J. Murdoch

发表

The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear

S. Wells, D. Henderson, V. Patterson, 2010, BMC Developmental Biology.

Cardiovascular Defects Associated With Abnormalities in Midline Development in the Loop-tail Mouse Mutant

N. Greene, A. Copp, D. Gerrelli, 2001, Circulation research.

Disruption of Planar Cell Polarity Signaling Results in Congenital Heart Defects and Cardiomyopathy Attributable to Early Cardiomyocyte Disorganization

Robert H. Anderson, A. Copp, D. Henderson, 2007, Circulation research.

Sequence and expression analysis of Nhlh1: a basic helix-loop-helix gene implicated in neurogenesis.

A. Copp, P. Stanier, N. Leblond-Bourget, 1999, Developmental genetics.

Retinal axon misrouting at the optic chiasm in mice with neural tube closure defects

A. Copp, C. Mason, F. Beermann, 2000, Genesis.

Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice

S. Wells, N. Greene, A. Copp, 2014, Disease Models & Mechanisms.

BCAP is a centriolar satellite protein and inhibitor of ciliogenesis

C. Wilkinson, J. Murdoch, Anila Iqbal, 2017, Journal of Cell Science.

Dishevelled: linking convergent extension with neural tube closure

N. Greene, A. Copp, J. Murdoch, 2003, Trends in Neurosciences.

Physical and transcriptional map of a 3-Mb region of mouse chromosome 1 containing the gene for the neural tube defect mutant loop-tail (Lp).

A. Copp, P. Stanier, J. Eddleston, 1999, Genomics.

Epidermal wound repair is regulated by the planar cell polarity signaling pathway.

S. Jane, J. Cunningham, S. Dworkin, 2010, Developmental cell.

Atypical Cadherins Celsr1-3 Differentially Regulate Migration of Facial Branchiomotor Neurons in Mice

S. Pfaff, Bernd Fritzsch, A. Goffinet, 2010, The Journal of Neuroscience.

Linkage mapping of Lims1l, the murine homolog of the human LIM domain gene PINCH, to mouse Chromosome 10

A. Copp, P. Stanier, J. Eddleston, 1998, Cytogenetic and Genome Research.

Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

Steve D. M. Brown, E. Fisher, K. Steel, 2003, Current Biology.

The genetic basis of mammalian neurulation

Andrew J. Copp, Jennifer N. Murdoch, N. Greene, 2003, Nature Reviews Genetics.

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–q23

S. Gregory, A. Copp, P. Stanier, 2001 .

Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification.

A. Copp, P. Stanier, C. Paternotte, 2001, Human molecular genetics.

Genomic organization and embryonic expression of igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia

A. Copp, D. Gerrelli, P. Stanier, 2003, Molecular and Cellular Neuroscience.

The relationship between sonic Hedgehog signaling, cilia, and neural tube defects.

A. Copp, J. Murdoch, 2010, Birth defects research. Part A, Clinical and molecular teratology.

Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.

A. Copp, P. Stanier, C. Paternotte, 2002, Genomics.

Microsoft Word-8224284-file00.docx

S. Wells, N. Greene, A. Copp, 2014 .

Secreted frizzled-related protein disrupts PCP in eye lens fiber cells that have polarised primary cilia.

Yanshu Wang, L. Wen, R. Stump, 2010, Developmental biology.

Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway

M. Stewart, V. Patterson, Christine Damrau, 2009, Human molecular genetics.

Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.

A. Copp, D. Henderson, P. Stanier, 2003, Human molecular genetics.

Circletail, a new mouse mutant with severe neural tube defects: chromosomal localization and interaction with the loop-tail mutation.

A. Copp, C. Mason, P. Stanier, 2001, Genomics.

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator

Jennifer N. Murdoch, Deborah J. Henderson, José Bragança, 2001, Nature Genetics.

Basal enrichment within neuroepithelia suggests novel function(s) for Celsr1 protein

P. Little, C. Moxon, C. Formstone, 2010, Molecular and Cellular Neuroscience.

The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis

A. Greenfield, C. Dean, L. Niswander, 2010, Human molecular genetics.

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates

J. Lupski, S. Fisher, D. Jagger, 2005, Nature Genetics.

Vangl2 Acts via RhoA Signaling to Regulate Polarized Cell Movements During Development of the Proximal Outflow Tract

A. Copp, D. Henderson, B. Chaudhry, 2005, Circulation research.

Alpha synuclein aggresomes inhibit ciliogenesis and multiple functions of the centrosome

C. Wilkinson, A. Fleming, M. Baldrighi, 2019, bioRxiv.

Non–Cell-Autonomous Roles for the Planar Cell Polarity Gene Vangl2 in Development of the Coronary Circulation

Kazuto Kobayashi, D. Henderson, V. Hildreth, 2008, Circulation research.

Scribble is required for normal epithelial cell–cell contacts and lumen morphogenesis in the mammalian lung

Jonathan J. Wilde, A. Greenfield, C. Dean, 2013, Developmental biology.

The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.

Bernd Fritzsch, M. Stewart, W. Bryant, 2012, Developmental biology.

Brainstem Respiratory Oscillators Develop Independently of Neuronal Migration Defects in the Wnt/PCP Mouse Mutant looptail

M. Thoby-Brisson, J. Champagnat, J. Bouvier, 2012, PloS one.

Asymmetric Localization of Vangl2 and Fz3 Indicate Novel Mechanisms for Planar Cell Polarity in Mammals

A. Forge, N. Copeland, N. Jenkins, 2006, The Journal of Neuroscience.

Alpha-synuclein aggresomes inhibit ciliogenesis and multiple functions of the centrosome

C. Wilkinson, A. Fleming, M. Baldrighi, 2020, Biology Open.

Neurulation and neural tube closure defects.

A. Copp, D. Gerrelli, A. Fleming, 2000, Methods in molecular biology.

Paralogous sm22alpha (Tagln) genes map to mouse chromosomes 1 and 9: further evidence for a paralogous relationship.

A. Copp, P. Stanier, J. Eddleston, 1998, Genomics.

Localization of the mouse gene encoding tyrosine kinase receptor type 10 on distal Chromosome 1

A. Copp, P. Stanier, J. Eddleston, 1997, Mammalian Genome.