(Q28246116)

2

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M M Abd El-Aziz

3

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M F El-Ashry

4

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L Abu-Safieh

5

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S S Bhattacharya

6

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G Antiñolo

Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus

7

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language of work or name

English

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publication date

January 2008

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published in

Annals of Human Genetics

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volume

72

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issue

Pt 1

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page(s)

26-34

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cites work

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Functional proteomics mapping of a human signaling pathway

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Smad-dependent and Smad-independent pathways in TGF-beta family signalling

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Localization of a gene (CORD7) for a dominant cone-rod dystrophy to chromosome 6q

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Evaluation of the ELOVL4 gene in families with retinitis pigmentosa linked to the RP25 locus

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Cloning, characterization, and chromosome mapping of the human GlcAT-S gene

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

21 April 2017

1 reference

https://api.crossref.org/works/10.1111/J.1469-1809.2007.00393.X

Exclusion of four candidate genes, KHDRBS2, PTP4A1, KIAA1411 and OGFRL1, as causative of autosomal recessive retinitis pigmentosa.

21 April 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X

Tandemly repeated DNA: why should anyone care?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X

Molecular genetics of human retinal dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X

A major locus for autosomal recessive retinitis pigmentosa on 6q, determined by homozygosity mapping of chromosomal regions that contain gamma-aminobutyric acid-receptor clusters

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X

Immunohistochemical localization of angiotensin-converting enzyme, angiotensin II and AT1 receptor in human ocular tissues

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X

Serotonin transporter: evolution and impact of polymorphic transcriptional regulation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X

Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1469-1809.2007.00393.X