MRC-Wellcome Trust Human Developmental Biology Resource : enabling studies of human developmental gene expressionLINDSAY, Susan; COPP, Andrew J.Trends in genetics (Regular ed.). 2005, Vol 21, Num 11, pp 586-590, issn 0168-9525, 5 p.Article

Fetal spina bifida in a mouse model : loss of neural function in uteroSTIEFEL, Dorothea; COPP, Andrew J; MEULI, Martin et al.Journal of neurosurgery. Pediatrics. 2007, Vol 106, Num 3, pp 213-221, issn 1933-0707, 9 p.Article

Defining a PARticular Pathway of Neural Tube ClosureCOPP, Andrew J; GREENE, Nicholas D. E.Developmental cell. 2010, Vol 18, Num 1, pp 1-2, issn 1534-5807, 2 p.Article

Knowledge and Periconceptional Use of Folic Acid for the Prevention of Neural Tube Defects in Ethnic Communities in the United Kingdom: Systematic Review and Meta-analysisPEAKE, Jordana N; COPP, Andrew J; SHAWE, Jill et al.Birth defects research. Clinical and molecular teratology. 2013, Vol 97, Num 7, pp 444-451, issn 1542-0752, 8 p.Article

Neural tube defects : Prevention by folic acid and other vitaminsCOPP, Andrew J; GREENE, Nicholas D. E.Indian journal of pediatrics. 2000, Vol 67, Num 12, pp 915-921, issn 0019-5456Conference Paper

The genetic basis of mammalian neurulationCOPP, Andrew J; GREENE, Nicholas D. E; MURDOCH, Jennifer N et al.Nature reviews. Genetics (Print). 2003, Vol 4, Num 10, pp 784-793, issn 1471-0056, 10 p.Article

Genetics of human neural tube defectsGREENE, Nicholas D. E; STANIER, Philip; COPP, Andrew J et al.Human molecular genetics (Print). 2009, Vol 18, issn 0964-6906, R113-R129, NS2Article

Dishevelled: linking convergent extension with neural tube closureCOPP, Andrew J; GREENE, Nicholas D. E; MURDOCH, Jennifer N et al.Trends in neurosciences (Regular edition). 2003, Vol 26, Num 9, pp 453-455, issn 0166-2236, 3 p.Article

Disruption of bardet-biedl syndrome ciliary proteins perturbs planar cell polarity in vertebratesROSS, Alison J; MAY-SIMERA, Helen; TAN, Perciliz L et al.Nature genetics. 2005, Vol 37, Num 10, pp 1135-1140, issn 1061-4036, 6 p.Article

FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorderLAI, Cecilia S. L; GERRELLI, Dianne; MONACO, Anthony P et al.Brain. 2003, Vol 126, pp 2455-2462, issn 0006-8950, 8 p., 11Article

Comparative physical and transcript maps of ∼1 Mb around loop-tail, a gene for severe neural tube defects on distal mouse chromosome 1 and human chromosome 1q22-q23DOUDNEY, Kit; MURDOCH, Jennifer N; PATERNOTTE, Caroline et al.Genomics (San Diego, Calif.). 2001, Vol 72, Num 2, pp 180-192, issn 0888-7543Article

Is LMNB1 a Susceptibility Gene for Neural Tube Defects in Humans?ROBINSON, Alexis; PARTRIDGE, Darren; GREENE, Nicholas D. E et al.Birth defects research. Clinical and molecular teratology. 2013, Vol 97, Num 6, pp 398-402, issn 1542-0752, 5 p.Article

Development of the vertebrate central nervous system : formation of the neural tubeGREENE, Nicholas D. E; COPP, Andrew J.Prenatal diagnosis. 2009, Vol 29, Num 4, pp 303-311, issn 0197-3851, 9 p.Article

Abnormal folate metabolism in foetuses affected by neural tube defectsDUNLEVY, Louisa P. E; CHITTY, Lyn S; BURREN, Katie A et al.Brain. 2007, Vol 130, pp 1043-1049, issn 0006-8950, 7 p., 4Article

The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formationDAWE, Helen R; SMITH, Ursula M; AFFORD, Simon C et al.Human molecular genetics (Print). 2007, Vol 16, Num 2, pp 173-186, issn 0964-6906, 14 p.Article

Vangl2 acts via rhoa signaling to regulate polarized cell movements during development of the proximal outflow tractPHILLIPS, Helen M; MURDOCH, Jennifer N; CHAUDHRY, Bill et al.Circulation research. 2005, Vol 96, Num 3, pp 292-299, issn 0009-7330, 8 p.Article

Mouse models of neural tube defects : Investigating preventive mechanismsGREENE, Nicholas D. E; COPP, Andrew J.American journal of medical genetics. 2005, Vol 135C, Num 1, pp 31-41, issn 0148-7299, 11 p.Conference Paper

Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specificationMURDOCH, Jennifer N; DOUDNEY, Kit; PATERNOTTE, Caroline et al.Human molecular genetics (Print). 2001, Vol 10, Num 22, pp 2593-2601, issn 0964-6906Article

Quantitative analysis of s-adenosylmethionine and s-adenosylhomocysteine in neurulation-stage mouse embryos by liquid chromatography tandem mass spectrometryBURREN, Katie A; MILLS, Kevin; COPP, Andrew J et al.Journal of chromatography. B. 2006, Vol 844, Num 1, pp 112-118, issn 1570-0232, 7 p.Article

Disruption of planar cell polarity signaling results in congenital heart defects and cardiomyopathy attributable to early cardiomyocyte disorganizationPHILLIPS, Helen M; HONG JUN RHEE; MURDOCH, Jennifer N et al.Circulation research. 2007, Vol 101, Num 2, pp 137-145, issn 0009-7330, 9 p.Article

Role of Sonic hedgehog in the development of the trachea and oesophagus. DiscussionIOANNIDES, Adonis S; HENDERSON, Deborah J; SPITZ, Lewis et al.Journal of pediatric surgery. 2003, Vol 38, Num 1, pp 29-36, issn 0022-3468, 8 p.Conference Paper

Cloning and characterization of Igsf9 in mouse and human: A new member of the immunoglobulin superfamily expressed in the developing nervous systemDOUDNEY, Kit; MURDOCH, Jennifer N; BRAYBROOK, Claire et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 5, pp 663-670, issn 0888-7543Article

Folic acid prevents exencephaly in Cited2 deficient miceMARTINEZ BARBERA, Juan Pedro; RODRIGUEZ, Tristan A; GREENE, Nicholas D. E et al.Human molecular genetics (Print). 2002, Vol 11, Num 3, pp 283-293, issn 0964-6906Article

Maternal diabetes increases the risk of caudal regression caused by retinoic acidCHAN, Billy W. H; CHAN, Kwok-Siu; KOIDE, Tsuyoshi et al.Diabetes (New York, NY). 2002, Vol 51, Num 9, pp 2811-2816, issn 0012-1797, 6 p.Article

Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humansNARISAWA, Ayumi; KOMATSUZAKI, Shoko; GRINHAM, James et al.Human molecular genetics (Print). 2012, Vol 21, Num 7, pp 1496-1503, issn 0964-6906, 8 p.Article