(Q84606524)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

review article

1 reference

title

[Development of the iridocorneal angle and congenital glaucoma] (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

publication date

1 July 2011

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

volume

108

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

page(s)

610-4, 616-7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21796509%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00347-010-2294-5

8 February 2020

exact match

0 references

cites work

Novel CYP1B1 and known PAX6 mutations in anterior segment dysgenesis (ASD).

1 reference

12 December 2020

Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases

1 reference

12 December 2020

Primary role of CYP1B1 in Indian juvenile-onset POAG patients

1 reference

12 December 2020

Multiple CYP1B1 mutations and incomplete penetrance in an inbred population segregating primary congenital glaucoma suggest frequent de novo events and a dominant modifier locus.

1 reference

12 December 2020

Null mutations in LTBP2 cause primary congenital glaucoma

1 reference

12 December 2020

Developmental immaturity of the trabecular meshwork in juvenile glaucoma.

1 reference

12 December 2020

Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma

1 reference

12 December 2020

TGFbeta2 in corneal morphogenesis during mouse embryonic development

1 reference

12 December 2020

Abnormal migration and distribution of neural crest cells in Pax6 heterozygous mutant eye, a model for human eye diseases.

1 reference

12 December 2020

The regulation of trabecular meshwork and ciliary muscle contractility

1 reference

12 December 2020

Characterization of the biochemical and structural phenotypes of four CYP1B1 mutations observed in individuals with primary congenital glaucoma

1 reference

12 December 2020

A compound heterozygous change found in Peters' anomaly.

1 reference

12 December 2020

The role of the actomyosin system in regulating trabecular fluid outflow

1 reference

12 December 2020

Modulation of extracellular matrix turnover in the trabecular meshwork

1 reference

12 December 2020

Fate maps of neural crest and mesoderm in the mammalian eye.

1 reference

12 December 2020

Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma

1 reference

12 December 2020

Update on the mechanism of action of topical prostaglandins for intraocular pressure reduction

1 reference

12 December 2020

Mutations in CYP1B1 cause primary congenital glaucoma by reduction of either activity or abundance of the enzyme.

1 reference

12 December 2020

Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21

1 reference

12 December 2020

A clinical and molecular genetic study of German patients with primary congenital glaucoma

1 reference

12 December 2020

Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucoma

1 reference

12 December 2020

The changing paradigm of outflow resistance generation: towards synergistic models of the JCT and inner wall endothelium.

1 reference

12 December 2020

Heterozygous loss-of-function variants in CYP1B1 predispose to primary open-angle glaucoma.

1 reference

12 December 2020

The trabecular meshwork outflow pathways: structural and functional aspects.

1 reference

12 December 2020

Retinoic acid signaling in mammalian eye development

1 reference

12 December 2020

Role of CYP1B1 in glaucoma

1 reference

12 December 2020

The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.

1 reference

12 December 2020

Evolving maps in craniofacial development.

1 reference

12 December 2020

Genotype and phenotype correlations in congenital glaucoma: CYP1B1 mutations, goniodysgenesis, and clinical characteristics

1 reference

12 December 2020