| Year |
Citation |
Score |
| 2021 |
Yu L, Lemay P, Ludlow AV, Guyot MC, Jones MA, Mohamed FF, Saroya GA, Panaretos C, Schneider E, Wang Y, Myers G, Khoriaty R, Li Q, Franceschi R, Engel JD, ... ... Justice MJ, et al. A new murine Rpl5(uL18) mutation provides a unique model of variably penetrant Diamond Blackfan Anemia. Blood Advances. PMID 34464976 DOI: 10.1182/bloodadvances.2021004658 |
0.344 |
|
| 2020 |
Enikanolaiye A, Ruston J, Zeng R, Taylor C, Schrock M, Buchovecky CM, Shendure J, Acar E, Justice MJ. Suppressor mutations in -null mice implicate the DNA damage response in Rett syndrome pathology. Genome Research. PMID 32317254 DOI: 10.1101/Gr.258400.119 |
0.465 |
|
| 2019 |
Qiu B, Ruston J, Granzier H, Justice MJ, Dowling JJ. Failure to identify modifiers of -related nemaline myopathy in two pre-clinical models of the disease. Biology Open. 8. PMID 31530540 DOI: 10.1242/Bio.044867 |
0.369 |
|
| 2019 |
Tracey LJ, Brooke-Bisschop T, Jansen PWTC, Campos EI, Vermeulen M, Justice MJ. The Pluripotency Regulator PRDM14 Requires Hematopoietic Regulator CBFA2T3 to Initiate Leukemia in Mice. Molecular Cancer Research : McR. PMID 31015254 DOI: 10.1158/1541-7786.Mcr-18-1327 |
0.347 |
|
| 2019 |
Vashi N, Justice MJ. Treating Rett syndrome: from mouse models to human therapies. Mammalian Genome : Official Journal of the International Mammalian Genome Society. PMID 30820643 DOI: 10.1007/S00335-019-09793-5 |
0.415 |
|
| 2018 |
Moore BA, Leonard BC, Sebbag L, Edwards SG, Cooper A, Imai DM, Straiton E, Santos L, Reilly C, Griffey SM, Bower L, Clary D, Mason J, Roux MJ, Meziane H, ... ... Justice MJ, et al. Identification of genes required for eye development by high-throughput screening of mouse knockouts. Communications Biology. 1: 236. PMID 30588515 DOI: 10.1038/s42003-018-0226-0 |
0.331 |
|
| 2018 |
Albrecht NE, Alevy J, Jiang D, Burger CA, Liu BI, Li F, Wang J, Kim SY, Hsu CW, Kalaga S, Udensi U, Asomugha C, Bohat R, Gaspero A, Justice MJ, et al. Rapid and Integrative Discovery of Retina Regulatory Molecules. Cell Reports. 24: 2506-2519. PMID 30157441 DOI: 10.1016/J.Celrep.2018.07.090 |
0.325 |
|
| 2018 |
Kyle SM, Vashi N, Justice MJ. Rett syndrome: a neurological disorder with metabolic components. Open Biology. 8. PMID 29445033 DOI: 10.1098/Rsob.170216 |
0.348 |
|
| 2017 |
Bowl MR, Simon MM, Ingham NJ, Greenaway S, Santos L, Cater H, Taylor S, Mason J, Kurbatova N, Pearson S, Bower LR, Clary DA, Meziane H, Reilly P, Minowa O, ... ... Justice MJ, et al. A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nature Communications. 8: 886. PMID 29026089 DOI: 10.1038/S41467-017-00595-4 |
0.36 |
|
| 2017 |
Nguyen AT, Prado MA, Schmidt PJ, Sendamarai AK, Wilson-Grady JT, Min M, Campagna DR, Tian G, Shi Y, Dederer V, Kawan M, Kuehnle N, Paulo JA, Yao Y, Weiss MJ, ... Justice MJ, et al. UBE2O remodels the proteome during terminal erythroid differentiation. Science (New York, N.Y.). 357. PMID 28774900 DOI: 10.1126/Science.Aan0218 |
0.32 |
|
| 2017 |
Allemang-Grand R, Ellegood J, Spencer Noakes L, Ruston J, Justice M, Nieman BJ, Lerch JP. Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes. Molecular Autism. 8: 32. PMID 28670438 DOI: 10.1186/S13229-017-0138-8 |
0.367 |
|
| 2017 |
Karp NA, Mason J, Beaudet AL, Benjamini Y, Bower L, Braun RE, Brown SDM, Chesler EJ, Dickinson ME, Flenniken AM, Fuchs H, Angelis MH, Gao X, Guo S, Greenaway S, ... ... Justice MJ, et al. Prevalence of sexual dimorphism in mammalian phenotypic traits. Nature Communications. 8: 15475. PMID 28650954 DOI: 10.1038/Ncomms15475 |
0.347 |
|
| 2017 |
Meehan TF, Conte N, West DB, Jacobsen JO, Mason J, Warren J, Chen CK, Tudose I, Relac M, Matthews P, Karp N, Santos L, Fiegel T, Ring N, Westerberg H, ... ... Justice MJ, et al. Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nature Genetics. PMID 28650483 DOI: 10.1038/Ng.3901 |
0.443 |
|
| 2016 |
Dharmadhikari AV, Sun JJ, Gogolewski K, Carofino BL, Ustiyan V, Hill M, Majewski T, Szafranski P, Justice MJ, Ray RS, Dickinson ME, Kalinichenko VV, Gambin A, Stankiewicz P. Lethal lung hypoplasia and vascular defects in mice with conditional Foxf1 overexpression. Biology Open. PMID 27638768 DOI: 10.1242/Bio.019208 |
0.355 |
|
| 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 |
0.465 |
|
| 2016 |
Kyle SM, Saha PK, Brown HM, Chan LC, Justice MJ. MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex. Human Molecular Genetics. PMID 27288453 DOI: 10.1093/Hmg/Ddw156 |
0.323 |
|
| 2016 |
Carofino BL, Ayanga B, Tracey LJ, Brooke-Bisschop T, Justice MJ. PRDM14 promotes RAG-dependent Notch1 driver mutations in mouse T-ALL. Biology Open. 5: 645-53. PMID 27106930 DOI: 10.1242/Bio.017699 |
0.363 |
|
| 2016 |
Justice MJ, Dhillon P. Using the mouse to model human disease: increasing validity and reproducibility. Disease Models & Mechanisms. 9: 101-3. PMID 26839397 DOI: 10.1242/Dmm.024547 |
0.326 |
|
| 2015 |
Carofino BL, Justice MJ. Tissue-Specific Regulation of Oncogene Expression Using Cre-Inducible ROSA26 Knock-In Transgenic Mice. Current Protocols in Mouse Biology. 5: 187-204. PMID 26069083 DOI: 10.1002/9780470942390.Mo140150 |
0.363 |
|
| 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 |
0.345 |
|
| 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 |
0.373 |
|
| 2013 |
Buchovecky CM, Hill MG, Borkey JM, Kyle SM, Justice MJ. Evaluation of Rett Syndrome Symptom Improvement by Metabolic Modulators in Mecp2-Mutant Mice. Current Protocols in Mouse Biology. 3: 187-204. PMID 26069093 DOI: 10.1002/9780470942390.Mo130157 |
0.366 |
|
| 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 |
0.451 |
|
| 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 |
0.367 |
|
| 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 |
0.391 |
|
| 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 |
0.328 |
|
| 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 |
0.348 |
|
| 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 |
0.304 |
|
| 2013 |
Beck TF, Shchelochkov OA, Yu Z, Kim BJ, Hernández-GarcÃa A, Zaveri HP, Bishop C, Overbeek PA, Stockton DW, Justice MJ, Scott DA. Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3. Plos One. 8: e58830. PMID 23536828 DOI: 10.1371/Journal.Pone.0058830 |
0.441 |
|
| 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 |
0.384 |
|
| 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 |
0.438 |
|
| 2013 |
Kim BJ, Zaveri HP, Shchelochkov OA, Yu Z, Hernández-García A, Seymour ML, Oghalai JS, Pereira FA, Stockton DW, Justice MJ, Lee B, Scott DA. An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions. Plos One. 8: e57460. PMID 23451234 DOI: 10.1371/Journal.Pone.0057460 |
0.413 |
|
| 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 |
0.447 |
|
| 2013 |
Beck TF, Veenma D, Shchelochkov OA, Yu Z, Kim BJ, Zaveri HP, van Bever Y, Choi S, Douben H, Bertin TK, Patel PI, Lee B, Tibboel D, de Klein A, Stockton DW, ... Justice MJ, et al. Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice. Human Molecular Genetics. 22: 1026-38. PMID 23221805 DOI: 10.1093/Hmg/Dds507 |
0.439 |
|
| 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 |
0.332 |
|
| 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 |
0.416 |
|
| 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 |
0.693 |
|
| 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 |
0.309 |
|
| 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 |
0.359 |
|
| 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 |
0.381 |
|
| 2011 |
Terzian T, Dumble M, Arbab F, Thaller C, Donehower LA, Lozano G, Justice MJ, Roop DR, Box NF. Rpl27a mutation in the sooty foot ataxia mouse phenocopies high p53 mouse models. The Journal of Pathology. 224: 540-52. PMID 21674502 DOI: 10.1002/Path.2891 |
0.399 |
|
| 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 |
0.43 |
|
| 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 |
0.346 |
|
| 2011 |
Dettman EJ, Simko SJ, Ayanga B, Carofino BL, Margolin JF, Morse HC, Justice MJ. Prdm14 initiates lymphoblastic leukemia after expanding a population of cells resembling common lymphoid progenitors. Oncogene. 30: 2859-73. PMID 21339739 DOI: 10.1038/Onc.2011.12 |
0.389 |
|
| 2011 |
Jiang Z, Zhu L, Hu L, Pautler R, Justice M, Belmont J. Differential requirement of ZIC3 function in cardiac development and X-linked heterotaxy Developmental Biology. 356: 235. DOI: 10.1016/J.Ydbio.2011.05.402 |
0.419 |
|
| 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 |
0.355 |
|
| 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 |
0.444 |
|
| 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 |
0.459 |
|
| 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 |
0.411 |
|
| 2010 |
Xu X, Kedlaya R, Higuchi H, Ikeda S, Justice MJ, Setaluri V, Ikeda A. Mutation in archain 1, a subunit of COPI coatomer complex, causes diluted coat color and Purkinje cell degeneration. Plos Genetics. 6: e1000956. PMID 20502676 DOI: 10.1371/Journal.Pgen.1000956 |
0.432 |
|
| 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 |
0.447 |
|
| 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 |
0.432 |
|
| 2009 |
Boles MK, Wilkinson BM, Maxwell A, Lai L, Mills AA, Nishijima I, Salinger AP, Moskowitz I, Hirschi KK, Liu B, Bradley A, Justice MJ. A mouse chromosome 4 balancer ENU-mutagenesis screen isolates eleven lethal lines. Bmc Genetics. 10: 12. PMID 19267930 DOI: 10.1186/1471-2156-10-12 |
0.382 |
|
| 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 |
0.336 |
|
| 2008 |
Salinger AP, Justice MJ. Mouse Mutagenesis Using N-Ethyl-N-Nitrosourea (ENU). Csh Protocols. 2008: pdb.prot4985. PMID 21356809 |
0.326 |
|
| 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 |
0.382 |
|
| 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 |
0.395 |
|
| 2008 |
Tian M, Campagna DR, Woodward LS, Justice MJ, Fleming MD. hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouse. Blood. 112: 4308-13. PMID 18780836 DOI: 10.1182/Blood-2007-09-111500 |
0.403 |
|
| 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 |
0.404 |
|
| 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 |
Tian M, Campagna DR, Langer N, Choe S, Paw BH, Justice MJ, Fleming MD. Rsp1 Is Indispensable for mRNA Stability during Erythroid Terminal Differentiation Blood. 112: 532-532. DOI: 10.1182/Blood.V112.11.532.532 |
0.355 |
|
| 2007 |
Castillo A, Morse HC, Godfrey VL, Naeem R, Justice MJ. Overexpression of Eg5 causes genomic instability and tumor formation in mice. Cancer Research. 67: 10138-47. PMID 17974955 DOI: 10.1158/0008-5472.Can-07-0326 |
0.351 |
|
| 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 |
0.42 |
|
| 2007 |
Zheng L, Baek HJ, Karsenty G, Justice MJ. Filamin B represses chondrocyte hypertrophy in a Runx2/Smad3-dependent manner. The Journal of Cell Biology. 178: 121-8. PMID 17606870 DOI: 10.1083/Jcb.200703113 |
0.355 |
|
| 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 |
0.378 |
|
| 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 |
0.392 |
|
| 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 |
0.358 |
|
| 2007 |
Zhu L, Peng JL, Harutyunyan KG, Garcia MD, Justice MJ, Belmont JW. Craniofacial, skeletal, and cardiac defects associated with altered embryonic murine Zic3 expression following targeted insertion of a PGK-NEO cassette. Frontiers in Bioscience : a Journal and Virtual Library. 12: 1680-90. PMID 17127413 |
0.321 |
|
| 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 |
0.334 |
|
| 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 |
0.401 |
|
| 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 |
0.315 |
|
| 2006 |
Bohnsack BL, Lai L, Northrop JL, Justice MJ, Hirschi KK. Visceral endoderm function is regulated by quaking and required for vascular development. Genesis (New York, N.Y. : 2000). 44: 93-104. PMID 16470614 DOI: 10.1002/Gene.20189 |
0.339 |
|
| 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 |
0.437 |
|
| 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 |
0.318 |
|
| 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 |
0.64 |
|
| 2005 |
Weiser KC, Justice MJ. Cancer biology: Sleeping Beauty awakens. Nature. 436: 184-6. PMID 16015313 DOI: 10.1038/436184A |
0.319 |
|
| 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 |
0.392 |
|
| 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 |
0.391 |
|
| 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 |
0.398 |
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| 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 |
0.354 |
|
| 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 |
0.702 |
|
| 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 |
0.381 |
|
| 2004 |
Justice MJ. From the atomic age to the genome project Genetica. 122: 3-7. PMID 15619956 DOI: 10.1007/S10709-004-1440-X |
0.432 |
|
| 2004 |
Yan J, Keener VW, Bi W, Walz K, Bradley A, Justice MJ, Lupski JR. Reduced penetrance of craniofacial anomalies as a function of deletion size and genetic background in a chromosome engineered partial mouse model for Smith-Magenis syndrome. Human Molecular Genetics. 13: 2613-24. PMID 15459175 DOI: 10.1093/Hmg/Ddh288 |
0.453 |
|
| 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 |
0.42 |
|
| 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 |
0.454 |
|
| 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 |
0.416 |
|
| 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 |
0.383 |
|
| 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 |
0.36 |
|
| 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 |
0.346 |
|
| 2004 |
Lorenzetti D, Antalffy B, Vogel H, Noveroske J, Armstrong D, Justice M. The neurological mutant quaking(viable) is Parkin deficient. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 15: 210-7. PMID 15014970 DOI: 10.1007/S00335-003-2333-5 |
0.466 |
|
| 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 |
0.398 |
|
| 2004 |
Justice MJ, Kile BT, Woodward LS. Inflammatory Disease and Abortive Platelet Shedding Caused by a Mutation in a Pivotal Regulator of Actin Dynamics in the redears Mouse. Blood. 104: 1606-1606. DOI: 10.1182/Blood.V104.11.1606.1606 |
0.399 |
|
| 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 |
0.328 |
|
| 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 |
0.437 |
|
| 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 |
0.475 |
|
| 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 |
0.485 |
|
| 2003 |
Behringer RR, Justice MJ. Genetic Screens in Mice for Androgen Disorders The Endocrinologist. 13: 243-246. DOI: 10.1097/01.Ten.0000081688.21823.30 |
0.313 |
|
| 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 |
0.389 |
|
| 2002 |
Cheunsuk S, Sparks R, Noveroske JK, Hsu T, Justice MJ, Gershwin ME, Gruen JR, Bowlus CL. Expression, genomic structure and mapping of the thymus specific protease prss16: a candidate gene for insulin dependent diabetes mellitus susceptibility. Journal of Autoimmunity. 18: 311-6. PMID 12144812 DOI: 10.1006/Jaut.2002.0593 |
0.416 |
|
| 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 |
0.465 |
|
| 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 |
0.335 |
|
| 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 |
0.411 |
|
| 2002 |
Headon DJ, Emmal SA, Ferguson BM, Tucker AS, Justice MJ, Sharpe PT, Zonana J, Overbeek PA. Gene defect in ectodermal dysplasia implicates a death domain adapter in development. Nature. 414: 913-6. PMID 11780064 DOI: 10.1038/414913A |
0.331 |
|
| 2002 |
Ohtoshi A, Nishijima I, Justice MJ, Behringer RR. Dmbx1, a novel evolutionarily conserved paired-like homeobox gene expressed in the brain of mouse embryos. Mechanisms of Development. 110: 241-4. PMID 11744391 DOI: 10.1016/S0925-4773(01)00587-1 |
0.399 |
|
| 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 |
0.424 |
|
| 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 |
0.391 |
|
| 2001 |
Kibar Z, Underhill DA, Canonne-Hergaux F, Gauthier S, Justice MJ, Gros P. Identification of a new chemically induced allele (Lp(m1Jus)) at the loop-tail locus: morphology, histology, and genetic mapping. Genomics. 72: 331-7. PMID 11401449 DOI: 10.1006/Geno.2000.6493 |
0.313 |
|
| 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 |
0.436 |
|
| 2000 |
Justice MJ. Capitalizing on large-scale mouse mutagenesis screens Nature Reviews Genetics. 1: 109-115. PMID 11253650 DOI: 10.1038/35038549 |
0.374 |
|
| 2000 |
Justice MJ, Carpenter DA, Favor J, Neuhauser-Klaus A, Hrabé de Angelis M, Soewarto D, Moser A, Cordes S, Miller D, Chapman V, Weber JS, Rinchik EM, Hunsicker PR, Russell WL, Bode VC. Effects of ENU dosage on mouse strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 484-8. PMID 10886010 DOI: 10.1007/S003350010094 |
0.301 |
|
| 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 |
0.341 |
|
| 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 |
0.312 |
|
| 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 |
0.438 |
|
| 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 |
0.396 |
|
| 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 |
0.425 |
|
| 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 |
0.486 |
|
| 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 |
0.312 |
|
| 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 |
0.418 |
|
| 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 |
0.406 |
|
| 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 |
0.425 |
|
| 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 |
0.342 |
|
| 1998 |
Woychik RP, Klebig ML, Justice MJ, Magnuson TR, Avner ED. Erratum: Functional genomics in the post-genome era (Mutation Research 400 (1998) (3-14) PII: 2002751098000232) Mutation Research. 422. DOI: 10.1016/S0027-5107(98)00218-8 |
0.325 |
|
| 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 |
0.453 |
|
| 1997 |
Perou CM, Perchellet A, Jago T, Pryor R, Kaplan J, Justice MJ. Comparative mapping in the beige-satin region of mouse chromosome 13. Genomics. 39: 136-46. PMID 9027500 DOI: 10.1006/Geno.1996.4478 |
0.39 |
|
| 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 |
0.432 |
|
| 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 |
0.474 |
|
| 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 |
0.304 |
|
| 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 |
0.387 |
|
| 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 |
0.397 |
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