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PrPSc Proteins

Abnormal isoform of PRION PROTEINS resulting from a posttranslational modification of the cellular prion protein (PRPC PROTEINS). PrPSc are disease-specific proteins seen in certain human and animal neurodegenerative diseases (PRION DISEASES).
Also Known As:
HaSp 33-37; PrP (CJD); PrP (GSS); PrP 33-35; PrP-res; Scrapie HaSp33-37 Protein; Scrapie PrP 33-35; Scrapie Virus; Sp 33-35; PrP res; Scrapie Agent; Scrapie PrP
Networked: 450 relevant articles (5 outcomes, 48 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Caughey, Byron: 19 articles (01/2017 - 03/2002)
2. Baron, Thierry: 13 articles (01/2014 - 01/2004)
3. Bencsik, Anna: 11 articles (02/2012 - 04/2004)
4. Shi, Qi: 8 articles (01/2017 - 10/2008)
5. Baron, Gerald S: 8 articles (02/2014 - 03/2002)
6. Dong, Xiao-Ping: 7 articles (01/2017 - 04/2009)
7. Biacabe, Anne-Gaëlle: 7 articles (01/2011 - 01/2004)
8. Priola, Suzette A: 7 articles (05/2009 - 09/2002)
9. Gambetti, Pierluigi: 6 articles (01/2017 - 12/2004)
10. Hughson, Andrew G: 6 articles (01/2016 - 08/2009)

Related Diseases

1. Scrapie
2. Prion Diseases (Transmissible Spongiform Encephalopathies)
3. Creutzfeldt-Jakob Syndrome (Creutzfeldt-Jakob Disease)
4. Disease Susceptibility (Diathesis)
5. Infections

Related Drugs and Biologics

1. Prion Proteins
2. Amphotericin B (Amphotericin)
3. MS 8209
4. Pharmaceutical Preparations
5. Peptide Hydrolases (Proteases)
6. Prions
7. PrPC Proteins
8. PrPSc Proteins
9. Amino Acids
10. Epitopes

Related Therapies and Procedures

1. Surgical Instruments (Clip)
2. Therapeutics
3. Intraocular Injections
4. Splenectomy
5. Intraperitoneal Injections