Compounds > asparagine

asparagine and Dementias, Transmissible

asparagine has been researched along with Dementias, Transmissible in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (20.00)	18.2507
2000's	1 (20.00)	29.6817
2010's	3 (60.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Kawahara, M; Sadakane, Y	1
Brown, E; Chakrabartty, A; Khan, MQ; Pai, EF; Sweeting, B	1
Arslan, F; Hong, JY; Kanneganti, V; Liebman, SW; Park, SK	1
Brandel, JP; Faucheux, BA; Haïk, S; Hauw, JJ; Laplanche, JL; Peoc'h, K; Privat, N	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 asparagine and Dementias, Transmissible

Article	Year
Implications of Metal Binding and Asparagine Deamidation for Amyloid Formation. International journal of molecular sciences, 2018, Aug-19, Volume: 19, Issue:8 Topics: alpha-Synuclein; Alzheimer Disease; Amyloid; Amyloid beta-Peptides; Animals; Asparagine; Humans; Iron; Lewy Body Disease; Metals; Prion Diseases; Prion Proteins	2018

Other Studies

4 other study(ies) available for asparagine and Dementias, Transmissible

Article	Year
N-terminal helix-cap in α-helix 2 modulates β-state misfolding in rabbit and hamster prion proteins. PloS one, 2013, Volume: 8, Issue:5 Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Asparagine; Circular Dichroism; Cricetinae; Hydrogen-Ion Concentration; Models, Molecular; Molecular Sequence Data; Mutation; Prion Diseases; Prions; Protein Conformation; Protein Folding; Protein Structure, Secondary; Rabbits; Sequence Alignment; Serine; Urea	2013
Heterologous aggregates promote de novo prion appearance via more than one mechanism. PLoS genetics, 2015, Volume: 11, Issue:1 Topics: Asparagine; Cytoplasm; Glutamine; Molecular Chaperones; Prion Diseases; Prions; Protein Aggregates; Protein Conformation; Saccharomyces cerevisiae; Vacuoles	2015
Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation. Annals of neurology, 2004, Volume: 56, Issue:6 Topics: Asparagine; Aspartic Acid; Brain; Humans; Mutation; Prion Diseases; PrPSc Proteins	2004
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