(Q36981827)

17 August 2017

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

1 reference

17 August 2017

photoreceptor protein

0 references

1 reference

N B Akhmedov

1 reference

17 August 2017

N I Piriev

1 reference

17 August 2017

B Chang

1 reference

17 August 2017

A L Rapoport

1 reference

17 August 2017

N L Hawes

1 reference

17 August 2017

P M Nishina

1 reference

17 August 2017

S Nusinowitz

1 reference

17 August 2017

J R Heckenlively

1 reference

17 August 2017

T H Roderick

1 reference

17 August 2017

C A Kozak

1 reference

17 August 2017

M Danciger

1 reference

17 August 2017

M T Davisson

1 reference

17 August 2017

D B Farber

1 reference

17 August 2017

language of work or name

English

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publication date

1 May 2000

1 reference

Proceedings of the National Academy of Sciences of the United States of America

17 August 2017

1 reference

17 August 2017

1 reference

17 August 2017

1 reference

17 August 2017

5551-5556

1 reference

Identification of a photoreceptor cell-specific nuclear receptor

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Increasing the complexity of coactivation in nuclear receptor signaling

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

A syndrome of severe mental retardation, spasticity, and tapetoretinal degeneration linked to chromosome 15q24

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosa.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Recessive mutations in the gene encoding the tubby-like protein TULP1 in patients with retinitis pigmentosa

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Linkage mapping in 29 Bardet-Biedl syndrome families confirms loci in chromosomal regions 11q13, 15q22.3-q23, and 16q21.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

A candidate gene for the mouse mutation tubby

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

The RXR heterodimers and orphan receptors

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

The nuclear receptor superfamily: the second decade

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

A type VII myosin encoded by the mouse deafness gene shaker-1

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Defective myosin VIIA gene responsible for Usher syndrome type 1B

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Isolation of a candidate cDNA for the gene causing retinal degeneration in the rd mouse

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Retinal degeneration in the rd mouse is caused by a defect in the beta subunit of rod cGMP-phosphodiesterase

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Multiplicity generates diversity in the retinoic acid signalling pathways

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Screening for mouse retinal degenerations. I. Correlation of indirect ophthalmoscopy, electroretinograms, and histology

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

The mouse homolog of the Gibbon ape leukemia virus receptor: genetic mapping and a possible receptor function in rodents

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Orphan nuclear receptors--new ligands and new possibilities.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Homozygous tandem duplication within the gene encoding the beta-subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25866

Mutations and polymorphisms in the human peripherin-RDS gene and their involvement in inherited retinal degeneration

4 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.97.10.5551

Mouse fundus photography and angiography: a catalogue of normal and mutant phenotypes

21 January 2018

1 reference

12 December 2020

Isolation of DNA from biological specimens without extraction with phenol

1 reference

12 December 2020

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

1 reference

12 December 2020

Molecular genetic markers spanning mouse chromosome 10

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.97.10.5551

1 reference

17 August 2017

0 references

1 reference

17 August 2017

PubMed publication ID

10805811

1 reference