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Development of the Human Pancreas From Foregut to Endocrine Commitment

Diabetes (New York, N.Y.), 2013-10, Vol.62 (10), p.3514-3522

2013

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

American journal of human genetics, 2015-10, Vol.97 (4), p.535-545

2015

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Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome

eLife, 2024-07, Vol.13

2024

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

Scientific reports, 2021-07, Vol.11 (1), p.15529-15529, Article 15529

2021

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

Frontiers in pediatrics, 2019-04, Vol.7, p.136-136

2019

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Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder

Frontiers in genetics, 2022-06, Vol.13, p.896125-896125

2022

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Heparanase 2 and Urofacial Syndrome, a Genetic Neuropathy

Advances in experimental medicine and biology, 2020, Vol.1221, p.807-819

2020

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

American journal of human genetics, 2017-12, Vol.101 (6), p.1021-1033

2017

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Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice

Neurourology and urodynamics, 2020-09, Vol.39 (7), p.1930-1938

2020

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

The Journal of pathology, 2019-12, Vol.249 (4), p.472-484

2019

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

Kidney international, 2019-05, Vol.95 (5), p.1138-1152

2019

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Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy

Journal of pediatric urology, 2021-10, Vol.17 (5), p.610-620

2021

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

Nephrology, dialysis, transplantation, 2016-04, Vol.31 (4), p.534-540

2016

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Ted Hughes, Nature and Culture

1, 2018

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

Human molecular genetics, 2014-08, Vol.23 (16), p.4302-4314

2014

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

Journal of tissue engineering and regenerative medicine, 2018-01, Vol.12 (1), p.252-264

2018

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Regulation of protein kinase D activity in adult myocardium: Novel counter-regulatory roles for protein kinase Cε and protein kinase A

Journal of molecular and cellular cardiology, 2007-12, Vol.43 (6), p.686-695

2007

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Neurogenic Defects Occur in LRIG2-Associated Urinary Bladder Disease

Kidney international reports, 2023-07, Vol.8 (7), p.1417-1429

2023

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Companion to Twentieth-Century Poetry

Roberts, Neil

1. Aufl., 2008

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

Journal of tissue engineering and regenerative medicine, 2016-02, Vol.10 (2), p.178-182

2016

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Stimulation of the plasma membrane Na+/H+ exchanger NHE1 by sustained intracellular acidosis. Evidence for a novel mechanism mediated by the ERK pathway

The Journal of biological chemistry, 2003-08, Vol.278 (34), p.31676-31684

2003

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Ted Hughes: From Cambridge to Collected

2013

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Specificity of action of bisindolylmaleimide protein kinase C inhibitors: do they inhibit the 70 kDa ribosomal S6 kinase in cardiac myocytes?

Biochemical pharmacology, 2004-11, Vol.68 (10), p.1923-1928

2004

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The tempo of Holocene climatic change in the eastern Mediterranean region: new high-resolution crater-lake sediment data from central Turkey

Holocene (Sevenoaks), 2001-01, Vol.11 (6), p.721-736

2001

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Specificity of action of bisindolylmaleimide protein kinase C inhibitors: do they inhibit the 70kDa ribosomal S6 kinase in cardiac myocytes?

Biochemical pharmacology, 2004-11, Vol.68 (10), p.1923-1928

2004

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Development of the Human Pancreas From Foregut to Endocrine Commitment

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

Human HPSE2 gene transfer ameliorates bladder pathophysiology in a mutant mouse model of urofacial syndrome

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

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

Expanding the HPSE2 Genotypic Spectrum in Urofacial Syndrome, A Disease Featuring a Peripheral Neuropathy of the Urinary Bladder

Heparanase 2 and Urofacial Syndrome, a Genetic Neuropathy

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

Dysfunctional bladder neurophysiology in urofacial syndrome Hpse2 mutant mice

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

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

Envisioning treating genetically-defined urinary tract malformations with viral vector-mediated gene therapy

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

Ted Hughes, Nature and Culture

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

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

Regulation of protein kinase D activity in adult myocardium: Novel counter-regulatory roles for protein kinase Cε and protein kinase A

Neurogenic Defects Occur in LRIG2-Associated Urinary Bladder Disease

Companion to Twentieth-Century Poetry

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

Stimulation of the plasma membrane Na+/H+ exchanger NHE1 by sustained intracellular acidosis. Evidence for a novel mechanism mediated by the ERK pathway

Ted Hughes: From Cambridge to Collected

Specificity of action of bisindolylmaleimide protein kinase C inhibitors: do they inhibit the 70 kDa ribosomal S6 kinase in cardiac myocytes?

The tempo of Holocene climatic change in the eastern Mediterranean region: new high-resolution crater-lake sediment data from central Turkey

Specificity of action of bisindolylmaleimide protein kinase C inhibitors: do they inhibit the 70kDa ribosomal S6 kinase in cardiac myocytes?

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