クロイツフェルト
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/09/14 12:35:08」(JST)
[Wiki en表示]
Creutzfeldt may mean:
- Hans Gerhard Creutzfeldt - German neuropathologist.
- Creutzfeldt-Jakob disease - degenerative CNS disorder, named after the authors who first described it.
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Prevalent mutations of human prion protein: a molecular modeling and molecular dynamics study.
- Behmard E, Abdolmaleki P, Asadabadi EB, Jahandideh S.SourceDepartment of Biophysics, Faculty of Biological Sciences, Tarbiat Modares University, P.O. Box: 14115/175, Tehran, Iran. parviz@modares.ac.ir.
- Journal of biomolecular structure & dynamics.J Biomol Struct Dyn.2011 Oct;29(2):379-89.
- Point mutations in the human prion protein gene, leading to amino acid substitutions in the human prion protein contribute to conversion of PrPC to PrPSc and amyloid formation, resulting in prion diseases such as familial Creutzfeldt-Jakob disease (CJD), Gerstmann-Straussler-Scheinker disease (GSS),
- PMID 21875156
- The Structural Stability of Wild-type Horse Prion Protein.
- Zhang J.SourceSchool of Sciences, Information Technology and Engineering, University of Ballarat, Mount Helen, Ballarat, Victoria 3353, Australia. jiapu_zhang@hotmail.com.
- Journal of biomolecular structure & dynamics.J Biomol Struct Dyn.2011 Oct;29(2):369-77.
- Prion diseases (e.g. Creutzfeldt-Jakob disease (CJD), variant CJD (vCJD), Gerstmann-Straussler-Scheinker syndrome (GSS), Fatal Familial Insomnia (FFI) and Kuru in humans, scrapie in sheep, bovine spongiform encephalopathy (BSE or 'mad-cow' disease) and chronic wasting disease (CWD) in cattles) are i
- PMID 21875155
Japanese Journal
- Ultrasensitive human prion detection in cerebrospinal fluid by real-time quaking-induced conversion.
- Atarashi Ryuichiro,Satoh Katsuya,Sano Kazunori,Fuse Takayuki,Yamaguchi Naohiro,Ishibashi Daisuke,Matsubara Takehiro,Nakagaki Takehiro,Yamanaka Hitoki,Shirabe Susumu,Yamada Masahito,Mizusawa Hidehiro,Kitamoto Tetsuyuki,Klug Genevieve,McGlade Amelia,Collins Steven J,Nishida Noriyuki
- Nature Medicine 17(2), 175-178, 2011-02
- … Here we developed a new PrP(Sc) amplification assay, called real-time quaking-induced conversion (RT-QUIC), which allows the detection of ≥1 fg of PrP(Sc) in diluted Creutzfeldt-Jakob disease (CJD) brain homogenate. …
- NAID 80021559565
- 臨床 クロイツフェルト・ヤコブ病の神経耳科学的所見
Related Links
- Creutzfeldt?Jakob disease or CJD is a degenerative neurological disorder (brain disease) that is incurable and invariably fatal. CJD is at times called a human form of mad cow disease, given that bovine spongiform encephalopathy is ...
Related Pictures
★リンクテーブル★
[★]
新変異型クロイツフェルト・ヤコブ病、新型クロイツフェルト・ヤコブ病
- 関
- CJD、Creutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、familial Creutzfeldt-Jakob disease、subacute spongiform encephalopathy
[★]
家族性クロイツフェルト・ヤコブ病
- 関
- CJD、Creutzfeldt-Jakob disease、Creutzfeldt-Jakob syndrome、new variant Creutzfeldt-Jakob disease、subacute spongiform encephalopathy
[★]
変異型クロイツフェルト・ヤコブ病
[★]
クロイツフェルト・ヤコブ病 CJD