| human | Q5 |
| P6178 | Dimensions author ID | 01031346656.06 |
| P8446 | Gateway to Research person ID | D980AA48-1397-4175-B214-4674CF0998C4 |
| P856 | official website | https://pureprojects.ppad.man.ac.uk/portal/en/researchers/neil-roberts(25f1d1f9-b5cc-4f47-aaac-4e6ede95b29b).html |
| P496 | ORCID iD | 0000-0002-6955-5536 |
| P69 | educated at | University of Manchester | Q230899 |
| P108 | employer | University of Manchester | Q230899 |
| P734 | family name | Roberts | Q1646493 |
| Roberts | Q1646493 | ||
| Roberts | Q1646493 | ||
| P735 | given name | Neil | Q5570878 |
| Neil | Q5570878 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q47315085 | ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder. |
| Q28829705 | Bridging the gap: functional healing of embryonic small intestine ex vivo |
| Q64054916 | Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies |
| Q40117499 | DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation. |
| Q37193414 | Development of the human pancreas from foregut to endocrine commitment. |
| Q96837675 | Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice |
| Q38770858 | Exogenous transforming growth factor-β1 enhances smooth muscle differentiation in embryonic mouse jejunal explants. |
| Q112609689 | Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder |
| Q26796508 | From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease |
| Q36133280 | Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 |
| Q42259092 | Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus |
| Q28283130 | LRIG2 mutations cause urofacial syndrome |
| Q64075952 | Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder |
| Q92538719 | Overactivity or blockade of transforming growth factor-β each generate a specific ureter malformation |
| Q37828896 | Understanding the role of SOX9 in acquired diseases: lessons from development |
| Q35228493 | Urinary tract effects of HPSE2 mutations |
| Q38119849 | Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation. |
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