Progressive polyuria without vasopressin neuron loss in a mouse model for familial neurohypophysial diabetes insipidus (Q45744978)

15 December 2017

title

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

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15 December 2017

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Masayuki Hayashi

1

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15 December 2017

Hiroshi Arima

2

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15 December 2017

Noriyuki Ozaki

3

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15 December 2017

Yoshiaki Morishita

4

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15 December 2017

Maiko Hiroi

5

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15 December 2017

Nobuaki Ozaki

6

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15 December 2017

Hiroshi Nagasaki

7

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15 December 2017

Noriaki Kinoshita

8

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15 December 2017

Masatsugu Ueda

9

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15 December 2017

Akira Shiota

10

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15 December 2017

Yutaka Oiso

11

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15 December 2017

publication date

18 March 2009

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15 December 2017

American Journal of Physiology - Regulatory, Integrative and Comparative Physiology

published in

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15 December 2017

volume

296

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15 December 2017

page(s)

R1641-9

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issue

5

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An immunochemical analysis of oxytocin and vasopressin prohormone processing in vivo

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Differential cellular handling of defective arginine vasopressin (AVP) prohormones in cells expressing mutations of the AVP gene associated with autosomal dominant and recessive familial neurohypophyseal diabetes insipidus

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Impaired trafficking of mutated AVP prohormone in cells expressing rare disease genes causing autosomal dominant familial neurohypophyseal diabetes insipidus

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Autophagy in hypothalamic neurones of rats expressing a familial neurohypophysial diabetes insipidus transgene.

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

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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

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

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

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

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Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

1 reference

15 December 2017

PubMed ID

19297548

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15 December 2017