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Genetic determinants of urolithiasis.

Genetic determinants of urolithiasis.

http://www.wikidata.org/entity/Q37512167

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Persistence of 1,25D-induced hypercalciuria in alendronate-treated genetic hypercalciuric stone-forming rats fed a low-calcium diet 1,25(OH)₂D₃ induces a mineralization defect and loss of bone mineral density in genetic hypercalciuric stone-forming rats Common and rare variants associated with kidney stones and biochemical traits.Effect of Potassium Citrate on Calcium Phosphate Stones in a Model of Hypercalciuria.Increased biological response to 1,25(OH)(2)D(3) in genetic hypercalciuric stone-forming rats.Kidney stones: a fetal origins hypothesis 1,25(OH)₂D₃-enhanced hypercalciuria in genetic hypercalciuric stone-forming rats fed a low-calcium diet Might E-cadherin promoter polymorphisms of rs16260 and rs5030625 associate with the risk of nephrolithiasis?When to suspect a genetic disorder in a patient with renal stones, and why.Geographic location is an important determinant of risk factors for stone disease.Epidemiology of stone disease across the world.Renal phosphate handling and inherited disorders of phosphate reabsorption: an update.Association study of DGKH gene polymorphisms with calcium oxalate stone in Chinese population.

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Genetic determinants of urolithiasis.

http://www.wikidata.org/entity/Q37512167

description

article científic

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article scientifique

@fr

articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 20 December 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

@cs

name

Genetic determinants of urolithiasis.

@en

Genetic determinants of urolithiasis.

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type

label

Genetic determinants of urolithiasis.

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Genetic determinants of urolithiasis.

@nl

prefLabel

Genetic determinants of urolithiasis.

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Genetic determinants of urolithiasis.

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NRNEPH.2011.211

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Nature Reviews Nephrology

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Genetic determinants of urolithiasis.

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Carla G Monico

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Dawn S Milliner

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Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome

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

Non-type I cystinuria caused by mutations in SLC7A9, encoding a subunit (bo,+AT) of rBAT

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

Mutations in DHDPSL are responsible for primary hyperoxaluria type III

SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phosphate homeostasis

Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I

Novel ATP6V1B1 and ATP6V0A4 mutations in autosomal recessive distal renal tubular acidosis with new evidence for hearing loss

Cystinuria caused by mutations in rBAT, a gene involved in the transport of cystine

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nrneph.2011.211

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151-162

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scholarly article

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10.1038/NRNEPH.2011.211

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