Search Results - Lucy B. Rowe
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Crossover Interference in the Mouse by Karl W. Broman, Lucy B. Rowe, Gary A. Churchill, Ken Paigen
Published 2002Artigo -
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Genome-wide mapping of unselected transcripts from extraembryonic tissue of 7.5-day mouse embryos reveals enrichment in the t-complex and under-representation on the X chromosome by Minoru S.H. Ko, Tracy A. Threat, X. Wang, Joseph Horton, Y. Cui, X. Wang, E.W. Pryor, Josephine R. Paris, J. Wells-Smith, J. Kitchen, Lucy B. Rowe, John J. Eppig, Toshimi Satoh, L. Brant, Hiroyuki Fujiwara, Shinichi Yotsumoto, Hiroshi Nakashima
Published 1998Artigo -
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The Genome of C57BL/6J “Eve”, the Mother of the Laboratory Mouse Genome Reference Strain by Vishal Sarsani, Narayanan Raghupathy, Ian T. Fiddes, Joel Armstrong, Françoise Thibaud‐Nissen, Oraya Zinder, Mohan Bolisetty, Kerstin Howe, Doug Hinerfeld, Xiaoan Ruan, Lucy B. Rowe, Mary Barter, Guruprasad Ananda, Benedict Paten, George M. Weinstock, Gary A. Churchill, Michael V. Wiles, Valérie Schneider, Anuj Srivastava, Laura G. Reinholdt
Published 2019Artigo -
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GPR179 Is Required for Depolarizing Bipolar Cell Function and Is Mutated in Autosomal-Recessive Complete Congenital Stationary Night Blindness by Neal S. Peachey, Thomas A. Ray, Ralph Florijn, Lucy B. Rowe, Trijntje Sjoerdsma, Susana Contreras‐Alcantara, Kenkichi Baba, Gianluca Tosini, Nikita Pozdeyev, P. Michael Iuvone, Pasano Bojang, Jillian N. Pearring, Huibert J. Simonsz, Maria van Genderen, David G. Birch, Elias I. Traboulsi, Allison Dorfman, Irma López, Huanan Ren, Andrew F.X. Goldberg, Patsy M. Nishina, Pierre Lachapelle, Maureen A. McCall, Robert K. Koenekoop, Arthur A. Bergen, Maarten Kamermans, Ronald G. Gregg
Published 2012Artigo -
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Mutations in CTNNA1 cause butterfly-shaped pigment dystrophy and perturbed retinal pigment epithelium integrity by Nicole T.M. Saksens, Mark P. Krebs, Frederieke E. Schoenmaker-Koller, Wanda L. Hicks, Minzhong Yu, Lan-Ying Shi, Lucy B. Rowe, Gayle B. Collin, Jeremy R. Charette, Stef J.F. Letteboer, Kornelia Neveling, Tamara W van Moorsel, Sleiman Abu-Ltaif, Elfride De Baere, Sophie Walraedt, Sandro Banfi, Francesca Simonelli, Frans P.M. Cremers, Camiel J.F. Boon, Ronald Roepman, Bart P. Leroy, Neal S. Peachey, Carel B. Hoyng, Patsy M. Nishina, Anneke I. den Hollander
Published 2015Artigo -
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Mutation discovery in mice by whole exome sequencing by Heather Fairfield, Griffith J Gilbert, Mary Barter, Rebecca R. Corrigan, Michelle Curtain, Yueming Ding, Mark D’Ascenzo, Daniel J. Gerhardt, Chao He, Wenhui Huang, Todd Richmond, Lucy B. Rowe, Frank J. Probst, David E. Bergstrom, Stephen A. Murray, Carol J. Bult, Joel E. Richardson, Benjamin T. Kile, Marta Gut, Jörg Hager, Snævar Sigurðsson, Evan Mauceli, Federica Di Palma, Kerstin Lindblad‐Toh, Michael L. Cunningham, Timothy C. Cox, Monica J. Justice, Mona S. Spector, Scott W. Lowe, Thomas Albert, Leah Rae Donahue, Jeffrey A. Jeddeloh, Jay Shendure, Laura G. Reinholdt
Published 2011Artigo -
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A Multi-Megabase Copy Number Gain Causes Maternal Transmission Ratio Distortion on Mouse Chromosome 2 by John P. Didion, Andrew P. Morgan, Amelia M.-F. Clayshulte, Rachel McMullan, Liran Yadgary, Petko M. Petkov, Timothy A. Bell, Daniel M. Gatti, James J. Crowley, Kunjie Hua, David L. Aylor, Ling Bai, Mark Calaway, Elissa J. Chesler, John E. French, Thomas R. Geiger, Terry J. Gooch, Theodore Garland, Alison H. Harrill, Kent W. Hunter, Leonard McMillan, Matt Holt, Darla R. Miller, Deborah A. O’Brien, Kenneth Paigen, Wenqi Pan, Lucy B. Rowe, Ginger D. Shaw, Petr Šimeček, Patrick F. Sullivan, Karen L. Svenson, George M. Weinstock, David W. Threadgill, Daniel Pomp, Gary A. Churchill, Fernando Pardo‐Manuel de Villena
Published 2015Artigo
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