(Q36823037)

16 August 2017

title

Characterization and mapping of the mouse NDP (Norrie disease) locus (Ndp). (English)

1 reference

16 August 2017

1 reference

3

1 reference

16 August 2017

Xandra O. Breakefield

series ordinal

4

object named as

X O Breakefield

1 reference

16 August 2017

E M Battinelli

1

1 reference

16 August 2017

Y Boyd

series ordinal

2

1 reference

16 August 2017

Z Y Chen

series ordinal

5

1 reference

16 August 2017

publication date

1 February 1996

1 reference

16 August 2017

number of pages

5

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inferred from page(s)

published in

Mammalian Genome

1 reference

16 August 2017

volume

7

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16 August 2017

issue

2

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16 August 2017

page(s)

93-97

1 reference

https://scigraph.springernature.com/pub.10.1007/s003359900026

16 August 2017

exact match

0 references

cites work

Isolation of a candidate gene for Norrie disease by positional cloning

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Mutations in the candidate gene for Norrie disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Organization and expression of eucaryotic split genes coding for proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Characterization of a YAC containing part or all of the Norrie disease locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Isolation and characterization of a candidate gene for Norrie disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Organization of the human monoamine oxidase genes and long-range physical mapping around them

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Characterization of a mutation within the NDP gene in a family with a manifesting female carrier

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Norrie disease gene: characterization of deletions and possible function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Novel sequences conserved on the human and mouse X chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

The properdin structural locus (Pfc) lies close to the locus for tissue inhibitor of metallothionine proteases (Timp) on the mouse X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Molecular modelling of the Norrie disease protein predicts a cystine knot growth factor tertiary structure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

DNA sequencing with chain-terminating inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Mutations in the Norrie disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Ligation-anchored PCR: a simple amplification technique with single-sided specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Identification of two new missense mutations (K58N and R121Q) in the Norrie disease (ND) gene in two Spanish families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Partial inversion of gene order within a homologous segment on the X chromosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS003359900026

Norrie disease resulting from a gene deletion: clinical features and DNA studies

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8835523

12 December 2020

inferred from PubMed ID database lookup

Norrie's disease. A congenital progressive oculo-acoustico-cerebral degeneration

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8835523

12 December 2020

inferred from PubMed ID database lookup

Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8835523

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S003359900026

1 reference

16 August 2017

1 reference