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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: 459 relevant articles (6 outcomes, 48 trials/studies)

Relationship Network

Bio-Agent Context: Research Results

Experts

1. Caughey, Byron: 20 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. Acquired CJD
5. Disease Susceptibility (Diathesis)

Related Drugs and Biologics

1. Prion Proteins
2. Prions
3. Amphotericin B (Amphotericin)
4. MS 8209
5. Peptide Hydrolases (Proteases)
6. PrPC Proteins
7. PrPSc Proteins
8. Amino Acids
9. Epitopes
10. Haemophilus influenzae type b-polysaccharide vaccine-diphtheria toxoid conjugate

Related Therapies and Procedures

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