; Humans; Methionine; Prion Diseases; Prion Proteins; Retrospective Studies; Sensitivity and Specificity; tau Proteins; United Kingdom; Zoonoses	2018
Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases. Neurobiology of aging, 2014, Volume: 35, Issue:5 Topics: Adult; Aged; Aged, 80 and over; Codon; Creutzfeldt-Jakob Syndrome; Female; Genotype; Humans; Immunoblotting; Insomnia, Fatal Familial; Male; Methionine; Middle Aged; Mutation; Phosphorylation; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Protein Isoforms; Protein Processing, Post-Translational; PrPC Proteins; PrPSc Proteins; Valine	2014
Prion protein expression and processing in human mononuclear cells: the impact of the codon 129 prion gene polymorphism. PloS one, 2009, Jun-04, Volume: 4, Issue:6 Topics: Brain; Codon; Enzyme-Linked Immunosorbent Assay; Genetic Predisposition to Disease; Genotype; Homozygote; Humans; Immunoblotting; Leukocytes, Mononuclear; Methionine; Polymorphism, Genetic; Prion Diseases; Prions; Reverse Transcriptase Polymerase Chain Reaction; Valine	2009
The structural intolerance of the PrP alpha-fold for polar substitution of the helix-3 methionines. Cellular and molecular life sciences : CMLS, 2010, Volume: 67, Issue:16 Topics: Amino Acid Substitution; Circular Dichroism; DNA Primers; Genetic Variation; Homoserine; Humans; Methionine; Models, Molecular; Norleucine; Prion Diseases; Prions; Protein Conformation; Protein Folding	2010
A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report. BMC neurology, 2010, Oct-25, Volume: 10 Topics: Aged; Blotting, Western; Brain; Codon; Endopeptidase K; Genotype; Humans; Male; Methionine; Phenotype; Prion Diseases; PrPSc Proteins; Valine	2010
Dynamic diagnosis of familial prion diseases supports the β2-α2 loop as a universal interference target. PloS one, 2011, Apr-28, Volume: 6, Issue:4 Topics: Binding Sites; Drug Design; Humans; Methionine; Molecular Dynamics Simulation; Mutation; Oxidation-Reduction; Prion Diseases; Prions; Protein Structure, Secondary; Solvents	2011
Clinical and genetic features of human prion diseases in Catalonia: 1993-2002. European journal of neurology, 2004, Volume: 11, Issue:10 Topics: 14-3-3 Proteins; Adult; Aged; Aged, 80 and over; Amyloid; Ataxia; Dementia; Electroencephalography; Female; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Protein Precursors; Retrospective Studies; Spain; Valine	2004
Genetic susceptibility to prion disease: new phenotypes? The Lancet. Neurology, 2005, Volume: 4, Issue:1 Topics: Animals; Cattle; Creutzfeldt-Jakob Syndrome; Encephalopathy, Bovine Spongiform; Genetic Predisposition to Disease; Homozygote; Humans; Methionine; Phenotype; Prion Diseases	2005
Neurodegenerative illness in transgenic mice expressing a transmembrane form of the prion protein. The Journal of neuroscience : the official journal of the Society for Neuroscience, 2005, Mar-30, Volume: 25, Issue:13 Topics: Animals; Animals, Newborn; Arginine; Blotting, Western; Brain; Cells, Cultured; Cerebellum; Cricetinae; Cricetulus; Detergents; Disease Models, Animal; Electrophoresis, Polyacrylamide Gel; Fluorescent Antibody Technique; Gene Expression; Glial Fibrillary Acidic Protein; Golgi Apparatus; Golgi Matrix Proteins; Immunoprecipitation; Leucine; Membrane Proteins; Methionine; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurodegenerative Diseases; Neurons; Octoxynol; Prion Diseases; Protein Structure, Tertiary; PrPSc Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Sulfur Isotopes; Time Factors; Type C Phospholipases; Valine	2005
The codon for the methionine at position 129 (M129) in the human prion protein provides an alternative initiation site for translation and renders individuals homozygous for M129 more susceptible to prion disease. Medical hypotheses, 2005, Volume: 65, Issue:5 Topics: Amino Acid Substitution; Animals; Clinical Trials as Topic; Codon, Initiator; DNA Mutational Analysis; Evidence-Based Medicine; Genetic Predisposition to Disease; Genetic Testing; Homozygote; Humans; Incidence; Methionine; Models, Genetic; Polymorphism, Genetic; Prion Diseases; Prions; Protein Biosynthesis; Risk Assessment; Risk Factors	2005
Role of N-terminal familial mutations in prion protein fibrillization and prion amyloid propagation in vitro. The Journal of biological chemistry, 2006, Mar-24, Volume: 281, Issue:12 Topics: Amyloid; Benzothiazoles; Escherichia coli; Genetic Predisposition to Disease; Humans; In Vitro Techniques; Kinetics; Methionine; Microscopy, Atomic Force; Molecular Conformation; Mutation; Plasmids; Polymorphism, Genetic; Prion Diseases; Prions; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Spectroscopy, Fourier Transform Infrared; Thiazoles; Time Factors; Valine	2006
Molecular heterosis of prion protein beta-oligomers. A potential mechanism of human resistance to disease. The Journal of biological chemistry, 2006, Nov-10, Volume: 281, Issue:45 Topics: Alleles; Amyloid; Benzothiazoles; Circular Dichroism; Heterozygote; Homozygote; Humans; Hybrid Vigor; Kinetics; Methionine; Prion Diseases; Prions; Thiazoles; Valine	2006
The normal distribution of PRNP codon 129 polymorphism in the Moroccan population (Arabs and Casablanca residents). Pathologie-biologie, 2008, Volume: 56, Issue:3 Topics: Arabs; Genotype; Humans; Methionine; Morocco; Normal Distribution; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Valine; White People	2008
[Prion protein coden 129 polymorphism (Val/Met) in a case of sporadic progressive multisystem degenerative disease]. Rinsho shinkeigaku = Clinical neurology, 1993, Volume: 33, Issue:6 Topics: Codon; Humans; Male; Methionine; Middle Aged; Nerve Degeneration; Polymorphism, Genetic; Prion Diseases; Prions; Valine	1993
Assays of protease-resistant prion protein and its formation. Methods in enzymology, 1999, Volume: 309 Topics: Animals; Brain; Cell-Free System; Cells, Cultured; Endopeptidases; Guanidine; Humans; Immunoblotting; Methionine; Precipitin Tests; Prion Diseases; Prions; Sulfur Radioisotopes	1999