(Q28142971)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10932181%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10 (English)

1 reference

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9 November 2019

4

1 reference

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9 November 2019

Jane Sowden

12

1 reference

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9 November 2019

author name string

Ferda Percin E

1

1 reference

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9 November 2019

Ploder LA

2

1 reference

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9 November 2019

Yu JJ

3

1 reference

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9 November 2019

Horsford DJ

5

1 reference

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9 November 2019

Rutherford A

6

1 reference

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9 November 2019

Bapat B

7

1 reference

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9 November 2019

Cox DW

8

1 reference

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9 November 2019

Duncan AM

9

1 reference

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9 November 2019

Kalnins VI

10

1 reference

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9 November 2019

Kocak-Altintas A

11

1 reference

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9 November 2019

Traboulsi E

13

1 reference

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9 November 2019

Sarfarazi M

14

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9 November 2019

McInnes RR

15

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9 November 2019

language of work or name

English

0 references

publication date

1 August 2000

1 reference

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9 November 2019

1 reference

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9 November 2019

volume

25

1 reference

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9 November 2019

page(s)

397-401

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9 November 2019

issue

4

1 reference

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X-linked clinical anophthalmos Localization of the gene to Xq27-Xq28

9 November 2019

cites work

1 reference

7 January 2021

Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11

1 reference

7 January 2021

A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.

1 reference

7 January 2021

Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3.

1 reference

7 January 2021

Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Inactivation of the zebrafish homologue of Chx10 by antisense oligonucleotides causes eye malformations similar to the ocular retardation phenotype.

1 reference

7 January 2021

Expression of Chx10 and Chx10-1 in the developing chicken retina.

1 reference

7 January 2021

Vsx-1 and Vsx-2: differential expression of two paired-like homeobox genes during zebrafish and goldfish retinogenesis

1 reference

7 January 2021

The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions

1 reference

7 January 2021

High resolution crystal structure of a paired (Pax) class cooperative homeodomain dimer on DNA

1 reference

7 January 2021

A sensitive method for the determination of protein-DNA binding specificities

1 reference

7 January 2021

Zinc fingers in sex determination: only one of the two C. elegans Tra-1 proteins binds DNA in vitro

1 reference

7 January 2021

Cooperative dimerization of paired class homeo domains on DNA.

1 reference

7 January 2021

Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse

1 reference

7 January 2021

Partial rescue of the ocular retardation phenotype by genetic modifiers

1 reference

7 January 2021

Basic local alignment search tool

1 reference

7 January 2021

Localization of the human 75-kDal Fe-S protein of NADH-coenzyme Q reductase gene (NDUFS1) to 2q33----q34

1 reference

7 January 2021

A comprehensive genetic map of the human genome based on 5,264 microsatellites

1 reference

7 January 2021

In situ hybridization with digoxigenin-labeled probes: sensitive and reliable detection method applied to myelinating rat brain

1 reference

7 January 2021

Mutation analysis of the ROM1 gene in retinitis pigmentosa.

1 reference

7 January 2021

Identifiers

DOI

10.1038/78071

2 references

Consolidated OpenCitations Corpus – April 2017

4002396

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10932181%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

4002396

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

4002396