Severe urinary concentrating defect in renal collecting duct-selective AQP2 conditional-knockout mice. - Wikidata - awgldk - TriplyDB

Severe urinary concentrating defect in renal collecting duct-selective AQP2 conditional-knockout mice.

Severe urinary concentrating defect in renal collecting duct-selective AQP2 conditional-knockout mice.

http://www.wikidata.org/entity/Q34498888

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Nuclear Receptor Regulation of Aquaporin-2 in the Kidney The Trafficking of the Water Channel Aquaporin-2 in Renal Principal Cells-a Potential Target for Pharmacological Intervention in Cardiovascular Diseases Serine 269 phosphorylated aquaporin-2 is targeted to the apical membrane of collecting duct principal cells Deletion of the prorenin receptor from the ureteric bud causes renal hypodysplasia.GATA2 regulates body water homeostasis through maintaining aquaporin 2 expression in renal collecting ducts.Regulation and dysregulation of aquaporins in water balance disorders.A role for VAMP8/endobrevin in surface deployment of the water channel aquaporin 2 PKCα regulates vasopressin-induced aquaporin-2 trafficking in mouse kidney collecting duct cells in vitro via altering microtubule assembly.Nephrogenic diabetes insipidus in mice caused by deleting COOH-terminal tail of aquaporin-2.Abnormal function of the vasopressin-cyclic-AMP-aquaporin2 axis during urine concentrating and diluting in patients with reduced renal function. A case control study.Characterization of the transcriptome, nucleotide sequence polymorphism, and natural selection in the desert adapted mouse Peromyscus eremicus.Aqp5 is a new transcriptional target of Dot1a and a regulator of Aqp2.Genetic ablation of aquaporin-2 in the mouse connecting tubules results in defective renal water handling.Identification of SPRED2 (sprouty-related protein with EVH1 domain 2) as a negative regulator of the hypothalamic-pituitary-adrenal axis.Hormonal regulation of ovarian bursa fluid in mice and involvement of aquaporins.Characterization of growth, glomerular number, and tubular proteins in the developing rhesus monkey kidney.Pathogenesis and treatment of autosomal-dominant nephrogenic diabetes insipidus caused by an aquaporin 2 mutation.Aquaporins as diagnostic and therapeutic targets in cancer: how far we are?Central diabetes insipidus associated with impaired renal aquaporin-1 expression in mice lacking liver X receptor β Disruption of prostaglandin E2 receptor EP4 impairs urinary concentration via decreasing aquaporin 2 in renal collecting ducts.Comparative functional analysis of aquaporins/glyceroporins in mammals and anurans.Aquaporin 2 promotes cell migration and epithelial morphogenesis.Autophagic degradation of aquaporin-2 is an early event in hypokalemia-induced nephrogenic diabetes insipidus Regulation of transport in the connecting tubule and cortical collecting duct Regulation of aquaporin-2 in the kidney: A molecular mechanism of body-water homeostasis.Acute regulation of aquaporin-2 phosphorylation at Ser-264 by vasopressin.Aquaporins: a promising target for drug development.Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Molecular regulation of kidney development.Creation of trophectoderm, the first epithelium, in mouse preimplantation development.Downregulation of UT-A1/UT-A3 is associated with urinary concentrating defect in glucocorticoid-excess state.Mouse models and the urinary concentrating mechanism in the new millennium.Hsp90 inhibitor partially corrects nephrogenic diabetes insipidus in a conditional knock-in mouse model of aquaporin-2 mutation.Physiology and pathophysiology of the vasopressin-regulated renal water reabsorption.Vasopressin and the regulation of aquaporin-2 Dissecting the roles of aquaporins in renal pathophysiology using transgenic mice.Localization and trafficking of aquaporin 2 in the kidney.Beta1-integrin is required for kidney collecting duct morphogenesis and maintenance of renal function.Congenital nephrogenic diabetes insipidus: what can we learn from mouse models?A selective EP4 PGE2 receptor agonist alleviates disease in a new mouse model of X-linked nephrogenic diabetes insipidus.

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Severe urinary concentrating defect in renal collecting duct-selective AQP2 conditional-knockout mice.

http://www.wikidata.org/entity/Q34498888

description

2006 nî lūn-bûn

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2006 թուականի Մարտին հրատարակուած գիտական յօդուած

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2006 թվականի մարտին հրատարակված գիտական հոդված

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2006年の論文

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Severe urinary concentrating d ...... QP2 conditional-knockout mice.

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Severe urinary concentrating d ...... QP2 conditional-knockout mice.

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Aleksandra Rojek

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Ernst-Martin Füchtbauer

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Jørgen Frøkiaer

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Søren Nielsen

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Tae-Hwan Kwon

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P2860

Vasopressin increases water permeability of kidney collecting duct by inducing translocation of aquaporin-CD water channels to plasma membrane

Sonic hedgehog regulates proliferation and differentiation of mesenchymal cells in the mouse metanephric kidney

Micropuncture study of the mammalian urinary concentrating mechanism: evidence for the countercurrent hypothesis

The connecting tubule: a functional subdivision of the rabbit distal nephron segments

Severely impaired urinary concentrating ability in transgenic mice lacking aquaporin-1 water channels

Aquaporins in the kidney: from molecules to medicine.

Perinatal lethality and defects in hindbrain development in mice homozygous for a targeted mutation of the zinc finger gene Krox20.

Collecting duct-specific gene inactivation of alphaENaC in the mouse kidney does not impair sodium and potassium balance.

Nephrogenic diabetes insipidus in mice lacking aquaporin-3 water channels.

Cellular and subcellular immunolocalization of vasopressin-regulated water channel in rat kidney.

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