Publications by Dr David Wilson - ePrints

Browsing publications by Dr David Wilson.

Newcastle Authors	Title	Year
Glenn Renforth Dr Lyndsey Butterworth Dr David Wilson	Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings	2009
Professor Fiona Oakley Dr David Wilson Professor Derek Mann Dr Neil Hanley	Ectopic SOX9 Mediates Extracellular Matrix Deposition Characteristic of Organ Fibrosis	2008
Lee Turnpenny Dr Stephen Ball Dr David Wilson	Beta cell differentiation during early human pancreas development	2004
Dr Kieren Hollingsworth Dr David Wilson	Magnetic resonance studies of liquid-soft solid mixing by extrusion	2004
Dr Karen Piper Hanley Lee Turnpenny Dr David Wilson Dr Stephen Ball Dr Neil Hanley et al.	Expression profile of PDX1 during human pancreas development	2002
Dr Elizabeth Jones Dr David Wilson Emerita Professor Susan Lindsay	Hepatic differentiation of murine embryonic stem cells	2002
Glenn Renforth Dr Neil Hanley Dr Karen Piper Hanley Dr Vincent Connolly Professor Mark Walker et al.	Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alstrom syndrome	2002
Dr Elizabeth Jones Dr David Wilson	A gene trap integration provides an early in situ marker for hepatic specification of the foregut endoderm	2001
Dr Helen Phillips Glenn Renforth Dr Matthew Jackson Dr Mark Clement-Jones Dr David Wilson et al.	Characterisation of a novel gene on distal 11q as a potential candidate for Hypoplastic Left Heart Syndrome	2001
Dr Elizabeth Jones Dr Mark Clement-Jones Emeritus Professor Oliver James Dr David Wilson	Differences between human and mouse alpha-fetoprotein expression during early development	2001
Dr Neil Hanley Dr David Wilson Dr Stephen Ball	Expression profiles of SF-1, DAX1, and CYP17 in the human fetal adrenal gland: Potential interactions in gene regulation	2001
Dr Elizabeth Jones Emerita Professor Susan Lindsay Dr David Wilson	Hepatic differentiation of murine embryonic stem cells	2001
Professor Helen Arthur Glenn Renforth Dr David Wilson Evelyn Torsney Dr Trevor Jowett et al.	Endoglin, an ancillary TGFβ receptor, is required for extraembryonic angiogenesis and plays a key role in heart development	2000
Dr Elizabeth Jones Dr Mark Clement-Jones Dr David Wilson	JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype	2000
Dr Elizabeth Jones Dr David Wilson	JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype	2000
Dr David Wilson Dr Ann Curtis Richard Charnley	Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis	2000
Dr Neil Hanley Dr Donna Hagan Dr Mark Clement-Jones Dr Stephen Ball Professor Tom Strachan et al.	SRY, SOX9, and DAX1 expression patterns during human sex determination and gonadal development	2000
Dr Elizabeth Jones Dr Mark Clement-Jones Emerita Professor Susan Lindsay Professor Tom Strachan Professor Steve Robson et al.	Embryonic alphafetoprotein expression: Significant human and mouse differences	1999
Dr Neil Hanley Dr Stephen Ball Dr Mark Clement-Jones Dr Donna Hagan Professor Tom Strachan et al.	Expression of steroidogenic factor 1 and Wilms' tumour 1 during early human gonadal development and sex determination	1999
Dr Neil Hanley Dr Karen Piper Hanley Dr Stephen Ball Dr Mark Clement-Jones Professor Tom Strachan et al.	High level SOX9 expression during development of the human embryonic pancreas is associated with abnormal islet formation in a case of Campomelic Dysplasia.	1999
Dr Ann Curtis Dr David Wilson Richard Charnley	Mutations in the cationic trypsinogen gene in patients with chronic pancreatitis	1999
Dr David Wilson Dr Ann Curtis Richard Charnley	Mutations of cationic trypsinogen in chronic pancreatitis [Reply]	1999
Professor Helen Arthur Dr David Wilson Evelyn Torsney Glenn Renforth Professor Sir John Burn et al.	Progress towards developing a mouse model of Hereditary Haemorrhagic Telangiectasia	1999
Dr Victor Ruiz-Perez Dr Donna Hagan Dr Sally Lynch Emerita Professor Susan Lindsay Dr David Wilson et al.	A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis	1998
Dr David Wilson Ian Cross Professor Judith Goodship Dr Sally Coulthard Dr Hugh Bain et al.	DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin	1991