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The emerging role of epigenetic mechanisms in the etiology of neural tube defects 由 Nicholas D. E. Greene, Philip Stanier, Gudrun E. Moore

出版 2011

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Genetics of human neural tube defects 由 Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp

出版 2009

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Revisão

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Neural tube defects: recent advances, unsolved questions, and controversies 由 Andrew J. Copp, Philip Stanier, Nicholas D. E. Greene

出版 2013

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Persistence of cytomegalovirus in mononuclear cells in peripheral blood from blood donors. 由 Philip Stanier, D.L. Taylor, Alan D. Kitchen, Nicholas M. Wales, Yvonne Tryhorn, A.S. Tyms

出版 1989

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Artigo

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The genetic aetiology of Silver-Russell syndrome 由 Sayeda Abu‐Amero, David Monk, Jennifer M. Frost, Michael Preece, Philip Stanier, Gudrun E. Moore

出版 2007

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Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression 由 David Monk, Philippe Arnaúd, Jennifer M. Frost, Frank Hills, Philip Stanier, Robert Feil, Gudrun E. Moore

出版 2009

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Limited evolutionary conservation of imprinting in the human placenta 由 David Monk, Philippe Arnaúd, Sophia Apostolidou, Frank Hills, Gavin Kelsey, Philip Stanier, Robert Feil, Gudrun E. Moore

出版 2006

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The Mn1 transcription factor acts upstream ofTbx22and preferentially regulates posterior palate growth in mice 由 Wenjing Liu, Yu Lan, Erwin Pauws, Magda A. Meester‐Smoor, Philip Stanier, Ellen C. Zwarthoff, Rulang Jiang

出版 2008

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Artigo

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Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies 由 Haiyan Zhou, Martin Brockington, Heinz Jungbluth, David Monk, Philip Stanier, Caroline A. Sewry, Gudrun E. Moore, Francesco Muntoni

出版 2006

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Artigo

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Maternal uniparental disomy 7 in Silver-Russell syndrome. 由 Michael A. Preece, Susan Price, V Davies, Louise E. Clough, Philip Stanier, Richard C. Trembath, Gudrun E. Moore

出版 1997

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Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects 由 Lucas Alvizi, Xiayi Ke, Luciano Abreu Brito, Rimante Seselgyte, Gudrun E. Moore, Philip Stanier, Maria Rita Passos‐Bueno

出版 2017

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Artigo

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Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the Unite... 由 Lydia J. Leon, Ronan Doyle, Ernest Diez Benavente, Taane G. Clark, Nigel Klein, Philip Stanier, Gudrun E. Moore

出版 2018

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Interactions between planar cell polarity genes cause diverse neural tube defects 由 J. Murdoch, Christine Damrau, Anju Paudyal, Debora Bogani, Sara Wells, Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp

出版 2014

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Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model 由 Peter Gustavsson, Nicholas D. E. Greene, Dina Lad, Erwin Pauws, Sandra C. de Castro, Philip Stanier, Andrew J. Copp

出版 2007

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Artigo

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Mutations in the planar cell polarity genesCELSR1andSCRIBare associated with the severe neural tube defect craniorachischisis 由 Alexis Robinson, Sarah Escuin, Kit Doudney, Michel Vekemans, Roger E. Stevenson, Nicholas D. E. Greene, Andrew J. Copp, Philip Stanier

出版 2011

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Artigo

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Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless. 由 Brandon J. Wainwright, Peter Scambler, Philip Stanier, Eila Watson, G. Bell, Carol Wicking, Xavier Estivill, Michael Courtney, A Boué, P. S. Pedersen

出版 1988

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Artigo

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Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome 由 David Monk, Emma Wakeling, Virginia K. Proud, Megan P. Hitchins, Sayeda Abu‐Amero, Philip Stanier, Michael A. Preece, Gudrun E. Moore

出版 2000

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Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes 由 Erwin Pauws, Aya Hoshino, Liz Bentley, Surendra Prajapati, Charles Keller, Peter Hammond, Juan Pedro Martı́nez-Barberá, Gudrun E. Moore, Philip Stanier

出版 2010

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Artigo

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Tbx22 null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes 由 Erwin Pauws, Aya Hoshino, Lucy Bentley, Suresh I. Prajapati, Charles Keller, Peter Hammond, Juan Pedro Martı́nez-Barberá, Gudrun E. Moore, Philip Stanier

出版 2009

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TBX22 Missense Mutations Found in Patients with X-Linked Cleft Palate Affect DNA Binding, Sumoylation, and Transcriptional Repression 由 Artemisia M. Andreou, Erwin Pauws, Marius C. Jones, Manvendra K. Singh, Markus Bussen, Kit Doudney, Gudrun E. Moore, Andreas Kispert, Jan J. Brosens, Philip Stanier

出版 2007

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The emerging role of epigenetic mechanisms in the etiology of neural tube defects 由 Nicholas D. E. Greene, Philip Stanier, Gudrun E. Moore

Genetics of human neural tube defects 由 Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp

Neural tube defects: recent advances, unsolved questions, and controversies 由 Andrew J. Copp, Philip Stanier, Nicholas D. E. Greene

Persistence of cytomegalovirus in mononuclear cells in peripheral blood from blood donors. 由 Philip Stanier, D.L. Taylor, Alan D. Kitchen, Nicholas M. Wales, Yvonne Tryhorn, A.S. Tyms

The genetic aetiology of Silver-Russell syndrome 由 Sayeda Abu‐Amero, David Monk, Jennifer M. Frost, Michael Preece, Philip Stanier, Gudrun E. Moore

Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression 由 David Monk, Philippe Arnaúd, Jennifer M. Frost, Frank Hills, Philip Stanier, Robert Feil, Gudrun E. Moore

Limited evolutionary conservation of imprinting in the human placenta 由 David Monk, Philippe Arnaúd, Sophia Apostolidou, Frank Hills, Gavin Kelsey, Philip Stanier, Robert Feil, Gudrun E. Moore

The Mn1 transcription factor acts upstream of<i>Tbx22</i>and preferentially regulates posterior palate growth in mice 由 Wenjing Liu, Yu Lan, Erwin Pauws, Magda A. Meester‐Smoor, Philip Stanier, Ellen C. Zwarthoff, Rulang Jiang

Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies 由 Haiyan Zhou, Martin Brockington, Heinz Jungbluth, David Monk, Philip Stanier, Caroline A. Sewry, Gudrun E. Moore, Francesco Muntoni

Maternal uniparental disomy 7 in Silver-Russell syndrome. 由 Michael A. Preece, Susan Price, V Davies, Louise E. Clough, Philip Stanier, Richard C. Trembath, Gudrun E. Moore

Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects 由 Lucas Alvizi, Xiayi Ke, Luciano Abreu Brito, Rimante Seselgyte, Gudrun E. Moore, Philip Stanier, Maria Rita Passos‐Bueno

Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the Unite... 由 Lydia J. Leon, Ronan Doyle, Ernest Diez Benavente, Taane G. Clark, Nigel Klein, Philip Stanier, Gudrun E. Moore

Interactions between planar cell polarity genes cause diverse neural tube defects 由 J. Murdoch, Christine Damrau, Anju Paudyal, Debora Bogani, Sara Wells, Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp

Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model 由 Peter Gustavsson, Nicholas D. E. Greene, Dina Lad, Erwin Pauws, Sandra C. de Castro, Philip Stanier, Andrew J. Copp

Mutations in the planar cell polarity genes<i>CELSR1</i>and<i>SCRIB</i>are associated with the severe neural tube defect craniorachischisis 由 Alexis Robinson, Sarah Escuin, Kit Doudney, Michel Vekemans, Roger E. Stevenson, Nicholas D. E. Greene, Andrew J. Copp, Philip Stanier

Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless. 由 Brandon J. Wainwright, Peter Scambler, Philip Stanier, Eila Watson, G. Bell, Carol Wicking, Xavier Estivill, Michael Courtney, A Boué, P. S. Pedersen

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome 由 David Monk, Emma Wakeling, Virginia K. Proud, Megan P. Hitchins, Sayeda Abu‐Amero, Philip Stanier, Michael A. Preece, Gudrun E. Moore

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The emerging role of epigenetic mechanisms in the etiology of neural tube defects 由 Nicholas D. E. Greene, Philip Stanier, Gudrun E. Moore

Genetics of human neural tube defects 由 Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp

Neural tube defects: recent advances, unsolved questions, and controversies 由 Andrew J. Copp, Philip Stanier, Nicholas D. E. Greene

Persistence of cytomegalovirus in mononuclear cells in peripheral blood from blood donors. 由 Philip Stanier, D.L. Taylor, Alan D. Kitchen, Nicholas M. Wales, Yvonne Tryhorn, A.S. Tyms

The genetic aetiology of Silver-Russell syndrome 由 Sayeda Abu‐Amero, David Monk, Jennifer M. Frost, Michael Preece, Philip Stanier, Gudrun E. Moore

Reciprocal imprinting of human GRB10 in placental trophoblast and brain: evolutionary conservation of reversed allelic expression 由 David Monk, Philippe Arnaúd, Jennifer M. Frost, Frank Hills, Philip Stanier, Robert Feil, Gudrun E. Moore

Limited evolutionary conservation of imprinting in the human placenta 由 David Monk, Philippe Arnaúd, Sophia Apostolidou, Frank Hills, Gavin Kelsey, Philip Stanier, Robert Feil, Gudrun E. Moore

The Mn1 transcription factor acts upstream of<i>Tbx22</i>and preferentially regulates posterior palate growth in mice 由 Wenjing Liu, Yu Lan, Erwin Pauws, Magda A. Meester‐Smoor, Philip Stanier, Ellen C. Zwarthoff, Rulang Jiang

Epigenetic Allele Silencing Unveils Recessive RYR1 Mutations in Core Myopathies 由 Haiyan Zhou, Martin Brockington, Heinz Jungbluth, David Monk, Philip Stanier, Caroline A. Sewry, Gudrun E. Moore, Francesco Muntoni

Maternal uniparental disomy 7 in Silver-Russell syndrome. 由 Michael A. Preece, Susan Price, V Davies, Louise E. Clough, Philip Stanier, Richard C. Trembath, Gudrun E. Moore

Differential methylation is associated with non-syndromic cleft lip and palate and contributes to penetrance effects 由 Lucas Alvizi, Xiayi Ke, Luciano Abreu Brito, Rimante Seselgyte, Gudrun E. Moore, Philip Stanier, Maria Rita Passos‐Bueno

Enrichment of Clinically Relevant Organisms in Spontaneous Preterm-Delivered Placentas and Reagent Contamination across All Clinical Groups in a Large Pregnancy Cohort in the Unite... 由 Lydia J. Leon, Ronan Doyle, Ernest Diez Benavente, Taane G. Clark, Nigel Klein, Philip Stanier, Gudrun E. Moore

Interactions between planar cell polarity genes cause diverse neural tube defects 由 J. Murdoch, Christine Damrau, Anju Paudyal, Debora Bogani, Sara Wells, Nicholas D. E. Greene, Philip Stanier, Andrew J. Copp

Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model 由 Peter Gustavsson, Nicholas D. E. Greene, Dina Lad, Erwin Pauws, Sandra C. de Castro, Philip Stanier, Andrew J. Copp

Mutations in the planar cell polarity genes<i>CELSR1</i>and<i>SCRIB</i>are associated with the severe neural tube defect craniorachischisis 由 Alexis Robinson, Sarah Escuin, Kit Doudney, Michel Vekemans, Roger E. Stevenson, Nicholas D. E. Greene, Andrew J. Copp, Philip Stanier

Isolation of a human gene with protein sequence similarity to human and murine int-1 and the Drosophila segment polarity mutant wingless. 由 Brandon J. Wainwright, Peter Scambler, Philip Stanier, Eila Watson, G. Bell, Carol Wicking, Xavier Estivill, Michael Courtney, A Boué, P. S. Pedersen

Duplication of 7p11.2-p13, Including GRB10, in Silver-Russell Syndrome 由 David Monk, Emma Wakeling, Virginia K. Proud, Megan P. Hitchins, Sayeda Abu‐Amero, Philip Stanier, Michael A. Preece, Gudrun E. Moore

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