(Q40966092)

English

Mutant vasopressin precursors that cause autosomal dominant neurohypophyseal diabetes insipidus retain dimerization and impair the secretion of wild-type proteins.

scientific article published on March 1999

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Mutant vasopressin precursors that cause autosomal dominant neurohypophyseal diabetes insipidus retain dimerization and impair the secretion of wild-type proteins (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

0 references

diabetes insipidus

1 reference

based on heuristic

inferred from title

neurohypophyseal diabetes insipidus

1 reference

based on heuristic

inferred from title

J. Larry Jameson

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

M Ito

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

R N Yu

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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publication date

1 March 1999

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Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Journal of Biological Chemistry

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

274

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12 November 2019

13

1 reference

Europe PubMed Central

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12 November 2019

9029-9037

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085151%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A single base substitution in the coding region for neurophysin II associated with familial central diabetes insipidus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Possible involvement of inefficient cleavage of preprovasopressin by signal peptidase as a cause for familial central diabetes insipidus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Two novel mutations in the coding region for neurophysin-II associated with familial central diabetes insipidus.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

A novel mutation in the coding region for neurophysin-II is associated with autosomal dominant neurohypophyseal diabetes insipidus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Identification of mutations of the arginine vasopressin-neurophysin II gene in two kindreds with familial central diabetes insipidus.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Identification of a novel nonsense mutation and a missense substitution in the vasopressin-neurophysin II gene in two Spanish kindreds with familial neurohypophyseal diabetes insipidus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Synthesis, Transport, and Release of Posterior Pituitary Hormones

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Genetic basis of familial neurohypophyseal diabetes insipidus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

HEREDITARY IDIOPATHIC DIABETES INSIPIDUS. A CASE REPORT WITH AUTOPSY FINDINGS.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Heredtary and idiopathic types of diabetes insipidus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Hereditary diabetes insipidus: an immunohistochemical study of the hypothalamus and pituitary gland

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Molecular basis of autosomal dominant neurohypophyseal diabetes insipidus. Cellular toxicity caused by the accumulation of mutant vasopressin precursors within the endoplasmic reticulum

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Functional inactivation of genes by dominant negative mutations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

DNA sequencing with chain-terminating inhibitors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

A new technique for the assay of infectivity of human adenovirus 5 DNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

DAX-1 inhibits SF-1-mediated transactivation via a carboxy-terminal domain that is deleted in adrenal hypoplasia congenita

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Structure-function relationships of the vasopressin prohormone domains

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Small peptides as analogs of oxytocin and vasopressin in their interactions with bovine neurophysin-II.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

Crystal structure of a bovine neurophysin II dipeptide complex at 2.8 A determined from the single-wavelength anomalous scattering signal of an incorporated iodine atom

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.13.9029

21 January 2018

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