The role of transient receptor potential channels in kidney disease (Q37527790)

20 August 2017

1 reference

title

The role of transient receptor potential channels in kidney disease (English)

1 reference

20 August 2017

Titia E Woudenberg-Vrenken

series ordinal

1

1 reference

20 August 2017

René J M Bindels

series ordinal

2

1 reference

20 August 2017

Joost G J Hoenderop

series ordinal

3

1 reference

20 August 2017

language of work or name

English

0 references

publication date

23 June 2009

1 reference

Nature Reviews Nephrology

20 August 2017

1 reference

20 August 2017

5

1 reference

20 August 2017

8

1 reference

20 August 2017

441-449

1 reference

https://scigraph.springernature.com/pub.10.1038/nrneph.2009.100

20 August 2017

0 references

cites work

TRP channels in disease

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Molecular determinants in TRPV5 channel assembly

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRP channels as cellular sensors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Transient receptor potential cation channels in disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Identification and localization of TRPC channels in the rat kidney

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Vasopressin-induced membrane trafficking of TRPC3 and AQP2 channels in cells of the rat renal collecting duct

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The epithelial Mg2+ channel transient receptor potential melastatin 6 is regulated by dietary Mg2+ content and estrogens

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Renal expression of osmotically responsive cation channel TRPV4 is restricted to water-impermeant nephron segments.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

OTRPC4, a nonselective cation channel that confers sensitivity to extracellular osmolarity

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Localization and regulation of the epithelial Ca2+ channel TRPV6 in the kidney.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Expression and characterization of human transient receptor potential melastatin 3 (hTRPM3).

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The transient receptor potential superfamily of ion channels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Canonical transient receptor potential 1 channel is involved in contractile function of glomerular mesangial cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPC channels as STIM1-regulated store-operated channels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Physiology and pathophysiology of canonical transient receptor potential channels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Diabetic nephropathy and retinopathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Vasopeptidase inhibition prevents nephropathy in Zucker diabetic fatty rats.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Progression of diabetic nephropathy. Insights from cell culture studies and animal models

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

HNF4 alpha and the Ca-channel TRPC1 are novel disease candidate genes in diabetic nephropathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Induction of TRPC6 channel in acquired forms of proteinuric kidney disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Cell swelling, heat, and chemical agonists use distinct pathways for the activation of the cation channel TRPV4.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Vertebrate and invertebrate TRPV-like mechanoreceptors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The TRPV4 channel: structure-function relationship and promiscuous gating behaviour.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Abnormal osmotic regulation in trpv4 -/- mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Impaired Pressure Sensation in Mice Lacking TRPV4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Impaired osmotic sensation in mice lacking TRPV4

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Control of epithelial transport via luminal P2 receptors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

ATP-induced inhibition of Na+, K+, Cl- cotransport in Madin-Darby canine kidney cells: lack of involvement of known purinoceptor-coupled signaling pathways

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPV4 mediates hypotonicity-induced ATP release by the thick ascending limb

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPP2 and TRPV4 form a polymodal sensory channel complex

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The versatile nature of the calcium-permeable cation channel TRPP2

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Disruption of TRPM6/TRPM7 complex formation by a mutation in the TRPM6 gene causes hypomagnesemia with secondary hypocalcemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Hypomagnesemia with secondary hypocalcemia is caused by mutations in TRPM6, a new member of the TRPM gene family

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Evidence for parathyroid failure in magnesium deficiency

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPM6 and TRPM7--Gatekeepers of human magnesium metabolism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Recent developments in intestinal magnesium absorption

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Hypomagnesemia with secondary hypocalcemia due to a missense mutation in the putative pore-forming region of TRPM6.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Molecular determinants of permeation through the cation channel TRPM6.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Functional characterization of homo- and heteromeric channel kinases TRPM6 and TRPM7

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPM6 forms the Mg2+ influx channel involved in intestinal and renal Mg2+ absorption

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The channel kinases TRPM6 and TRPM7 are functionally nonredundant

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Hereditary etiologies of hypomagnesemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Epidermal growth factor receptor monoclonal antibodies for the treatment of metastatic colorectal cancer

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Phase I study of cetuximab, erlotinib, and bevacizumab in patients with advanced solid tumors

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Dual inhibition of the epidermal growth factor receptor pathway with cetuximab and erlotinib: a phase I study in patients with advanced solid malignancies

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Deletion of Trpm7 disrupts embryonic development and thymopoiesis without altering Mg2+ homeostasis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Polycystic kidney disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Clinical practice. Autosomal dominant polycystic kidney disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Treatment of autosomal dominant polycystic kidney disease (ADPKD): the new horizon for children with ADPKD.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Autosomal dominant polycystic kidney disease: recent advances in pathogenesis and treatment

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Understanding pathogenic mechanisms in polycystic kidney disease provides clues for therapy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Comparison of phenotypes of polycystic kidney disease types 1 and 2. European PKD1-PKD2 Study Group

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Late onset of renal and hepatic cysts in Pkd1-targeted heterozygotes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Perinatal lethality with kidney and pancreas defects in mice with a targetted Pkd1 mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Polycystins 1 and 2 mediate mechanosensation in the primary cilium of kidney cells

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Comparative analysis of the polycystic kidney disease 1 (PKD1) gene reveals an integral membrane glycoprotein with multiple evolutionary conserved domains

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Polycystin-2 is an intracellular calcium release channel

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The hypercalciurias. Causes, parathyroid functions, and diagnostic criteria

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Thiazide-induced hypocalciuria is accompanied by a decreased expression of Ca2+ transport proteins in kidney.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Coordinated control of renal Ca(2+) transport proteins by parathyroid hormone

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The role of 1 alpha, 25-dihydroxyvitamin D in the mediation of intestinal hyperabsorption of calcium in primary hyperparathyroidism and absorptive hypercalciuria

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

An Experimental Human Model of 1,25-Dihydroxyvitamin D-Mediated Hypercalciuria*

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Renal Ca2+ wasting, hyperabsorption, and reduced bone thickness in mice lacking TRPV5

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Epithelial Ca(2+) channel (ECAC1) in autosomal dominant idiopathic hypercalciuria.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPV5 gene polymorphisms in renal hypercalciuria.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Hormone-stimulated Ca2+ reabsorption in rabbit kidney cortical collecting system is cAMP-independent and involves a phorbol ester-insensitive PKC isotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Epithelial Ca2+ and Mg2+ channels in health and disease

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The beta-glucuronidase klotho hydrolyzes and activates the TRPV5 channel

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

The beta-glucuronidase klotho exclusively activates the epithelial Ca2+ channels TRPV5 and TRPV6.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Marked disturbance of calcium homeostasis in mice with targeted disruption of the Trpv6 calcium channel gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

TRPV6 exhibits unusual patterns of polymorphism and divergence in worldwide populations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Gain-of-function haplotype in the epithelial calcium channel TRPV6 is a risk factor for renal calcium stone formation.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Rescue of the pseudo-vitamin D deficiency rickets phenotype of CYP27B1-deficient mice by treatment with 1,25-dihydroxyvitamin D3: biochemical, histomorphometric, and biomechanical analyses

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

25-hydroxyvitamin D 1alpha-hydroxylase: structure of the mouse gene, chromosomal assignment, and developmental expression.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Effects of vitamin D receptor inactivation on the expression of calbindins and calcium metabolism

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Duodenal calcium absorption in vitamin D receptor-knockout mice: functional and molecular aspects

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Modulation of renal Ca2+ transport protein genes by dietary Ca2+ and 1,25-dihydroxyvitamin D3 in 25-hydroxyvitamin D3-1alpha-hydroxylase knockout mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Gene structure and regulation of the murine epithelial calcium channels ECaC1 and 2

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Molecular and functional characterization of the melastatin-related cation channel TRPM3.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Alternative splicing switches the divalent cation selectivity of TRPM3 channels

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Transient receptor potential M3 channels are ionotropic steroid receptors in pancreatic beta cells.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Minireview: aquaporin 2 trafficking.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Homer 1 mediates store- and inositol 1,4,5-trisphosphate receptor-dependent translocation and retrieval of TRPC3 to the plasma membrane.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Dietary Sodium Loading Increases Arterial Pressure in Afferent Renal–Denervated Rats

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

A novel mechanism contributing to development of Dahl salt-sensitive hypertension: role of the transient receptor potential vanilloid type 1.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Deletion of transient receptor potential vanilloid type 1 receptors exaggerates renal damage in deoxycorticosterone acetate-salt hypertension

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Sympathetic hyperactivity in chronic renal failure: a wake-up call

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEPH.2009.100

Targeted inactivation of the 25-hydroxyvitamin D(3)-1(alpha)-hydroxylase gene (CYP27B1) creates an animal model of pseudovitamin D-deficiency rickets

31 March 2020

1 reference

12 December 2020

Rodent models of nephropathy associated with type II diabetes.

1 reference

12 December 2020

1 reference

12 December 2020

Calciotropic and magnesiotropic TRP channels

1 reference

12 December 2020

Diabetic nephropathy: from mechanisms to rational therapies.

1 reference

12 December 2020

Localization of the epithelial Ca(2+) channel in rabbit kidney and intestine

1 reference

12 December 2020

Primary hypomagnesemia with secondary hypocalcemia in an infant

1 reference

12 December 2020

Calcitonin gene-related peptide and its receptors: molecular genetics, physiology, pathophysiology, and therapeutic potentials

1 reference

12 December 2020

Identifiers

DOI

10.1038/NRNEPH.2009.100

1 reference

20 August 2017

1 reference