Systematic reconstruction of cellular trajectories across mouse embryogenesis von Qiu, Chengxiang, Cao, Junyue, Martin, Beth K., Li, Tony, Welsh, Ian C., Srivatsan, Sanjay, Huang, Xingfan, Calderon, Diego, Noble, William Stafford, Disteche, Christine M., Murray, Stephen A., Spielmann, Malte, Moens, Cecilia B., Trapnell, Cole, Shendure, Jay

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Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder von Long, Hannah K., Osterwalder, Marco, Welsh, Ian C., Hansen, Karissa, Davies, James O.J., Liu, Yiran E., Koska, Mervenaz, Adams, Alexander T., Aho, Robert, Arora, Neha, Ikeda, Kazuya, Williams, Ruth M., Sauka-Spengler, Tatjana, Porteus, Matthew H., Mohun, Tim, Dickel, Diane E., Swigut, Tomek, Hughes, Jim R., Higgs, Douglas R., Visel, Axel, Selleri, Licia, Wysocka, Joanna

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The Left-Right Pitx2 Pathway Drives Organ-Specific Arterial and Lymphatic Development in the Intestine von Mahadevan, Aparna, Welsh, Ian C., Sivakumar, Aravind, Gludish, David W., Shilvock, Abigail R., Noden, Drew M., Huss, David, Lansford, Rusty, Kurpios, Natasza A.

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Integration of Left-Right Pitx2 Transcription and Wnt Signaling Drives Asymmetric Gut Morphogenesis via Daam2 von Welsh, Ian C., Thomsen, Michael, Gludish, David W., Alfonso-Parra, Catalina, Bai, Yan, Martin, James F., Kurpios, Natasza A.

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Signaling integration in the rugae growth zone directs sequential SHH signaling center formation during the rostral outgrowth of the palate von Welsh, Ian C., O'Brien, Timothy P.

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Chromatin Architecture of the Pitx2 Locus Requires CTCF- and Pitx2-Dependent Asymmetry that Mirrors Embryonic Gut Laterality von Welsh, Ian C., Kwak, Hojoong, Chen, Frances L., Werner, Melissa, Shopland, Lindsay S., Danko, Charles G., Lis, John T., Zhang, Min, Martin, James F., Kurpios, Natasza A.

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A single-cell time-lapse of mouse prenatal development from gastrula to birth von Qiu, Chengxiang, Martin, Beth K., Welsh, Ian C., Daza, Riza M., Le, Truc-Mai, Huang, Xingfan, Nichols, Eva K., Taylor, Megan L., Fulton, Olivia, O’Day, Diana R., Gomes, Anne Roshella, Ilcisin, Saskia, Srivatsan, Sanjay, Deng, Xinxian, Disteche, Christine M., Noble, William Stafford, Hamazaki, Nobuhiko, Moens, Cecilia B., Kimelman, David, Cao, Junyue, Schier, Alexander F., Spielmann, Malte, Murray, Stephen A., Trapnell, Cole, Shendure, Jay

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Evidence for a Conserved Function in Synapse Formation Reveals Phr1 as a Candidate Gene for Respiratory Failure in Newborn Mice von Burgess, Robert W., Peterson, Kevin A., Johnson, Michael J., Roix, Jeffrey J., Welsh, Ian C., O'Brien, Timothy P.

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The spontaneous mouse mutant low set ears (Lse) is caused by tandem duplication of Fgf3 and Fgf4 von Luzzio, Alana, Edie, Sarah, Palmer, Kristina, Caddle, L. Brianna, Urban, Rachel, Goodwin, Leslie O., Welsh, Ian C., Reinholdt, Laura G., Bergstrom, David E., Cox, Timothy C., Donahue, Leah Rae, Murray, Stephen A.

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Mouse H6 Homeobox 1 (Hmx1) mutations cause cranial abnormalities and reduced body mass von Munroe, Robert J, Prabhu, Vinay, Acland, Greg M, Johnson, Kenneth R, Harris, Belinda S, O'Brien, Tim P, Welsh, Ian C, Noden, Drew M, Schimenti, John C

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Pbx loss in cranial neural crest, unlike in epithelium, results in cleft palate only and a broader midface von Welsh, Ian C., Hart, James, Brown, Joel M., Hansen, Karissa, Rocha Marques, Marcelo, Aho, Robert J., Grishina, Irina, Hurtado, Romulo, Herzlinger, Doris, Ferretti, Elisabetta, Garcia‐Garcia, Maria J., Selleri, Licia

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Notch signaling regulates left-right asymmetry determination by inducing Nodal expression von Krebs, Luke T, Iwai, Naomi, Nonaka, Shigenori, Welsh, Ian C, Lan, Yu, Jiang, Rulang, Saijoh, Yukio, O'Brien, Timothy P, Hamada, Hiroshi, Gridley, Thomas

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Reproductive and Developmental Genomics Retreat at Cornell University, 2012 von Lyndaker, Amy M., Modzelewski, Andrew J., Welsh, Ian C.

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Development of an Enhanced GFP-Based Dual-Color Reporter to Facilitate Genetic Screens for the Recovery of Mutations in Mice von Frank, Aubrey C., Meyers, Kimberly A., Welsh, Ian C., O'Brien, Timothy P.

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Analysis of the Gene Regulatory Program Induced by the Homeobox Transcription Factor Distal-less 3 in Mouse Placenta von Han, Li, Dias Figueiredo, Monica, Berghorn, Kathie A, Iwata, Terri N, Clark-Campbell, Patricia A, Welsh, Ian C, Wang, Wei, O’Brien, Timothy P, Lin, David M, Roberson, Mark S

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A dosage-dependent role for Spry2 in growth and patterning during palate development von Welsh, Ian C., Hagge-Greenberg, Aaron, O’Brien, Timothy P.

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Mendelian gene identification through mouse embryo viability screening von Cacheiro, Pilar, Westerberg, Carl Henrik, Mager, Jesse, Dickinson, Mary E, Nutter, Lauryl M J, Muñoz-Fuentes, Violeta, Hsu, Chih-Wei, Van den Veyver, Ignatia B, Flenniken, Ann M, McKerlie, Colin, Murray, Stephen A, Teboul, Lydia, Heaney, Jason D, Lloyd, K C Kent, Lanoue, Louise, Braun, Robert E, White, Jacqueline K, Creighton, Amie K, Laurin, Valerie, Guo, Ruolin, Qu, Dawei, Wells, Sara, Cleak, James, Bunton-Stasyshyn, Rosie, Stewart, Michelle, Harrisson, Jackie, Mason, Jeremy, Haseli Mashhadi, Hamed, Parkinson, Helen, Mallon, Ann-Marie, Smedley, Damian

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Loss of Late Primitive Streak Mesoderm and Interruption of Left–Right Morphogenesis in the Ednrbs-1Acrg Mutant Mouse von Welsh, Ian C., O'Brien, Timothy P.

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Integration of L-R Pitx2 transcription and Wnt signaling drives asymmetric gut morphogenesis via Daam2 von Welsh, Ian C., Thomsen, Michael, Gludish, David W., Alfonso-Parra, Catalina, Bai, Yan, Martin, James F., Kurpios, Natasza A.

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Loss of late primitive streak mesoderm and interruption of left-right morphogenesis in the Ednrb(s-1Acrg) mutant mouse von Welsh, I C, O'Brien, T P

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