Publications by authors named "Harris Morrison"

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ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.
Mark T Handley, Kaalak Reddy, Jimi Wills, Elisabeth Rosser, Archith Kamath, Harris Morrison

PLoS Genet· March 2019

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Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) Syndrome in Humans and Mice.
Joe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, Lisa McKie, Lihadh Al-Gazali, Harris Morrison

PLoS Genet· December 2018

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Coronary Artery Formation Is Driven by Localized Expression of R-spondin3.
Fabio Da Silva, Ana Sofia Rocha, Fariba Jian Motamedi, Filippo Massa, Cem Basboga, Harris Morrison

Cell Rep· August 2017

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A novel mouse model of Warburg Micro syndrome reveals roles for RAB18 in eye development and organisation of the neuronal cytoskeleton.
Sarah M Carpanini, Lisa McKie, Derek Thomson, Ann K Wright, Sarah L Gordon, Harris Morrison

Dis Model Mech· June 2014

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FRA2A is a CGG repeat expansion associated with silencing of AFF3.
Sofie Metsu, Liesbeth Rooms, Jacqueline Rainger, Martin S Taylor, Hemant Bengani, Harris Morrison

PLoS Genet· April 2014

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Fine tuning of craniofacial morphology by distant-acting enhancers.
Catia Attanasio, Alex S Nord, Yiwen Zhu, Matthew J Blow, Zirong Li, Harris Morrison

Science· October 2013

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Glucocorticoid receptor is required for foetal heart maturation.
Eva A Rog-Zielinska, Adrian Thomson, Christopher J Kenyon, David G Brownstein, Carmel M Moran, Harris Morrison

Hum Mol Genet· August 2013

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Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH.
Joe Rainger, Hemant Bengani, Leigh Campbell, Eve Anderson, Kishan Sokhi, Harris Morrison

Hum Mol Genet· September 2012

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MCS9.7 enhancer activity is highly, but not completely, associated with expression of Irf6 and p63.
Walid D Fakhouri, Lindsey Rhea, Tianli Du, Eileen Sweezer, Harris Morrison

Dev Dyn· February 2012

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Enhancer-adoption as a mechanism of human developmental disease.
Laura A Lettice, Sarah Daniels, Elizabeth Sweeney, Shanmugasundaram Venkataraman, Paul S Devenney, Harris Morrison

Hum Mutat· December 2011

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Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.
Joe Rainger, Ellen van Beusekom, Jacqueline K Ramsay, Lisa McKie, Lihadh Al-Gazali, Harris Morrison

PLoS Genet· July 2011

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The podocyte protein nephrin is required for cardiac vessel formation.
Nicole Wagner, Harris Morrison, Sophie Pagnotta, Jean-Francois Michiels, Yannick Schwab

Hum Mol Genet· June 2011

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Human-specific gain of function in a developmental enhancer.
Shyam Prabhakar, Axel Visel, Jennifer A Akiyama, Malak Shoukry, Keith D Lewis, Harris Morrison

Science· September 2008

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Localization and fate of Fgf10-expressing cells in the adult mouse brain implicate Fgf10 in control of neurogenesis.
Mohammad K Hajihosseini, Stijn De Langhe, Eva Lana-Elola, Harris Morrison, Neil Sparshott

Mol Cell Neurosci· April 2008

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Three-dimensional imaging of Drosophila melanogaster.
Leeanne McGurk, Harris Morrison, Liam P Keegan, James Sharpe, Mary A O'Connell

PLoS One· September 2007

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Tomographic molecular imaging and 3D quantification within adult mouse organs.
Tomas Alanentalo, Amir Asayesh, Harris Morrison, Christina E Lorén, Dan Holmberg

Nat Methods· January 2007

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Visualizing plant development and gene expression in three dimensions using optical projection tomography.
Karen Lee, Jerome Avondo, Harris Morrison, Lilian Blot, Margaret Stark

Plant Cell· September 2006

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Foxg1 is required for specification of ventral telencephalon and region-specific regulation of dorsal telencephalic precursor proliferation and apoptosis.
Ben Martynoga, Harris Morrison, David J Price, John O Mason

Dev Biol· July 2005

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Allele-specific underacetylation of histone H4 downstream from promoters is associated with X-inactivation in human cells.
Harris Morrison, Peter Jeppesen

Chromosome Res· June 2003

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Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals.
Ian G Cowell, Rebecca Aucott, Shantha K Mahadevaiah, Paul S Burgoyne, Neville Huskisson, Harris Morrison

Chromosoma· March 2002

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