(Q46839093)

25 December 2017

title

Mouse models of ocular diseases (English)

1 reference

25 December 2017

author name string

Chang B

1

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25 December 2017

Hawes NL

2

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25 December 2017

Hurd RE

3

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25 December 2017

Wang J

4

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25 December 2017

Howell D

5

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25 December 2017

Davisson MT

6

1 reference

25 December 2017

Roderick TH

7

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25 December 2017

Nusinowitz S

8

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25 December 2017

Heckenlively JR

9

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25 December 2017

publication date

1 September 2005

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25 December 2017

published in

Visual neuroscience

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25 December 2017

volume

22

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25 December 2017

issue

5

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25 December 2017

page(s)

587-593

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25 December 2017

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Mouse model of subretinal neovascularization with choroidal anastomosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Mouse model for Usher syndrome: linkage mapping suggests homology to Usher type I reported at human chromosome 11p15.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Motor neuron degeneration of mice is a model of neuronal ceroid lipofuscinosis (Batten's disease)

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

A deletion in a photoreceptor-specific nuclear receptor mRNA causes retinal degeneration in the rd7 mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Fierce: a new mouse deletion of Nr2e1; violent behaviour and ocular abnormalities are background-dependent

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Excess cone cell proliferation due to lack of a functional NR2E3 causes retinal dysplasia and degeneration in rd7/rd7 mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Genetic and physical maps of the mouse rd3 locus; exclusion of the ortholog of USH2A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Lop12, a mutation in mouse Crygd causing lens opacity similar to human Coppock cataract

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

The bst locus on mouse chromosome 16 is associated with age-related subretinal neovascularization

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Retinal degeneration mutants in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

A new dominant retinal degeneration (Rd4) associated with a chromosomal inversion in the mouse.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

A Gja8 (Cx50) point mutation causes an alteration of alpha 3 connexin (Cx46) in semi-dominant cataracts of Lop10 mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

A candidate gene for the mouse mutation tubby

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Chromosomal localization of a new mouse lens opacity gene (lop18)

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Mfrp, a gene encoding a frizzled related protein, is mutated in the mouse retinal degeneration 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

7 January 2021

New mouse primary retinal degeneration (rd-3)

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

7 January 2021

PCR-amplification of simple sequence repeat variants from pooled DNA samples for rapidly mapping new mutations of the mouse

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

7 January 2021

Aberrant actin cytoskeleton leads to accelerated proliferation of corneal epithelial cells in mice deficient for destrin (actin depolymerizing factor)

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

7 January 2021

Congenital ocular blindness in children, 1945 to 1984

1 reference

https://api.crossref.org/works/10.1017%2FS0952523805225075

7 January 2021

10.1017/S0952523805225075

Identifiers

DOI

1 reference

25 December 2017

PubMed ID

16332269

1 reference

25 December 2017