(Q24311359)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

main subject

photoreceptor protein

0 references

Cone-rod homeobox

1 reference

animal organ morphogenesis

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Stephen W. Scherer

11

1 reference

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7 November 2019

author name string

C Y Gregory-Evans

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

T Furukawa

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Papaioannou

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

J Looser

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

L Ploder

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

J Bellingham

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

D Ng

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

J A Herbrick

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A Duncan

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

L C Tsui

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A Loutradis-Anagnostou

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

S G Jacobson

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

C L Cepko

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

S S Bhattacharya

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

R R McInnes

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

language of work or name

English

0 references

publication date

1 November 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

91

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

543-553

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

7 November 2019

cites work

1 reference

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7 January 2021

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

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7 January 2021

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7 January 2021

An integrated metric physical map of human chromosome 19.

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7 January 2021

A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13

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7 January 2021

Mutation analysis of the ROM1 gene in retinitis pigmentosa.

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7 January 2021

Retinitis pigmentosa: unfolding its mystery

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7 January 2021

Retinal photoreceptor dystrophies LI. Edward Jackson Memorial Lecture

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7 January 2021

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

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7 January 2021

Cell fate determination in the vertebrate retina

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7 January 2021

Nuclear targeting sequences--a consensus?

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7 January 2021

Molecular genetics of retinitis pigmentosa

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7 January 2021

Assignment of the gene for the cytochrome c1 subunit of the mitochondrial cytochrome bc1 complex (CYC1) to human chromosome 8q24.3

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7 January 2021

Genetic linkage of cone-rod retinal dystrophy to chromosome 19q and evidence for segregation distortion

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7 January 2021

Chromosome 19q cone-rod retinal dystrophy. Ocular phenotype

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7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

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7 January 2021

The orthodenticle gene encodes a novel homeo domain protein involved in the development of the Drosophila nervous system and ocellar visual structures.

1 reference

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7 January 2021

Transcription factor genes and the developing eye: a genetic perspective

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7 January 2021

Structure of the segmentation gene paired and the Drosophila PRD gene set as part of a gene network

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7 January 2021

Vision in Leber congenital amaurosis

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7 January 2021

rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina

1 reference

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7 January 2021

Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

1 reference

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7 January 2021

Pituitary homeobox 2, a novel member of the bicoid-related family of homeobox genes, is a potential regulator of anterior structure formation.

1 reference

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7 January 2021

An STS-based map of the human genome

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7 January 2021

Retinopathy induced in mice by targeted disruption of the rhodopsin gene

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7 January 2021

A new bacteriophage P1-derived vector for the propagation of large human DNA fragments

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7 January 2021

Localisation of a gene for dominant cone-rod dystrophy (CORD6) to chromosome 17p

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7 January 2021

Crystal structure of an engrailed homeodomain-DNA complex at 2.8 A resolution: a framework for understanding homeodomain-DNA interactions

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7 January 2021

An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs

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7 January 2021

Strategies for multilocus linkage analysis in humans

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7 January 2021

High-resolution chromosomal localization of the beta-gene of the human beta-globin gene complex by in situ hybridization

1 reference

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7 January 2021

Developmental expression of a novel murine homeobox gene (Chx10): evidence for roles in determination of the neuroretina and inner nuclear layer.

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7 January 2021

The Rx homeobox gene is essential for vertebrate eye development

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7 January 2021

Mouse Otx2 functions in the formation and patterning of rostral head.

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7 January 2021

Insight into the microphthalmia gene

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7 January 2021

Current views on eye development

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7 January 2021

Retinal-specific guanylate cyclase gene mutations in Leber's congenital amaurosis

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7 January 2021

Avoiding recomputation in linkage analysis.

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7 January 2021

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

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7 January 2021

Clinical subtypes of cone-rod dystrophy

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7 January 2021

Mammalian hairy and Enhancer of split homolog 1 regulates differentiation of retinal neurons and is essential for eye morphogenesis

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7 January 2021

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7 January 2021

A method for constructing radiation hybrid maps of whole genomes

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7 January 2021

Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211.

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

2417605

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9390563%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

2417605

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2417605