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

von Arkell, Ruth M., Tam, Patrick P. L.
Veröffentlicht 2012

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

von Thomsen, Nicole, Ali, Radiya G., Ahmed, Jehangir N., Arkell, Ruth M.
Veröffentlicht 2012

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

von Ahmed, Jehangir N., Diamand, Koula E. M., Bellchambers, Helen M., Arkell, Ruth M.
Veröffentlicht in Sci Rep (2020)

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

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

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

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

von 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.
Veröffentlicht 2013

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

von 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
Veröffentlicht in eLife (2021)

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

von 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.
Veröffentlicht 2005

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

von 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.
Veröffentlicht 2013

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

von 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.
Veröffentlicht in PLoS Genet (2015)

Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data

von 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
Veröffentlicht in Am J Hum Genet (2020)