707 results on '"Woolf, Adrian S."'
Search Results
2. Predicting congenital renal tract malformation genes using machine learning
3. Modelling human lower urinary tract malformations in zebrafish
4. Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations
5. Genetic imputation of kidney transcriptome, proteome and multi-omics illuminates new blood pressure and hypertension targets
6. Bi-allelic variants in CELSR3 are implicated in central nervous system and urinary tract anomalies
7. Author response: Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome
8. Neurogenic Defects Occur in LRIG2-Associated Urinary Bladder Disease
9. The term CAKUT has outlived its usefulness: the case for the prosecution
10. A unique subset of pericystic endothelium associates with aberrant microvascular remodelling and impaired blood perfusion early in polycystic kidney disease
11. A genome-wide association study with tissue transcriptomics identifies genetic drivers for classic bladder exstrophy
12. Building human renal tracts
13. Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome.
14. Contributors
15. Nephrogenesis in health and disease
16. Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome
17. Heparanase 2 and Urofacial Syndrome, a Genetic Neuropathy
18. When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta‐analysis
19. Uncovering genetic mechanisms of hypertension through multi-omic analysis of the kidney
20. Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformations
21. Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder
22. Vascular Endothelial Growth Factor C for Polycystic Kidney Diseases
23. Loss-of-function variants in myocardin cause congenital megabladder in humans and mice
24. When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta‐analysis.
25. Human HPSE2gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome
26. Formation of Mature Nephrons by Implantation of Human Pluripotent Stem Cell-Derived Progenitors into Mice
27. Human pluripotent stem cell-derived kidney organoids reveal tubular epithelial pathobiology of heterozygous HNF1B-associated dysplastic kidney malformations
28. Serum-Free Organ Culture of the Embryonic Mouse Ureter
29. A questionnaire survey of radiological diagnosis and management of renal dysplasia in children
30. PS-BPB06-5: URINARY CELL TRANSCRIPTOMICS: A NON-INVASIVE EXPRESSION READOUT OF KIDNEY GENES OF RELEVANCE TO HYPERTENSION
31. Neurogenic defects underlie functional bladder outflow tract obstruction associated with biallelic variants inLRIG2
32. Molecular insights into genome-wide association studies of chronic kidney disease-defining traits
33. Three-dimensional imaging and single-cell transcriptomics of the human kidney implicate perturbation of lymphatics in alloimmunity
34. Exploration of the single-cell transcriptomic landscape identifies aberrant glomerular cell crosstalk in a murine model of WT1 kidney disease
35. Monocyte-derived peritoneal macrophages protect C57BL/6 mice against surgery-induced adhesions
36. Definition, diagnosis and clinical management of non-obstructive kidney dysplasia: a consensus statement by the ERKNet Working Group on Kidney Malformations
37. Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder
38. Embryology
39. International multi-centre study of pregnancy outcomes with interleukin-1 inhibitors
40. Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease
41. MO374: Urinary Cell Transcriptomics Provides a Non-Invasive Readout of Kidney Genes Essential to Renal Health and Disease
42. Narrowing the chromosome 22q11.2 locus duplicated in bladder exstrophy-epispadias complex
43. A paradoxical teratogenic mechanism for retinoic acid
44. HPSE2, LRIG2, and the Urofacial Syndrome
45. Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects
46. Building Human Renal Tracts
47. Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation
48. Genetics of human congenital urinary bladder disease
49. From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease
50. Diverse ancestry whole-genome sequencing association study identifies TBX5 and PTK7 as susceptibility genes for posterior urethral valves.
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