Localization of the Norrie disease gene mRNA by in situ hybridization. (Q48133081)

9 February 2018

title

Localization of the Norrie disease gene mRNA by in situ hybridization. (English)

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9 February 2018

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Hartzer MK

1

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9 February 2018

Cheng M

series ordinal

2

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9 February 2018

Liu X

series ordinal

3

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9 February 2018

Shastry BS

series ordinal

4

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9 February 2018

publication date

1 July 1999

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9 February 2018

published in

Brain Research Bulletin

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9 February 2018

volume

49

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9 February 2018

page(s)

355-358

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9 February 2018

issue

5

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9 February 2018

describes a project that uses

in situ hybridization

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Isolation of a candidate gene for Norrie disease by positional cloning

inferred from title

cites work

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https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

An animal model for Norrie disease (ND): gene targeting of the mouse ND gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Isolation and characterization of a candidate gene for Norrie disease

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Norrie disease and MAO genes: nearest neighbors

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

X-linked exudative vitreoretinopathy caused by an arginine to leucine substitution (R121L) in the Norrie disease protein

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Missense mutations in the NDP gene in patients with a less severe course of Norrie disease

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Mutations in the Norrie disease gene

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Linkage and candidate gene analysis of X-linked familial exudative vitreoretinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Identification of novel missense mutations in the Norrie disease gene associated with one X-linked and four sporadic cases of familial exudative vitreoretinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

Norrie disease in a family with a manifesting female carrier.

1 reference

https://api.crossref.org/works/10.1016%2FS0361-9230%2899%2900071-4

7 January 2021

10.1016/S0361-9230(99)00071-4

Identifiers

DOI

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9 February 2018

PubMed ID

10452356

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9 February 2018