Compounds > proline

proline and Dementias, Transmissible

proline has been researched along with Dementias, Transmissible in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (33.33)18.2507
2000's3 (50.00)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cortes, CJ; Dearmond, SJ; Mallik, S; Mastrianni, JA; Tunnell, E; Wollman, R1
Jodoin, J; Laroche-Pierre, S; LeBlanc, AC1
Agarwal, S; Gill, AC; Goldmann, W; Graham, JF; Kirby, L1
Mizusawa, H; Shiraishi, A; Yamada, M1
Barrow, CJ; Beyreuther, K; Cappai, R; Collins, SJ; Jobling, MF; Masters, CL; Stewart, L; Thyer, JM; White, AR1
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, M1

Reviews

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

ArticleYear
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

5 other study(ies) available for proline and Dementias, Transmissible

ArticleYear
A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformation.
    Neurology, 2008, Oct-28, Volume: 71, Issue:18

    Topics: Adult; Amino Acid Substitution; Brain; Family Health; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Male; Middle Aged; Mutation; Prion Diseases; Prion Proteins; Prions; Proline; Protein Conformation; PrPSc Proteins; Serine

2008
Helix 3 is necessary and sufficient for prion protein's anti-Bax function.
    Journal of neurochemistry, 2009, Volume: 108, Issue:4

    Topics: Alanine; Amino Acid Sequence; Amino Acid Substitution; Animals; Apoptosis; bcl-2-Associated X Protein; Cell Line, Tumor; Cells, Cultured; Cytoprotection; Humans; Mice; Neoplasms; Nerve Degeneration; Prion Diseases; Proline; Protein Structure, Secondary; PrPC Proteins

2009
Inverse correlation of thermal lability and conversion efficiency for five prion protein polymorphic variants.
    Biochemistry, 2010, Feb-23, Volume: 49, Issue:7

    Topics: Amino Acid Substitution; Animals; Cell-Free System; Deer; Genetic Predisposition to Disease; Genetic Variation; Immunity, Innate; Leucine; Mice; Peptide Fragments; Polymorphism, Genetic; Prion Diseases; Prions; Proline; Protein Conformation; Protein Denaturation; Protein Folding; Protein Stability; Sheep; Temperature

2010
Early and persistent sensory-psychiatric symptoms in an inherited prion disease with a PrP P105L mutation.
    Journal of neurology, 2002, Volume: 249, Issue:12

    Topics: Female; Humans; Leucine; Male; Middle Aged; Mutation; Pedigree; Prion Diseases; Prions; Proline

2002
Familial prion disease mutation alters the secondary structure of recombinant mouse prion protein: implications for the mechanism of prion formation.
    Biochemistry, 1999, Mar-16, Volume: 38, Issue:11

    Topics: Amino Acid Substitution; Animals; Circular Dichroism; Drug Resistance; Endopeptidase K; Escherichia coli; Leucine; Mice; Mice, Inbred BALB C; Prion Diseases; Prions; Proline; Protein Structure, Secondary; Recombinant Proteins

1999