Compounds > valine

valine and Dementias, Transmissible

valine has been researched along with Dementias, Transmissible in 17 studies

Research

Studies (17)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	3 (17.65)	18.2507
2000's	7 (41.18)	29.6817
2010's	6 (35.29)	24.3611
2020's	1 (5.88)	2.80

Authors

Authors	Studies
Engelke, AD; Fodor, E; Krausz, SL; Sangeetham, SB; Tatzelt, J; Welker, E	1
Brandel, JP; Cali, I; Cobb, BA; Gambetti, P; Haïk, S; Kitamoto, T; Kong, Q; Langeveld, J; Laplanche, JL; Laude, H; Li, B; Moudjou, M; Petersen, RB; Xiao, X; Yuan, J; Zhan, Y; Zou, WQ	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
Arteagoitia, JM; Atarés, B; Bilbao, MJ; de Pancorbo, MM; Ferrer, I; Garrido, JM; Juste, RA; Rodríguez-Martínez, AB; Zarranz, JJ	1
Hashizume, Y; Ieda, T; Ito, M; Iwasaki, Y; Kitamoto, T; Mori, K; Nagaoka, M; Yoshida, M	1
Biljan, I; Giachin, G; Ilc, G; Legname, G; Plavec, J; Raspadori, A; Zhukov, I	1
Cortez, LM; Kumar, J; Renault, L; Sim, VL; Young, HS	1
Domínguez, A; Graus, F; Nos, C; Saiz, A; Sanchez-Valle, R; Yagüe, J	1
Ghetti, B; Harris, DA; Piccardo, P; Stewart, RS	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
Budka, H; Ertsey, C; Flicker, H; Jelencsik, I; Kovács, GG; László, L; Majtényi, C; Strain, L; Szirmai, I	1
Brown, P; Cortelli, P; Goldfarb, LG; Julien, J; LeBlanc, AC; Montagna, P; Pendelbury, WW; Petersen, RB; Tabaton, M; Vital, C	1

Reviews

1 review(s) available for valine and Dementias, Transmissible

Article	Year
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

16 other study(ies) available for valine and Dementias, Transmissible

Article	Year
The G127V variant of the prion protein interferes with dimer formation in vitro but not in cellulo. Scientific reports, 2021, 02-04, Volume: 11, Issue:1 Topics: Amino Acid Substitution; Cloning, Molecular; Escherichia coli; Gene Expression; Genetic Vectors; Glycine; HeLa Cells; Humans; Luminescent Proteins; Molecular Dynamics Simulation; Mutation; Prion Diseases; Prion Proteins; Protein Multimerization; PrPSc Proteins; Recombinant Fusion Proteins; Recombinant Proteins; Red Fluorescent Protein; Valine	2021
Glycoform-selective prion formation in sporadic and familial forms of prion disease. PloS one, 2013, Volume: 8, Issue:3 Topics: Brain; Cell Line; Cell Membrane; Creutzfeldt-Jakob Syndrome; Endopeptidase K; Endoplasmic Reticulum; Glycosylation; Humans; Polysaccharides; Prion Diseases; Prions; Proteolysis; Valine	2013
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
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
An autopsied case of V180I Creutzfeldt-Jakob disease presenting with panencephalopathic-type pathology and a characteristic prion protein type. Neuropathology : official journal of the Japanese Society of Neuropathology, 2011, Volume: 31, Issue:5 Topics: Aged; Autopsy; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Fatal Outcome; Female; Humans; Isoleucine; Prion Diseases; Subacute Sclerosing Panencephalitis; Valine	2011
Toward the molecular basis of inherited prion diseases: NMR structure of the human prion protein with V210I mutation. Journal of molecular biology, 2011, Sep-30, Volume: 412, Issue:4 Topics: Amino Acid Sequence; Amino Acid Substitution; Genetic Predisposition to Disease; Humans; Hydrophobic and Hydrophilic Interactions; Isoleucine; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Nuclear Magnetic Resonance, Biomolecular; Prion Diseases; Prions; Protein Folding; Protein Structure, Secondary; Protein Structure, Tertiary; Signal Transduction; Valine	2011
Mouse prion protein polymorphism Phe-108/Val-189 affects the kinetics of fibril formation and the response to seeding: evidence for a two-step nucleation polymerization mechanism. The Journal of biological chemistry, 2013, Feb-15, Volume: 288, Issue:7 Topics: Alleles; Animals; Benzothiazoles; Circular Dichroism; Dose-Response Relationship, Drug; Kinetics; Mice; Microscopy, Electron; Phenylalanine; Polymers; Polymorphism, Genetic; Prion Diseases; Prions; Protein Conformation; Recombinant Proteins; Thiazoles; Time Factors; Valine	2013
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
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
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
Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family. Journal of neurology, neurosurgery, and psychiatry, 2001, Volume: 70, Issue:6 Topics: Adult; Alanine; Brain; Female; Humans; Hungary; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Pedigree; Phenotype; Prion Diseases; Prions; Valine	2001
Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism. Science (New York, N.Y.), 1992, Oct-30, Volume: 258, Issue:5083 Topics: Adult; Asparagine; Chromosomes, Human, Pair 20; Codon; Creutzfeldt-Jakob Syndrome; DNA; Genotype; Humans; Middle Aged; Mutation; Phenotype; Polymorphism, Genetic; Prion Diseases; Prions; Valine	1992