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Heredtary and idiopathic types of diabetes insipidus.

作者信息

Green J R, Buchan G C, Alvord E C, Swanson A G

出版信息

Brain. 1967 Sep;90(3):707-14. doi: 10.1093/brain/90.3.707.

DOI:10.1093/brain/90.3.707
PMID:6058149
Abstract
摘要

相似文献

1
Heredtary and idiopathic types of diabetes insipidus.
Brain. 1967 Sep;90(3):707-14. doi: 10.1093/brain/90.3.707.
2
Evidence for oxytocin synthesis after electrolytic destruction f the paraventricular nucleus in rats withereditary hypothalamic diabetes insipidus.遗传性下丘脑性尿崩症大鼠室旁核电解毁损后催产素合成的证据。
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3
Neurohypophysial hormones in the pars nervosa of the mouse with hereditary nephrogenic diabetes insipidus.
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Hereditary diabetes insipidus: an immunohistochemical study of the hypothalamus and pituitary gland.遗传性尿崩症：下丘脑和垂体的免疫组织化学研究
Acta Neuropathol. 1991;81(3):345-8. doi: 10.1007/BF00305879.
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Vasopressin-resistant diabetes insipidus associated with cytological changes in the supraoptic and paraventricular nuclei.与视上核和室旁核细胞学改变相关的抗血管加压素性尿崩症
Lancet. 1961 Sep 2;2(7201):522-5. doi: 10.1016/s0140-6736(61)92959-2.
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Influence of neurosecretion on the activity of median eminence and pars intermedia in hereditary nephrogenic diabetes insipidus mice with bilateral supraoptic lesions.
Z Zellforsch Mikrosk Anat. 1972;125(4):460-79. doi: 10.1007/BF00306654.
7
The hypothalamohypophyseal neurosecretory system in mice with vasopressin-resistant urinary concENTRATING DEFECTS.
Gen Comp Endocrinol. 1970 Aug;15(1):59-69. doi: 10.1016/0016-6480(70)90097-3.
8
Fine structural features of the neural lobe of the hypophysis of the rat with homozygous diabetes insipidus (Brattleboro strain).
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[Hereditary hypothalamic diabetes insipidus].[遗传性下丘脑性尿崩症]
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Morphological basis of the phasic course of posttraumatic diabetes insipidus.创伤后尿崩症阶段性病程的形态学基础。
Bull Exp Biol Med. 1974 Jun;76(12):1475-8. doi: 10.1007/BF00787568.

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Misfolding of Mutated Vasopressin Causes ER-Retention and Activation of ER-Stress Markers in Neuro-2a Cells.突变的血管加压素错误折叠导致神经母细胞瘤2a细胞内质网滞留及内质网应激标志物激活。
Open Neuroendocrinol J. 2011;4:136-146. doi: 10.2174/1876528901104010136.
7
Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin-neurophysin II gene.常染色体显性遗传神经垂体性尿崩症一家系的临床和分子分析及其与加压素-神经垂体素 II 基因新错义突变的关系。
Endocrine. 2012 Aug;42(1):208-13. doi: 10.1007/s12020-012-9606-2. Epub 2012 Feb 4.
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Structural Requirements for Sorting Pro-Vasopressin to the Regulated Secretory Pathway in a Neuronal Cell Line.在神经元细胞系中，将前血管加压素分选至调节性分泌途径的结构要求。
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Apoptosis of supraoptic AVP neurons is involved in the development of central diabetes insipidus after hypophysectomy in rats.视上核抗利尿激素（AVP）神经元的凋亡参与大鼠垂体切除术后中枢性尿崩症的发生发展。
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A novel heterozygous missense mutation in the vasopressin moiety is identified in a Japanese person with neurohypophyseal diabetes insipidus.在一名患有神经垂体性尿崩症的日本人中，发现了血管加压素部分的一种新型杂合错义突变。
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