Dr Irina Neganova
Dr Stuart Atkinson
Dr George Anyfantis
Dr Owen Hughes
Professor Tom Strachan
et al.A role for NANOG in G1 to S transition in human embryonic stem cells through direct binding of CDK6 and CDC25A2009 Dr Rebecca Stewart
Dr Chunbo Yang
Dr George Anyfantis
Dr Nicholas Hole
Professor Tom Strachan
et al.Silencing of the expression of pluripotent driven-reporter genes stably transfected into human pluripotent cells2008Dr Vlad Seitan
Dr Andrew Banks
Dr Steven Laval
Dr Sarah Newbury
Professor Tom Strachan
et al.Metazoan Scc4 homologs link sister chromatid cohesion to cell and axon migration guidance2006Dr Subrot Sarma
Dr Janet Kerwin
Mark Scott
Professor Tom Strachan
Emerita Professor Susan Lindsay
et al.3D modelling, gene expression mapping and post-mapping image analysis in the developing human brain2005Petra Stojkovic
Professor Majlinda Lako
Dr Rebecca Stewart
Professor Lyle Armstrong
Jerome Evans
et al.An autogeneic feeder cell system that efficiently supports growth of undifferentiated human embryonic stem cells2005Petra Stojkovic
Professor Majlinda Lako
Dr Rebecca Stewart
Professor Lyle Armstrong
Professor Mary Herbert
et al.An Autogeneic Feeder Cell System That Efficiently Supports Growth of Undifferentiated Human Embryonic Stem Cells2005Professor Tom Strachan
Cornelia de Lange Syndrome and the link between chromosomal function, DNA repair and developmental gene regulation2005Dr Louise Hyslop
Professor Miodrag Stojkovic
Professor Lyle Armstrong
Theresia Walter
Petra Stojkovic
et al.Downregulation of NANOG induces differentiation of human embryonic stem cells to extraembryonic lineages2005Dr Sajjad Ahmad
Professor Lyle Armstrong
Professor Miodrag Stojkovic
Ian Dimmick
Dr Louise Hyslop
et al.The identification and characterisation of human corneal epithelial progenitors on the basis of high aldehyde dehydrogenase activity2005Dr Janet Kerwin
Mark Scott
Professor Steve Robson
Professor Tom Strachan
Emerita Professor Susan Lindsay
et al.3 dimensional modelling of early human brain development using optical projection tomography2004 Professor Steve Robson
Dr Janet Kerwin
Mark Scott
Professor Tom Strachan
Emerita Professor Susan Lindsay
et al.3-dimensional modelling of human development using optical projection tomography2004Dr Emma Tonkin
Pieter Eichhorn
Burhan Imamwerdi
Emerita Professor Susan Lindsay
Dr Michael Jackson
et al.A giant novel gene undergoing extensive alternative splicing is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.32004Dr Lorraine Eley
Lee Turnpenny
Dr Laura Yates
Scott Craighead
David Morgan
et al.A perspective on inversin2004Professor Miodrag Stojkovic
Professor Majlinda Lako
Petra Stojkovic
Dr Rebecca Stewart
Professor Lyle Armstrong
et al.Derivation of human embryonic stem cells from day-8 blastocysts recovered after three-step in vitro culture2004Professor Miodrag Stojkovic
Professor Majlinda Lako
Professor Tom Strachan
Professor Alison Murdoch
Derivation, growth and applications of human embryonic stem cells2004Dr Sajjad Ahmad
Dr Louise Hyslop
Professor Colin Jahoda
Professor Tom Strachan
Professor Majlinda Lako
et al.From embryo to eye - Human embryonic stem cell markers OCT-4 and NANOG are localised to adult limbal epithelium2004Emerita Professor Susan Lindsay
Mark Scott
Dr Subrot Sarma
Moira Crosier
Dr Steven Lisgo
et al.Human developmental gene expression: an important link between disorder and understanding2004Dr Emma Tonkin
Tzu-Jou Wang
Dr Steven Lisgo
Professor Tom Strachan
NIPBL, encoding a homolog of fungal Scc2-type sister chromatid cohesion proteins and fly Nipped-B, is mutated in Cornelia de Lange syndrome2004Dr Subrot Sarma
Emerita Professor Susan Lindsay
Professor Tom Strachan
Professor Steve Robson
Stability of RNA in human embryos stored over long periods of time2004Dr Emma Tonkin
Emerita Professor Susan Lindsay
Professor Tom Strachan
A giant gone encoding a developmentally regulated novel member of the M28 peptidase family is severed by a Cornelia de Lange-associated translocation breakpoint at 3q26.32003Professor Tom Strachan
Dr Emma Tonkin
Genome-wide linkage analysis identifies five candidate gene regions in the Cornelia de Lange syndrome (CdLS)2003Professor Judith Goodship
Professor Tom Strachan
Inversin mutations cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination2003Professor Judith Goodship
Professor Tom Strachan
Mutations in Inversin cause Nephronophthisis type 2, linking cystic kidney disease to the function of primary cilia and left-right axis determination2003Professor Judith Goodship
Professor Tom Strachan
Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination2003Professor Tom Strachan
Towards effective and rewarding data sharing2003Dr Maria Lastowska
Simon Cotterill
Natalie Bown
Professor John Lunec
Professor Tom Strachan
et al.Breakpoint position on 17q identifies the most aggressive neuroblastoma tumors2002Dr Steven Lisgo
Professor Deborah Henderson
Professor Tom Strachan
Emerita Professor Susan Lindsay
Craniofacial expression of human and murine TBX22 correlates with the cleft palate and ankyloglossia phenotype observed in CPx patients2002David Morgan
Dr Lorraine Eley
Professor John Sayer
Professor Tom Strachan
Dr Laura Yates
et al.Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle2002Catriona Munro
Professor Tom Strachan
Hailey-Hailey disease: Molecular and clinical characterization of novel mutations in the ATP2C1 gene2002Dr Emma Tonkin
Dr Donna Hagan
Weiping Li
Professor Tom Strachan
Identification and characterisation of novel mammalian homologues of Drosophila polyhomeotic permits new insights into relationships between members of the polyhomeotic family2002Professor Judith Goodship
Lee Turnpenny
Professor Tom Strachan
The left-right determinant inversin has highly conserved ankyrin repeat and IQ domains and interacts with calmodulin2002Dr Emma Tonkin
Pieter Eichhorn
Dr Donna Hagan
Dr Meryl Lusher
Dr Maggie Ireland
et al.A novel gene is disrupted by a Cornelia de Lange-associated translocation breakpoint at 3q26.32001Dr Emma Tonkin
Professor Tom Strachan
Exclusion of linkage to the CDL1 gene region on chromosome 3q26.3 in some familial cases of Cornelia de Lange Syndrome2001Dr Maria Lastowska
Dr Nicholas Bown
Professor John Lunec
Professor Tom Strachan
Professor Andrew Pearson
et al.Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma2001Dr Maria Lastowska
Dr Nicholas Bown
Professor John Lunec
Professor Tom Strachan
Professor Andrew Pearson
et al.Molecular cytogenetic definition of 17q translocation breakpoints in neuroblastoma2001Dr Sally Lynch
Ying Wang
Professor Tom Strachan
Professor Sir John Burn
Emerita Professor Susan Lindsay
et al.Autosomal dominant sacral agenesis: Currarino syndrome2000Professor Tom Strachan
Clinical and molecular correlates of somatic mosaicism in neurofibromatosis 22000Simon Carter
Dr Eugene Healy
Professor Tom Strachan
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca2+ pump2000Emerita Professor Susan Lindsay
Professor Steve Robson
Professor Tom Strachan
Human-mouse differences in the embryonic expression patterns of developmental control genes and disease genes2000Dr Donna Hagan
Alison Ross
Professor Tom Strachan
Dr Sally Lynch
Dr Victor Ruiz-Perez
et al.Mutation analysis and embryonic expression of the HLXB9 Currarino syndrome gene2000Dr Donna Hagan
Alison Ross
Professor Tom Strachan
Dr Victor Ruiz-Perez
Emerita Professor Susan Lindsay
et al.Mutation analysis anti embryonic expression of the HLXB9 currarino syndrome gene2000Dr 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 development2000Dr Mark Clement-Jones
Professor Steve Robson
Professor Tom Strachan
Emerita Professor Susan Lindsay
The short stature homeobox gene SHOX is involved in skeletal abnormalities in Turner syndrome2000Dr Victor Ruiz-Perez
Simon Carter
Dr Eugene Healy
Carole Todd
Professor Jonathan Rees
et al.ATP2A2 mutations in Darier's disease: Variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class1999Dr Victor Ruiz-Perez
Simon Carter
Dr Eugene Healy
Professor Jonathan Rees
Professor Tom Strachan
et al.Classical and variant Darier disease due to mutation in ATP2A21999Dr 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 differences1999Dr Victor Ruiz-Perez
Simon Carter
Carole Todd
Professor Jonathan Rees
Professor Tom Strachan
et al.Expression of SERCA2 isoforms in skin, and mutations in Darier's disease1999Dr 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 determination1999Emerita Professor Susan Lindsay
Dr Mark Clement-Jones
Professor Steve Robson
Professor Tom Strachan
Expression of the short stature homeobox gene, SHOX, correlates with skeletal abnormalities in Turner syndromece1999Dr Meryl Lusher
Dr Maggie Ireland
Professor Tom Strachan
Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes1999Dr 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.1999Professor Tom Strachan
Human Molecular Genetics1999Dr Donna Hagan
Dr Steven Lisgo
Professor Tom Strachan
Dr Mark Clement-Jones
Professor Steve Robson
et al.Mapping gene expression domains and neuronal cell differentiation during human embryonic forebrain development1999Professor Majlinda Lako
Professor Tom Strachan
Mutation screening in British 21-hydroxylase deficiency families and development of novel microsatellite based approaches to prenatal diagnosis1999Dr Victor Ruiz-Perez
Professor Tom Strachan
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease1999Professor Tom Strachan
Probability of bilateral disease in people presenting with a unilateral vestibular schwannoma1999Dr Emma Tonkin
Professor Tom Strachan
The Cornelia de Lange syndrome; Cytogenetic and molecular analysis, with exclusion of linkage to chromosome 3q in some familial cases1999Dr 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 agenesis1998Dr Maria Lastowska
Dr Nicholas Bown
Professor John Lunec
Professor Tom Strachan
Professor Andrew Pearson
et al.Molecular cytogenetic delineation of 17q translocation breakpoints in neuroblastoma cell lines1998Simon Carter
Dr Victor Ruiz-Perez
Professor Jonathan Rees
Professor Tom Strachan
Refined genetic mapping of the Darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region1998