Fine Tuning of Craniofacial Morphology by Distant-Acting Enhancers
Attanasio, Catia, Nord, Alex S., Zhu, Yiwen, Blow, Matthew J., Li, Zirong, Liberton, Denise K., Morrison, Harris, Plajzer-Frick, Ingrid, Holt, Amy, Hosseini, Roya, Phouanenavong, Sengthavy, Akiyama, Jennifer A., Shoukry, Malak, Afzal, Veena, Rubin, Edward M., FitzPatrick, David R., Ren, Bing, Hallgrímsson, Benedikt, Pennacchio, Len A., Visel, Axel
Published in Science (American Association for the Advancement of Science) (25.10.2013)
Published in Science (American Association for the Advancement of Science) (25.10.2013)
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Human-Specific Gain of Function in a Developmental Enhancer
Prabhakar, Shyam, Visel, Axel, Akiyama, Jennifer A, Shoukry, Malak, Lewis, Keith D, Holt, Amy, Plajzer-Frick, Ingrid, Morrison, Harris, FitzPatrick, David R, Afzal, Veena, Pennacchio, Len A, Rubin, Edward M, Noonan, James P
Published in Science (American Association for the Advancement of Science) (05.09.2008)
Published in Science (American Association for the Advancement of Science) (05.09.2008)
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Journal Article
Tomographic molecular imaging and 3D quantification within adult mouse organs
Sharpe, James, Ahlgren, Ulf, Alanentalo, Tomas, Asayesh, Amir, Morrison, Harris, Lorén, Christina E, Holmberg, Dan
Published in Nature methods (01.01.2007)
Published in Nature methods (01.01.2007)
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Journal Article
ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy
Handley, Mark T, Reddy, Kaalak, Wills, Jimi, Rosser, Elisabeth, Kamath, Archith, Halachev, Mihail, Falkous, Gavin, Williams, Denise, Cox, Phillip, Meynert, Alison, Raymond, Eleanor S, Morrison, Harris, Brown, Stephen, Allan, Emma, Aligianis, Irene, Jackson, Andrew P, Ramsahoye, Bernard H, von Kriegsheim, Alex, Taylor, Robert W, Finch, Andrew J, FitzPatrick, David R
Published in PLoS genetics (11.03.2019)
Published in PLoS genetics (11.03.2019)
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Journal Article
Enhancer-adoption as a mechanism of human developmental disease
Lettice, Laura A., Daniels, Sarah, Sweeney, Elizabeth, Venkataraman, Shanmugasundaram, Devenney, Paul S., Gautier, Philippe, Morrison, Harris, Fantes, Judy, Hill, Robert E., FitzPatrick, David R.
Published in Human mutation (01.12.2011)
Published in Human mutation (01.12.2011)
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FRA2A is a CGG repeat expansion associated with silencing of AFF3
Metsu, Sofie, Rooms, Liesbeth, Rainger, Jacqueline, Taylor, Martin S, Bengani, Hemant, Wilson, David I, Chilamakuri, Chandra Sekhar Reddy, Morrison, Harris, Vandeweyer, Geert, Reyniers, Edwin, Douglas, Evelyn, Thompson, Geoffrey, Haan, Eric, Gecz, Jozef, Fitzpatrick, David R, Kooy, R Frank
Published in PLoS genetics (01.04.2014)
Published in PLoS genetics (01.04.2014)
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Three-dimensional imaging of Drosophila melanogaster
McGurk, Leeanne, Morrison, Harris, Keegan, Liam P, Sharpe, James, O'Connell, Mary A
Published in PloS one (05.09.2007)
Published in PloS one (05.09.2007)
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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
Carpanini, Sarah M, McKie, Lisa, Thomson, Derek, Wright, Ann K, Gordon, Sarah L, Roche, Sarah L, Handley, Mark T, Morrison, Harris, Brownstein, David, Wishart, Thomas M, Cousin, Michael A, Gillingwater, Thomas H, Aligianis, Irene A, Jackson, Ian J
Published in Disease models & mechanisms (01.06.2014)
Published in Disease models & mechanisms (01.06.2014)
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Heterochromatin, HP1 and methylation at lysine 9 of histone H3 in animals
Cowell, Ian G, Aucott, Rebecca, Mahadevaiah, Shantha K, Burgoyne, Paul S, Huskisson, Neville, Bongiorni, Silvia, Prantera, Giorgio, Fanti, Laura, Pimpinelli, Sergio, Wu, Rong, Gilbert, David M, Shi, Wei, Fundele, Reinald, Morrison, Harris, Jeppesen, Peter, Singh, Prim B
Published in Chromosoma (01.03.2002)
Published in Chromosoma (01.03.2002)
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Journal Article
Localization and fate of Fgf10-expressing cells in the adult mouse brain implicate Fgf10 in control of neurogenesis
Hajihosseini, Mohammad K., Langhe, Stijn De, Lana-Elola, Eva, Morrison, Harris, Sparshott, Neil, Kelly, Robert, Sharpe, James, Rice, David, Bellusci, Saverio
Published in Molecular and cellular neuroscience (01.04.2008)
Published in Molecular and cellular neuroscience (01.04.2008)
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Journal Article
Human X Inactivation Center Induces Random X Chromosome Inactivation in Male Transgenic Mice
Migeon, Barbara R., Kazi, Ethan, Haisley-Royster, Camille, Hu, Jie, Reeves, Roger, Call, Linda, Lawler, Ann, Moore, Clara S., Morrison, Harris, Jeppesen, Peter
Published in Genomics (San Diego, Calif.) (15.07.1999)
Published in Genomics (San Diego, Calif.) (15.07.1999)
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Journal Article
Glucocorticoid receptor is required for foetal heart maturation
Rog-Zielinska, Eva A, Thomson, Adrian, Kenyon, Christopher J, Brownstein, David G, Moran, Carmel M, Szumska, Dorota, Michailidou, Zoi, Richardson, Jennifer, Owen, Elizabeth, Watt, Alistair, Morrison, Harris, Forrester, Lesley M, Bhattacharya, Shoumo, Holmes, Megan C, Chapman, Karen E
Published in Human molecular genetics (15.08.2013)
Published in Human molecular genetics (15.08.2013)
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Journal Article
MCS9.7 enhancer activity is highly, but not completely, associated with expression of Irf6 and p63
Fakhouri, Walid D., Rhea, Lindsey, Du, Tianli, Sweezer, Eileen, Morrison, Harris, Fitzpatrick, David, Yang, Baoli, Dunnwald, Martine, Schutte, Brian C.
Published in Developmental dynamics (01.02.2012)
Published in Developmental dynamics (01.02.2012)
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Journal Article
Miller (Genée―Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH
RAINGER, Joe, BENGANI, Hemant, MERCER, Catherine, MCKENZIE, Kathryn, LENGFELD, Tobias, QUEROKL, Blanca Gener, BRANNEY, Peter, MCKAY, Stewart, MORRISON, Harris, MEDINA, Bethan, ROBERTSON, Morag, KOHLHASE, Jurgen, CAMPBELL, Leigh, GORDON, Colin, KIRK, Jean, WIECZOREK, Dagmar, FITZPATRICK, David R, ANDERSON, Eve, SOKHI, Kishan, LAM, Wayne, RIESS, Angelika, ANSARI, Morad, SMITHSON, Sarah, LEES, Melissa
Published in Human molecular genetics (15.09.2012)
Published in Human molecular genetics (15.09.2012)
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Journal Article
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice
Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, Fitzpatrick, David R
Published in PLoS genetics (01.07.2011)
Published in PLoS genetics (01.07.2011)
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Journal Article
Correction: Loss of the BMP Antagonist, SMOC-1, Causes Ophthalmo-Acromelic
Rainger, Joe, van Beusekom, Ellen, Ramsay, Jacqueline K, McKie, Lisa, Al-Gazali, Lihadh, Pallotta, Rosanna, Saponari, Anita, Branney, Peter, Fisher, Malcolm, Morrison, Harris, Bicknell, Louise, Gautier, Philippe, Perry, Paul, Sokhi, Kishan, Sexton, David, Bardakjian, Tanya M, Schneider, Adele S, Elcioglu, Nursel, Ozkinay, Ferda, Koenig, Rainer, Mégarbané, Andre, Semerci, C. Nur, Khan, Ayesha, Zafar, Saemah, Hennekam, Raoul, Sousa, Sérgio B, Ramos, Lina, Garavelli, Livia, Furga, Andrea Superti, Wischmeijer, Anita, Jackson, Ian J, Gillessen-Kaesbach, Gabriele, Brunner, Han G, Wieczorek, Dagmar, van Bokhoven, Hans, FitzPatrick, David R
Published in PLoS genetics (26.12.2018)
Published in PLoS genetics (26.12.2018)
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The podocyte protein nephrin is required for cardiac vessel formation
WAGNER, Nicole, MORRISON, Harris, PAGNOTTA, Sophie, MICHIELS, Jean-Francois, SCHWAB, Yannick, TRYGGVASON, Karl, SCHEDL, Andreas, WAGNER, Kay-Dietrich
Published in Human molecular genetics (01.06.2011)
Published in Human molecular genetics (01.06.2011)
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