Inhibition of retinoic acid signaling impairs cranial and spinal neural tube closure in mice lacking the Grainyhead-like 3 transcription factor von Deng, Zihao, Carpinelli, Marina R., Butt, Tariq, Magor, Graham W., Perkins, Andrew C., Jane, Stephen M.

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Critical roles for c-Myb in lymphoid priming and early B-cell development von Greig, Kylie T., de Graaf, Carolyn A., Murphy, James M., Carpinelli, Marina R., Pang, Swee Heng Milon, Frampton, Jon, Kile, Benjamin T., Hilton, Douglas J., Nutt, Stephen L.

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A new mouse model of Canavan leukodystrophy displays hearing impairment due to central nervous system dysmyelination von Carpinelli, Marina R, Voss, Anne K, Manning, Michael G, Perera, Ashwyn A, Cooray, Anne A, Kile, Benjamin T, Burt, Rachel A

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Thrombocytopenia and Kidney Disease in Mice with a Mutation in the C1galt1 Gene von Alexander, Warren S., Viney, Elizabeth M., Zhang, Jian-Guo, Metcalf, Donald, Kauppi, Maria, Hyland, Craig D., Carpinelli, Marina R., Stevenson, William, Croker, Ben A., Hilton, Adrienne A., Ellis, Sarah, Selan, Carly, Nandurkar, Harshal H., Goodnow, Christopher C., Kile, Benjamin T., Nicola, Nicos A., Roberts, Andrew W., Hilton, Douglas J.

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Delineating the roles of Grhl2 in craniofacial development through tissue‐specific conditional deletion and epistasis approaches in mouse von Vries, Michael, Owens, Harley G., Carpinelli, Marina R., Partridge, Darren, Kersbergen, Ariena, Sutherland, Kate D., Auden, Alana, Anderson, Peter J., Jane, Stephen M., Dworkin, Sebastian

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Vitamin D-deficient diet rescues hearing loss in Klotho mice von Carpinelli, Marina R., Wise, Andrew K., Burt, Rachel A.

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An Ethyl-Nitrosourea-Induced Point Mutation in Phex Causes Exon Skipping, X-Linked Hypophosphatemia, and Rickets von Carpinelli, Marina R., Wicks, Ian P., Sims, Natalie A., O'Donnell, Kristy, Hanzinikolas, Katherine, Burt, Rachel, Foote, Simon J., Bahlo, Melanie, Alexander, Warren S., Hilton, Douglas J.

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Anomalous megakaryocytopoiesis in mice with mutations in the c-Myb gene von Metcalf, Donald, Carpinelli, Marina R., Hyland, Craig, Mifsud, Sandra, DiRago, Ladina, Nicola, Nicos A., Hilton, Douglas J., Alexander, Warren S.

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Genetic Modifier Screens in Mice von Carpinelli, Marina R., Burt, Rachel A., Kile, Benjamin T.

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Inactivation of Zeb1 in GRHL2-deficient mouse embryos rescues mid-gestation viability and secondary palate closure von Carpinelli, Marina R, de Vries, Michael E, Auden, Alana, Butt, Tariq, Deng, Zihao, Partridge, Darren D, Miles, Lee B, Georgy, Smitha R, Haigh, Jody J, Darido, Charbel, Brabletz, Simone, Brabletz, Thomas, Stemmler, Marc P, Dworkin, Sebastian, Jane, Stephen M

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Two ENU-Induced Alleles of Atp2b2 Cause Deafness in Mice. e67479 von Carpinelli, Marina R, Manning, Michael G, Kile, Benjamin T, Rachel, A Burt

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The Bcl-2 Protein Family Is Essential for Platelet Survival In Vivo von Mason, Kylie D., Carpinelli, Marina R., Collinge, Janelle E., Hilton, Adrienne A., Fletcher, Jamie I., Roberts, Andrew W., Metcalf, Donald, Huang, David C.S., Kile, Benjamin T.

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