Compounds > isoleucine

isoleucine and Creutzfeldt-Jakob Syndrome

isoleucine has been researched along with Creutzfeldt-Jakob Syndrome in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (12.50)18.2507
2000's3 (37.50)29.6817
2010's4 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Akagi, A; Iwasaki, Y; Kitamoto, T; Mimuro, M; Yamada, M; Yoshida, M1
Hamaguchi, T; Hizume, M; Ito, Y; Kitamoto, T; Kobayashi, A; Mizusawa, H; Ohgami, T; Sanjo, N; Satoh, K; Yamada, M; Yokota, T1
Hashizume, Y; Ieda, T; Ito, M; Iwasaki, Y; Kitamoto, T; Mori, K; Nagaoka, M; Yoshida, M1
Calero, M; Calero, O; Cuadrado-Corrales, N; de Pedro-Cuesta, J; Díaz-Hurtado, M; Ipiens, JR; López-Gastón, JI; Muñoz-Nieto, M; Ramón y Cajal, S; Ramonet, N1
Inada, H; Kato, R; Kobayashi, M; Nagasaka, T; Nitta, K; Ohta, E; Shimokawa, C; Shindo, K; Shiozawa, Z; Togashi, S1
Beaudry, P; Chatelain, J; Dussaucy, M; Jouvet, A; Laplanche, JL; Launay, JM; Planques, B; Ripoll, L; Salzmann, M1
Attane, F; Beaudry, P; Besson, G; Delasnerie-Lauprêtre, N; Hannequin, D; Laplanche, JL; Manivet, P; Peoc'h, K1
Barnham, KJ; Barrow, CJ; Norton, RS; Thompson, AJ1

Other Studies

8 other study(ies) available for isoleucine and Creutzfeldt-Jakob Syndrome

ArticleYear
Pathological progression of genetic Creutzfeldt-Jakob disease with a PrP V180I mutation.
    Prion, 2018, 01-02, Volume: 12, Issue:1

    Topics: Aged; Aged, 80 and over; Brain; Creutzfeldt-Jakob Syndrome; Disease Progression; Gliosis; Glutamic Acid; Humans; Isoleucine; Methionine; Middle Aged; Mutation; Prion Proteins; Vacuoles; Valine

2018
Biochemical features of genetic Creutzfeldt-Jakob disease with valine-to-isoleucine substitution at codon 180 on the prion protein gene.
    Biochemical and biophysical research communications, 2018, 02-19, Volume: 496, Issue:4

    Topics: Aged, 80 and over; Amino Acid Substitution; Codon; Creutzfeldt-Jakob Syndrome; Female; Genetic Markers; Genetic Predisposition to Disease; Humans; Isoleucine; Male; Neocortex; Prion Proteins; Valine

2018
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
A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes.
    Journal of neurology, 2013, Volume: 260, Issue:1

    Topics: 14-3-3 Proteins; Aged; Aged, 80 and over; Alzheimer Disease; Autopsy; Creutzfeldt-Jakob Syndrome; Glial Fibrillary Acidic Protein; Humans; Isoleucine; Male; Models, Molecular; Mutation; Phenotype; Prion Proteins; Prions; Spain; Valine

2013
Autopsy-proven Creutzfeldt-Jakob disease with a codon 180 mutation showing dissociation between diffusion-weighted magnetic resonance imaging and single-photon emission computed tomography findings: Is this a suggestive finding in long survival?
    European neurology, 2006, Volume: 56, Issue:1

    Topics: Aged; Autopsy; Cerebral Cortex; Creutzfeldt-Jakob Syndrome; Diffusion Magnetic Resonance Imaging; Female; Humans; Isoleucine; Methionine; Mutation; Prions; Tomography, Emission-Computed, Single-Photon; Valine

2006
A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease.
    Neurology, 1993, Volume: 43, Issue:10

    Topics: Aged; Aged, 80 and over; Amino Acid Sequence; Base Sequence; Brain; Codon; Creutzfeldt-Jakob Syndrome; DNA; DNA Primers; Humans; Isoleucine; Middle Aged; Molecular Sequence Data; Nerve Tissue Proteins; Oligonucleotide Probes; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Prions; PrPSc Proteins; Reference Values; Valine

1993
Identification of three novel mutations (E196K, V203I, E211Q) in the prion protein gene (PRNP) in inherited prion diseases with Creutzfeldt-Jakob disease phenotype.
    Human mutation, 2000, Volume: 15, Issue:5

    Topics: Aged; Amino Acid Substitution; Amyloid; Creutzfeldt-Jakob Syndrome; Female; Glutamic Acid; Glutamine; Humans; Isoleucine; Lysine; Male; Middle Aged; Mutation, Missense; Phenotype; Prion Proteins; Prions; Protein Precursors; Valine

2000
The Val-210-Ile pathogenic Creutzfeldt-Jakob disease mutation increases both the helical and aggregation propensities of a sequence corresponding to helix-3 of PrP(C).
    Biochimica et biophysica acta, 2001, Jan-12, Volume: 1544, Issue:1-2

    Topics: Amino Acid Sequence; Circular Dichroism; Creutzfeldt-Jakob Syndrome; Isoleucine; Molecular Sequence Data; Mutation; Nuclear Magnetic Resonance, Biomolecular; Protein Structure, Secondary; PrPC Proteins; Valine

2001