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1.
Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease.
Pediatr Nephrol
; 30(9): 1459-65, 2015 Sep.
Article
in English
| MEDLINE | ID: mdl-25739341
2.
Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations.
Stem Cell Reports
; 2024 May 13.
Article
in English
| MEDLINE | ID: mdl-38788724
3.
Galectin-3 associates with the primary cilium and modulates cyst growth in congenital polycystic kidney disease.
Am J Pathol
; 169(6): 1925-38, 2006 Dec.
Article
in English
| MEDLINE | ID: mdl-17148658
4.
P2X(7) receptors are expressed during mouse nephrogenesis and in collecting duct cysts of the cpk/cpk mouse.
Exp Nephrol
; 10(1): 34-42, 2002.
Article
in English
| MEDLINE | ID: mdl-11803203
5.
Unilateral renal agenesis and the congenital solitary functioning kidney: developmental, genetic and clinical perspectives.
BJU Int
; 99(1): 17-21, 2007 Jan.
Article
in English
| MEDLINE | ID: mdl-16956352
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