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Browsing publications by Dr David Wilson.

Newcastle AuthorsTitleYearFull text
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 findings2009
Professor Fiona Oakley
Dr David Wilson
Professor Derek Mann
Dr Neil Hanley
Ectopic SOX9 Mediates Extracellular Matrix Deposition Characteristic of Organ Fibrosis2008
Lee Turnpenny
Dr Stephen Ball
Dr David Wilson
Beta cell differentiation during early human pancreas development2004
Dr Kieren Hollingsworth
Dr David Wilson
Magnetic resonance studies of liquid-soft solid mixing by extrusion2004
Dr Karen Piper Hanley
Lee Turnpenny
Dr David Wilson
Dr Stephen Ball
Dr Neil Hanley
et al.
Expression profile of PDX1 during human pancreas development2002
Dr Elizabeth Jones
Dr David Wilson
Emerita Professor Susan Lindsay
Hepatic differentiation of murine embryonic stem cells2002
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 syndrome2002
Dr Elizabeth Jones
Dr David Wilson
A gene trap integration provides an early in situ marker for hepatic specification of the foregut endoderm2001
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 Syndrome2001
Dr Elizabeth Jones
Dr Mark Clement-Jones
Emeritus Professor Oliver James
Dr David Wilson
Differences between human and mouse alpha-fetoprotein expression during early development2001
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 regulation2001
Dr Elizabeth Jones
Emerita Professor Susan Lindsay
Dr David Wilson
Hepatic differentiation of murine embryonic stem cells2001
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 development2000
Dr Elizabeth Jones
Dr Mark Clement-Jones
Dr David Wilson
JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype2000
Dr Elizabeth Jones
Dr David Wilson
JAGGED1 expression in human embryos: correlation with the Alagille syndrome phenotype2000
Dr David Wilson
Dr Ann Curtis
Richard Charnley
Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis2000
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 development2000
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 differences1999
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 determination1999
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 pancreatitis1999
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 Telangiectasia1999
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 agenesis1998
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 origin1991