List of works - Neil A Roberts

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.

scientific article published in December 2017

Bridging the gap: functional healing of embryonic small intestine ex vivo

scientific article

Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies

scientific article published on 11 April 2019

DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation.

scientific article

Development of the human pancreas from foregut to endocrine commitment.

scientific article published on 29 April 2013

Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice

scientific article published on 01 July 2020

Exogenous transforming growth factor-β1 enhances smooth muscle differentiation in embryonic mouse jejunal explants.

scientific article published on 13 January 2017

Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder

scientific article published on 30 July 2021

From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease

scientific article

Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 ⬇️

scientific article

Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus

scientific article published on April 2014

LRIG2 mutations cause urofacial syndrome

scientific article

Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder

scientific article published on 08 March 2019

Overactivity or blockade of transforming growth factor-β each generate a specific ureter malformation

scientific article published on 01 October 2019

Understanding the role of SOX9 in acquired diseases: lessons from development

scientific article published on 13 January 2011

Urinary tract effects of HPSE2 mutations

scientific article

Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation.

scientific article published on 09 July 2013

List of works by Neil A Roberts

ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder.

Bridging the gap: functional healing of embryonic small intestine ex vivo

Congenital Disorders of the Human Urinary Tract: Recent Insights From Genetic and Molecular Studies

DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation.

Development of the human pancreas from foregut to endocrine commitment.

Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice

Exogenous transforming growth factor-β1 enhances smooth muscle differentiation in embryonic mouse jejunal explants.

Experimental long-term diabetes mellitus alters the transcriptome and biomechanical properties of the rat urinary bladder

From gene discovery to new biological mechanisms: heparanases and congenital urinary bladder disease

Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6 ⬇️

Heparanase 2, mutated in urofacial syndrome, mediates peripheral neural development in Xenopus

LRIG2 mutations cause urofacial syndrome

Lrig2 and Hpse2, mutated in urofacial syndrome, pattern nerves in the urinary bladder

Overactivity or blockade of transforming growth factor-β each generate a specific ureter malformation

Understanding the role of SOX9 in acquired diseases: lessons from development

Urinary tract effects of HPSE2 mutations

Urofacial syndrome: a genetic and congenital disease of aberrant urinary bladder innervation.