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Hexosaminidase B

A mammalian beta-hexosaminidase isoform that is comprized of hexosaminidase beta subunits. Deficiency of hexosaminidase B due to mutations in the gene encoding the hexosaminidase beta subunit is a case of SANDHOFF DISEASE.
Also Known As:
Hex B
Networked: 66 relevant articles (0 outcomes, 7 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Zwierz, Krzysztof: 7 articles (01/2014 - 03/2008)
2. Waszkiewicz, Napoleon: 5 articles (01/2014 - 01/2011)
3. Kępka, Alina: 4 articles (01/2014 - 01/2011)
4. Szajda, Sławomir Dariusz: 4 articles (01/2014 - 09/2009)
5. Chojnowska, Sylwia: 3 articles (01/2014 - 09/2010)
6. Zalewska-Szajda, Beata: 3 articles (01/2014 - 01/2012)
7. Tutor, J Carlos: 3 articles (09/2005 - 01/2003)
8. Casal, J Antonio: 3 articles (09/2005 - 01/2003)
9. Ładny, Jerzy Robert: 2 articles (01/2014 - 01/2013)
10. Zalewska, Anna: 2 articles (09/2013 - 01/2013)

Related Diseases

1. Alcoholism (Alcohol Abuse)
2. Neoplasms (Cancer)
3. Sandhoff Disease (Sandhoff's Disease)
4. Carcinoma (Carcinomatosis)
5. Colonic Neoplasms (Colon Cancer)

Related Drugs and Biologics

1. Hexosaminidase A (Hex A)
2. Isoenzymes
3. Protein Isoforms (Isoforms)
4. Glycoside Hydrolases (Endoglycosidases)
5. Hexosaminidases (Hexosaminidase)
6. Glucuronidase
7. Insulin (Novolin)
8. Galactosidases
9. alpha-L-Fucosidase (Fucosidase)
10. Creatinine

Related Therapies and Procedures

1. Oral Administration