31 results on '"Woolf, Adrian S."'
Search Results
2. Modelling human lower urinary tract malformations in zebrafish
3. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
4. The term CAKUT has outlived its usefulness: the case for the prosecution
5. Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder
6. Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney
7. Molecular insights into genome-wide association studies of chronic kidney disease-defining traits
8. Publisher Correction: Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
9. Genome-wide linkage and association study implicates the 10q26 region as a major genetic contributor to primary nonsyndromic vesicoureteric reflux
10. ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development
11. TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons
12. Measures of kidney function by minimally invasive techniques correlate with histological glomerular damage in SCID mice with adriamycin-induced nephropathy
13. Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease
14. Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation
15. Genetics of human congenital urinary bladder disease
16. Angiogenesis and autosomal dominant polycystic kidney disease
17. Expression of Fraser syndrome genes in normal and polycystic murine kidneys
18. Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutations
19. Similar renal outcomes in children with ADPKD diagnosed by screening or presenting with symptoms
20. Renal malformations associated with mutations of developmental genes: messages from the clinic
21. Genetic analyses reveal a requirement for Dicer1 in the mouse urogenital tract
22. Renal tract malformations: perspectives for nephrologists
23. Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs
24. Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein
25. The Life of the Human Kidney Before Birth: Its Secrets Unfold
26. Emerging roles of obstruction and mutations in renal malformations
27. Molecular bases of human kidney malformations
28. Expression of Hepatocyte Growth Factor/Scatter Factor and Its Receptor, MET, Suggests Roles in Human Embryonic Organogenesis
29. Taxol inhibits progression of congenital polycystic kidney disease
30. Genetically engineered kidneys
31. Do glomerular hemodynamic adaptations influence the progression of human renal disease?
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