Initiating head development in mouse embryos: integrating signalling and transcriptional activity

Por Arkell, Ruth M., Tam, Patrick P. L.
Publicado em 2012

High Resolution Melt Analysis (HRMA); a Viable Alternative to Agarose Gel Electrophoresis for Mouse Genotyping

Por Thomsen, Nicole, Ali, Radiya G., Ahmed, Jehangir N., Arkell, Ruth M.
Publicado em 2012

Systematized reporter assays reveal ZIC protein regulatory abilities are Subclass-specific and dependent upon transcription factor binding site context

Por Ahmed, Jehangir N., Diamand, Koula E. M., Bellchambers, Helen M., Arkell, Ruth M.
Publicado no Sci Rep (2020)

A murine Zic3 transcript with a premature termination codon evades nonsense-mediated decay during axis formation

Por Ahmed, Jehangir N., Ali, Radiya G., Warr, Nicholas, Wilson, Heather M., Bellchambers, Helen M., Barratt, Kristen S., Thompson, Amelia J., Arkell, Ruth M.
Publicado em 2013

The Role of Zic Genes in Inner Ear Development in the Mouse: Exploring Mutant Mouse Phenotypes

Por Chervenak, Andrew P., Bank, Lisa M., Thomsen, Nicole, Glanville-Jones, Hannah C, Skibo, Jonathan, Millen, Kathleen J., Arkell, Ruth M., Barald, Kate F.
Publicado em 2014

Genome-Wide ENU Mutagenesis in Combination with High Density SNP Analysis and Exome Sequencing Provides Rapid Identification of Novel Mouse Models of Developmental Disease

Por Caruana, Georgina, Farlie, Peter G., Hart, Adam H., Bagheri-Fam, Stefan, Wallace, Megan J., Dobbie, Michael S., Gordon, Christopher T., Miller, Kerry A., Whittle, Belinda, Abud, Helen E., Arkell, Ruth M., Cole, Timothy J., Harley, Vincent R., Smyth, Ian M., Bertram, John F.
Publicado em 2013

Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen

Por Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, Haines, Heather, McKeone, Richard, Cadman, Matthew, Pieles, Guido, Schneider, Jürgen E., Bhattacharya, Shoumo, Hardy, Andrea, Nolan, Patrick M., Tripodis, Nikos, Depew, Michael J., Chandrasekara, Ramya, Duncan, Gimara, Sharpe, Paul T., Greenfield, Andy, Denny, Paul, Brown, Steve D. M., Ragoussis, Jiannis, Arkell, Ruth M.
Publicado em 2005

Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

Por Watkins-Chow, Dawn E., Cooke, Joanna, Pidsley, Ruth, Edwards, Andrew, Slotkin, Rebecca, Leeds, Karen E., Mullen, Raymond, Baxter, Laura L., Campbell, Thomas G., Salzer, Marion C., Biondini, Laura, Gibney, Gretchen, Phan Dinh Tuy, Françoise, Chelly, Jamel, Morris, H. Douglas, Riegler, Johannes, Lythgoe, Mark F., Arkell, Ruth M., Loreni, Fabrizio, Flint, Jonathan, Pavan, William J., Keays, David A.
Publicado em 2013

Correction: Mutation of the Diamond-Blackfan Anemia Gene Rps7 in Mouse Results in Morphological and Neuroanatomical Phenotypes

Por Watkins-Chow, Dawn E., Cooke, Joanna, Pidsley, Ruth, Edwards, Andrew, Slotkin, Rebecca, Leeds, Karen E., Mullen, Raymond, Baxter, Laura L., Campbell, Thomas G., Salzer, Marion C., Biondini, Laura, Gibney, Gretchen, Tuy, Françoise Phan Dinh, Chelly, Jamel, Morris, H. Douglas, Riegler, Johannes, Lythgoe, Mark F., Arkell, Ruth M., Loreni, Fabrizio, Flint, Jonathan, Pavan, William J., Keays, David A.
Publicado no PLoS Genet (2015)

Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data

Por Easteal, Simon, Arkell, Ruth M., Balboa, Renzo F., Bellingham, Shayne A., Brown, Alex D., Calma, Tom, Cook, Matthew C., Davis, Megan, Dawkins, Hugh J.S., Dinger, Marcel E., Dobbie, Michael S., Farlow, Ashley, Gwynne, Kylie G., Hermes, Azure, Hoy, Wendy E., Jenkins, Misty R., Jiang, Simon H., Kaplan, Warren, Leslie, Stephen, Llamas, Bastien, Mann, Graham J., McMorran, Brendan J., McWhirter, Rebekah E., Meldrum, Cliff J., Nagaraj, Shivashankar H., Newman, Saul J., Nunn, Jack S., Ormond-Parker, Lyndon, Orr, Neil J., Paliwal, Devashi, Patel, Hardip R., Pearson, Glenn, Pratt, Greg R., Rambaldini, Boe, Russell, Lynette W., Savarirayan, Ravi, Silcocks, Matthew, Skinner, John C., Souilmi, Yassine, Vinuesa, Carola G., Baynam, Gareth
Publicado no Am J Hum Genet (2020)