Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

CYP1B1, a developmental gene with a potential role in glaucoma therapy.

Xenobiotica; the fate of foreign compounds in biological systems - 1 Aug 2009

Choudhary D, Jansson I, Schenkman J B

Abstract excerpt

The association of CYP1B1 gene alterations in primary congenital glaucoma individuals has been known for about a decade. Recent evidence has shown the involvement of CYP1B1 mutations in a number of forms of glaucoma and anterior segment disorders. This suggests a wide role for CYP1B1 in ocular ph...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aryl Hydrocarbon Hydroxylases
Share to Cornea
Share to Cytochrome P-450 CYP1B1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Diseases, Inborn

Share to Glaucoma

Share to Stem Cell Transplantation

Share to Trabecular Meshwork

Source

Identifiers

PMID: 19622003
DOI: 10.1080/00498250903000198

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19622003-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

CYP1B1, a developmental gene with a potential role in glaucoma therapy.PMID 19622003Read ↗

Role of CYP1B1 in glaucoma.Semantic proximity Read ↗

Primary congenital glaucoma and the involvement of CYP1B1Semantic proximity Read ↗

Congenital glaucoma and CYP1B1: an old story revisited.Semantic proximity Read ↗

Molecular genetics of primary congenital glaucoma.Semantic proximity Read ↗

Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism Genes.Semantic proximity Read ↗

Null cyp1b1 Activity in Zebrafish Leads to Variable Craniofacial Defects Associated with Altered Expression of Extracellular Matrix and Lipid Metabolism GenesSemantic proximity Read ↗

Updates on the molecular genetics of primary congenital glaucoma (Review)Semantic proximity Read ↗

The p.Gly61Glu Mutation in CYP1B1 Affects the Extracellular Matrix in Glaucoma Patients.Semantic proximity Read ↗

Ultrastructural abnormalities of the trabecular meshwork extracellular matrix in Cyp1b1-deficient mice.Semantic proximity Read ↗

Analysis of CYP1B1 in pediatric and adult glaucoma and other ocular phenotypes.Semantic proximity Read ↗

Novel compound heterozygous mutations in CYP1B1 identified in a Chinese family with developmental glaucoma.Semantic proximity Read ↗

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi ArabiaSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.