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CYP1B1 gene

Known as: CP1B, Cytochrome P450, Family 1, Subfamily B, Polypeptide 1 Gene, CYP1B1 
This gene plays a role in eye development, steroid catabolism and xenobiotic metabolism.
National Institutes of Health

Papers overview

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2010
2010
The overexpression of the cysteine protease calpain is associated with many diseases, including brain trauma, spinal cord injury… 
2009
2009
Cytochrome P450 1B1 (CYP1B1), a phase I enzyme, is involved in the activation of a broad spectrum of procarcinogens. An… 
2008
2008
Purpose The gene coding cytochrome P4501B1 (CYP1B1) has been shown to be a major cause of primary congenital glaucoma in the… 
2006
2006
Background: Mutations and polymorphisms have been identified in the CYP1B1 gene; while mutations that affect the conserved core… 
Highly Cited
2004
Highly Cited
2004
Peters anomaly (PA) and primary congenital glaucoma (PCG) are genetically and phenotypically distinct conditions. Mutations in… 
Highly Cited
2003
Highly Cited
2003
Aim: To investigate the phenotypes associated with cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary… 
1999
1999
A 57-kDa protein whose expression in rat adrenocortical microsomes is increased after weaning has been identified as cytochrome… 
1998
1998
A PCR-based test has been developed that makes it possible to detect a G to A substitution in the cytochrome P4501B1 gene. This…