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493 results

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Page 1
Mouse gestation length is genetically determined.
Murray SA, Morgan JL, Kane C, Sharma Y, Heffner CS, Lake J, Donahue LR. Murray SA, et al. PLoS One. 2010 Aug 25;5(8):e12418. doi: 10.1371/journal.pone.0012418. PLoS One. 2010. PMID: 20811634 Free PMC article.
Mouse resources for craniofacial research.
Murray SA. Murray SA. Genesis. 2011 Apr;49(4):190-9. doi: 10.1002/dvg.20722. Epub 2011 Apr 1. Genesis. 2011. PMID: 21309071 Free PMC article. Review.
Mutation discovery in mice by whole exome sequencing.
Fairfield H, Gilbert GJ, Barter M, Corrigan RR, Curtain M, Ding Y, D'Ascenzo M, Gerhardt DJ, He C, Huang W, Richmond T, Rowe L, Probst FJ, Bergstrom DE, Murray SA, Bult C, Richardson J, Kile BT, Gut I, Hager J, Sigurdsson S, Mauceli E, Di Palma F, Lindblad-Toh K, Cunningham ML, Cox TC, Justice MJ, Spector MS, Lowe SW, Albert T, Donahue LR, Jeddeloh J, Shendure J, Reinholdt LG. Fairfield H, et al. Among authors: murray sa. Genome Biol. 2011 Sep 14;12(9):R86. doi: 10.1186/gb-2011-12-9-r86. Genome Biol. 2011. PMID: 21917142 Free PMC article.
Maternal synchronization of gestational length and lung maturation.
Besnard V, Wert SE, Ikegami M, Xu Y, Heffner C, Murray SA, Donahue LR, Whitsett JA. Besnard V, et al. Among authors: murray sa. PLoS One. 2011;6(11):e26682. doi: 10.1371/journal.pone.0026682. Epub 2011 Nov 9. PLoS One. 2011. PMID: 22096492 Free PMC article.
Transcriptional programs controlling perinatal lung maturation.
Xu Y, Wang Y, Besnard V, Ikegami M, Wert SE, Heffner C, Murray SA, Donahue LR, Whitsett JA. Xu Y, et al. Among authors: murray sa. PLoS One. 2012;7(8):e37046. doi: 10.1371/journal.pone.0037046. Epub 2012 Aug 20. PLoS One. 2012. PMID: 22916088 Free PMC article.
Beyond knockouts: cre resources for conditional mutagenesis.
Murray SA, Eppig JT, Smedley D, Simpson EM, Rosenthal N. Murray SA, et al. Mamm Genome. 2012 Oct;23(9-10):587-99. doi: 10.1007/s00335-012-9430-2. Epub 2012 Aug 29. Mamm Genome. 2012. PMID: 22926223 Free PMC article.
Kidney adysplasia and variable hydronephrosis, a new mutation affecting the odd-skipped related 1 gene in the mouse, causes variable defects in kidney development and hydronephrosis.
Davisson MT, Cook SA, Akeson EC, Liu D, Heffner C, Gudis P, Fairfield H, Murray SA. Davisson MT, et al. Among authors: murray sa. Am J Physiol Renal Physiol. 2015 Jun 15;308(12):F1335-42. doi: 10.1152/ajprenal.00410.2014. Epub 2015 Apr 1. Am J Physiol Renal Physiol. 2015. PMID: 25834070 Free PMC article.
Exome sequencing reveals pathogenic mutations in 91 strains of mice with Mendelian disorders.
Fairfield H, Srivastava A, Ananda G, Liu R, Kircher M, Lakshminarayana A, Harris BS, Karst SY, Dionne LA, Kane CC, Curtain M, Berry ML, Ward-Bailey PF, Greenstein I, Byers C, Czechanski A, Sharp J, Palmer K, Gudis P, Martin W, Tadenev A, Bogdanik L, Pratt CH, Chang B, Schroeder DG, Cox GA, Cliften P, Milbrandt J, Murray S, Burgess R, Bergstrom DE, Donahue LR, Hamamy H, Masri A, Santoni FA, Makrythanasis P, Antonarakis SE, Shendure J, Reinholdt LG. Fairfield H, et al. Genome Res. 2015 Jul;25(7):948-57. doi: 10.1101/gr.186882.114. Epub 2015 Apr 27. Genome Res. 2015. PMID: 25917818 Free PMC article.
493 results