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  • Bauschatz JD,Curtain MM,Davisson MT,Lane PW,Donahue LR. 2003. In collaboration: The Jackson laboratory craniofacial resource. Crit Rev Eukaryot Gene Expr 13: 107108.
  • Beaty TH,Murray JC,Marazita ML,Munger RG,Ruczinski I,Hetmanski JB,Liang KY,Wu T,Murray T,Fallin MD,Redett RA,Raymond G,Schwender H,Jin SC,Cooper ME,Dunnwald M,Mansilla MA,Leslie E,Bullard S,Lidral AC,Moreno LM,Menezes R,Vieira AR,Petrin A,Wilcox AJ,Lie RT,Jabs EW,Wu-Chou YH,Chen PK,Wang H,Ye X,Huang S,Yeow V,Chong SS,Jee SH,Shi B,Christensen K,Melbye M,Doheny KF,Pugh EW,Ling H,Castilla EE,Czeizel AE,Ma L,Field LL,Brody L,Pangilinan F,Mills JL,Molloy AM,Kirke PN,Scott JM,Arcos-Burgos M,Scott AF. 2010. A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. Nat Genet 42: 525529.
  • Beckers J,Wurst W,de Angelis MH. 2009. Towards better mouse models: Enhanced genotypes, systemic phenotyping and envirotype modelling. Nat Rev Genet 10: 371380.
  • Bjork BC,Turbe-Doan A,Prysak M,Herron BJ,Beier DR. 2010. Prdm16 is required for normal palatogenesis in mice. Hum Mol Genet 19: 774789.
  • Blake JA,Bult CJ,Kadin JA,Richardson JE,Eppig JT. 2010. The mouse genome database (MGD): Premier model organism resource for mammalian genomics and genetics. Nucleic Acids Res 39: 842848.
  • Brown SD,Chambon P,de Angelis MH. 2005. EMPReSS: Standardized phenotype screens for functional annotation of the mouse genome. Nat Genet 37: 1155.
  • Brown SD,Wurst W,Kuhn R,Hancock JM. 2009. The functional annotation of mammalian genomes: The challenge of phenotyping. Annu Rev Genet 43: 305333.
  • Chesler EJ,Miller DR,Branstetter LR,Galloway LD,Jackson BL,Philip VM,Voy BH,Culiat CT,Threadgill DW,Williams RW,Churchill GA,Johnson DK,Manly KF. 2008. The collaborative cross at Oak Ridge National Laboratory: Developing a powerful resource for systems genetics. Mamm Genome 19: 382389.
  • Churchill GA,Airey DC,Allayee H,Angel JM,Attie AD,Beatty J,Beavis WD,Belknap JK,Bennett B,Berrettini W,Bleich A,Bogue M,Broman KW,Buck KJ,Buckler E,Burmeister M,Chesler EJ,Cheverud JM,Clapcote S,Cook MN,Cox RD,Crabbe JC,Crusio WE,Darvasi A,Deschepper CF,Doerge RW,Farber CR,Forejt J,Gaile D,Garlow SJ,Geiger H,Gershenfeld H,Gordon T,Gu J,Gu W,de Haan G,Hayes NL,Heller C,Himmelbauer H,Hitzemann R,Hunter K,Hsu HC,Iraqi FA,Ivandic B,Jacob HJ,Jansen RC,Jepsen KJ,Johnson DK,Johnson TE,Kempermann G,Kendziorski C,Kotb M,Kooy RF,Llamas B,Lammert F,Lassalle JM,Lowenstein PR,Lu L,Lusis A,Manly KF,Marcucio R,Matthews D,Medrano JF,Miller DR,Mittleman G,Mock BA,Mogil JS,Montagutelli X,Morahan G,Morris DG,Mott R,Nadeau JH,Nagase H,Nowakowski RS,O'Hara BF,Osadchuk AV,Page GP,Paigen B,Paigen K,Palmer AA,Pan HJ,Peltonen-Palotie L,Peirce J,Pomp D,Pravenec M,Prows DR,Qi Z,Reeves RH,Roder J,Rosen GD,Schadt EE,Schalkwyk LC,Seltzer Z,Shimomura K,Shou S,Sillanpaa MJ,Siracusa LD,Snoeck HW,Spearow JL,Svenson K,Tarantino LM,Threadgill D,Toth LA,Valdar W,de Villena FP,Warden C,Whatley S,Williams RW,Wiltshire T,Yi N,Zhang D,Zhang M,Zou F. 2004. The collaborative cross: A community resource for the genetic analysis of complex traits. Nat Genet 36: 11331137.
  • Collins FS,Finnell RH,Rossant J,Wurst W. 2007a. A new partner for the international knockout mouse consortium. Cell 129: 235.
  • Collins FS,Rossant J,Wurst W. 2007b. A mouse for all reasons. Cell 128: 913.
  • D'Ascenzo M,Meacham C,Kitzman J,Middle C,Knight J,Winer R,Kukricar M,Richmond T,Albert TJ,Czechanski A,Donahue LR,Affourtit J,Jeddeloh JA,Reinholdt L. 2009. Mutation discovery in the mouse using genetically guided array capture and resequencing. Mamm Genome 20: 424436.
  • Davisson MT,Taft RA. 2006. Strategies for managing an ever increasing mutant mouse repository. Brain Res 1091: 255257.
  • Diehl SR,Erickson RP. 1997. Genome scan for teratogen-induced clefting susceptibility loci in the mouse: Evidence of both allelic and locus heterogeneity distinguishing cleft lip and cleft palate. Proc Natl Acad Sci USA 94: 52315236.
  • Donahue LR,Chang B,Mohan S,Miyakoshi N,Wergedal JE,Baylink DJ,Hawes NL,Rosen CJ,Ward-Bailey P,Zheng QY,Bronson RT,Johnson KR,Davisson MT. 2003. A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis. J Bone Miner Res 18: 16121621.
  • Eppig JT,Strivens M. 1999. Finding a mouse: The international mouse strain resource (IMSR). Trends Genet 15: 8182.
  • Finger JH,Smith CM,Hayamizu TF,McCright IJ,Eppig JT,Kadin JA,Richardson JE,Ringwald M. 2010. The mouse gene expression database (GXD): 2011 update. Nucleic Acids Res 39S1: D835D841.
  • Friedel RH,Seisenberger C,Kaloff C,Wurst W. 2007. EUCOMM—The European conditional mouse mutagenesis program. Brief Funct Genomic Proteomic 6: 180185.
  • Gondo Y. 2008. Trends in large-scale mouse mutagenesis: From genetics to functional genomics. Nat Rev Genet 9: 803810.
  • Gong S,Doughty M,Harbaugh CR,Cummins A,Hatten ME,Heintz N,Gerfen CR. 2007. Targeting Cre recombinase to specific neuron populations with bacterial artificial chromosome constructs. J Neurosci 27: 98179823.
  • Grieder FB. 2002. Mutant mouse regional resource center program: A resource for distribution of mouse models for biomedical research. Comp Med 52: 203.
  • Gritli-Linde A. 2008. The etiopathogenesis of cleft lip and cleft palate: Usefulness and caveats of mouse models. Curr Top Dev Biol 84: 37138.
  • Jiang R,Bush JO,Lidral AC. 2006. Development of the upper lip: Morphogenetic and molecular mechanisms. Dev Dyn 235: 11521166.
  • Juriloff DM,Harris MJ,McMahon AP,Carroll TJ,Lidral AC. 2006. Wnt9b is the mutated gene involved in multifactorial nonsyndromic cleft lip with or without cleft palate in A/WySn mice, as confirmed by a genetic complementation test. Birth Defects Res A Clin Mol Teratol 76: 574579.
  • Lorenz-Depiereux B,Guido VE,Johnson KR,Zheng QY,Gagnon LH,Bauschatz JD,Davisson MT,Washburn LL,Donahue LR,Strom TM,Eicher EM. 2004. New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice. Mamm Genome 15: 151161.
  • Madisen L,Zwingman TA,Sunkin SM,Oh SW,Zariwala HA,Gu H,Ng LL,Palmiter RD,Hawrylycz MJ,Jones AR,Lein ES,Zeng H. 2010. A robust and high-throughput Cre reporting and characterization system for the whole mouse brain. Nat Neurosci 13: 133140.
  • Mangold E,Ludwig KU,Birnbaum S,Baluardo C,Ferrian M,Herms S,Reutter H,de Assis NA,Chawa TA,Mattheisen M,Steffens M,Barth S,Kluck N,Paul A,Becker J,Lauster C,Schmidt G,Braumann B,Scheer M,Reich RH,Hemprich A,Potzsch S,Blaumeiser B,Moebus S,Krawczak M,Schreiber S,Meitinger T,Wichmann HE,Steegers-Theunissen RP,Kramer FJ,Cichon S,Propping P,Wienker TF,Knapp M,Rubini M,Mossey PA,Hoffmann P,Nothen MM. 2010. Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. Nat Genet 42: 2426.
  • Mao M,Thedens DR,Chang B,Harris BS,Zheng QY,Johnson KR,Donahue LR,Anderson MG. 2009. The podosomal-adaptor protein SH3PXD2B is essential for normal postnatal development. Mamm Genome 20: 462475.
  • Moore M,Committe IS. 2010. The international mouse phenotyping consortium: Initial business plan. Available at http://nihroadmap.nih.gov/kompz/IMPC-Business-Plan.
  • Nagy A,Mar L. 2001. Creation and use of a Cre recombinase transgenic database. Methods Mol Biol 158: 95106.
  • Nagy A,Mar L,Watts G. 2009. Creation and use of a cre recombinase transgenic database. Methods Mol Biol 530: 365378.
  • Odgren PR,Pratt CH,Mackay CA,Mason-Savas A,Curtain M,Shopland L,Ichicki T,Sundberg JP,Donahue LR. 2010. Disheveled hair and ear (Dhe), a spontaneous mouse Lmna mutation modeling human laminopathies. PLoS One 5: e9959.
  • Peters LL,Robledo RF,Bult CJ,Churchill GA,Paigen BJ,Svenson KL. 2007. The mouse as a model for human biology: A resource guide for complex trait analysis. Nat Rev Genet 8: 5869.
  • Ringwald M,Iyer V,Mason JC,Stone KR,Tadepally HD,Kadin JA,Bult CJ,Eppig JT,Oakley DJ,Briois S,Stupka E,Maselli V,Smedley D,Liu S,Hansen J,Baldock R,Hicks GG,Skarnes WC. 2010. The IKMC web portal: A central point of entry to data and resources from the international knockout mouse consortium. Nucleic Acids Res 39S1: D849D855.
  • Rizzo MA,Springer GH,Granada B,Piston DW. 2004. An improved cyan fluorescent protein variant useful for FRET. Nat Biotechnol 22: 445449.
  • Smedley D,Salimova E,Rosenthal N. 2010. Cre recombinase resources for conditional mouse mutagenesis. Methods. Epub ahead of print doi: 10.1016/j. physletb.2003.10.071
  • Soriano P. 1999. Generalized lacZ expression with the ROSA26 Cre reporter strain. Nat Genet 21: 7071.
  • Stottmann RW,Bjork BC,Doyle JB,Beier DR. 2010. Identification of a Van der Woude syndrome mutation in the cleft palate 1 mutant mouse. Genesis 48: 303308.
  • Szymczak AL,Workman CJ,Wang Y,Vignali KM,Dilioglou S,Vanin EF,Vignali DA. 2004. Correction of multi-gene deficiency in vivo using a single “self-cleaving” 2A peptide-based retroviral vector. Nat Biotechnol 22: 589594.
  • Valenzuela DM,Murphy AJ,Frendewey D,Gale NW,Economides AN,Auerbach W,Poueymirou WT,Adams NC,Rojas J,Yasenchak J,Chernomorsky R,Boucher M,Elsasser AL,Esau L,Zheng J,Griffiths JA,Wang X,Su H,Xue Y,Dominguez MG,Noguera I,Torres R,Macdonald LE,Stewart AF,DeChiara TM,Yancopoulos GD. 2003. High-throughput engineering of the mouse genome coupled with high-resolution expression analysis. Nat Biotechnol 21: 652659.
  • Visel A,Blow MJ,Li Z,Zhang T,Akiyama JA,Holt A,Plajzer-Frick I,Shoukry M,Wright C,Chen F,Afzal V,Ren B,Rubin EM,Pennacchio LA. 2009. ChIP-seq accurately predicts tissue-specific activity of enhancers. Nature 457: 854858.
  • Visel A,Prabhakar S,Akiyama JA,Shoukry M,Lewis KD,Holt A,Plajzer-Frick I,Afzal V,Rubin EM,Pennacchio LA. 2008. Ultraconservation identifies a small subset of extremely constrained developmental enhancers. Nat Genet 40: 158160.
  • Warming S,Costantino N,Court DL,Jenkins NA,Copeland NG. 2005. Simple and highly efficient BAC recombineering using galK selection. Nucleic Acids Res 33: e36.
  • Wilkinson P,Sengerova J,Matteoni R,Chen CK,Soulat G,Ureta-Vidal A,Fessele S,Hagn M,Massimi M,Pickford K,Butler RH,Marschall S,Mallon AM,Pickard A,Raspa M,Scavizzi F,Fray M,Larrigaldie V,Leyritz J,Birney E,Tocchini-Valentini GP,Brown S,Herault Y,Montoliu L,de Angelis MH,Smedley D. 2010. EMMA—Mouse mutant resources for the international scientific community. Nucleic Acids Res 38: D570D576.