Norrie disease protein (norrin) forms disulfide-linked oligomers associated with the extracellular matrix (Q73960070)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9407136%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

title

Norrie disease protein (norrin) forms disulfide-linked oligomers associated with the extracellular matrix (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9407136%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

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J Perez-Vilar

1

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8 November 2019

R L Hill

series ordinal

2

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8 November 2019

language of work or name

English

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publication date

1 December 1997

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Journal of Biological Chemistry

8 November 2019

published in

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8 November 2019

volume

272

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8 November 2019

issue

52

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8 November 2019

page(s)

33410-33415

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Isolation of a candidate gene for Norrie disease by positional cloning

8 November 2019

cites work

1 reference

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Isolation and characterization of a candidate gene for Norrie disease

21 January 2018

1 reference

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Mutations in the Norrie disease gene

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Two new mutations in exon 3 of theNDP gene: S73X and S101F associated with severe and less severe ocular phenotype, respectively

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

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

21 January 2018

1 reference

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An integumentary mucin (FIM-B.1) from Xenopus laevis homologous with von Willebrand factor.

21 January 2018

1 reference

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Characterization of a mucin cDNA clone isolated from HT-29 mucus-secreting cells. The 3' end of MUC5AC?

21 January 2018

1 reference

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Genomic organization of the 3' region of the human mucin gene MUC5B.

21 January 2018

1 reference

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The carboxyl-terminal sequence of the human secretory mucin, MUC6. Analysis Of the primary amino acid sequence

21 January 2018

1 reference

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Norrie disease gene: characterization of deletions and possible function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

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/10.1074%2FJBC.272.52.33410

The cystine-knot growth-factor superfamily

21 January 2018

1 reference

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Identification of disulfide-bridged substructures within human von Willebrand factor

21 January 2018

1 reference

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Assembly and routing of von Willebrand factor variants: the requirements for disulfide-linked dimerization reside within the carboxy-terminal 151 amino acids

21 January 2018

1 reference

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Porcine submaxillary mucin forms disulfide-bonded dimers between its carboxyl-terminal domains

21 January 2018

1 reference

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Site-directed mutagenesis of virtually any plasmid by eliminating a unique site

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

Transformation-sensitive protein associated with the cell substratum of chicken embryo fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

Morphological appearance, growth behavior and migratory activity of human tumor cells maintained on extracellular matrix versus plastic

21 January 2018

1 reference

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Brefeldin A: insights into the control of membrane traffic and organelle structure

21 January 2018

1 reference

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Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

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/10.1074%2FJBC.272.52.33410

Mutations in the Norrie disease gene: a new mutation in a Japanese family

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.272.52.33410

21 January 2018

Identifiers

DOI

10.1074/JBC.272.52.33410

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9407136%20AND%20SRC:MED&resulttype=core&format=json

8 November 2019

1 reference