Warning: Undefined array key "mm" in /www/wwwroot/www.ai-bt.com/si.php on line 10 Deprecated: trim(): Passing null to parameter #1 ($string) of type string is deprecated in /www/wwwroot/www.ai-bt.com/si.php on line 10 Molecular studies of prion diseases.

Literature DB >> 9932423

Molecular studies of prion diseases.

J Safar¹, S B Prusiner.

Abstract

Entities: Disease Gene

Mesh：

Substances：
Prions
Protein Isoforms

Year: 1998 PMID： 9932423 DOI： 10.1016/s0079-6123(08)64030-3

Source DB: PubMed Journal: Prog Brain Res ISSN： 0079-6123 Impact factor: 2.453

Keyword Cloud
Cited

× No keyword cloud information.

10 in total

1. Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β.

Authors: Mark L Cohen; Chae Kim; Tracy Haldiman; Mohamed ElHag; Prachi Mehndiratta; Termsarasab Pichet; Frances Lissemore; Michelle Shea; Yvonne Cohen; Wei Chen; Janis Blevins; Brian S Appleby; Krystyna Surewicz; Witold K Surewicz; Martha Sajatovic; Curtis Tatsuoka; Shulin Zhang; Ping Mayo; Mariusz Butkiewicz; Jonathan L Haines; Alan J Lerner; Jiri G Safar
Journal: Brain Date: 2015-02-15 Impact factor: 13.501

2. Distinct populations of highly potent TAU seed conformers in rapidly progressing Alzheimer's disease.

Authors: Chae Kim; Tracy Haldiman; Sang-Gyun Kang; Lenka Hromadkova; Zhuang Zhuang Han; Wei Chen; Frances Lissemore; Alan Lerner; Rohan de Silva; Mark L Cohen; David Westaway; Jiri G Safar
Journal: Sci Transl Med Date: 2022-01-05 Impact factor: 19.319

3. Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection.

Authors: Tracy Haldiman; Chae Kim; Yvonne Cohen; Wei Chen; Janis Blevins; Liuting Qing; Mark L Cohen; Jan Langeveld; Glenn C Telling; Qingzhong Kong; Jiri G Safar
Journal: J Biol Chem Date: 2013-08-23 Impact factor: 5.157

4. Green fluorescent protein as a reporter of prion protein folding.

Authors: Snezana Vasiljevic; Junyuan Ren; YongXiu Yao; Kevin Dalton; Catherine S Adamson; Ian M Jones
Journal: Virol J Date: 2006-08-29 Impact factor: 4.099

5. The Features of Genetic Prion Diseases Based on Chinese Surveillance Program.

Authors: Qi Shi; Wei Zhou; Cao Chen; Bao-Yun Zhang; Kang Xiao; Xiu-Chun Zhang; Xiao-Jing Shen; Qing Li; Li-Quan Deng; Jian-Hua Dong; Wen-Qing Lin; Pu Huang; Wei-Jia Jiang; Jie Lv; Jun Han; Xiao-Ping Dong
Journal: PLoS One Date: 2015-10-21 Impact factor: 3.240

6. Co-occurrence of chronic traumatic encephalopathy and prion disease.

Authors: Satish Kumar Nemani; Silvio Notari; Ignazio Cali; Victor E Alvarez; Diane Kofskey; Mark Cohen; Robert A Stern; Brian Appleby; Joseph Abrams; Lawrence Schonberger; Ann McKee; Pierluigi Gambetti
Journal: Acta Neuropathol Commun Date: 2018-12-18 Impact factor: 7.801

Molecular studies of prion diseases.

1. Rapidly progressive Alzheimer's disease features distinct structures of amyloid-β.

2. Distinct populations of highly potent TAU seed conformers in rapidly progressing Alzheimer's disease.

3. Co-existence of distinct prion types enables conformational evolution of human PrPSc by competitive selection.

4. Green fluorescent protein as a reporter of prion protein folding.

5. The Features of Genetic Prion Diseases Based on Chinese Surveillance Program.

6. Co-occurrence of chronic traumatic encephalopathy and prion disease.

Review 7. Implications of prion adaptation and evolution paradigm for human neurodegenerative diseases.

8. Structurally distinct external solvent-exposed domains drive replication of major human prions.

9. Myositis facilitates preclinical accumulation of pathological prion protein in muscle.

Review 10. Emerging Role of Cellular Prion Protein in the Maintenance and Expansion of Glioma Stem Cells.