Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages

por Seda, Marian, Peskett, Emma, Demetriou, Charalambos, Bryant, Dale, Moore, Gudrun E., Stanier, Philip, Jenkins, Dagan
Publicado 2019

A new biological and clinical resource for research into pregnancy complications: The Baby Bio Bank

por Leon, Lydia J., Solanky, Nita, Stalman, Susanne E., Demetriou, Charalambos, Abu-Amero, Sayeda, Stanier, Philip, Regan, Lesley, Moore, Gudrun E.
Publicado 2016

Analysis of CDKN1C in fetal growth restriction and pregnancy loss

por Suntharalingham, Jenifer P., Ishida, Miho, Buonocore, Federica, del Valle, Ignacio, Solanky, Nita, Demetriou, Charalambos, Regan, Lesley, Moore, Gudrun E., Achermann, John C.
Publicado 2020

Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo

por Derakhshan, Maria, Kessler, Noah J, Ishida, Miho, Demetriou, Charalambos, Brucato, Nicolas, Moore, Gudrun E, Fall, Caroline H D, Chandak, Giriraj R, Ricaut, Francois-Xavier, Prentice, Andrew M, Hellenthal, Garrett, Silver, Matt J
Publicado 2022

Paternally Expressed, Imprinted Insulin-Like Growth Factor-2 in Chorionic Villi Correlates Significantly with Birth Weight

por Demetriou, Charalambos, Abu-Amero, Sayeda, Thomas, Anna C., Ishida, Miho, Aggarwal, Reena, Al-Olabi, Lara, Leon, Lydia J., Stafford, Jaime L., Syngelaki, Argyro, Peebles, Donald, Nicolaides, Kypros H., Regan, Lesley, Stanier, Philip, Moore, Gudrun E.
Publicado 2014

The role and interaction of imprinted genes in human fetal growth

por Moore, Gudrun E., Ishida, Miho, Demetriou, Charalambos, Al-Olabi, Lara, Leon, Lydia J., Thomas, Anna C., Abu-Amero, Sayeda, Frost, Jennifer M., Stafford, Jaime L., Chaoqun, Yao, Duncan, Andrew J., Baigel, Rachel, Brimioulle, Marina, Iglesias-Platas, Isabel, Apostolidou, Sophia, Aggarwal, Reena, Whittaker, John C., Syngelaki, Argyro, Nicolaides, Kypros H., Regan, Lesley, Monk, David, Stanier, Philip
Publicado 2015

Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations

por Bryant, Dale, Seda, Marian, Peskett, Emma, Maurer, Constance, Pomeranz, Gideon, Ghosh, Marcus, Hawkins, Thomas A., Cleak, James, Datta, Sanchari, Hariri, Hanaa, Eckert, Kaitlyn M., Jafree, Daniyal J., Walsh, Claire, Demetriou, Charalambos, Ishida, Miho, Alemán-Charlet, Cristina, Vestito, Letizia, Seselgyte, Rimante, McDonald, Jeffrey G., Bitner-Glindzicz, Maria, Hemberger, Myriam, Rihel, Jason, Teboul, Lydia, Henne, W. Mike, Jenkins, Dagan, Moore, Gudrun E., Stanier, Philip
Publicado 2020

PTPN11 Mosaicism Causes a Spectrum of Pigmentary and Vascular Neurocutaneous Disorders and Predisposes to Melanoma

por Polubothu, Satyamaanasa, Bender, Nicole, Muthiah, Siobhan, Zecchin, Davide, Demetriou, Charalambos, Martin, Sara Barberan, Malhotra, Sony, Travnickova, Jana, Zeng, Zhiqiang, Böhm, Markus, Barbarot, Sebastien, Cottrell, Catherine, Davies, Olivia, Baselga, Eulalia, Burrows, Nigel P., Carmignac, Virginie, Diaz, Joey Santiago, Fink, Christine, Haenssle, Holger A., Happle, Rudolf, Harland, Mark, Majerowski, Jacquelyn, Vabres, Pierre, Vincent, Marie, Newton-Bishop, Julia A., Bishop, D. Tim, Siegel, Dawn, Patton, E. Elizabeth, Topf, Maya, Rajan, Neil, Drolet, Beth, Kinsler, Veronica A.
Publicado 2023