Evidence that the cysteine-rich domain of Drosophila Frizzled family receptors is dispensable for transducing Wingless

von Chen, Chiann-mun, Strapps, Walter, Tomlinson, Andrew, Struhl, Gary
Veröffentlicht 2004

A Comparison of Exogenous Promoter Activity at the ROSA26 Locus Using a PhiC31 Integrase Mediated Cassette Exchange Approach in Mouse ES Cells

von Chen, Chiann-mun, Krohn, Jon, Bhattacharya, Shoumo, Davies, Benjamin
Veröffentlicht 2011

Detecting cardiac contractile activity in the early mouse embryo using multiple modalities

von Chen, Chiann-Mun, Miranda, António M. A., Bub, Gil, Srinivas, Shankar
Veröffentlicht in Front Physiol (2015)

Calcium handling precedes cardiac differentiation to initiate the first heartbeat

von Tyser, Richard CV, Miranda, Antonio MA, Chen, Chiann-mun, Davidson, Sean M, Srinivas, Shankar, Riley, Paul R
Veröffentlicht in eLife (2016)

A cell-autonomous role of Cited2 in controlling myocardial and coronary vascular development

von MacDonald, Simon T., Bamforth, Simon D., Bragança, José, Chen, Chiann-Mun, Broadbent, Carol, Schneider, Jürgen E., Schwartz, Robert J., Bhattacharya, Shoumo
Veröffentlicht 2013

Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency

von MacDonald, Simon T., Bamforth, Simon D., Chen, Chiann-Mun, Farthing, Cassandra R., Franklyn, Angela, Broadbent, Carol, Schneider, Jürgen E., Saga, Yumiko, Lewandoski, Mark, Bhattacharya, Shoumo
Veröffentlicht 2008

Functional Significance of SRJ Domain Mutations in CITED2

von Chen, Chiann-mun, Bentham, Jamie, Cosgrove, Catherine, Braganca, Jose, Cuenda, Ana, Bamforth, Simon D., Schneider, Jürgen E., Watkins, Hugh, Keavney, Bernard, Davies, Benjamin, Bhattacharya, Shoumo
Veröffentlicht 2012

A Requirement for Zic2 in the Regulation of Nodal Expression Underlies the Establishment of Left-Sided Identity

von Dykes, Iain M., Szumska, Dorota, Kuncheria, Linta, Puliyadi, Rathi, Chen, Chiann-mun, Papanayotou, Costis, Lockstone, Helen, Dubourg, Christèle, David, Véronique, Schneider, Jurgen E., Keane, Thomas M., Adams, David J., Brown, Steve D. M., Mercier, Sandra, Odent, Sylvie, Collignon, Jérôme, Bhattacharya, Shoumo
Veröffentlicht in Sci Rep (2018)

NKX2-5 mutations causative for congenital heart disease retain functionality and are directed to hundreds of targets

von Bouveret, Romaric, Waardenberg, Ashley J, Schonrock, Nicole, Ramialison, Mirana, Doan, Tram, de Jong, Danielle, Bondue, Antoine, Kaur, Gurpreet, Mohamed, Stephanie, Fonoudi, Hananeh, Chen, Chiann-mun, Wouters, Merridee A, Bhattacharya, Shoumo, Plachta, Nicolas, Dunwoodie, Sally L, Chapman, Gavin, Blanpain, Cédric, Harvey, Richard P
Veröffentlicht in eLife (2015)