(Q33906416)

29 July 2017

0 references

Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria (English)

1 reference

dyschromatosis symmetrica hereditaria

29 July 2017

main subject

0 references

author name string

Yoshinori Miyamura

1

1 reference

29 July 2017

Tamio Suzuki

2

1 reference

29 July 2017

Michihiro Kono

3

1 reference

29 July 2017

Katsuhiko Inagaki

4

1 reference

29 July 2017

Shiro Ito

5

1 reference

29 July 2017

Noriyuki Suzuki

6

1 reference

29 July 2017

Yasushi Tomita

7

1 reference

29 July 2017

language of work or name

English

0 references

publication date

11 August 2003

1 reference

American Journal of Human Genetics

29 July 2017

published in

1 reference

29 July 2017

volume

73

1 reference

29 July 2017

issue

3

1 reference

29 July 2017

page(s)

693-699

1 reference

A gene locus responsible for dyschromatosis symmetrica hereditaria (DSH) maps to chromosome 6q24.2-q25.2.

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Requirement of the RNA editing deaminase ADAR1 gene for embryonic erythropoiesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Regulation of alternative splicing by RNA editing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Regulation of serotonin-2C receptor G-protein coupling by RNA editing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

RNA editing of hepatitis delta virus antigenome by dsRNA-adenosine deaminase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Faster sequential genetic linkage computations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

RNA editing of AMPA receptor subunit GluR-B: a base-paired intron-exon structure determines position and efficiency

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Control of kinetic properties of AMPA receptor channels by nuclear RNA editing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Genomic organization and chromosomal location of the human dsRNA adenosine deaminase gene: the enzyme for glutamate-activated ion channel RNA editing

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Strategies for multilocus linkage analysis in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

A double-stranded RNA unwinding activity introduces structural alterations by means of adenosine to inosine conversions in mammalian cells and Xenopus eggs

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Deletion of the c-kit protooncogene in the human developmental defect piebald trait

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Mutation of the KIT (mast/stem cell growth factor receptor) protooncogene in human piebaldism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

In utero manipulation of coat color formation by a monoclonal anti-c-kit antibody: two distinct waves of c-kit-dependency during melanocyte development.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Widespread inosine-containing mRNA in lymphocytes regulated by ADAR1 in response to inflammation.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Exclusion of linkage between dyschromatosis symmetrica hereditaria and chromosome 9.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Avoiding recomputation in linkage analysis.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180697

Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11-1q21

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12916015

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An unwinding activity that covalently modifies its double-stranded RNA substrate

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12916015

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12916015

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/378209

1 reference

29 July 2017

1 reference

29 July 2017

1 reference