(Q30978189)

27 June 2017

title

AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus (English)

1 reference

27 June 2017

1 reference

Doga Turkkahraman

1

1 reference

27 June 2017

Emel Saglar

series ordinal

2

1 reference

27 June 2017

Tugce Karaduman

series ordinal

3

1 reference

27 June 2017

Hatice Mergen

series ordinal

4

1 reference

27 June 2017

publication date

2 July 2015

1 reference

27 June 2017

1 reference

27 June 2017

volume

18

1 reference

27 June 2017

issue

6

1 reference

27 June 2017

page(s)

898-904

1 reference

https://scigraph.springernature.com/pub.10.1007/s11102-015-0668-z

27 June 2017

exact match

0 references

cites work

Nucleotide sequence of cloned cDNA encoding bovine arginine vasopressin–neurophysin II precursor

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Endoplasmic reticulum stress in vasopressin neurons of familial diabetes insipidus model mice: aggregate formation and mRNA poly(A) tail shortening

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Progressive decline of vasopressin secretion in familial autosomal dominant neurohypophyseal diabetes insipidus presenting a novel mutation in the vasopressin‐neurophysin II gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

SWISS-MODEL: modelling protein tertiary and quaternary structure using evolutionary information

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

The SWISS-MODEL Repository and associated resources

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Automated comparative protein structure modeling with SWISS-MODEL and Swiss-PdbViewer: a historical perspective.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Synthesis, Transport, and Release of Posterior Pituitary Hormones

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

A murine model of autosomal dominant neurohypophyseal diabetes insipidus reveals progressive loss of vasopressin-producing neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Identification of a novel mutation in the arginine vasopressin-neurophysin II gene affecting the sixth intrachain disulfide bridge of the neurophysin II moiety

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

A missense mutation encoding cys(67) --> gly in neurophysin ii is associated with early onset autosomal dominant neurohypophyseal diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Progressive polyuria without vasopressin neuron loss in a mouse model for familial neurohypophysial diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

A novel variation in the AVP gene resulting in familial neurohypophyseal diabetes insipidus in a large Italian kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Clinical features and molecular analysis of arginine-vasopressin neurophysin II gene in long-term follow-up patients with idiopathic central diabetes insipidus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11102-015-0668-Z

The human vasopressin gene is linked to the oxytocin gene and is selectively expressed in a cultured lung cancer cell line

21 January 2018

1 reference

12 December 2020

Effects of aging on vasopressin production in a kindred with autosomal dominant neurohypophyseal diabetes insipidus due to the DeltaE47 neurophysin mutation

1 reference

12 December 2020

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

1 reference

12 December 2020

Identification of 13 new mutations in the vasopressin-neurophysin II gene in 17 kindreds with familial autosomal dominant neurohypophyseal diabetes insipidus

1 reference

12 December 2020

10.1007/S11102-015-0668-Z

Identifiers

DOI

1 reference

27 June 2017

1 reference