Ngā hua rapu - Bowen, Margot E.

The role of p53 in developmental syndromes mā Bowen, Margot E, Attardi, Laura D

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Puma- and Caspase9-mediated apoptosis is dispensable for p53-driven neural crest-based developmental defects mā Bowen, Margot E., Mulligan, Abigail S., Sorayya, Aryo, Attardi, Laura D.

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Efficient Mapping and Cloning of Mutations in Zebrafish by Low-Coverage Whole-Genome Sequencing mā Bowen, Margot E., Henke, Katrin, Siegfried, Kellee R., Warman, Matthew L., Harris, Matthew P.

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SHP2 Regulates Chondrocyte Terminal Differentiation, Growth Plate Architecture and Skeletal Cell Fates mā Bowen, Margot E., Ayturk, Ugur M., Kurek, Kyle C., Yang, Wentian, Warman, Matthew L.

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The p53 family members have distinct roles during mammalian embryonic development mā Van Nostrand, Jeanine L, Bowen, Margot E, Vogel, Hannes, Barna, Maria, Attardi, Laura D

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Presphenoidal synchondrosis fusion in DBA/2J mice mā Adams, Allysa, McBratney-Owen, Brandeis, Newby, Brittany, Bowen, Margot E., Olsen, Bjorn R., Warman, Matthew L.

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Single Cell Transcriptomics Reveal Abnormalities in Neurosensory Patterning of the Chd7 Mutant Mouse Ear mā Durruthy-Durruthy, Robert, Sperry, Ethan D., Bowen, Margot E., Attardi, Laura D., Heller, Stefan, Martin, Donna M.

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Siva plays a critical role in mouse embryonic development mā Jacobs, Suzanne B. R., Van Nostrand, Jeanine L., Bowen, Margot E., Baker, Julie C., Attardi, Laura D.

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The spatiotemporal pattern and intensity of p53 activation during embryogenesis dictates phenotypic diversity in p53-driven developmental syndromes mā Bowen, Margot E., McClendon, Jacob, Long, Hannah K., Sorayya, Aryo, Van Nostrand, Jeanine L., Wysocka, Joanna, Attardi, Laura D.

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Integrated K+ channel and K+Cl- cotransporter function are required for the coordination of size and proportion during development mā Lanni, Jennifer S., Peal, David, Ekstrom, Laura, Chen, Haining, Stanclift, Caroline, Bowen, Margot E., Mercado, Adriana, Gamba, Gerardo, Kahle, Kristopher T., Harris, Matthew, P.

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Tissue–selective effects of nucleolar stress and rDNA damage in developmental disorders mā Calo, Eliezer, Gu, Bo, Bowen, Margot E., Aryan, Fardin, Zalc, Antoine, Liang, Jialiang, Flynn, Ryan A., Swigut, Tomek, Chang, Howard Y., Attardi, Laura D., Wysocka, Joanna

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Sclerostin Inhibition Reverses Skeletal Fragility in an Lrp5-Deficient Mouse Model of OPPG Syndrome mā Kedlaya, Rajendra, Veera, Shreya, Horan, Daniel J., Moss, Rachel E., Ayturk, Ugur M., Jacobsen, Christina M., Bowen, Margot E., Paszty, Chris, Warman, Matthew L., Robling, Alexander G.

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A p53-dependent translational program directs tissue-selective phenotypes in a model of ribosomopathies mā Tiu, Gerald C., Kerr, Craig H., Forester, Craig M., Krishnarao, Pallavi S., Rosenblatt, Hannah D., Raj, Nitin, Lantz, Travis C., Zhulyn, Olena, Bowen, Margot E., Shokat, Leila, Attardi, Laura D., Ruggero, Davide, Barna, Maria

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Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome mā Kurek, Kyle C., Luks, Valerie L., Ayturk, Ugur M., Alomari, Ahmad I., Fishman, Steven J., Spencer, Samantha A., Mulliken, John B., Bowen, Margot E., Yamamoto, Guilherme L., Kozakewich, Harry P.W., Warman, Matthew L.

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SHP2 regulates skeletal cell fate by modifying SOX9 expression and transcriptional activity mā Zuo, Chunlin, Wang, Lijun, Kamalesh, Raghavendra M., Bowen, Margot E., Moore, Douglas C., Dooner, Mark S., Reginato, Anthony M., Wu, Qian, Schorl, Christoph, Song, Yueming, Warman, Matthew L., Neel, Benjamin G., Ehrlich, Michael G., Yang, Wentian

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Loss-of-Function Mutations in PTPN11 Cause Metachondromatosis, but Not Ollier Disease or Maffucci Syndrome mā Bowen, Margot E., Boyden, Eric D., Holm, Ingrid A., Campos-Xavier, Belinda, Bonafé, Luisa, Superti-Furga, Andrea, Ikegawa, Shiro, Cormier-Daire, Valerie, Bovée, Judith V., Pansuriya, Twinkal C., de Sousa, Sérgio B., Savarirayan, Ravi, Andreucci, Elena, Vikkula, Miikka, Garavelli, Livia, Pottinger, Caroline, Ogino, Toshihiko, Sakai, Akinori, Regazzoni, Bianca M., Wuyts, Wim, Sangiorgi, Luca, Pedrini, Elena, Zhu, Mei, Kozakewich, Harry P., Kasser, James R., Seidman, Jon G., Kurek, Kyle C., Warman, Matthew L.

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