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

por Arkell, Ruth M., Tam, Patrick P. L.
Publicado 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 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 en 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 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 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 2013

Disruption of entire Cables2 locus leads to embryonic lethality by diminished Rps21 gene expression and enhanced p53 pathway

por Dinh, Tra Thi Huong, Iseki, Hiroyoshi, Mizuno, Seiya, Iijima-Mizuno, Saori, Tanimoto, Yoko, Daitoku, Yoko, Kato, Kanako, Hamada, Yuko, Hasan, Ammar Shaker Hamed, Suzuki, Hayate, Murata, Kazuya, Muratani, Masafumi, Ema, Masatsugu, Kim, Jun-Dal, Ishida, Junji, Fukamizu, Akiyoshi, Kato, Mitsuyasu, Takahashi, Satoru, Yagami, Ken-ichi, Wilson, Valerie, Arkell, Ruth M, Sugiyama, Fumihiro
Publicado en eLife (2021)

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 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 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 en 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 en Am J Hum Genet (2020)