Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families (Q61386395)

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English	Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families	article

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instance of

scholarly article

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stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

title

Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

main subject

retinitis pigmentosa

1 reference

based on heuristic

inferred from title

author

Diana Valverde

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

Susana Balcells

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

D Grinberg

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

Carmen Ayuso

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

author name string

M Bayés

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

L Vilageliu

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

J Benítez

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

M Beneyto

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

M Baiget

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

R Gonzàlez-Duarte

series ordinal

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

publication date

1 July 1995

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stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

volume

96

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

page(s)

89-94

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stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

cites work

Missense rhodopsin mutation in a family with recessive RP

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dinucleotide repeat polymorphism at the human recoverin RCVI gene locus on chromosome 17p.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of the DNA of patients with retinitis pigmentosa with a cellular retinaldehyde binding protein cDNA

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Population genetic studies of retinitis pigmentosa.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic and physical mapping of human recoverin: a gene expressed in retinal photoreceptors.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Strategies for multilocus linkage analysis in humans

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recoverin's role: conclusion withdrawn

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A second-generation linkage map of the human genome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple salting out procedure for extracting DNA from human nucleated cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical findings and common symptoms in retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of genes coding for S-antigen, interstitial retinol binding protein, and the alpha-subunit of cone transducin in patients with retinitis pigmentosa.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evaluation of the gene encoding the gamma subunit of rod phosphodiesterase in retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the gene for pigment epithelium-derived factor (PEDF) to chromosome 17p13.1 and expression in cultured human retinoblastoma cells

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deficiencies in sight with the candidate gene approach

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A null mutation in the rhodopsin gene causes rod photoreceptor dysfunction and autosomal recessive retinitis pigmentosa

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation of human retinal genes: recoverin cDNA and gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Retinitis pigmentosa. The Friedenwald Lecture

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recoverin: a Calcium Sensitive Activator of Retinal Rod Guanylate Cyclase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An extended genetic linkage map and an "index" map for human chromosome 17.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human retinal guanylate cyclase (GUC2D) maps to chromosome 17p13.1.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Three microsatellite polymorphisms at the recoverin locus on chromosome 17.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7607661

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00214192

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

Dimensions Publication ID

1041858834

0 references

PubMed publication ID

7607661

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7607661

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7607661%20AND%20SRC:MED&resulttype=core&format=json

retrieved

21 October 2019

 

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