Hox proteins drive cell segregation and non-autonomous apical remodelling during hindbrain segmentation

por Prin, Fabrice, Serpente, Patricia, Itasaki, Nobue, Gould, Alex P.
Publicado 2014

Control of skeletal morphogenesis by the Hippo-YAP/TAZ pathway

por Vanyai, Hannah K., Prin, Fabrice, Guillermin, Oriane, Marzook, Bishara, Boeing, Stefan, Howson, Alexander, Saunders, Rebecca E., Snoeks, Thomas, Howell, Michael, Mohun, Timothy J., Thompson, Barry
Publicado 2020

A staging system for correct phenotype interpretation of mouse embryos harvested on embryonic day 14 (E14.5)

por Geyer, Stefan H., Reissig, Lukas, Rose, Julia, Wilson, Robert, Prin, Fabrice, Szumska, Dorota, Ramirez‐Solis, Ramiro, Tudor, Catherine, White, Jacqui, Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2017

Hypoglossal Nerve Abnormalities as Biomarkers for Central Nervous System Defects in Mouse Lines Producing Embryonically Lethal Offspring

por Reissig, Lukas F., Seyedian Moghaddam, Atieh, Prin, Fabrice, Wilson, Robert, Galli, Antonella, Tudor, Catherine, White, Jaqueline K., Geyer, Stefan H., Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2021

Visualising the Cardiovascular System of Embryos of Biomedical Model Organisms with High Resolution Episcopic Microscopy (HREM)

por Weninger, Wolfgang J., Maurer-Gesek, Barbara, Reissig, Lukas F., Prin, Fabrice, Wilson, Robert, Galli, Antonella, Adams, David J., White, Jacqueline K., Mohun, Timothy J., Geyer, Stefan H.
Publicado 2018

Artefacts in Volume Data Generated with High Resolution Episcopic Microscopy (HREM)

por Reissig, Lukas F., Geyer, Stefan H., Rose, Julia, Prin, Fabrice, Wilson, Robert, Szumska, Dorota, Galli, Antonella, Tudor, Catherine, White, Jacqueline K., Mohun, Tim J., Weninger, Wolfgang J.
Publicado 2021

Detailed characterizations of cranial nerve anatomy in E14.5 mouse embryos/fetuses and their use as reference for diagnosing subtle, but potentially lethal malformations in mutants

por Reissig, Lukas F., Geyer, Stefan H., Winkler, Viola, Preineder, Ester, Prin, Fabrice, Wilson, Robert, Galli, Antonella, Tudor, Catherine, White, Jaqueline K., Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2022

The venous system of E14.5 mouse embryos—reference data and examples for diagnosing malformations in embryos with gene deletions

por Geyer, Stefan H., Maurer‐Gesek, Barbara, Reissig, Lukas F., Rose, Julia, Prin, Fabrice, Wilson, Robert, Galli, Antonella, Tudor, Catherine, White, Jacqueline K., Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2021

Morphology, topology and dimensions of the heart and arteries of genetically normal and mutant mouse embryos at stages S21–S23

por Geyer, Stefan H., Reissig, Lukas F., Hüsemann, Markus, Höfle, Cordula, Wilson, Robert, Prin, Fabrice, Szumska, Dorota, Galli, Antonella, Adams, David J., White, Jacqui, Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2017

Placental Inflammation Leads to Abnormal Embryonic Heart Development

por Ward, Eleanor J., Bert, Serena, Fanti, Silvia, Malone, Kerri M., Maughan, Robert T., Gkantsinikoudi, Christina, Prin, Fabrice, Volpato, Lia Karina, Piovezan, Anna Paula, Graham, Gerard J., Dufton, Neil P., Perretti, Mauro, Marelli-Berg, Federica M., Nadkarni, Suchita
Publicado 2022

Lem2 is essential for cardiac development by maintaining nuclear integrity

por Ross, Jacob A, Arcos-Villacis, Nathaly, Battey, Edmund, Boogerd, Cornelis, Orellana, Constanza Avalos, Marhuenda, Emilie, Swiatlowska, Pamela, Hodzic, Didier, Prin, Fabrice, Mohun, Tim, Catibog, Norman, Tapia, Olga, Gerace, Larry, Iskratsch, Thomas, Shah, Ajay M, Stroud, Matthew J
Publicado 2023

Highly variable penetrance of abnormal phenotypes in embryonic lethal knockout mice

por Wilson, Robert, Geyer, Stefan H., Reissig, Lukas, Rose, Julia, Szumska, Dorota, Hardman, Emily, Prin, Fabrice, McGuire, Christina, Ramirez-Solis, Ramiro, White, Jacqui, Galli, Antonella, Tudor, Catherine, Tuck, Elizabeth, Mazzeo, Cecilia Icoresi, Smith, James C., Robertson, Elizabeth, Adams, David J., Mohun, Timothy, Weninger, Wolfgang J.
Publicado 2017

The Col4a2(em1(IMPC)Wtsi) mouse line: lessons from the Deciphering the Mechanisms of Developmental Disorders program

por Reissig, Lukas F., Herdina, Anna Nele, Rose, Julia, Maurer-Gesek, Barbara, Lane, Jenna L., Prin, Fabrice, Wilson, Robert, Hardman, Emily, Galli, Antonella, Tudor, Catherine, Tuck, Elizabeth, Icoresi-Mazzeo, Cecilia, White, Jacqueline K., Ryder, Ed, Gleeson, Diane, Adams, David J., Geyer, Stefan H., Mohun, Timothy J., Weninger, Wolfgang J.
Publicado 2019

A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development

por De Franco, Elisa, Watson, Rachel A., Weninger, Wolfgang J., Wong, Chi C., Flanagan, Sarah E., Caswell, Richard, Green, Angela, Tudor, Catherine, Lelliott, Christopher J., Geyer, Stefan H., Maurer-Gesek, Barbara, Reissig, Lukas F., Lango Allen, Hana, Caliebe, Almuth, Siebert, Reiner, Holterhus, Paul Martin, Deeb, Asma, Prin, Fabrice, Hilbrands, Robert, Heimberg, Harry, Ellard, Sian, Hattersley, Andrew T., Barroso, Inês
Publicado 2019

Maternal iron deficiency perturbs embryonic cardiovascular development in mice

por Kalisch-Smith, Jacinta I., Ved, Nikita, Szumska, Dorota, Munro, Jacob, Troup, Michael, Harris, Shelley E., Rodriguez-Caro, Helena, Jacquemot, Aimée, Miller, Jack J., Stuart, Eleanor M., Wolna, Magda, Hardman, Emily, Prin, Fabrice, Lana-Elola, Eva, Aoidi, Rifdat, Fisher, Elizabeth M. C., Tybulewicz, Victor L. J., Mohun, Timothy J., Lakhal-Littleton, Samira, De Val, Sarah, Giannoulatou, Eleni, Sparrow, Duncan B.
Publicado 2021

PKN2 deficiency leads both to prenatal ‘congenital’ cardiomyopathy and defective angiotensin II stress responses

por Marshall, Jacqueline J.T., Cull, Joshua J., Alharbi, Hajed O., Zaw Thin, May, Cooper, Susanna T.E., Barrington, Christopher, Vanyai, Hannah, Snoeks, Thomas, Siow, Bernard, Suáarez-Bonnet, Alejandro, Herbert, Eleanor, Stuckey, Daniel J., Cameron, Angus J.M., Prin, Fabrice, Cook, Andrew C., Priestnall, Simon L., Chotani, Sonia, Rackham, Owen J. L., Meijles, Daniel N., Mohun, Tim, Clerk, Angela, Parker, Peter J.
Publicado 2022

SMCHD1 has separable roles in chromatin architecture and gene silencing that could be targeted in disease

por Tapia del Fierro, Andres, den Hamer, Bianca, Benetti, Natalia, Jansz, Natasha, Chen, Kelan, Beck, Tamara, Vanyai, Hannah, Gurzau, Alexandra D., Daxinger, Lucia, Xue, Shifeng, Ly, Thanh Thao Nguyen, Wanigasuriya, Iromi, Iminitoff, Megan, Breslin, Kelsey, Oey, Harald, Krom, Yvonne D., van der Hoorn, Dinja, Bouwman, Linde F., Johanson, Timothy M., Ritchie, Matthew E., Gouil, Quentin A., Reversade, Bruno, Prin, Fabrice, Mohun, Timothy, van der Maarel, Silvère M., McGlinn, Edwina, Murphy, James M., Keniry, Andrew, de Greef, Jessica C., Blewitt, Marnie E.
Publicado 2023