methionine has been researched along with Encephalopathy, Kuru 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 | 5 (71.43) | 29.6817 |
| 2010's | 1 (14.29) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Berghoff, AS; Hortobágyi, T; Kovacs, GG; Ströbel, T; Trummert, A; Unterberger, U | 1 |
| Alpers, M; Beck, JA; Campbell, T; Collinge, J; Fisher, EM; Goldstein, D; Mead, S; Poulter, M; Stumpf, MP; Uphill, JB; Whitfield, J | 1 |
| Cervenakova, L; Gajdusek, DC; Goldfarb, LG | 1 |
| Li, H; Lo, RY; Shyu, WC | 1 |
| Kamitani, T; Kawauchi, Y; Kishida, H; Kitamoto, T; Yagishita, S | 1 |
| Brown, P; Cervenáková, L; Gajdusek, DC; Garruto, R; Goldfarb, LG; Lee, HS | 1 |
| Alpers, MP; Brown, P; Cervenáková, L; Gajdusek, DC; Garruto, RM; Goldfarb, LG; Lee, HS | 1 |
1 review(s) available for methionine and Encephalopathy, Kuru
| Article | Year |
|---|---|
Genetic studies in relation to kuru: an overview.
Topics: Animals; Cattle; Creutzfeldt-Jakob Syndrome; Genetic Predisposition to Disease; Genotype; Humans; Kuru; Methionine; Papua New Guinea; Phenotype; Prions; Risk Factors | 2004 |
6 other study(ies) available for methionine and Encephalopathy, Kuru
| Article | Year |
|---|---|
Atypical sporadic CJD-MM phenotype with white matter kuru plaques associated with intranuclear inclusion body and argyrophilic grain disease.
Topics: Aged; Brain; Creutzfeldt-Jakob Syndrome; Encephalopathy, Bovine Spongiform; Humans; Intranuclear Inclusion Bodies; Kuru; Male; Methionine; Phenotype; Tauopathies; White Matter | 2015 |
Balancing selection at the prion protein gene consistent with prehistoric kurulike epidemics.
Topics: Adult; Animals; Cannibalism; Child; Codon; Creutzfeldt-Jakob Syndrome; Disease Outbreaks; Ethnicity; Female; Gene Frequency; Haplotypes; Heterozygote; History, 19th Century; History, 20th Century; History, Ancient; Homozygote; Humans; Immunity, Innate; Kuru; Linkage Disequilibrium; Male; Methionine; Middle Aged; Mutation; Papua New Guinea; Polymorphism, Genetic; PrPC Proteins; Selection, Genetic; Valine | 2003 |
Long-duration sCJD with PRNP codon 129 methionine homozygosity and cerebral cortical plaques.
Topics: Adult; Amyloid; Brain Diseases; Codon; Creutzfeldt-Jakob Syndrome; Female; Genetic Predisposition to Disease; Homozygote; Humans; Kuru; Methionine; Mutation; Plaque, Amyloid; Prion Proteins; Prions; Protein Precursors; Time Factors | 2006 |
Autopsy case of Creutzfeldt-Jakob disease with Met/Val heterozygosity at codon 129 and type 1 protease-resistant prion protein presenting some florid-type plaques and many Kuru plaques in the cerebellum.
Topics: Autopsy; Blotting, Western; Cerebellum; Creutzfeldt-Jakob Syndrome; Female; Genotype; Humans; Kuru; Methionine; Middle Aged; Peptide Hydrolases; Plaque, Amyloid; Polymerase Chain Reaction; Polymorphism, Genetic; Prions; Valine | 2006 |
Phenotype-genotype studies in kuru: implications for new variant Creutzfeldt-Jakob disease.
Topics: Adolescent; Adult; Age of Onset; Amyloid; Child; Chromosomes, Human, Pair 20; Codon; Creutzfeldt-Jakob Syndrome; DNA; Female; Genetic Variation; Genotype; Humans; Kuru; Male; Methionine; Middle Aged; Papua New Guinea; Phenotype; Point Mutation; Prion Proteins; Prions; Protein Precursors; Retrospective Studies; Valine | 1998 |
Increased susceptibility to Kuru of carriers of the PRNP 129 methionine/methionine genotype.
Topics: Amyloid; Child; Child, Preschool; Codon; Disease Outbreaks; Female; Genetic Predisposition to Disease; Genotype; Humans; Infant; Kuru; Male; Methionine; Mutation; New Guinea; Polymorphism, Genetic; Prion Proteins; Prions; Protein Precursors; Sequence Analysis, DNA | 2001 |