Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease (Q45291040)

11 December 2017

title

Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease (English)

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11 December 2017

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6

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11 December 2017

Riess O

1

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11 December 2017

Noerremoelle A

2

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11 December 2017

Collins C

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11 December 2017

Mah D

4

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11 December 2017

Weber B

5

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11 December 2017

publication date

1 May 1992

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11 December 2017

language of work or name

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11 December 2017

volume

1

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11 December 2017

issue

2

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11 December 2017

page(s)

104-108

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Recombination events suggest potential sites for the Huntington's disease gene

11 December 2017

cites work

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https://api.crossref.org/works/10.1038%2FNG0592-104

The mouse gene retinal degeneration (rd) may reduce the number of neurons present in the adult hippocampal dentate gyrus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

Multiple mutations in highly conserved residues are found in mildly affected cystic fibrosis patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

Complete cDNA sequences of mouse rod photoreceptor cGMP phosphodiesterase α- and β-subunits, and identification of β′-, a putative β-subunit isozyme produced by alternative splicing of the β-subunit gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

The alpha 1-antitrypsin gene and its deficiency states

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

Transcription of the dystrophin gene in human muscle and non-muscle tissue

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

Deletion of Huntington's disease-linked G8 (D4S10) locus in Wolf-Hirschhorn syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Mapping of cosmid clones in Huntington's disease region of chromosome 4.

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Non-random association between alleles detected at D4S95 and D4S98 and the Huntington's disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Identification of multiple CpG islands and associated conserved sequences in a candidate region for the Huntington disease gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Genomic organization and complete sequence of the human gene encoding the beta-subunit of the cGMP phosphodiesterase and its localisation to 4p 16.3

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

cGMP phosphodiesterase of retinal rods is regulated by two inhibitory subunits

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase beta-subunit gene of the rd mouse

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Physical maps of 4p16.3, the area expected to contain the Huntington disease mutation

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Isolation of an additional member of the fibroblast growth factor receptor family, FGFR-3

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4.

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Huntington disease-linked locus D4S111 exposed as the alpha-L-iduronidase gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

New mutation to Huntington's disease

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Expression of the cystic fibrosis transmembrane conductance regulator gene in cells of non-epithelial origin

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Detection of specific sequences among DNA fragments separated by gel electrophoresis

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

https://api.crossref.org/works/10.1038%2FNG0592-104

1 reference

7 January 2021

Protocols for an improved detection of point mutations by SSCP

1 reference

https://api.crossref.org/works/10.1038%2FNG0592-104

7 January 2021

Identifiers

DOI

10.1038/NG0592-104

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Dimensions Publication ID

11 December 2017

1005769699

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