Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+. - Wikidata - thesis-toulmin - TriplyDB

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

http://www.wikidata.org/entity/Q37603366

about

Molecular pathophysiology of Bartter's and Gitelman's syndromes.Developmental changes in renal tubular transport-an overview.Genetic causes of hypomagnesemia, a clinical overview Reduced renal calcium excretion in the absence of sclerostin expression: evidence for a novel calcium-regulating bone kidney axis.Regulation of magnesium balance: lessons learned from human genetic disease Epigenetic profiles of pre-diabetes transitioning to type 2 diabetes and nephropathy.Calcium Extrusion Pump PMCA4: A New Player in Renal Calcium Handling?A Novel Homozygous Mutation in the Transient Receptor Potential Melastatin 6 Gene: A Case Report.The role of calbindin-D28k on renal calcium and magnesium handling during treatment with loop and thiazide diuretics.Activation of the Ca(2+)-sensing receptor increases renal claudin-14 expression and urinary Ca(2+) excretion.Molecular basis of epithelial Ca2+ and Mg2+ transport: insights from the TRP channel family.Calcium regulation of tight junction permeability.Alterations in vitamin D metabolite, parathyroid hormone and fibroblast growth factor-23 concentrations in sclerostin-deficient mice permit the maintenance of a high bone mass.Intestinal absorption and renal reabsorption of calcium throughout postnatal development.Effect of diuretics on renal tubular transport of calcium and magnesium.Increased expression of renal TRPM6 compensates for Mg(2+) wasting during furosemide treatment.Coordinated regulation of TRPV5-mediated Ca²⁺ transport in primary distal convolution cultures.Regulation of calcium reabsorption along the rat nephron: a modeling study.A model of calcium transport along the rat nephron.Ultrastructural and immunohistochemical localization of plasma membrane Ca2+-ATPase 4 in Ca2+-transporting epithelia.Magnesium: Nutrition and Homoeostasis.

P2860

Q30487704-9BAF638F-B048-4F9A-B16E-435678547A83 Q33639194-43A248D3-CDDC-456B-B338-40D3108028FC Q33715342-71CF9DA8-3DCF-4232-8929-7E066DC4B188 Q34260123-BBA4B48D-78DF-4236-9C65-D437765211EB Q35683775-D0414BBA-00EC-4773-A348-FCEBA6E2FCCA Q35932565-B1AA1D67-8179-49A6-B40B-960DE5F2F2F9 Q35996158-B883792E-AC47-433A-8A60-A2C77F693371 Q36721996-AE15BA95-3E26-46E4-AC60-A47DCCEFB9C2 Q36955336-8F334E8D-3217-4FA0-9D0D-4DC19D294A1A Q37123850-705A66D2-9DDC-4D42-B1AE-D8D8B90303FE Q37805923-CC584B8E-8669-451E-8CFF-130597D57C9C Q38021499-B6EA392E-94F2-438E-A186-3EE1ED4B35B4 Q38275068-BD87D05E-0A5F-49F6-8237-F3D8ADB42D63 Q38739265-6CA9A5F0-DDA8-4BDD-B375-89161235D2C4 Q39169297-E0CD861D-E897-4E8C-8F61-49355D38B24B Q39721762-788E6640-5D82-4F82-9B03-7EA45C44C966 Q50460870-A2C81A07-A908-4F7C-86E7-69D34E233F26 Q50993061-7F102E54-FA4D-497C-A5C0-A6A7D7A48786 Q51202269-03941DB2-5A55-41A5-82D3-241B630C4638 Q53423937-4D78D13D-8C74-4594-9982-DFFE8D542F10 Q55222414-7B05A6DB-D8BC-4C02-9329-DAF2A04367D6

P2860

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

http://www.wikidata.org/entity/Q37603366

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 28 September 2009

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

@en

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

@nl

type

label

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

@en

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

@nl

prefLabel

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

@en

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+.

@nl

P1433

Q37603366-019DCC60-D2DC-4EBE-8226-B8E1917E7343

P1476

Q37603366-74E3FC93-5910-4C68-8B0B-5E20E8A026AD

P2093

Q37603366-1B5504AC-FCE3-4D26-BF2F-DFCD2716F843

Q37603366-29EAFB39-7E80-41A2-BDAF-ADDB411C27C7

P2860

Q37603366-05D841F8-A6DF-4477-8B28-432B9C4DD4D2

Q37603366-0CC4EC81-4CB9-48BD-8124-2889115DC684

Q37603366-0F9A87B0-E0BE-432F-B562-B8ECDF43036D

Q37603366-0FADBF1B-FE2D-42FD-BBB9-BE877D046136

Q37603366-11A3F70A-6050-497E-9FF1-CBED65367D2B

Q37603366-11FF3D27-7DB3-4281-A12F-87101ABCDCF1

Q37603366-155A481F-1751-4A3E-9A63-5A372B349092

Q37603366-15C6BC60-33DA-4BA2-AF11-B8913E60F21D

Q37603366-15F9B2C2-D90E-4EAF-B0EF-BB681B9C8251

Q37603366-169F0267-FA88-4811-B619-BB8B0665268F

P304

Q37603366-555B56FA-C8C7-47D9-AE7A-6934E2EB9EF9

P31

Q37603366-E8F25939-574F-4C40-83CC-A7BB662E1408

P356

Q37603366-B9082944-4A5F-4A7D-BA39-608645A333B2

P407

Q37603366-765AC2E7-9455-452C-A440-FEE8C22CA5AB

P433

Q37603366-2C69EAC7-2A77-46FC-8807-4DDADA180971

P478

Q37603366-92C41512-B436-4D4B-844A-E5765A85518C

P50

Q37603366-E9713887-037A-4EA6-B3DA-195644666094

P577

Q37603366-17E0BEF3-0CDC-4161-9478-F536ED3EA527

P698

Q37603366-76FC4430-5846-457C-9066-F2585317E2B0

P356

P1433

Clinical Science

P1476

Hereditary tubular transport disorders: implications for renal handling of Ca2+ and Mg2+

@en

P2093

Joost G Hoenderop

http://www.w3.org/2001/XMLSchema#string

René J Bindels

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the gene encoding B1 subunit of H+-ATPase cause renal tubular acidosis with sensorineural deafness

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption

Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearing

The thiazide-sensitive Na-Cl cotransporter is regulated by a WNK kinase signaling complex

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

Autosomal dominant hypocalcaemia caused by a Ca(2+)-sensing receptor gene mutation

A common molecular basis for three inherited kidney stone diseases

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

Dent Disease with mutations in OCRL1

P304

1-18

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1042/CS20090086

http://www.w3.org/2001/XMLSchema#string

P407

P433

1

http://www.w3.org/2001/XMLSchema#string

P478

118

http://www.w3.org/2001/XMLSchema#string

P50

P577

2009-09-28T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

19780717

http://www.w3.org/2001/XMLSchema#string