Differentiation of zebrafish melanophores depends on transcription factors AP2 alpha and AP2 epsilon
Van Otterloo, Eric, Li, Wei, Bonde, Gregory, Day, Kristopher M, Hsu, Mei-Yu, Cornell, Robert A
Published in PLoS genetics (01.09.2010)
Published in PLoS genetics (01.09.2010)
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Vnd/ nkx, ind/ gsh, and msh/ msx: conserved regulators of dorsoventral neural patterning?
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Book Review
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Cooperation between melanoma cell states promotes metastasis through heterotypic cluster formation
Campbell, Nathaniel R., Rao, Anjali, Hunter, Miranda V., Sznurkowska, Magdalena K., Briker, Luzia, Zhang, Maomao, Baron, Maayan, Heilmann, Silja, Deforet, Maxime, Kenny, Colin, Ferretti, Lorenza P., Huang, Ting-Hsiang, Perlee, Sarah, Garg, Manik, Nsengimana, Jérémie, Saini, Massimo, Montal, Emily, Tagore, Mohita, Newton-Bishop, Julia, Middleton, Mark R., Corrie, Pippa, Adams, David J., Rabbie, Roy, Aceto, Nicola, Levesque, Mitchell P., Cornell, Robert A., Yanai, Itai, Xavier, Joao B., White, Richard M.
Published in Developmental cell (25.10.2021)
Published in Developmental cell (25.10.2021)
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Irf6 directly regulates Klf17 in zebrafish periderm and Klf4 in murine oral epithelium, and dominant-negative KLF4 variants are present in patients with cleft lip and palate
Liu, Huan, Leslie, Elizabeth J, Jia, Zhonglin, Smith, Tiffany, Eshete, Mekonen, Butali, Azeez, Dunnwald, Martine, Murray, Jeffrey, Cornell, Robert A
Published in Human molecular genetics (15.02.2016)
Published in Human molecular genetics (15.02.2016)
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TFAP2 paralogs regulate midfacial development in part through a conserved ALX genetic pathway
Nguyen, Timothy T, Mitchell, Jennyfer M, Kiel, Michaela D, Kenny, Colin P, Li, Hong, Jones, Kenneth L, Cornell, Robert A, Williams, Trevor J, Nichols, James T, Van Otterloo, Eric
Published in Development (Cambridge) (01.01.2024)
Published in Development (Cambridge) (01.01.2024)
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Vesicular monoamine transporter 2 (SLC18A2) regulates monoamine turnover and brain development in zebrafish
Baronio, Diego, Chen, Yu‐Chia, Decker, Amanda R., Enckell, Louise, Fernández‐López, Blanca, Semenova, Svetlana, Puttonen, Henri A. J., Cornell, Robert A., Panula, Pertti
Published in Acta Physiologica (01.01.2022)
Published in Acta Physiologica (01.01.2022)
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Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genes
Lansdon, Lisa A., Dickinson, Amanda, Arlis, Sydney, Liu, Huan, Hlas, Arman, Hahn, Alyssa, Bonde, Greg, Long, Abby, Standley, Jennifer, Tyryshkina, Anastasia, Wehby, George, Lee, Nanette R., Daack-Hirsch, Sandra, Mohlke, Karen, Girirajan, Santhosh, Darbro, Benjamin W., Cornell, Robert A., Houston, Douglas W., Murray, Jeffrey C., Manak, J. Robert
Published in American journal of human genetics (05.01.2023)
Published in American journal of human genetics (05.01.2023)
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TFAP2 paralogs facilitate chromatin access for MITF at pigmentation and cell proliferation genes
Kenny, Colin, Dilshat, Ramile, Seberg, Hannah E, Van Otterloo, Eric, Bonde, Gregory, Helverson, Annika, Franke, Christopher M, Steingrímsson, Eiríkur, Cornell, Robert A
Published in PLoS genetics (17.05.2022)
Published in PLoS genetics (17.05.2022)
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Journal Article
A single nucleotide polymorphism associated with isolated cleft lip and palate, thyroid cancer and hypothyroidism alters the activity of an oral epithelium and thyroid enhancer near FOXE1
Lidral, Andrew C, Liu, Huan, Bullard, Steven A, Bonde, Greg, Machida, Junichiro, Visel, Axel, Uribe, Lina M Moreno, Li, Xiao, Amendt, Brad, Cornell, Robert A
Published in Human molecular genetics (15.07.2015)
Published in Human molecular genetics (15.07.2015)
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Mutations in GDF11 and the extracellular antagonist, Follistatin, as a likely cause of Mendelian forms of orofacial clefting in humans
Cox, Timothy C., Lidral, Andrew C., McCoy, Jason C., Liu, Huan, Cox, Liza L., Zhu, Ying, Anderson, Ryan D., Moreno Uribe, Lina M., Anand, Deepti, Deng, Mei, Richter, Chika T., Nidey, Nichole L., Standley, Jennifer M., Blue, Elizabeth E., Chong, Jessica X., Smith, Joshua D., Kirk, Edwin P., Venselaar, Hanka, Krahn, Katy N., Bokhoven, Hans, Zhou, Huiqing, Cornell, Robert A., Glass, Ian A., Bamshad, Michael J., Nickerson, Deborah A., Murray, Jeffrey C., Lachke, Salil A., Thompson, Thomas B., Buckley, Michael F., Roscioli, Tony
Published in Human mutation (01.10.2019)
Published in Human mutation (01.10.2019)
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Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans
Lansdon, Lisa A, Darbro, Benjamin W, Petrin, Aline L, Hulstrand, Alissa M, Standley, Jennifer M, Brouillette, Rachel B, Long, Abby, Mansilla, M Adela, Cornell, Robert A, Murray, Jeffrey C, Houston, Douglas W, Manak, J Robert
Published in Genetics (Austin) (01.01.2018)
Published in Genetics (Austin) (01.01.2018)
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The fate of human malignant melanoma cells transplanted into zebrafish embryos: Assessment of migration and cell division in the absence of tumor formation
Lee, Lisa M.J., Seftor, Elisabeth A., Bonde, Gregory, Cornell, Robert A., Hendrix, Mary J.C.
Published in Developmental dynamics (01.08.2005)
Published in Developmental dynamics (01.08.2005)
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Aberrant CpG methylation of the TFAP2A gene constitutes a mechanism for loss of TFAP2A expression in human metastatic melanoma
Hallberg, Andrea R, Vorrink, Sabine U, Hudachek, Danielle R, Cramer-Morales, Kimberly, Milhem, Mohammed M, Cornell, Robert A, Domann, Frederick E
Published in Epigenetics (01.12.2014)
Published in Epigenetics (01.12.2014)
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Notch in the pathway: The roles of Notch signaling in neural crest development
Cornell, Robert A., Eisen, Judith S.
Published in Seminars in cell & developmental biology (01.12.2005)
Published in Seminars in cell & developmental biology (01.12.2005)
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