(Q53726981)

English

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice.

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scholarly article

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Interacting loci cause severe iris atrophy and glaucoma in DBA/2J mice. (English)

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

author name string

Chang B

1

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Smith RS

2

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Hawes NL

3

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Anderson MG

4

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Zabaleta A

5

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Savinova O

6

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Roderick TH

7

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Heckenlively JR

8

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Davisson MT

9

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

John SW

10

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

language of work or name

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publication date

1 April 1999

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

Nature Genetics

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

21

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Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

405-409

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

4

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

https://scigraph.springernature.com/pub.10.1038/7741

0 references

Number of people with glaucoma worldwide

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

A gene responsible for the pigment dispersion syndrome maps to chromosome 7q35-q36

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of pigment dispersion syndrome in a population undergoing glaucoma screening

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Pigmentary dispersion syndrome and pigmentary glaucoma. A prospective study of the natural history.

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Long-term analysis of pigmentary dispersion syndrome and pigmentary glaucoma.

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk factors for the development and severity of glaucoma in the pigment dispersion syndrome.

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Progressive essential iris atrophy, Chandler's syndrome, and the iris nevus (Cogan-Reese) syndrome: A spectrum of disease

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Unusual aspects of progressive essential iris atrophy

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Corneal Edema in Essential Iris Atrophy

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

The forkhead transcription factor gene FKHL7 is responsible for glaucoma phenotypes which map to 6p25

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage of posterior polymorphous corneal dystrophy to 20q11

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

A cDNA encoding tyrosinase-related protein maps to the brown locus in mouse

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locus

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Light is a dominant mouse mutation resulting in premature cell death

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Rufous oculocutaneous albinism in southern African Blacks is caused by mutations in the TYRP1 gene

1 reference

https://api.crossref.org/works/10.1038%2F7741

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

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1 reference

Europe PubMed Central

18 May 2018

http://europepmc.org/abstract/MED/10192392

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