PAX2 in human kidney malformations and disease.

PAX2 in human kidney malformations and disease.

Item
http://www.wikidata.org/entity/Q37964437
Mutations in PAX2 associate with adult-onset FSGSExpressional alterations in functional ultra-conserved non-coding RNAs in response to all-trans retinoic acid--induced differentiation in neuroblastoma cells.Lhx4 deficiency: increased cyclin-dependent kinase inhibitor expression and pituitary hypoplasia.Repair after nephron ablation reveals limitations of neonatal neonephrogenesisDNA methylation promotes paired box 2 expression via myeloid zinc finger 1 in endometrial cancer.Congenital anomalies of the kidney and urinary tract: an embryogenetic review.Diverse Renal Phenotypes Observed in a Single Family with a Genetic Mutation in Paired Box Protein 2.PAX2 polymorphisms and congenital abnormalities of the kidney and urinary tract in a Brazilian pediatric population: evidence for a role in vesicoureteral refluxEngineered Kidney Tubules for Modeling Patient-Specific Diseases and Drug Discovery
P2860

PAX2 in human kidney malformations and disease.

Item
http://www.wikidata.org/entity/Q37964437
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
PAX2 in human kidney malformations and disease.
@en
PAX2 in human kidney malformations and disease.
@nl
type
label
PAX2 in human kidney malformations and disease.
@en
PAX2 in human kidney malformations and disease.
@nl
prefLabel
PAX2 in human kidney malformations and disease.
@en
PAX2 in human kidney malformations and disease.
@nl
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P698
P356
P1433
P1476
PAX2 in human kidney malformations and disease
@en
P2093
P2860
P2888
P304
P31
P356
P433
P478
P50
P577
P698