(Q42665432)

4 November 2017

title

Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice (English)

1 reference

4 November 2017

1 reference

1

1 reference

4 November 2017

Richard S Smith

2

1 reference

4 November 2017

Norman L Hawes

3

1 reference

4 November 2017

Adriana Zabaleta

4

1 reference

4 November 2017

Bo Chang

5

1 reference

4 November 2017

Janey L Wiggs

6

1 reference

4 November 2017

Simon W M John

7

1 reference

4 November 2017

language of work or name

English

0 references

publication date

17 December 2001

1 reference

4 November 2017

1 reference

4 November 2017

volume

30

1 reference

4 November 2017

issue

1

1 reference

4 November 2017

page(s)

81-85

1 reference

https://scigraph.springernature.com/pub.10.1038/ng794

4 November 2017

exact match

0 references

cites work

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

1 reference

7 January 2021

Prevalence of pigment dispersion syndrome in a population undergoing glaucoma screening

1 reference

7 January 2021

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

1 reference

7 January 2021

Characterization of a new melanocyte-specific gene (QNR-71) expressed in v-myc-transformed quail neuroretina.

1 reference

7 January 2021

nmb, a novel gene, is expressed in low-metastatic human melanoma cell lines and xenografts

1 reference

7 January 2021

Intracellular sorting and targeting of melanosomal membrane proteins: identification of signals for sorting of the human brown locus protein, gp75

1 reference

7 January 2021

Strong homophilic interactions of the Ig-like domains of polycystin-1, the protein product of an autosomal dominant polycystic kidney disease gene, PKD1

1 reference

7 January 2021

Sandy: a new mouse model for platelet storage pool deficiency

1 reference

7 January 2021

Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher.

1 reference

7 January 2021

Genetic modification of glaucoma associated phenotypes between AKXD-28/Ty and DBA/2J mice

1 reference

7 January 2021

Light is a dominant mouse mutation resulting in premature cell death

1 reference

7 January 2021

Genetic variations in the fine structure and ontogeny of mouse melanin granules

1 reference

7 January 2021

Tyrosinase stabilization by Tyrp1 (the brown locus protein).

1 reference

7 January 2021

Murine and human b locus pigmentation genes encode a glycoprotein (gp75) with catalase activity

1 reference

7 January 2021

1 reference

7 January 2021

Human tyrosinase related protein-1 (TRP-1) does not function as a DHICA oxidase activity in contrast to murine TRP-1.

1 reference

7 January 2021

The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness

1 reference

7 January 2021

The incidence and time-course of latanoprost-induced iridial pigmentation as a function of eye color.

1 reference

7 January 2021

Latanoprost-induced increase of tyrosinase transcription in iridial melanocytes

1 reference

7 January 2021

Transcriptional activation of tyrosinase and TRP-1 by p53 links UV irradiation to the protective tanning response

1 reference

7 January 2021

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

1 reference

7 January 2021

Identifiers

DOI

10.1038/NG794

1 reference

Dimensions Publication ID

4 November 2017

1050453704

0 references

1 reference