(Q77810067)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

title

Mutation analysis of codons 345 and 347 of rhodopsin gene in Indian retinitis pigmentosa patients (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference

M Dikshit

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

R Agarwal

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

publication date

1 August 2001

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

volume

80

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

page(s)

111-116

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11910130%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf02728336

8 December 2019

exact match

0 references

cites work

Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene

1 reference

12 December 2020

Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from Europe

1 reference

12 December 2020

Further screening of the rhodopsin gene in patients with autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

[The Pro347Leu mutation of the rhodopsin gene in a Spanish family with autosomal dominant pigmentary retinosis]

1 reference

12 December 2020

Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsin.

1 reference

12 December 2020

Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

A rapid procedure for extracting genomic DNA from leukocytes

1 reference

12 December 2020

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

1 reference

12 December 2020

Ocular findings in patients with autosomal dominant retinitis pigmentosa and rhodopsin, proline-347-leucine

1 reference

12 December 2020

A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Dominant retinitis pigmentosa associated with two rhodopsin gene mutations. Leu-40-Arg and an insertion disrupting the 5'-splice junction of exon 5.

1 reference

12 December 2020

Diffuse loss of rod function in autosomal dominant retinitis pigmentosa with pro-347-leu mutation of rhodopsin.

1 reference

12 December 2020

A large deletion at the 3' end of the rhodopsin gene in an Italian family with a diffuse form of autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Retinal genetics: a nullifying effect for rhodopsin

1 reference

12 December 2020

Evaluation of patients with retinitis pigmentosa receiving electric stimulation, ozonated blood, and ocular surgery in Cuba

1 reference

12 December 2020

Clinical and ERG data in a family with autosomal dominant RP and Pro-347-Arg mutation in the rhodopsin gene

1 reference

12 December 2020

Molecular Analysis and Genetic Mapping of the Rhodopsin Gene in Families with Autosomal Dominant Retinitis Pigmentosa

1 reference

12 December 2020

Ocular findings in patients with autosomal dominant retinitis pigmentosa and Cys110Phe, Arg135Gly, and Gln344stop mutations of rhodopsin

1 reference

12 December 2020

Deletions in exon 5 of the human rhodopsin gene causing a shift in the reading frame and autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

A photoreceptor gene mutation in an indigenous black African family with retinitis pigmentosa identified using a rapid screening approach for common rhodopsin mutations.

1 reference

12 December 2020

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)

1 reference

12 December 2020

Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa

1 reference

12 December 2020

Rhodopsin mutation proline347-to-alanine in a family with autosomal dominant retinitis pigmentosa indicates an important role for proline at position 347

1 reference

12 December 2020

Retinitis pigmentosa genetics: a study in Indian population

1 reference

12 December 2020

Transgenic mice carrying the dominant rhodopsin mutation P347S: evidence for defective vectorial transport of rhodopsin to the outer segments

1 reference

12 December 2020

Molecular genetic study of autosomal dominant retinitis pigmentosa in Lithuanian patients

1 reference

12 December 2020

[A molecular biological study on retinitis pigmentosa]

1 reference

12 December 2020

Defective intracellular transport is the molecular basis of rhodopsin-dependent dominant retinal degeneration

1 reference

12 December 2020

Analysis of rhodopsin gene in patients with retinitis pigmentosa using allele-specific polymerase chain reaction

1 reference

12 December 2020