(Q38360930)

2 September 2017

Analysis of phosducin as a candidate gene for retinopathies (English)

1 reference

2 September 2017

Ara-Iwata F

1

1 reference

2 September 2017

Jacobson SG

2

1 reference

2 September 2017

Gass JD

3

1 reference

2 September 2017

Hotta Y

4

1 reference

2 September 2017

Fujiki K

5

1 reference

2 September 2017

Hayakawa M

6

1 reference

2 September 2017

Inana G

7

1 reference

2 September 2017

1 March 1996

1 reference

2 September 2017

1 reference

2 September 2017

17

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2 September 2017

3-14

1 reference

2 September 2017

1

1 reference

A novel complex from bovine visual cells of a 33,000-dalton phosphoprotein with beta- and gamma-transducin: purification and subunit structure

2 September 2017

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

The photoreceptor-specific 33 kDa phosphoprotein of mammalian retina: generation of monospecific antibodies and localization by immunocytochemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Rat pineal gland phosducin: cDNA isolation, nucleotide sequence, and chromosomal assignment in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Phosducin is a protein kinase A-regulated G-protein regulator

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Assignment of the phosducin (PDC) gene to human chromosome 1q25-1q32.1 by somatic cell hybridization and in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Analysis of the human, bovine and rat 33-kDa proteins and cDNA in retina and pineal gland

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Isolation and analysis of the human MEKA gene encoding a retina-specific protein

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Localization of two genes for Usher syndrome type I to chromosome 11.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

A gene for Usher syndrome type I (USH1A) maps to chromosome 14q

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Localization of Usher syndrome type II to chromosome 1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Mapping recessive ophthalmic diseases: linkage of the locus for Usher syndrome type II to a DNA marker on chromosome 1q.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Genetic heterogeneity of Usher syndrome type II

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Defective myosin VIIA gene responsible for Usher syndrome type 1B

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

Mapping of the choroideremia-like (CHML) gene at 1q42-qter and mutation analysis in patients with Usher syndrome type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

How do eucaryotic ribosomes select initiation regions in messenger RNA?

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816819609057863

10.3109/13816819609057863

21 January 2018

Identifiers

DOI

1 reference

2 September 2017

1 reference