(Q39782823)

English

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

scientific article published on April 1997

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scholarly article

1 reference

Europe PubMed Central

14 September 2017

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

1 reference

Europe PubMed Central

14 September 2017

endoplasmic reticulum

0 references

0 references

author name string

Ito M

1

1 reference

Europe PubMed Central

14 September 2017

Jameson JL

2

1 reference

Europe PubMed Central

14 September 2017

Ito M

3

1 reference

Europe PubMed Central

14 September 2017

language of work or name

0 references

publication date

1 April 1997

1 reference

Europe PubMed Central

14 September 2017

Journal of Clinical Investigation

1 reference

Europe PubMed Central

14 September 2017

99

1 reference

Europe PubMed Central

14 September 2017

1897-1905

1 reference

Europe PubMed Central

14 September 2017

8

1 reference

Europe PubMed Central

14 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

A recurring dominant negative mutation causes autosomal dominant growth hormone deficiency--a clinical research center study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

The toxicity in vitro of beta-amyloid protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Vasopressin function in familial cranial diabetes insipidus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Cell death: the significance of apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Synthesis, Transport, and Release of Posterior Pituitary Hormones

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Complete assignment of neurophysin disulfides indicates pairing in two separate domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Accumulation of PiZ alpha 1-antitrypsin causes liver damage in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Functional inactivation of genes by dominant negative mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Movement of proteins through the Golgi stack: a molecular dissection of vesicular transport.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

Mutation of the signal peptide-encoding region of the preproparathyroid hormone gene in familial isolated hypoparathyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

A missense mutation in the vasopressin-neurophysin precursor gene cosegregates with human autosomal dominant neurohypophyseal diabetes insipidus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

The mechanism of Z alpha 1-antitrypsin accumulation in the liver

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

The Golgi complex: in vitro veritas?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

DNA sequencing with chain-terminating inhibitors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

22 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

25 September 2017

Glu-47, which forms a salt bridge between neurophysin-II and arginine vasopressin, is deleted in patients with familial central diabetes insipidus.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

Heterologous biosynthesis and processing of preprovasopressin in Neuro2A neuroblastoma cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

Therapeutic levels of sodium valproate inhibit mitotic indices in cells of neural origin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

Intracellular degradation of the transport-impaired human PiZ alpha 1-antitrypsin variant. Biochemical mapping of the degradative event among compartments of the secretory pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

Determination of the length of the histological stages of apoptosis in normal liver and in altered hepatic foci of rats.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

Expression of porcine pro-opiomelanocortin in mouse neuroblastoma (Neuro2A) cells: targeting of the foreign neuropeptide to dense-core vesicles

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

The anticonvulsant valproate teratogen restricts the glial cell cycle at a defined point in the mid-G1 phase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

17 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

20 August 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

20 August 2018

The Alzheimer's A beta peptide induces neurodegeneration and apoptotic cell death in transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

20 August 2018

Targeting and processing of pro-opiomelanocortin in neuronal cell lines

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=508014

20 August 2018

Obstructive Lung Disease and Trypsin Inhibitors in α1-Antitrypsin Deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ultrastructure of mouse neuroblastoma cells in tissue culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Radioimmunoassay of vasopressin in familial cental diabetes insipidus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Binding of neurohypophyseal peptides to neurophysin dimer promotes formation of compact and spherical complexes

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two cases of hereditary diabetes insipidus, with an autopsy finding in one

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal assignment of human sequences encoding arginine vasopressin-neurophysin II and growth hormone releasing factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural requirements of peptide hormone binding for peptide-potentiated self-association of bovine neurophysin II

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of a novel arginine vasopressin defect by dideoxy fingerprinting

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial neurohypophyseal diabetes insipidus associated with a signal peptide mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A de novo mutation in the coding sequence for neurophysin-II (Pro24-->Leu) is associated with onset and transmission of autosomal dominant neurohypophyseal diabetes insipidus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel point mutation in the translation initiation codon of the pre-pro-vasopressin-neurophysin II gene: cosegregation with morphological abnormalities and clinical symptoms in autosomal dominant neurohypophyseal diabetes insipidus

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A new type of familial central diabetes insipidus caused by a single base substitution in the neurophysin II coding region of the vasopressin gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/9109434

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1172/JCI119357

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

1 reference

Europe PubMed Central

14 September 2017

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