A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa (Q24305284)

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scientific article published on December 12, 1991

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Language	Label	Description	Also known as
English	A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa	scientific article published on December 12, 1991

Statements

instance of

scholarly article

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title

A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosa (English)

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A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosa (English)

1 reference

stated in

Crossref

DOI

10.1038/354478A0

reference URL

https://api.crossref.org/works/10.1038/354478A0

retrieved

15 November 2022

main subject

Peripherin 2

1 reference

stated in

GOA release 2020-03-11

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

chromosomal deletion syndrome

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

membrane glycoprotein

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

nerve tissue protein

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

author name string

G. J. Farrar

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

P. Kenna

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

S. A. Jordan

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

R. Kumar-Singh

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

M. M. Humphries

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

E. M. Sharp

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

D. M. Sheils

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

P. Humphries

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1749427

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1749427

retrieved

15 November 2022

language of work or name

English

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publication date

12 December 1991

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full work available at URL

http://www.nature.com/articles/354478a0

1 reference

stated in

Crossref

DOI

10.1038/354478A0

reference URL

https://api.crossref.org/works/10.1038/354478A0

retrieved

15 November 2022

http://www.nature.com/articles/354478a0.pdf

file format

PDF

1 reference

stated in

Crossref

DOI

10.1038/354478A0

reference URL

https://api.crossref.org/works/10.1038/354478A0

retrieved

15 November 2022

published in

Nature

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volume

354

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issue

6353

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page(s)

478-80

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cites work

A study of retinitis pigmentosa in the City of Birmingham. I Prevalence

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Prevalence of retinitis pigmentosa in Maine

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations within the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNA

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular cloning, primary structure, and orientation of the vertebrate photoreceptor cell protein peripherin in the rod outer segment disk membrane

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A new H-2-linked mutation, rds, causing retinal degeneration in the mouse

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Absence of receptor outer segments in the retina of rds mutant mice

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Development and degeneration of retina in rds mutant mice: electron microscopy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Nucleotide and predicted protein sequence of rat retinal degeneration slow (rds).

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

A dot-blot screening procedure for mutated ras oncogenes using synthetic oligodeoxynucleotides

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of RAS gene mutations in acute myeloid leukemia by polymerase chain reaction and oligonucleotide probes

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2F354478A0

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/354478A0

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Dimensions Publication ID

1044783150

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PubMed publication ID

1749427

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