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Monica Justice

TitleSenior Scientist
InstitutionThe Hospital for Sick Children
DepartmentGenetics and Genome Biology
Address555 University Avenue
Toronto ON M5G 1X8
Phone416-813-1500
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    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Enikanolaiye A, Ruston J, Zeng R, Taylor C, Schrock M, Buchovecky CM, Shendure J, Acar E, Justice MJ. Suppressor mutations in Mecp2-null mice implicate the DNA damage response in Rett syndrome pathology. Genome Res. 2020 Apr; 30(4):540-552. PMID: 32317254.
      View in: PubMed
    2. 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, Scott DA. Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice. Hum Mol Genet. 2020 Apr 15; 29(6):1054. PMID: 32016392.
      View in: PubMed
    3. Justice MJ, Hmeljak J, Sankaran VG, Socolovsky M, Zon LI. From blood development to disease: a paradigm for clinical translation. Dis Model Mech. 2020 01 09; 13(1). PMID: 31836582.
      View in: PubMed
    4. Qiu B, Ruston J, Granzier H, Justice MJ, Dowling JJ. Failure to identify modifiers of NEBULIN-related nemaline myopathy in two pre-clinical models of the disease. Biol Open. 2019 Sep 18; 8(9). PMID: 31530540.
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    5. Tracey LJ, Justice MJ. Off to a Bad Start: Cancer Initiation by Pluripotency Regulator PRDM14. Trends Genet. 2019 07; 35(7):489-500. PMID: 31130394.
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    6. 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. Mol Cancer Res. 2019 07; 17(7):1468-1479. PMID: 31015254.
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    7. Justice MJ. DMM Prize 2018 winner: Wenqing Zhou. Dis Model Mech. 2019 03 26; 12(3). PMID: 30923050.
      View in: PubMed
    8. 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, Herault Y, McKerlie C, Flenniken AM, Nutter LMJ, Berberovic Z, Owen C, Newbigging S, Adissu H, Eskandarian M, Hsu CW, Kalaga S, Udensi U, Asomugha C, Bohat R, Gallegos JJ, Seavitt JR, Heaney JD, Beaudet AL, Dickinson ME, Justice MJ, Philip V, Kumar V, Svenson KL, Braun RE, Wells S, Cater H, Stewart M, Clementson-Mobbs S, Joynson R, Gao X, Suzuki T, Wakana S, Smedley D, Seong JK, Tocchini-Valentini G, Moore M, Fletcher C, Karp N, Ramirez-Solis R, White JK, de Angelis MH, Wurst W, Thomasy SM, Flicek P, Parkinson H, Brown SDM, Meehan TF, Nishina PM, Murray SA, Krebs MP, Mallon AM, Kent Lloyd KC, Murphy CJ, Moshiri A. Erratum: Author Correction: Identification of genes required for eye development by high-throughput screening of mouse knockouts. Commun Biol. 2019; 2:97. PMID: 30854487.
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    9. Vashi N, Justice MJ. Treating Rett syndrome: from mouse models to human therapies. Mamm Genome. 2019 06; 30(5-6):90-110. PMID: 30820643.
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    10. Hmeljak J, Justice MJ. From gene to treatment: supporting rare disease translational research through model systems. Dis Model Mech. 2019 02 22; 12(2). PMID: 30819728.
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    11. 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, Herault Y, McKerlie C, Flenniken AM, Nutter LMJ, Berberovic Z, Owen C, Newbigging S, Adissu H, Eskandarian M, Hsu CW, Kalaga S, Udensi U, Asomugha C, Bohat R, Gallegos JJ, Seavitt JR, Heaney JD, Beaudet AL, Dickinson ME, Justice MJ, Philip V, Kumar V, Svenson KL, Braun RE, Wells S, Cater H, Stewart M, Clementson-Mobbs S, Joynson R, Gao X, Suzuki T, Wakana S, Smedley D, Seong JK, Tocchini-Valentini G, Moore M, Fletcher C, Karp N, Ramirez-Solis R, White JK, de Angelis MH, Wurst W, Thomasy SM, Flicek P, Parkinson H, Brown SDM, Meehan TF, Nishina PM, Murray SA, Krebs MP, Mallon AM, Lloyd KCK, Murphy CJ, Moshiri A. Identification of genes required for eye development by high-throughput screening of mouse knockouts. Commun Biol. 2018; 1:236. PMID: 30588515.
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    12. 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, Westenskow PD, Yamamoto S, Seavitt JR, Beaudet AL, Dickinson ME, Samuel MA. Rapid and Integrative Discovery of Retina Regulatory Molecules. Cell Rep. 2018 08 28; 24(9):2506-2519. PMID: 30157441.
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    13. Kyle SM, Vashi N, Justice MJ. Rett syndrome: a neurological disorder with metabolic components. Open Biol. 2018 02; 8(2). PMID: 29445033.
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    14. 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, Clary D, Cleak J, Daly MJ, Denegre JM, Doe B, Dolan ME, Edie Helmut Fuchs SM, Gailus-Durner V, Galli A, Gambadoro A, Gallegos J, Guo S, Horner NR, Hsu CW, Johnson SJ, Kalaga S, Keith LC, Lanoue L, Lawson TN, Lek M, Mark M, Marschall S, Mason J, McElwee ML, Nutter SNLMJ, Peterson KA, Ramirez-Solis R, Rowland DJ, Ryder E, Samocha KE, Seavitt JR, Selloum M, Szoke-Kovacs Z, Tamura M, Trainor AG, Tudose I, Wakana S, Warren J, Wendling O, West DB, Wong L, Yoshiki A, Wurst W, MacArthur DG, Tocchini-Valentini GP, Gao X, Flicek P, Bradley A, Skarnes WC, Justice MJ, Parkinson HE, Moore M, Wells S, Braun RE, Svenson KL, de Angelis MH, Herault Y, Mohun T, Mallon AM, Henkelman RM, Brown SDM, Adams DJ, Lloyd KCK, McKerlie C, Beaudet AL, Murray MBSA. Corrigendum: High-throughput discovery of novel developmental phenotypes. Nature. 2017 11 16; 551(7680):398. PMID: 29144450.
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    15. 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, Kelsey L, Tocchini-Valentini GP, Gao X, Bradley A, Skarnes WC, Moore M, Beaudet AL, Justice MJ, Seavitt J, Dickinson ME, Wurst W, de Angelis MH, Herault Y, Wakana S, Nutter LMJ, Flenniken AM, McKerlie C, Murray SA, Svenson KL, Braun RE, West DB, Lloyd KCK, Adams DJ, White J, Karp N, Flicek P, Smedley D, Meehan TF, Parkinson HE, Teboul LM, Wells S, Steel KP, Mallon AM, Brown SDM. A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Nat Commun. 2017 10 12; 8(1):886. PMID: 29026089.
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    16. 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, Gygi SP, Fleming MD, Finley D. UBE2O remodels the proteome during terminal erythroid differentiation. Science. 2017 08 04; 357(6350). PMID: 28774900.
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    17. 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, Heller R, Herault Y, Justice MJ, Kurbatova N, Lelliott CJ, Lloyd KCK, Mallon AM, Mank JE, Masuya H, McKerlie C, Meehan TF, Mott RF, Murray SA, Parkinson H, Ramirez-Solis R, Santos L, Seavitt JR, Smedley D, Sorg T, Speak AO, Steel KP, Svenson KL, Wakana S, West D, Wells S, Westerberg H, Yaacoby S, White JK. Prevalence of sexual dimorphism in mammalian phenotypic traits. Nat Commun. 2017 06 26; 8:15475. PMID: 28650954.
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    18. 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. Mol Autism. 2017; 8:32. PMID: 28670438.
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    19. 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, Greenaway S, Sneddon D, Morgan H, Codner GF, Stewart ME, Brown J, Horner N, Haendel M, Washington N, Mungall CJ, Reynolds CL, Gallegos J, Gailus-Durner V, Sorg T, Pavlovic G, Bower LR, Moore M, Morse I, Gao X, Tocchini-Valentini GP, Obata Y, Cho SY, Seong JK, Seavitt J, Beaudet AL, Dickinson ME, Herault Y, Wurst W, de Angelis MH, Lloyd KCK, Flenniken AM, Nutter LMJ, Newbigging S, McKerlie C, Justice MJ, Murray SA, Svenson KL, Braun RE, White JK, Bradley A, Flicek P, Wells S, Skarnes WC, Adams DJ, Parkinson H, Mallon AM, Brown SDM, Smedley D. Disease model discovery from 3,328 gene knockouts by The International Mouse Phenotyping Consortium. Nat Genet. 2017 Aug; 49(8):1231-1238. PMID: 28650483.
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    20. 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. Biol Open. 2016 Nov 15; 5(11):1595-1606. PMID: 27638768.
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    21. 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, Clary D, Cleak J, Daly MJ, Denegre JM, Doe B, Dolan ME, Edie SM, Fuchs H, Gailus-Durner V, Galli A, Gambadoro A, Gallegos J, Guo S, Horner NR, Hsu CW, Johnson SJ, Kalaga S, Keith LC, Lanoue L, Lawson TN, Lek M, Mark M, Marschall S, Mason J, McElwee ML, Newbigging S, Nutter LM, Peterson KA, Ramirez-Solis R, Rowland DJ, Ryder E, Samocha KE, Seavitt JR, Selloum M, Szoke-Kovacs Z, Tamura M, Trainor AG, Tudose I, Wakana S, Warren J, Wendling O, West DB, Wong L, Yoshiki A, MacArthur DG, Tocchini-Valentini GP, Gao X, Flicek P, Bradley A, Skarnes WC, Justice MJ, Parkinson HE, Moore M, Wells S, Braun RE, Svenson KL, de Angelis MH, Herault Y, Mohun T, Mallon AM, Henkelman RM, Brown SD, Adams DJ, Lloyd KC, McKerlie C, Beaudet AL, Bucan M, Murray SA. High-throughput discovery of novel developmental phenotypes. Nature. 2016 09 22; 537(7621):508-514. PMID: 27626380.
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    22. Kyle SM, Saha PK, Brown HM, Chan LC, Justice MJ. MeCP2 co-ordinates liver lipid metabolism with the NCoR1/HDAC3 corepressor complex. Hum Mol Genet. 2016 07 15; 25(14):3029-3041. PMID: 27288453.
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    23. Carofino BL, Ayanga B, Tracey LJ, Brooke-Bisschop T, Justice MJ. PRDM14 promotes RAG-dependent Notch1 driver mutations in mouse T-ALL. Biol Open. 2016 May 15; 5(5):645-53. PMID: 27106930.
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    24. Justice MJ, Dhillon P. Using the mouse to model human disease: increasing validity and reproducibility. Dis Model Mech. 2016 Feb; 9(2):101-3. PMID: 26839397.
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    25. Carofino BL, Justice MJ. Tissue-Specific Regulation of Oncogene Expression Using Cre-Inducible ROSA26 Knock-In Transgenic Mice. Curr Protoc Mouse Biol. 2015 Jun 01; 5(2):187-204. PMID: 26069083.
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    26. 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, Gambin A, Belmont J, Stankiewicz P. Comparative analyses of lung transcriptomes in patients with alveolar capillary dysplasia with misalignment of pulmonary veins and in foxf1 heterozygous knockout mice. PLoS One. 2014; 9(4):e94390. PMID: 24722050.
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    27. Buchovecky CM, Hill MG, Borkey JM, Kyle SM, Justice MJ. Evaluation of Rett Syndrome Symptom Improvement by Metabolic Modulators in Mecp2-Mutant Mice. Curr Protoc Mouse Biol. 2013 Dec 19; 3(4):187-204. PMID: 26069093.
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    28. Justice MJ, Buchovecky CM, Kyle SM, Djukic A. A role for metabolism in Rett syndrome pathogenesis: New clinical findings and potential treatment targets. Rare Dis. 2013; 1:e27265. PMID: 25003017.
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    29. 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. 2013; 8(11):e80408. PMID: 24303013.
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    30. 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. Hum Mol Genet. 2014 Apr 01; 23(7):1687-99. PMID: 24203697.
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    31. 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). Dis Model Mech. 2013 Nov; 6(6):1494-506. PMID: 24046360.
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    32. 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. Nat Genet. 2013 Sep; 45(9):1013-20. PMID: 23892605.
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    33. Justice M. Of mice and men, and medicine: an interview with Monica Justice. Dis Model Mech. 2013 Jul; 6(4):871-3. PMID: 23828642.
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    34. 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, Potocki L, Zapata G, Hernandez PP, Ramocki MB, Santos-Cortez RL, Wang G, York MK, Justice MJ, Chu ZD, Bader PI, Omo-Griffith L, Madduri NS, Scharer G, Crawford HP, Yanatatsaneejit P, Eifert A, Kerr J, Bacino CA, Franklin AI, Goin-Kochel RP, Simpson G, Immken L, Haque ME, Stosic M, Williams MD, Morgan TM, Pruthi S, Omary R, Boyadjiev SA, Win KK, Thida A, Hurles M, Hibberd ML, Khor CC, Van Vinh Chau N, Gallagher TE, Mutirangura A, Stankiewicz P, Beaudet AL, Maletic-Savatic M, Rosenfeld JA, Shaffer LG, Davis EE, Belmont JW, Dunstan S, Simmons CP, Bonnen PE, Leal SM, Katsanis N, Lupski JR, Lalani SR. TM4SF20 ancestral deletion and susceptibility to a pediatric disorder of early language delay and cerebral white matter hyperintensities. Am J Hum Genet. 2013 Aug 08; 93(2):197-210. PMID: 23810381.
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    35. Cagan RL, Justice MJ, Tidmarsh GF. Bridging the gap between basic and applied biology: towards preclinical translation. Dis Model Mech. 2013 May; 6(3):559-61. PMID: 23616075.
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    36. Nakamura H, Cook RN, Justice MJ. Mouse Tenm4 is required for mesoderm induction. BMC Dev Biol. 2013 Mar 25; 13:9. PMID: 23521771.
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    37. 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. Dis Model Mech. 2013 May; 6(3):571-9. PMID: 23519032.
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    38. Beck TF, Shchelochkov OA, Yu Z, Kim BJ, Hernández-García 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. 2013; 8(3):e58830. PMID: 23536828.
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    39. 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. 2013; 8(2):e57460. PMID: 23451234.
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    40. 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. 2013 Jun; 98(6):854-61. PMID: 23300183.
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    41. Buchovecky CM, Hill MG, Borkey JM, Kyle SM, Justice MJ. A protocol for evaluation of Rett Syndrome symptom improvement by metabolic modulators in Mecp2-mutant mice. Curr Protoc Mouse Biol. 2013; 2013. PMID: 25506514.
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    42. 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 Genet. 2012 Dec 12; 13:106. PMID: 23231322.
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    43. 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, Scott DA. Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice. Hum Mol Genet. 2013 Mar 01; 22(5):1026-38. PMID: 23221805.
      View in: PubMed
    44. 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. Hum Mol Genet. 2013 Mar 01; 22(5):879-89. PMID: 23184148.
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    45. 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, Schaevitz LR, St Hillaire-Clarke C, Young JL, Zoghbi HY, Mamounas LA. Preclinical research in Rett syndrome: setting the foundation for translational success. Dis Model Mech. 2012 Nov; 5(6):733-45. PMID: 23115203.
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    46. 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 (Basel). 2012 Dec 01; 4(4):1050-1066. PMID: 23487523.
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    47. 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. J Neurosci. 2012 Aug 01; 32(31):10574-86. PMID: 22855807.
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    48. Larina IV, Larin KV, Justice MJ, Dickinson ME. Optical Coherence Tomography for live imaging of mammalian development. Curr Opin Genet Dev. 2011 Oct; 21(5):579-84. PMID: 21962442.
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    49. 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. Mutation discovery in mice by whole exome sequencing. Genome Biol. 2011 Sep 14; 12(9):R86. PMID: 21917142.
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    50. 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. 2011; 6(8):e22956. PMID: 21857973.
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    51. 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. J Pathol. 2011 Aug; 224(4):540-52. PMID: 21674502.
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    52. Justice MJ, Siracusa LD, Stewart AF. Technical approaches for mouse models of human disease. Dis Model Mech. 2011 May; 4(3):305-10. PMID: 21558063.
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    53. 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. 2011 Jun 23; 30(25):2859-73. PMID: 21339739.
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    54. 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. Dev Dyn. 2011 Apr; 240(4):839-49. PMID: 21404367.
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    55. 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 Genet. 2010 Jun 10; 6(6):e1000985. PMID: 20548961.
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    56. 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. Hum Mol Genet. 2010 Aug 15; 19(16):3105-13. PMID: 20511334.
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    57. 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 Genet. 2010 May 20; 6(5):e1000956. PMID: 20502676.
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    58. Justice MJ, Hirschi KK. The role of quaking in mammalian embryonic development. Adv Exp Med Biol. 2010; 693:82-92. PMID: 21189687.
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    59. Probst FJ, Justice MJ. Mouse mutagenesis with the chemical supermutagen ENU. Methods Enzymol. 2010; 477:297-312. PMID: 20699147.
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    60. 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, Funato Y, Miki H, Marin-Garcia P, Matthews L, Coffey AJ, Parker A, Hubbard TJ, Rogers J, Bradley A, Adams DJ, Justice MJ. Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin. PLoS Genet. 2009 Dec; 5(12):e1000759. PMID: 20011118.
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    61. 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. Proc Natl Acad Sci U S A. 2009 Oct 06; 106(40):17055-60. PMID: 19805151.
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    62. 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 Genet. 2009 Mar 06; 10:12. PMID: 19267930.
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    63. 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. J Neurosci. 2009 Mar 04; 29(9):2733-41. PMID: 19261867.
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    64. Dettman EJ, Justice MJ. The zinc finger SET domain gene Prdm14 is overexpressed in lymphoblastic lymphomas with retroviral insertions at Evi32. PLoS One. 2008; 3(11):e3823. PMID: 19043588.
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    65. Tian M, Campagna DR, Woodward LS, Justice MJ, Fleming MD. hem6: an ENU-induced recessive hypochromic microcytic anemia mutation in the mouse. Blood. 2008 Nov 15; 112(10):4308-13. PMID: 18780836.
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    66. Justice MJ. Removing the cloak of invisibility: phenotyping the mouse. Dis Model Mech. 2008 Sep-Oct; 1(2-3):109-12. PMID: 19048073.
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    67. Probst FJ, Cooper ML, Cheung SW, Justice MJ. Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome. J Hered. 2008 Sep-Oct; 99(5):512-7. PMID: 18499648.
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    68. 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, Beales PL. Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome. Proc Natl Acad Sci U S A. 2008 May 06; 105(18):6714-9. PMID: 18443298.
      View in: PubMed
    69. Salinger AP, Justice MJ. Mouse Mutagenesis Using N-Ethyl-N-Nitrosourea (ENU). CSH Protoc. 2008 Apr 01; 2008:pdb.prot4985. PMID: 21356809.
      View in: PubMed
    70. Castillo A, Morse HC, Godfrey VL, Naeem R, Justice MJ. Overexpression of Eg5 causes genomic instability and tumor formation in mice. Cancer Res. 2007 Nov 01; 67(21):10138-47. PMID: 17974955.
      View in: PubMed
    71. 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. Mamm Genome. 2007 Oct; 18(10):709-22. PMID: 17926094.
      View in: PubMed
    72. Zheng L, Baek HJ, Karsenty G, Justice MJ. Filamin B represses chondrocyte hypertrophy in a Runx2/Smad3-dependent manner. J Cell Biol. 2007 Jul 02; 178(1):121-8. PMID: 17606870.
      View in: PubMed
    73. 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. 2007 Oct 01; 110(7):2371-80. PMID: 17515402.
      View in: PubMed
    74. Castillo A, Justice MJ. The kinesin related motor protein, Eg5, is essential for maintenance of pre-implantation embryogenesis. Biochem Biophys Res Commun. 2007 Jun 08; 357(3):694-9. PMID: 17449012.
      View in: PubMed
    75. Hentges KE, Pollock DD, Liu B, Justice MJ. Regional variation in the density of essential genes in mice. PLoS Genet. 2007 May 04; 3(5):e72. PMID: 17480122.
      View in: PubMed
    76. 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. Front Biosci. 2007 Jan 01; 12:1680-90. PMID: 17127413.
      View in: PubMed
    77. 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. Mamm Genome. 2006 Dec; 17(12):1162-71. PMID: 17143585.
      View in: PubMed
    78. 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. Hum Genet. 2006 Sep; 120(2):211-26. PMID: 16794820.
      View in: PubMed
    79. 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. EMBO J. 2006 Mar 22; 25(6):1406-17. PMID: 16511562.
      View in: PubMed
    80. 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 Expr Patterns. 2006 Aug; 6(6):653-65. PMID: 16466971.
      View in: PubMed
    81. Bohnsack BL, Lai L, Northrop JL, Justice MJ, Hirschi KK. Visceral endoderm function is regulated by quaking and required for vascular development. Genesis. 2006 Feb; 44(2):93-104. PMID: 16470614.
      View in: PubMed
    82. Noveroske JK, Hardy R, Dapper JD, Vogel H, Justice MJ. A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination. Mamm Genome. 2005 Sep; 16(9):672-82. PMID: 16245024.
      View in: PubMed
    83. Dapper JD, Justice MJ. Defining the breakpoints of the quaking(viable) mouse mutation reveals a duplication from a Parkin intron. Mov Disord. 2005 Oct; 20(10):1369-74. PMID: 16001410.
      View in: PubMed
    84. Basilio A, Justice M, Harris G, Bills G, Collado J, de la Cruz M, Diez MT, Hernandez P, Liberator P, Nielsen kahn J, Pelaez F, Platas G, Schmatz D, Shastry M, Tormo JR, Andersen GR, Vicente F. The discovery of moriniafungin, a novel sordarin derivative produced by Morinia pestalozzioides. Bioorg Med Chem. 2006 Jan 15; 14(2):560-6. PMID: 16183294.
      View in: PubMed
    85. Weiser KC, Justice MJ. Cancer biology: Sleeping Beauty awakens. Nature. 2005 Jul 14; 436(7048):184-6. PMID: 16015313.
      View in: PubMed
    86. Lossie AC, Meehan TP, Castillo A, Zheng L, Weiser KC, Strivens MA, Justice MJ. 18th international mouse genome conference. Mamm Genome. 2005 Jul; 16(7):471-5. PMID: 16151691.
      View in: PubMed
    87. 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. Hum Mol Genet. 2005 Apr 15; 14(8):983-95. PMID: 15746153.
      View in: PubMed
    88. 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. 2005 Feb 10; 24(7):1220-30. PMID: 15580294.
      View in: PubMed
    89. 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. Mol Endocrinol. 2005 Apr; 19(4):972-81. PMID: 15625238.
      View in: PubMed
    90. Lossie AC, Nakamura H, Thomas SE, Justice MJ. Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation. Genetics. 2005 Jan; 169(1):285-99. PMID: 15489520.
      View in: PubMed
    91. 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. Hum Mol Genet. 2004 Nov 01; 13(21):2613-24. PMID: 15459175.
      View in: PubMed
    92. 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. Proc Natl Acad Sci U S A. 2004 Sep 14; 101(37):13560-5. PMID: 15345741.
      View in: PubMed
    93. 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. 2004 Sep; 122(1):51-64. PMID: 15619961.
      View in: PubMed
    94. Justice MJ. From the atomic age to the Genome Project. Genetica. 2004 Sep; 122(1):3-7. PMID: 15619956.
      View in: PubMed
    95. Hentges KE, Justice MJ. Checks and balancers: balancer chromosomes to facilitate genome annotation. Trends Genet. 2004 Jun; 20(6):252-9. PMID: 15145578.
      View in: PubMed
    96. Lorenzetti D, Bishop CE, Justice MJ. Deletion of the Parkin coregulated gene causes male sterility in the quaking(viable) mouse mutant. Proc Natl Acad Sci U S A. 2004 Jun 01; 101(22):8402-7. PMID: 15148410.
      View in: PubMed
    97. Hentges KE, Kyttälä M, Justice MJ, Peltonen L. Comparative physical maps of the human and mouse Meckel syndrome critical regions. Mamm Genome. 2004 Apr; 15(4):252-64. PMID: 15112103.
      View in: PubMed
    98. 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. 2004 Apr 16; 304(5669):445-8. PMID: 15031436.
      View in: PubMed
    99. Lorenzetti D, Antalffy B, Vogel H, Noveroske J, Armstrong D, Justice M. The neurological mutant quaking(viable) is Parkin deficient. Mamm Genome. 2004 Mar; 15(3):210-7. PMID: 15014970.
      View in: PubMed
    100. 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. Dev Cell. 2004 Mar; 6(3):423-35. PMID: 15030764.
      View in: PubMed
    101. 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. Biol Reprod. 2004 May; 70(5):1317-24. PMID: 14711786.
      View in: PubMed
    102. George A, Morse HC, Justice MJ. The homeobox gene Hex induces T-cell-derived lymphomas when overexpressed in hematopoietic precursor cells. Oncogene. 2003 Oct 02; 22(43):6764-73. PMID: 14555989.
      View in: PubMed
    103. 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. Mol Cell Biol. 2003 Oct; 23(19):6798-808. PMID: 12972600.
      View in: PubMed
    104. 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. 2003 Sep 04; 425(6953):81-6. PMID: 12955145.
      View in: PubMed
    105. Kile BT, Mason-Garrison CL, Justice MJ. Sex and strain-related differences in the peripheral blood cell values of inbred mouse strains. Mamm Genome. 2003 Jan; 14(1):81-5. PMID: 12532271.
      View in: PubMed
    106. Hentges KE, Yarlagadda SP, Justice MJ. Tnfrsf13c (Baffr) is mis-expressed in tumors with murine leukemia virus insertions at Lvis22. Genomics. 2002 Aug; 80(2):204-12. PMID: 12160734.
      View in: PubMed
    107. Tsai TF, Chen KS, Weber JS, Justice MJ, Beaudet AL. Evidence for translational regulation of the imprinted Snurf-Snrpn locus in mice. Hum Mol Genet. 2002 Jul 01; 11(14):1659-68. PMID: 12075010.
      View in: PubMed
    108. 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. J Autoimmun. 2002 Jun; 18(4):311-6. PMID: 12144812.
      View in: PubMed
    109. Noveroske JK, Lai L, Gaussin V, Northrop JL, Nakamura H, Hirschi KK, Justice MJ. Quaking is essential for blood vessel development. Genesis. 2002 Mar; 32(3):218-30. PMID: 11892011.
      View in: PubMed
    110. 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. Nat Genet. 2002 Feb; 30(2):185-9. PMID: 11818962.
      View in: PubMed
    111. Ohtoshi A, Nishijima I, Justice MJ, Behringer RR. Dmbx1, a novel evolutionarily conserved paired-like homeobox gene expressed in the brain of mouse embryos. Mech Dev. 2002 Jan; 110(1-2):241-4. PMID: 11744391.
      View in: PubMed
    112. 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. 2001 Dec 20-27; 414(6866):913-6. PMID: 11780064.
      View in: PubMed
    113. Panitkin SY, Ajitanand NN, Alexander J, Anderson M, Best D, Brady FP, Case T, Caskey W, Cebra D, Chance J, Chung P, Cole B, Crowe K, Das A, Draper J, Gilkes M, Gushue S, Heffner M, Hirsch A, Hjort E, Huo L, Justice M, Kaplan M, Keane D, Kintner J, Klay J, Krofcheck D, Lacey R, Lauret J, Lisa MA, Liu H, Liu YM, McGrath R, Milosevich Z, Odyniec G, Olson D, Pinkenburg C, Porile N, Rai G, Ritter HG, Romero J, Scharenberg R, Schroeder LS, Srivastava B, Stone NT, Symons TJ, Wang S, Wells R, Whitfield J, Wienold T, Witt R, Wood L, Yang X, Zhang WN, Zhang Y, Brown DA, Danielewicz P. Model-independent source imaging using two-pion correlations in (2 to 8)a GeV Au+Au collisions. Phys Rev Lett. 2001 Sep 10; 87(11):112304. PMID: 11531518.
      View in: PubMed
    114. 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. Biochem Biophys Res Commun. 2001 Aug 10; 286(1):133-40. PMID: 11485319.
      View in: PubMed
    115. 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. Nat Genet. 2001 Jul; 28(3):251-5. PMID: 11431695.
      View in: PubMed
    116. 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. 2001 Apr; 29(4):163-71. PMID: 11309849.
      View in: PubMed
    117. 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. 2001 Mar 15; 72(3):331-7. PMID: 11401449.
      View in: PubMed
    118. 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, Guenet JL, Hicks G, Hrabe de Angelis M, Jackson I, Jacob HJ, Jenkins N, Johnson D, Justice M, Kay S, Kingsley D, Lehrach H, Magnuson T, Meisler M, Poustka A, Rinchik EM, Rossant J, Russell LB, Schimenti J, Shiroishi T, Skarnes WC, Soriano P, Stanford W, Takahashi JS, Wurst W, Zimmer A. Sequence interpretation. Functional annotation of mouse genome sequences. Science. 2001 Feb 16; 291(5507):1251-5. PMID: 11233449.
      View in: PubMed
    119. Brayton C, Justice M, Montgomery CA. Evaluating mutant mice: anatomic pathology. Vet Pathol. 2001 Jan; 38(1):1-19. PMID: 11199155.
      View in: PubMed
    120. Justice MJ. Capitalizing on large-scale mouse mutagenesis screens. Nat Rev Genet. 2000 Nov; 1(2):109-15. PMID: 11253650.
      View in: PubMed
    121. Swiergiel JJ, Funderburgh JL, Justice MJ, Conrad GW. Developmental eye and neural tube defects in the eye blebs mouse. Dev Dyn. 2000 Sep; 219(1):21-7. PMID: 10974668.
      View in: PubMed
    122. 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. Mamm Genome. 2000 Jul; 11(7):484-8. PMID: 10886010.
      View in: PubMed
    123. Noveroske JK, Weber JS, Justice MJ. The mutagenic action of N-ethyl-N-nitrosourea in the mouse. Mamm Genome. 2000 Jul; 11(7):478-83. PMID: 10886009.
      View in: PubMed
    124. Denny P, Justice MJ. Mouse as the measure of man? Trends Genet. 2000 Jul; 16(7):283-7. PMID: 10858655.
      View in: PubMed
    125. Weber JS, Salinger A, Justice MJ. Optimal N-ethyl-N-nitrosourea (ENU) doses for inbred mouse strains. Genesis. 2000 Apr; 26(4):230-3. PMID: 10748459.
      View in: PubMed
    126. Hansen GM, Skapura D, Justice MJ. Genetic profile of insertion mutations in mouse leukemias and lymphomas. Genome Res. 2000 Feb; 10(2):237-43. PMID: 10673281.
      View in: PubMed
    127. 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. Anal Biochem. 2000 Jan 01; 277(1):157-60. PMID: 10610701.
      View in: PubMed
    128. 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. Mamm Genome. 2000 Jan; 11(1):58-63. PMID: 10602994.
      View in: PubMed
    129. Hansen GM, Justice MJ. Activation of Hex and mEg5 by retroviral insertion may contribute to mouse B-cell leukemia. Oncogene. 1999 Nov 11; 18(47):6531-9. PMID: 10597256.
      View in: PubMed
    130. 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. 1999 May 01; 57(3):333-41. PMID: 10328999.
      View in: PubMed
    131. Davis AP, Woychik RP, Justice MJ. Effective chemical mutagenesis in FVB/N mice requires low doses of ethylnitrosourea. Mamm Genome. 1999 Mar; 10(3):308-10. PMID: 10051330.
      View in: PubMed
    132. Hansen GM, Tackles D, Schwartz C, Justice MJ. A mouse chromosome 19 genetic map including the Lvis1 viral insertion site. Genomics. 1999 Mar 01; 56(2):228-31. PMID: 10051411.
      View in: PubMed
    133. Justice MJ, Noveroske JK, Weber JS, Zheng B, Bradley A. Mouse ENU mutagenesis. Hum Mol Genet. 1999; 8(10):1955-63. PMID: 10469849.
      View in: PubMed
    134. Davis AP, Justice MJ. Mouse alleles: if you've seen one, you haven't seen them all. Trends Genet. 1998 Nov; 14(11):438-41. PMID: 9825669.
      View in: PubMed
    135. 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. 1998 Aug 15; 52(1):110-1. PMID: 10348636.
      View in: PubMed
    136. Woychik RP, Klebig ML, Justice MJ, Magnuson TR, Avner ED, Avrer ED. Functional genomics in the post-genome era. Mutat Res. 1998 May 25; 400(1-2):3-14. PMID: 9685569.
      View in: PubMed
    137. Davis AP, Justice MJ. Meeting report: 11th International Mouse Genome Conference. Mamm Genome. 1998 May; 9(5):345-8. PMID: 9545489.
      View in: PubMed
    138. Hansen GM, Justice MJ. Pten, a candidate tumor suppressor gene, maps to mouse chromosome 19. Mamm Genome. 1998 Jan; 9(1):88-90. PMID: 9434957.
      View in: PubMed
    139. Davis AP, Justice MJ. An Oak Ridge legacy: the specific locus test and its role in mouse mutagenesis. Genetics. 1998 Jan; 148(1):7-12. PMID: 9475716.
      View in: PubMed
    140. 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. 1997 Dec; 13(4):423-36. PMID: 9480786.
      View in: PubMed
    141. Perou CM, Perchellet A, Jago T, Pryor R, Kaplan J, Justice MJ. Comparative mapping in the beige-satin region of mouse chromosome 13. Genomics. 1997 Jan 15; 39(2):136-46. PMID: 9027500.
      View in: PubMed
    142. Justice MJ, Stephenson DA. Mouse chromosome 13. Mamm Genome. 1997; 7 Spec No:S223-37. PMID: 9233396.
      View in: PubMed
    143. 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. Nat Genet. 1996 Jul; 13(3):303-8. PMID: 8673129.
      View in: PubMed
    144. Perou CM, Justice MJ, Pryor RJ, Kaplan J. Complementation of the beige mutation in cultured cells by episomally replicating murine yeast artificial chromosomes. Proc Natl Acad Sci U S A. 1996 Jun 11; 93(12):5905-9. PMID: 8650191.
      View in: PubMed
    145. 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. Mamm Genome. 1996 Jun; 7(6):417-9. PMID: 8662222.
      View in: PubMed
    146. 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. Nat Genet. 1996 Mar; 12(3):260-5. PMID: 8589716.
      View in: PubMed
    147. Justice MJ, Stephenson DA. Encyclopedia of the mouse genome V. Mouse chromosome 13. Mamm Genome. 1996; 6 Spec No:S232-44. PMID: 8800768.
      View in: PubMed
    148. Funderburgh JL, Funderburgh ML, Hevelone ND, Stech ME, Justice MJ, Liu CY, Kao WW, Conrad GW. Sequence, molecular properties, and chromosomal mapping of mouse lumican. Invest Ophthalmol Vis Sci. 1995 Oct; 36(11):2296-303. PMID: 7558724.
      View in: PubMed
    149. Liu CY, Zhu G, Converse R, Kao CW, Nakamura H, Tseng SC, Mui MM, Seyer J, Justice MJ, Stech ME, et al. Characterization and chromosomal localization of the cornea-specific murine keratin gene Krt1.12. J Biol Chem. 1994 Oct 07; 269(40):24627-36. PMID: 7523376.
      View in: PubMed
    150. Justice MJ, Morse HC, Jenkins NA, Copeland NG. Identification of Evi-3, a novel common site of retroviral integration in mouse AKXD B-cell lymphomas. J Virol. 1994 Mar; 68(3):1293-300. PMID: 8107195.
      View in: PubMed
    151. Justice MJ, Stephenson DA. Mouse chromosome 13. Mamm Genome. 1994; 5 Spec No:S196-206. PMID: 7719006.
      View in: PubMed
    152. 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. 1993 Apr; 16(1):278-81. PMID: 8486374.
      View in: PubMed
    153. Justice MJ, Stephenson DA. Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 13. Mamm Genome. 1993; 4 Spec No:S192-202. PMID: 8268673.
      View in: PubMed
    154. Justice MJ, Gilbert DJ, Kinzler KW, Vogelstein B, Buchberg AM, Ceci JD, Matsuda Y, Chapman VM, Patriotis C, Makris A, et al. A molecular genetic linkage map of mouse chromosome 18 reveals extensive linkage conservation with human chromosomes 5 and 18. Genomics. 1992 Aug; 13(4):1281-8. PMID: 1354644.
      View in: PubMed
    155. Justice MJ, Jenkins NA, Copeland NG. Recombinant inbred mouse strains: models for disease study. Trends Biotechnol. 1992 Apr; 10(4):120-6. PMID: 1368097.
      View in: PubMed
    156. Justice MJ, Stephenson DA. Mouse chromosome 13. Mamm Genome. 1992; 3 Spec No:S195-205. PMID: 1498432.
      View in: PubMed
    157. Oettinger HF, Streeter H, Lose E, Copeland NG, Gilbert DJ, Justice MJ, Jenkins NA, Mohandas T, Bernfield M. Chromosome mapping of the murine syndecan gene. Genomics. 1991 Oct; 11(2):334-8. PMID: 1769649.
      View in: PubMed
    158. Jenkins NA, Justice MJ, Gilbert DJ, Chu ML, Copeland NG. Nidogen/entactin (Nid) maps to the proximal end of mouse chromosome 13 linked to beige (bg) and identifies a new region of homology between mouse and human chromosomes. Genomics. 1991 Feb; 9(2):401-3. PMID: 1672300.
      View in: PubMed
    159. Taylor BA, Justice MJ, Reeves R. Mouse chromosome 10. Mamm Genome. 1991; 1 Spec No:S146-57. PMID: 1799797.
      View in: PubMed
    160. Justice MJ, Stephenson DA. Mouse chromosome 13. Mamm Genome. 1991; 1 Spec No:S205-20. PMID: 1799801.
      View in: PubMed
    161. Justice MJ, Siracusa LD, Gilbert DJ, Heisterkamp N, Groffen J, Chada K, Silan CM, Copeland NG, Jenkins NA. A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross. Genetics. 1990 Aug; 125(4):855-66. PMID: 1975791.
      View in: PubMed
    162. Justice MJ, Bode VC. ENU-induced allele of brachyury (Tkt1) exhibits a developmental lethal phenotype similar to the original brachyury (T) mutation. J Exp Zool. 1990 Jun; 254(3):286-95. PMID: 2345346.
      View in: PubMed
    163. Dickinson ME, Kobrin MS, Silan CM, Kingsley DM, Justice MJ, Miller DA, Ceci JD, Lock LF, Lee A, Buchberg AM, et al. Chromosomal localization of seven members of the murine TGF-beta superfamily suggests close linkage to several morphogenetic mutant loci. Genomics. 1990 Mar; 6(3):505-20. PMID: 1970330.
      View in: PubMed
    164. 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. 1990 Mar; 6(3):491-504. PMID: 1970329.
      View in: PubMed
    165. Justice MJ, Silan CM, Ceci JD, Buchberg AM, Copeland NG, Jenkins NA. A molecular genetic linkage map of mouse chromosome 13 anchored by the beige (bg) and satin (sa) loci. Genomics. 1990 Feb; 6(2):341-51. PMID: 2307475.
      View in: PubMed
    166. Ceci JD, Justice MJ, Lock LF, Jenkins NA, Copeland NG. An interspecific backcross linkage map of mouse chromosome 8. Genomics. 1990 Jan; 6(1):72-9. PMID: 1968046.
      View in: PubMed
    167. Mock BA, Nordan RP, Justice MJ, Kozak C, Jenkins NA, Copeland NG, Clark SC, Wong GG, Rudikoff S. The murine Il-6 gene maps to the proximal region of chromosome 5. J Immunol. 1989 Feb 15; 142(4):1372-6. PMID: 2563387.
      View in: PubMed
    168. Hill RE, Jones PF, Rees AR, Sime CM, Justice MJ, Copeland NG, Jenkins NA, Graham E, Davidson DR. A new family of mouse homeo box-containing genes: molecular structure, chromosomal location, and developmental expression of Hox-7.1. Genes Dev. 1989 Jan; 3(1):26-37. PMID: 2565278.
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    169. Justice MJ, Bode VC. Genetic analysis of mouse t haplotypes using mutations induced by ethylnitrosourea mutagenesis: the order of T and qk is inverted in t mutants. Genetics. 1988 Oct; 120(2):533-43. PMID: 3197958.
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    170. Justice MJ, Bode VC. Three ENU-induced alleles of the murine quaking locus are recessive embryonic lethal mutations. Genet Res. 1988 Apr; 51(2):95-102. PMID: 3410318.
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    171. Justice MJ, Bode VC. Induction of new mutations in a mouse t-haplotype using ethylnitrosourea mutagenesis. Genet Res. 1986 Jun; 47(3):187-92. PMID: 3744044.
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