(Q24305284)

chromosomal deletion syndrome

inferred from title

1 reference

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

15 November 2022

membrane glycoprotein

1 reference

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

15 November 2022

nerve tissue protein

1 reference

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

15 November 2022

G. J. Farrar

1 reference

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

15 November 2022

P. Kenna

1 reference

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

15 November 2022

S. A. Jordan

1 reference

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

15 November 2022

R. Kumar-Singh

1 reference

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

15 November 2022

M. M. Humphries

1 reference

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

15 November 2022

E. M. Sharp

1 reference

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

15 November 2022

D. M. Sheils

1 reference

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

15 November 2022

P. Humphries

1 reference

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

full work available at URL

15 November 2022

language of work or name

English

0 references

publication date

12 December 1991

0 references

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

1 reference

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

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

15 November 2022

1 reference

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

15 November 2022

0 references

354

0 references

issue

6353

0 references

page(s)

478-80

0 references

cites work

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

1 reference

7 January 2021

Prevalence of retinitis pigmentosa in Maine

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Rhodopsin mutations in autosomal dominant retinitis pigmentosa

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

Dimensions Publication ID

Identifiers

DOI

10.1038/354478A0

0 references

1044783150

0 references