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Journal Abstract Search

190 related items for PubMed ID: 15366372

  • 1. Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptor.
    Lee D, Cross SH, Strunk KE, Morgan JE, Bailey CL, Jackson IJ, Threadgill DW.
    Mamm Genome; 2004 Jul; 15(7):525-36. PubMed ID: 15366372
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  • 2. Placental and embryonic growth restriction in mice with reduced function epidermal growth factor receptor alleles.
    Dackor J, Caron KM, Threadgill DW.
    Genetics; 2009 Sep; 183(1):207-18. PubMed ID: 19564486
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  • 7. A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.
    Longo-Guess C, Gagnon LH, Bergstrom DE, Johnson KR.
    Hear Res; 2007 Dec; 234(1-2):21-8. PubMed ID: 17967520
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  • 10. N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.
    Rinchik EM, Carpenter DA.
    Genetics; 1999 May; 152(1):373-83. PubMed ID: 10224267
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  • 11. Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Na(v)1.6) and a genetically linked retinal mutation, rd13.
    Buchner DA, Seburn KL, Frankel WN, Meisler MH.
    Mamm Genome; 2004 May; 15(5):344-51. PubMed ID: 15170223
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  • 13. Activation of neu by missense point mutation in the transmembrane domain in schwannomas induced in C3H/HeNCr mice by transplacental exposure to N-nitrosoethylurea.
    Buzard GS, Enomoto T, Anderson LM, Perantoni AO, Devor DE, Rice JM.
    J Cancer Res Clin Oncol; 1999 Dec; 125(12):653-9. PubMed ID: 10592097
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  • 14. Mutation in Sos1 dominantly enhances a weak allele of the EGFR, demonstrating a requirement for Sos1 in EGFR signaling and development.
    Wang DZ, Hammond VE, Abud HE, Bertoncello I, McAvoy JW, Bowtell DD.
    Genes Dev; 1997 Feb 01; 11(3):309-20. PubMed ID: 9030684
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  • 15. Mutant frequencies and loss of heterozygosity induced by N-ethyl-N-nitrosourea in the thymidine kinase gene of L5178Y/TK(+/-)-3.7.2C mouse lymphoma cells.
    Chen T, Harrington-Brock K, Moore MM.
    Mutagenesis; 2002 Mar 01; 17(2):105-9. PubMed ID: 11880538
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  • 16. Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice.
    Michaud EJ, Culiat CT, Klebig ML, Barker PE, Cain KT, Carpenter DJ, Easter LL, Foster CM, Gardner AW, Guo ZY, Houser KJ, Hughes LA, Kerley MK, Liu Z, Olszewski RE, Pinn I, Shaw GD, Shinpock SG, Wymore AM, Rinchik EM, Johnson DK.
    BMC Genomics; 2005 Nov 21; 6():164. PubMed ID: 16300676
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  • 17. Reduced EGFR causes abnormal valvular differentiation leading to calcific aortic stenosis and left ventricular hypertrophy in C57BL/6J but not 129S1/SvImJ mice.
    Barrick CJ, Roberts RB, Rojas M, Rajamannan NM, Suitt CB, O'Brien KD, Smyth SS, Threadgill DW.
    Am J Physiol Heart Circ Physiol; 2009 Jul 21; 297(1):H65-75. PubMed ID: 19448146
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  • 18. An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.
    Barbaric I, Perry MJ, Dear TN, Rodrigues Da Costa A, Salopek D, Marusic A, Hough T, Wells S, Hunter AJ, Cheeseman M, Brown SD.
    Physiol Genomics; 2008 Feb 19; 32(3):311-21. PubMed ID: 17986521
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  • 19. An ENU-induced mutation of Nrg1 causes dilated pupils and a reduction in muscarinic receptors in the sphincter pupillae.
    Chen B, Li K, Zhang F, Zhai G, Gong W, Qiang S, Xue Z.
    PLoS One; 2011 Feb 19; 6(9):e25176. PubMed ID: 21949880
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  • 20. W mutant mice with mild or severe developmental defects contain distinct point mutations in the kinase domain of the c-kit receptor.
    Reith AD, Rottapel R, Giddens E, Brady C, Forrester L, Bernstein A.
    Genes Dev; 1990 Mar 19; 4(3):390-400. PubMed ID: 1692559
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