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CYP1B1 gene
Known as:
CP1B
, Cytochrome P450, Family 1, Subfamily B, Polypeptide 1 Gene
, CYP1B1
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This gene plays a role in eye development, steroid catabolism and xenobiotic metabolism.
National Institutes of Health
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Related topics
Related topics
9 relations
CYP1A1 gene
CYP1B1 protein, human
Eye Development
Iron Chelation
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Serum metabolomic profiles reveal the impact of BuZangTongLuo formula on metabolic pathways in diabetic mice with hindlimb ischemia.
Junping Zheng
,
Yanlei Guo
,
+5 authors
Hongtao Liu
Journal of Ethnopharmacology
2020
Corpus ID: 218520101
2010
2010
Molecular modeling studies of peptide inhibitors highlight the importance of conformational prearrangement for inhibition of calpain.
Wanting Jiao
,
D. Q. Mcdonald
,
J. Coxon
,
E. Parker
Biochemistry
2010
Corpus ID: 24869307
The overexpression of the cysteine protease calpain is associated with many diseases, including brain trauma, spinal cord injury…
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2009
2009
Influence of the Cyp1B1 L432V Gene Polymorphism and Exposure to Tobacco Smoke on Cyp1B1 mRNA Expression in Human Leukocytes
S. Helmig
,
Bahar Hadzaad
,
Juliane Döhrel
,
J. Schneider
Drug Metabolism And Disposition
2009
Corpus ID: 17188583
Cytochrome P450 1B1 (CYP1B1), a phase I enzyme, is involved in the activation of a broad spectrum of procarcinogens. An…
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2009
2009
Frequency of common CYP1B1 polymorphic variations in Delhi population of Northern India.
Vivek Kumar
,
Satyender Singh
,
R. Ahmed
,
B. Banerjee
,
T. Ahmed
,
S. T. Pasha
Environmental Toxicology and Pharmacology
2009
Corpus ID: 37938113
2008
2008
Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol
Fatemeh Suri
,
Reza Kalhor
,
+9 authors
E. Elahi
Molecular Vision
2008
Corpus ID: 8091649
Purpose The gene coding cytochrome P4501B1 (CYP1B1) has been shown to be a major cause of primary congenital glaucoma in the…
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2006
2006
Molecular Analysis of the CYP1B1 Gene: Identification of Novel Truncating Mutations in Patients with Primary Congenital Glaucoma
Olga M. Messina-Baas
,
L. González-Huerta
,
+4 authors
S. Cuevas-Covarrubias
Ophthalmic Research
2006
Corpus ID: 22161879
Background: Mutations and polymorphisms have been identified in the CYP1B1 gene; while mutations that affect the conserved core…
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Highly Cited
2004
Highly Cited
2004
Molecular basis of Peters anomaly in Saudi Arabia
Deepak P. Edward
,
Ali A. Rajhi
,
R. Lewis
,
Stacey M. Curry
,
Zong-ying Wang
,
B. Bejjani
Ophthalmic Genetics
2004
Corpus ID: 25882311
Peters anomaly (PA) and primary congenital glaucoma (PCG) are genetically and phenotypically distinct conditions. Mutations in…
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Highly Cited
2003
Highly Cited
2003
Phenotype of cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary congenital glaucoma
Y. Ohtake
,
T. Tanino
,
+6 authors
Y. Mashima
British Journal of Ophthalmology
2003
Corpus ID: 19443262
Aim: To investigate the phenotypes associated with cytochrome P4501B1 gene (CYP1B1) mutations in Japanese patients with primary…
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1999
1999
Developmental expression and regulation of adrenocortical cytochrome P4501B1 in the rat.
P. B. Brake
,
M. Arai
,
Suzie As-Sanie
,
C. Jefcoate
,
E. Widmaier
Endocrinology
1999
Corpus ID: 9322799
A 57-kDa protein whose expression in rat adrenocortical microsomes is increased after weaning has been identified as cytochrome…
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1998
1998
[Molecular diagnosis of mutations responsible for recurrent and severe forms of primary congenital glaucoma].
M. Plášilová
,
A. Gerinec
,
V. Ferák
Czech and Slovak Ophthalmology
1998
Corpus ID: 40209385
A PCR-based test has been developed that makes it possible to detect a G to A substitution in the cytochrome P4501B1 gene. This…
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