isoleucine and Dementias, Transmissible

isoleucine has been researched along with Dementias, Transmissible in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
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

Other Studies

2 other study(ies) available for isoleucine and Dementias, Transmissible

Article	Year
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

Article

Year

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