Monica J. Justice - Publications

The University of Tennessee, Knoxville, TN, United States 
Molecular Biology, Genetics

109 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Dickinson ME, Flenniken AM, Ji X, Teboul L, Wong MD, White JK, Meehan TF, Weninger WJ, Westerberg H, Adissu H, Baker CN, Bower L, Brown JM, Caddle LB, Chiani F, ... ... Justice MJ, et al. High-throughput discovery of novel developmental phenotypes. Nature. PMID 27626380 DOI: 10.1038/Nature19356  0.32
2016 Justice MJ, Dhillon P. Using the mouse to model human disease: Increasing validity and reproducibility Dmm Disease Models and Mechanisms. 9: 101-103. DOI: 10.1242/dmm.024547  0.32
2014 Sen P, Dharmadhikari AV, Majewski T, Mohammad MA, Kalin TV, Zabielska J, Ren X, Bray M, Brown HM, Welty S, Thevananther S, Langston C, Szafranski P, Justice MJ, Kalinichenko VV, et al. Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice. Plos One. 9: e94390. PMID 24722050 DOI: 10.1371/Journal.Pone.0094390  0.32
2014 Allache R, Lachance S, Guyot MC, De Marco P, Merello E, Justice MJ, Capra V, Kibar Z. Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway. Human Molecular Genetics. 23: 1687-99. PMID 24203697 DOI: 10.1093/Hmg/Ddt558  0.32
2014 Allache R, Lachance S, Guyot MC, de Marco P, Merello E, Justice MJ, Capra V, Kibar Z. Corrigendum to Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway [Human molecular genetics 23, 7, (2013) 1687-1699] DOI: 10.1093/hmg/ddt558 Human Molecular Genetics. 23: 4185. DOI: 10.1093/Hmg/Ddu192  0.32
2013 Probst FJ, Corrigan RR, Del Gaudio D, Salinger AP, Lorenzo I, Gao SS, Chiu I, Xia A, Oghalai JS, Justice MJ. A point mutation in the gene for asparagine-linked glycosylation 10B (Alg10b) causes nonsyndromic hearing impairment in mice (Mus musculus). Plos One. 8: e80408. PMID 24303013 DOI: 10.1371/Journal.Pone.0080408  0.32
2013 Carofino BL, Ayanga B, Justice MJ. A mouse model for inducible overexpression of Prdm14 results in rapid-onset and highly penetrant T-cell acute lymphoblastic leukemia (T-ALL) Dmm Disease Models and Mechanisms. 6: 1494-1506. PMID 24046360 DOI: 10.1242/Dmm.012575  0.32
2013 Buchovecky CM, Turley SD, Brown HM, Kyle SM, McDonald JG, Liu B, Pieper AA, Huang W, Katz DM, Russell DW, Shendure J, Justice MJ. A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome. Nature Genetics. 45: 1013-20. PMID 23892605 DOI: 10.1038/Ng.2714  0.32
2013 Justice M. Of mice and men, and medicine: an interview with Monica Justice Disease Models &Amp; Mechanisms. 6: 871-873. PMID 23828642 DOI: 10.1242/Dmm.011809  0.32
2013 Wiszniewski W, Hunter JV, Hanchard NA, Willer JR, Shaw C, Tian Q, Illner A, Wang X, Cheung SW, Patel A, Campbell IM, Gelowani V, Hixson P, Ester AR, Azamian MS, ... ... Justice MJ, et al. TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. American Journal of Human Genetics. 93: 197-210. PMID 23810381 DOI: 10.1016/J.Ajhg.2013.05.027  0.32
2013 Cagan RL, Justice MJ, Tidmarsh GF. Bridging the gap between basic and applied biology: towards preclinical translation. Disease Models & Mechanisms. 6: 559-61. PMID 23616075 DOI: 10.1242/Dmm.012450  0.32
2013 Nakamura H, Cook RN, Justice MJ. Mouse Tenm4 is required for mesoderm induction. Bmc Developmental Biology. 13: 9. PMID 23521771 DOI: 10.1186/1471-213X-13-9  0.32
2013 Adams D, Baldock R, Bhattacharya S, Copp AJ, Dickinson M, Greene ND, Henkelman M, Justice M, Mohun T, Murray SA, Pauws E, Raess M, Rossant J, Weaver T, West D. Bloomsbury report on mouse embryo phenotyping: recommendations from the IMPC workshop on embryonic lethal screening. Disease Models & Mechanisms. 6: 571-9. PMID 23519032 DOI: 10.1242/Dmm.011833  0.32
2013 Bartnikas TB, Steinbicker AU, Campagna DR, Blevins S, Woodward LS, Herrera C, Bloch KD, Justice MJ, Fleming MD. Identification and characterization of a novel murine allele of Tmprss6. Haematologica. 98: 854-61. PMID 23300183 DOI: 10.3324/Haematol.2012.074617  0.32
2013 Jiang Z, Zhu L, Hu L, Slesnick TC, Pautler RG, Justice MJ, Belmont JW. Zic3 is required in the extra-cardiac perinodal region of the lateral plate mesoderm for left-right patterning and heart development. Human Molecular Genetics. 22: 879-89. PMID 23184148 DOI: 10.1093/Hmg/Dds494  0.32
2013 Adams D, Baldock R, Bhattacharya S, Copp AJ, Dickinson M, Greene NDE, Henkelman M, Justice M, Mohun T, Murray SA, Pauws E, Raess M, Rossant J, Weaver T, West D. Bloomsbury report on mouse embryo phenotyping: Recommendations from the IMPC workshop on embryonic lethal screening (DMM Disease Models and Mechanisms 6, (571-579)) Dmm Disease Models and Mechanisms. 6: 1049. DOI: 10.1242/dmm.012898  0.32
2012 Simko SJ, Voicu H, Carofino BL, Justice MJ. Mouse Lymphoblastic Leukemias Induced by Aberrant Prdm14 Expression Demonstrate Widespread Copy Number Alterations Also Found in Human ALL. Cancers. 4: 1050-1066. PMID 23487523 DOI: 10.3390/Cancers4041050  0.32
2012 Lossie AC, Lo CL, Baumgarner KM, Cramer MJ, Garner JP, Justice MJ. ENU mutagenesis reveals that Notchless homolog 1 (Drosophila) affects Cdkn1a and several members of the Wnt pathway during murine pre-implantation development. Bmc Genetics. 13: 106. PMID 23231322 DOI: 10.1186/1471-2156-13-106  0.32
2012 Katz DM, Berger-Sweeney JE, Eubanks JH, Justice MJ, Neul JL, Pozzo-Miller L, Blue ME, Christian D, Crawley JN, Giustetto M, Guy J, Howell CJ, Kron M, Nelson SB, Samaco RC, et al. Preclinical research in Rett syndrome: setting the foundation for translational success. Disease Models & Mechanisms. 5: 733-45. PMID 23115203 DOI: 10.1242/Dmm.011007  0.32
2012 Han HJ, Allen CC, Buchovecky CM, Yetman MJ, Born HA, Marin MA, Rodgers SP, Song BJ, Lu HC, Justice MJ, Probst FJ, Jankowsky JL. Strain background influences neurotoxicity and behavioral abnormalities in mice expressing the tetracycline transactivator. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 32: 10574-86. PMID 22855807 DOI: 10.1523/Jneurosci.0893-12.2012  0.32
2011 Larina IV, Larin KV, Justice MJ, Dickinson ME. Optical Coherence Tomography for live imaging of mammalian development. Current Opinion in Genetics & Development. 21: 579-84. PMID 21962442 DOI: 10.1016/J.Gde.2011.09.004  0.32
2011 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, ... ... Justice MJ, et al. Mutation discovery in mice by whole exome sequencing. Genome Biology. 12: R86. PMID 21917142 DOI: 10.1186/Gb-2011-12-9-R86  0.32
2011 Zheng L, Michelson Y, Freger V, Avraham Z, Venken KJ, Bellen HJ, Justice MJ, Wides R. Drosophila Ten-m and filamin affect motor neuron growth cone guidance. Plos One. 6: e22956. PMID 21857973 DOI: 10.1371/Journal.Pone.0022956  0.32
2011 Justice MJ, Siracusa LD, Stewart AF. Technical approaches for mouse models of human disease Dmm Disease Models and Mechanisms. 4: 305-310. PMID 21558063 DOI: 10.1242/Dmm.000901  0.32
2011 Guyot MC, Bosoi CM, Kharfallah F, Reynolds A, Drapeau P, Justice M, Gros P, Kibar Z. A novel hypomorphic Looptail allele at the planar cell polarity Vangl2 gene. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 240: 839-49. PMID 21404367 DOI: 10.1002/Dvdy.22577  0.32
2010 Justice MJ, Hirschi KK. The role of quaking in mammalian embryonic development. Advances in Experimental Medicine and Biology. 693: 82-92. PMID 21189687 DOI: 10.1007/978-1-4419-7005-3_6  0.32
2010 Probst FJ, Justice MJ. Mouse mutagenesis with the chemical supermutagen ENU. Methods in Enzymology. 477: 297-312. PMID 20699147 DOI: 10.1016/S0076-6879(10)77015-4  0.32
2010 Saleem AN, Chen YH, Baek HJ, Hsiao YW, Huang HW, Kao HJ, Liu KM, Shen LF, Song IW, Tu CP, Wu JY, Kikuchi T, Justice MJ, Yen JJ, Chen YT. Mice with alopecia, osteoporosis, and systemic amyloidosis due to mutation in Zdhhc13, a gene coding for palmitoyl acyltransferase. Plos Genetics. 6: e1000985. PMID 20548961 DOI: 10.1371/Journal.Pgen.1000985  0.32
2010 Kamp A, Peterson MA, Svenson KL, Bjork BC, Hentges KE, Rajapaksha TW, Moran J, Justice MJ, Seidman JG, Seidman CE, Moskowitz IP, Beier DR. Genome-wide identification of mouse congenital heart disease loci. Human Molecular Genetics. 19: 3105-13. PMID 20511334 DOI: 10.1093/Hmg/Ddq211  0.32
2009 Boles MK, Wilkinson BM, Wilming LG, Liu B, Probst FJ, Harrow J, Grafham D, Hentges KE, Woodward LP, Maxwell A, Mitchell K, Risley MD, Johnson R, Hirschi K, Lupski JR, ... ... Justice MJ, et al. Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin. Plos Genetics. 5: e1000759. PMID 20011118 DOI: 10.1371/Journal.Pgen.1000759  0.32
2009 Zhang Z, Shen X, Gude DR, Wilkinson BM, Justice MJ, Flickinger CJ, Herr JC, Eddy EM, Strauss JF. MEIG1 is essential for spermiogenesis in mice. Proceedings of the National Academy of Sciences of the United States of America. 106: 17055-60. PMID 19805151 DOI: 10.1073/Pnas.0906414106  0.32
2009 Sharkey LM, Cheng X, Drews V, Buchner DA, Jones JM, Justice MJ, Waxman SG, Dib-Hajj SD, Meisler MH. The ataxia3 mutation in the N-terminal cytoplasmic domain of sodium channel Na(v)1.6 disrupts intracellular trafficking. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 2733-41. PMID 19261867 DOI: 10.1523/Jneurosci.6026-08.2009  0.32
2008 Justice MJ. Removing the cloak of invisibility: Phenotyping the mouse Dmm Disease Models and Mechanisms. 1: 109-112. PMID 19048073 DOI: 10.1242/Dmm.001057  0.32
2008 Dettman EJ, Justice MJ. The zinc finger SET domain gene Prdm14 Is overexpressed in lymphoblastic lymphomas with retroviral insertions at Evi32 Plos One. 3. PMID 19043588 DOI: 10.1371/Journal.Pone.0003823  0.32
2008 Probst FJ, Cooper ML, Cheung SW, Justice MJ. Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome. The Journal of Heredity. 99: 512-7. PMID 18499648 DOI: 10.1093/Jhered/Esn027  0.32
2008 Tobin JL, Di Franco M, Eichers E, May-Simera H, Garcia M, Yan J, Quinlan R, Justice MJ, Hennekam RC, Briscoe J, Tada M, Mayor R, Burns AJ, Lupski JR, Hammond P, et al. Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome. Proceedings of the National Academy of Sciences of the United States of America. 105: 6714-9. PMID 18443298 DOI: 10.1073/Pnas.0707057105  0.32
2008 Salinger AP, Justice MJ. Mouse mutagenesis using N-ethyl-N-nitrosourea (ENU) Cold Spring Harbor Protocols. 3. DOI: 10.1101/pdb.prot4985  0.32
2007 Weiser KC, Liu B, Hansen GM, Skapura D, Hentges KE, Yarlagadda S, Morse Iii HC, Justice MJ. Retroviral insertions in the VISION database identify molecular pathways in mouse lymphoid leukemia and lymphoma. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 18: 709-22. PMID 17926094 DOI: 10.1007/S00335-007-9060-2  0.32
2007 Kile BT, Panopoulos AD, Stirzaker RA, Hacking DF, Tahtamouni LH, Willson TA, Mielke LA, Henley KJ, Zhang JG, Wicks IP, Stevenson WS, Nurden P, Watowich SS, Justice MJ. Mutations in the cofilin partner Aip1/Wdr1 cause autoinflammatory disease and macrothrombocytopenia. Blood. 110: 2371-80. PMID 17515402 DOI: 10.1182/Blood-2006-10-055087  0.32
2007 Hentges KE, Pollock DD, Liu B, Justice MJ. Regional variation in the density of essential genes in mice. Plos Genetics. 3: e72. PMID 17480122 DOI: 10.1371/Journal.Pgen.0030072  0.32
2007 Castillo A, Justice MJ. The kinesin related motor protein, Eg5, is essential for maintenance of pre-implantation embryogenesis Biochemical and Biophysical Research Communications. 357: 694-699. PMID 17449012 DOI: 10.1016/J.Bbrc.2007.04.021  0.32
2006 Meehan TP, Tabeta K, Du X, Woodward LS, Firozi K, Beutler B, Justice MJ. Point mutations in the melanocortin-4 receptor cause variable obesity in mice. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 17: 1162-71. PMID 17143585 DOI: 10.1007/S00335-006-0073-Z  0.32
2006 Eichers ER, Abd-El-Barr MM, Paylor R, Lewis RA, Bi W, Lin X, Meehan TP, Stockton DW, Wu SM, Lindsay E, Justice MJ, Beales PL, Katsanis N, Lupski JR. Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity. Human Genetics. 120: 211-26. PMID 16794820 DOI: 10.1007/S00439-006-0197-Y  0.32
2006 Frese KK, Latorre IJ, Chung SH, Caruana G, Bernstein A, Jones SN, Donehower LA, Justice MJ, Garner CC, Javier RT. Oncogenic function for the Dlg1 mammalian homolog of the Drosophila discs-large tumor suppressor. The Embo Journal. 25: 1406-17. PMID 16511562 DOI: 10.1038/Sj.Emboj.7601030  0.32
2006 Hentges KE, Nakamura H, Furuta Y, Yu Y, Thompson DM, O'Brien W, Bradley A, Justice MJ. Novel lethal mouse mutants produced in balancer chromosome screens. Gene Expression Patterns : Gep. 6: 653-65. PMID 16466971 DOI: 10.1016/J.Modgep.2005.11.015  0.32
2005 Noveroske JK, Hardy R, Dapper JD, Vogel H, Justice MJ. A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 672-82. PMID 16245024 DOI: 10.1007/S00335-005-0035-X  0.32
2005 Lossie AC, Meehan TP, Castillo A, Zheng L, Weiser KC, Strivens MA, Justice MJ. 18th international mouse genome conference. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 471-5. PMID 16151691 DOI: 10.1007/S00335-004-4001-9  0.32
2005 Weiser KC, Justice MJ. Cancer biology: Sleeping Beauty awakens. Nature. 436: 184-6. PMID 16015313 DOI: 10.1038/436184A  0.32
2005 Dapper JD, Justice MJ. Defining the breakpoints of the quaking(viable) mouse mutation reveals a duplication from a Parkin intron. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 1369-74. PMID 16001410 DOI: 10.1002/mds.20595  0.32
2005 Bi W, Ohyama T, Nakamura H, Yan J, Visvanathan J, Justice MJ, Lupski JR. Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome. Human Molecular Genetics. 14: 983-95. PMID 15746153 DOI: 10.1093/Hmg/Ddi085  0.32
2005 Pask AJ, Kanasaki H, Kaiser UB, Conn PM, Janovick JA, Stockton DW, Hess DL, Justice MJ, Behringer RR. A novel mouse model of hypogonadotrophic hypogonadism: N-ethyl-N-nitrosourea-induced gonadotropin-releasing hormone receptor gene mutation. Molecular Endocrinology (Baltimore, Md.). 19: 972-81. PMID 15625238 DOI: 10.1210/Me.2004-0192  0.32
2005 Hentges KE, Weiser KC, Schountz T, Woodward LS, Morse HC, Justice MJ. Evi3, a zinc-finger protein related to EBFAZ, regulates EBF activity in B-cell leukemia. Oncogene. 24: 1220-30. PMID 15580294 DOI: 10.1038/Sj.Onc.1208243  0.32
2005 Lossie AC, Nakamura H, Thomas SE, Justice MJ. Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation. Genetics. 169: 285-99. PMID 15489520 DOI: 10.1534/Genetics.104.034967  0.32
2004 Clark AT, Goldowitz D, Takahashi JS, Vitaterna MH, Siepka SM, Peters LL, Frankel WN, Carlson GA, Rossant J, Nadeau JH, Justice MJ. Implementing large-scale ENU mutagenesis screens in North America. Genetica. 122: 51-64. PMID 15619961 DOI: 10.1007/S10709-004-1436-6  0.32
2004 Justice MJ. From the atomic age to the genome project Genetica. 122: 3-7. PMID 15619956 DOI: 10.1007/S10709-004-1440-X  0.32
2004 Smyth I, Du X, Taylor MS, Justice MJ, Beutler B, Jackson IJ. The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis Proceedings of the National Academy of Sciences of the United States of America. 101: 13560-13565. PMID 15345741 DOI: 10.1073/Pnas.0402760101  0.32
2004 Lorenzetti D, Bishop CE, Justice MJ. Deletion of the Parkin coregulated gene causes male sterility in the quaking(viable) mouse mutant. Proceedings of the National Academy of Sciences of the United States of America. 101: 8402-7. PMID 15148410 DOI: 10.1073/Pnas.0401832101  0.32
2004 Hentges KE, Justice MJ. Checks and balancers: Balancer chromosomes to facilitate genome annotation Trends in Genetics. 20: 252-259. PMID 15145578 DOI: 10.1016/J.Tig.2004.04.004  0.32
2004 Hentges KE, Kyttälä M, Justice MJ, Peltonen L. Comparative physical maps of the human and mouse Meckel syndrome critical regions Mammalian Genome. 15: 252-264. PMID 15112103 DOI: 10.1007/S00335-003-2303-Y  0.32
2004 Singer JB, Hill AE, Burrage LC, Olszens KR, Song J, Justice M, O'Brien WE, Conti DV, Witte JS, Lander ES, Nadeau JH. Genetic dissection of complex traits with chromosome substitution strains of mice. Science (New York, N.Y.). 304: 445-8. PMID 15031436 DOI: 10.1126/Science.1093139  0.32
2004 Bialek P, Kern B, Yang X, Schrock M, Sosic D, Hong N, Wu H, Yu K, Ornitz DM, Olson EN, Justice MJ, Karsenty G. A twist code determines the onset of osteoblast differentiation. Developmental Cell. 6: 423-35. PMID 15030764 DOI: 10.1016/S1534-5807(04)00058-9  0.32
2004 Clark AT, Firozi K, Justice MJ. Mutations in a novel locus on mouse chromosome 11 resulting in male infertility associated with defects in microtubule assembly and sperm tail function. Biology of Reproduction. 70: 1317-24. PMID 14711786 DOI: 10.1095/Biolreprod.103.020628  0.32
2003 George A, Morse HC, Justice MJ. The homeobox gene Hex induces T-cell-derived lymphomas when overexpressed in hematopoietic precursor cells. Oncogene. 22: 6764-73. PMID 14555989 DOI: 10.1038/Sj.Onc.1206822  0.32
2003 Yan J, Walz K, Nakamura H, Carattini-Rivera S, Zhao Q, Vogel H, Wei N, Justice MJ, Bradley A, Lupski JR. COP9 signalosome subunit 3 is essential for maintenance of cell proliferation in the mouse embryonic epiblast. Molecular and Cellular Biology. 23: 6798-808. PMID 12972600 DOI: 10.1128/Mcb.23.19.6798-6808.2003  0.32
2003 Kile BT, Hentges KE, Clark AT, Nakamura H, Salinger AP, Liu B, Box N, Stockton DW, Johnson RL, Behringer RR, Bradley A, Justice MJ. Functional genetic analysis of mouse chromosome 11. Nature. 425: 81-6. PMID 12955145 DOI: 10.1038/Nature01865  0.32
2003 Kile BT, Mason-Garrison CL, Justice MJ. Sex and strain-related differences in the peripheral blood cell values of inbred mouse strains Mammalian Genome. 14: 81-85. PMID 12532271 DOI: 10.1007/S00335-002-2160-0  0.32
2003 Klysik J, Justice MJ, Bradley A. Chromosome engineering and ENU mutagenesis: Their use for defining gene function Current Genomics. 4: 37-50. DOI: 10.2174/1389202033350155  0.32
2002 Hentges KE, Yarlagadda SP, Justice MJ. Tnfrsf13c (Baffr) is mis-expressed in tumors with murine leukemia virus insertions at Lvis22 Genomics. 80: 204-212. PMID 12160734 DOI: 10.1006/Geno.2002.6812  0.32
2002 Tsai TF, Chen KS, Weber JS, Justice MJ, Beaudet AL. Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice. Human Molecular Genetics. 11: 1659-68. PMID 12075010 DOI: 10.1093/Hmg/11.14.1659  0.32
2002 Noveroske JK, Lai L, Gaussin V, Northrop JL, Nakamura H, Hirschi KK, Justice MJ. Quaking is essential for blood vessel development. Genesis (New York, N.Y. : 2000). 32: 218-30. PMID 11892011 DOI: 10.1002/Gene.10060  0.32
2002 Herron BJ, Lu W, Rao C, Liu S, Peters H, Bronson RT, Justice MJ, McDonald JD, Beier DR. Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis. Nature Genetics. 30: 185-9. PMID 11818962 DOI: 10.1038/Ng812  0.32
2001 Ohtoshi A, Justice MJ, Behringer RR. Isolation and characterization of Vsx1, a novel mouse CVC paired-like homeobox gene expressed during embryogenesis and in the retina Biochemical and Biophysical Research Communications. 286: 133-140. PMID 11485319 DOI: 10.1006/Bbrc.2001.5372  0.32
2001 Kibar Z, Vogan KJ, Groulx N, Justice MJ, Underhill DA, Gros P. Ltap, a mammalian homolog of Drosophila Strabismus/Van Gogh, is altered in the mouse neural tube mutant Loop-tail. Nature Genetics. 28: 251-5. PMID 11431695 DOI: 10.1038/90081  0.32
2001 Hong HK, Noveroske JK, Headon DJ, Liu T, Sy MS, Justice MJ, Chakravarti A. The winged helix/forkhead transcription factor Foxq1 regulates differentiation of hair in satin mice. Genesis (New York, N.Y. : 2000). 29: 163-71. PMID 11309849 DOI: 10.1002/Gene.1020  0.32
2001 Nadeau JH, Balling R, Barsh G, Beier D, Brown SD, Bucan M, Camper S, Carlson G, Copeland N, Eppig J, Fletcher C, Frankel WN, Ganten D, Goldowitz D, Goodnow C, ... ... Justice M, et al. Sequence interpretation. Functional annotation of mouse genome sequences. Science (New York, N.Y.). 291: 1251-5. PMID 11233449 DOI: 10.1126/Science.1058244  0.32
2000 Justice MJ. Capitalizing on large-scale mouse mutagenesis screens Nature Reviews Genetics. 1: 109-115. PMID 11253650 DOI: 10.1038/35038549  0.32
2000 Swiergiel JJ, Funderburgh JL, Justice MJ, Conrad GW. Developmental eye and neural tube defects in the eye blebs mouse. Developmental Dynamics : An Official Publication of the American Association of Anatomists. 219: 21-7. PMID 10974668 DOI: 10.1002/1097-0177(2000)9999:9999<::Aid-Dvdy1030>3.0.Co;2-S  0.32
2000 Noveroske JK, Weber JS, Justice MJ. The mutagenic action of N-ethyl-N-nitrosourea in the mouse Mammalian Genome. 11: 478-483. PMID 10886009 DOI: 10.1007/S003350010093  0.32
2000 Denny P, Justice MJ. Mouse as the measure of man? Trends in Genetics. 16: 283-287. PMID 10858655 DOI: 10.1016/S0168-9525(00)02039-4  0.32
2000 Weber JS, Salinger A, Justice MJ. Optimal N-ethyl-N-nitrosourea (ENU) doses for inbred mouse strains Genesis. 26: 230-233. PMID 10748459 DOI: 10.1002/(Sici)1526-968X(200004)26:4<230::Aid-Gene20>3.0.Co;2-S  0.32
2000 Hansen GM, Skapura D, Justice MJ. Genetic profile of insertion mutations in mouse leukemias and lymphomas Genome Research. 10: 237-243. PMID 10673281 DOI: 10.1101/Gr.10.2.237  0.32
2000 Dunn WC, Jacobson SC, Waters LC, Kroutchinina N, Khandurina J, Foote RS, Justice MJ, Stubbs LJ, Ramsey JM. PCR amplification and analysis of simple sequence length polymorphisms in mouse DNA using a single microchip device. Analytical Biochemistry. 277: 157-60. PMID 10610701 DOI: 10.1006/Abio.1999.4397  0.32
2000 Simpson EH, Suffolk R, Bell JA, Jordan SA, Johnson DK, Hunsicker PR, Weber JS, Justice MJ, Jackson IJ. A comparative transcript map and candidates for mutant phenotypes in the Tyrp1 (brown) deletion complex homologous to human 9p21-23. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 58-63. PMID 10602994 DOI: 10.1007/S003350010011  0.32
1999 Hansen GM, Justice MJ. Activation of Hex and mEg5 by retroviral insertion may contribute to mouse B-cell leukemia Oncogene. 18: 6531-6539. PMID 10597256 DOI: 10.1038/Sj.Onc.1203023  0.32
1999 Justice MJ, Noveroske JK, Weber JS, Zheng B, Bradley A. Mouse ENU mutagenesis Human Molecular Genetics. 8: 1955-1963. PMID 10469849 DOI: 10.1093/Hmg/8.10.1955  0.32
1999 Cox RD, Hugill A, Shedlovsky A, Noveroske JK, Best S, Justice MJ, Lehrach H, Dove WF. Contrasting effects of ENU induced embryonic lethal mutations of the quaking gene Genomics. 57: 333-341. PMID 10328999 DOI: 10.1006/Geno.1999.5804  0.32
1999 Hansen GM, Tackles D, Schwartz C, Justice MJ. A mouse chromosome 19 genetic map including the Lvis1 viral insertion site Genomics. 56: 228-231. PMID 10051411 DOI: 10.1006/Geno.1998.5708  0.32
1999 Davis AP, Woychik RP, Justice MJ. Effective chemical mutagenesis in FVB/N mice requires low doses of ethylnitrosourea Mammalian Genome. 10: 308-310. PMID 10051330 DOI: 10.1007/S003359900992  0.32
1998 Davis AP, Justice MJ. Mouse alleles: If you've seen one, you haven't seen them all Trends in Genetics. 14: 438-441. PMID 9825669 DOI: 10.1016/S0168-9525(98)01579-0  0.32
1998 Funderburgh JL, Perchellet AL, Swiergiel J, Conrad GW, Justice MJ. Keratocan (Kera), a corneal keratan sulfate proteoglycan, maps to the distal end of mouse chromosome 10 Genomics. 52: 110-1. PMID 9740679 DOI: 10.1006/Geno.1998.5355  0.32
1998 Woychik RP, Klebig ML, Justice MJ, Magnuson TR, Avner ED, Avrer ED. Functional genomics in the post-genome era. Mutation Research. 400: 3-14. PMID 9685569 DOI: 10.1016/S0027-5107(98)00023-2  0.32
1998 Davis AP, Justice MJ. Meeting report: 11th International Mouse Genome Conference Mammalian Genome. 9: 345-348. PMID 9545489 DOI: 10.1007/S003359900767  0.32
1998 Hansen GM, Justice MJ. Pten, a candidate tumor suppressor gene, maps to mouse chromosome 19 Mammalian Genome. 9: 88-90. PMID 9434957 DOI: 10.1007/S003359900690  0.32
1997 Justice MJ, Zheng B, Woychik RP, Bradley A. Using targeted large deletions and high-efficiency N-ethyl-N-nitrosourea mutagenesis for functional analyses of the mammalian genome Methods: a Companion to Methods in Enzymology. 13: 423-436. PMID 9480786 DOI: 10.1006/Meth.1997.0548  0.32
1996 Perou CM, Moore KJ, Nagle DL, Misumi DJ, Woolf EA, McGrail SH, Holmgren L, Brody TH, Dussault BJ, Monroe CA, Duyk GM, Pryor RJ, Li L, Justice MJ, Kaplan J. Identification of the murine beige gene by YAC complementation and positional cloning Nature Genetics. 13: 303-309. PMID 8673129 DOI: 10.1038/Ng0796-303  0.32
1996 Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH. Location of the 9257 and ataxia mutations on mouse chromosome 18. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 417-9. PMID 8662222 DOI: 10.1007/S003359900124  0.32
1996 Perou CM, Justice MJ, Pryor RJ, Kaplan J. Complementation of the beige mutation in cultured cells by episomally replicating murine yeast artificial chromosomes Proceedings of the National Academy of Sciences of the United States of America. 93: 5905-5909. PMID 8650191 DOI: 10.1073/Pnas.93.12.5905  0.32
1996 Ebersole TA, Chen Q, Justice MJ, Artzt K. The quaking gene product necessary in embryogenesis and myelination combines features of RNA binding and signal transduction proteins Nature Genetics. 12: 260-265. PMID 8589716 DOI: 10.1038/ng0396-260  0.32
1994 Justice MJ, Stephenson DA. Mouse chromosome 13 Mammalian Genome : Official Journal of the International Mammalian Genome Society. 5. PMID 7719006 DOI: 10.1007/BF00648431  0.32
1993 Porter BE, Justice MJ, Copeland NG, Jenkins NA, Hunter DD, Merlie JP, Sanes JR. S-laminin: mapping to mouse chromosome 9 and expression in the linked mutants tippy and ducky. Genomics. 16: 278-81. PMID 8486374 DOI: 10.1006/Geno.1993.1178  0.32
1993 Justice MJ, Stephenson DA. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 13 Mammalian Genome : Official Journal of the International Mammalian Genome Society. 4. PMID 8268673 DOI: 10.1007/BF00360839  0.32
1992 Justice MJ, Jenkins NA, Copeland NG. Recombinant inbred mouse strains: models for disease study Trends in Biotechnology. 10: 120-126. PMID 1368097 DOI: 10.1016/0167-7799(92)90193-Y  0.32
1992 Justice MJ, Gilbert DJ, Kinzler KW, Vogelstein B, Buchberg AM, Ceci JD, Matsuda Y, Chapman VM, Patriotis C, Makris A. A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18. Genomics. 13: 1281-8. PMID 1354644 DOI: 10.1016/0888-7543(92)90047-V  0.32
1991 Taylor BA, Justice MJ, Reeves R. Mouse chromosome 10. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 1: S146-57. PMID 1799797 DOI: 10.1007/Bf00656491  0.32
1990 Justice MJ, Bode VC. ENU-induced allele of brachyury (T(kt1)) exhibits a developmental lethal phenotype similar to the original brachyury (T) mutation Journal of Experimental Zoology. 254: 286-295. PMID 2345346 DOI: 10.1002/jez.1402540307  0.32
1990 Dickinson ME, Kobrin MS, Silan CM, Kingsley DM, Justice MJ, Miller DA, Ceci JD, Lock LF, Lee A, Buchberg AM. Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci. Genomics. 6: 505-20. PMID 1970330 DOI: 10.1016/0888-7543(90)90480-I  0.32
1990 Siracusa LD, Silan CM, Justice MJ, Mercer JA, Bauskin AR, Ben-Neriah Y, Duboule D, Hastie ND, Copeland NG, Jenkins NA. A molecular genetic linkage map of mouse chromosome 2. Genomics. 6: 491-504. PMID 1970329 DOI: 10.1016/0888-7543(90)90479-E  0.32
1988 Justice MJ, Bode VC. Three ENU-induced alleles of the murine quaking locus are recessive embryonic lethal mutations Genetical Research. 51: 95-102. PMID 3410318 DOI: 10.1017/S0016672300024101  0.32
1986 Justice MJ, Bode VC. Induction of new mutations in a mouse t-haplotype using ethylnitrosourea mutagenesis Genetical Research. 47: 187-192. PMID 3744044 DOI: 10.1017/S0016672300023119  0.32
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