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    Results: 1 to 20 of 122

    1.

    Mouse segmental duplication and copy number variation.

    She X, Cheng Z, Zöllner S, Church DM, Eichler EE.

    Nat Genet. 2008 Jul;40(7):909-14. Epub 2008 May 22.PMID: 18500340 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Significant gene content variation characterizes the genomes of inbred mouse strains.

    Cutler G, Marshall LA, Chin N, Baribault H, Kassner PD.

    Genome Res. 2007 Dec;17(12):1743-54. Epub 2007 Nov 7.PMID: 17989247 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Analysis of segmental duplications and genome assembly in the mouse.

    Bailey JA, Church DM, Ventura M, Rocchi M, Eichler EE.

    Genome Res. 2004 May;14(5):789-801.PMID: 15123579 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    A high-resolution map of segmental DNA copy number variation in the mouse genome.

    Graubert TA, Cahan P, Edwin D, Selzer RR, Richmond TA, Eis PS, Shannon WD, Li X, McLeod HL, Cheverud JM, Ley TJ.

    PLoS Genet. 2007 Jan 5;3(1):e3. Epub 2006 Nov 22.PMID: 17206864 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Recent segmental and gene duplications in the mouse genome.

    Cheung J, Wilson MD, Zhang J, Khaja R, MacDonald JR, Heng HH, Koop BF, Scherer SW.

    Genome Biol. 2003;4(8):R47. Epub 2003 Jul 9.PMID: 12914656 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH.

    de Bustos C, Díaz de Ståhl T, Piotrowski A, Mantripragada KK, Buckley PG, Darai E, Hansson CM, Grigelionis G, Menzel U, Dumanski JP.

    Genomics. 2006 Aug;88(2):152-62. Epub 2006 May 18.PMID: 16713171 [PubMed - indexed for MEDLINE]Related articles

    7.

    Lineage-specific biology revealed by a finished genome assembly of the mouse.

    Church DM, Goodstadt L, Hillier LW, Zody MC, Goldstein S, She X, Bult CJ, Agarwala R, Cherry JL, DiCuccio M, Hlavina W, Kapustin Y, Meric P, Maglott D, Birtle Z, Marques AC, Graves T, Zhou S, Teague B, Potamousis K, Churas C, Place M, Herschleb J, Runnheim R, Forrest D, Amos-Landgraf J, Schwartz DC, Cheng Z, Lindblad-Toh K, Eichler EE, Ponting CP; Mouse Genome Sequencing Consortium.

    PLoS Biol. 2009 May 5;7(5):e1000112. Epub 2009 May 26.PMID: 19468303 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Structure and expression of mobile ETnII retroelements and their coding-competent MusD relatives in the mouse.

    Baust C, Gagnier L, Baillie GJ, Harris MJ, Juriloff DM, Mager DL.

    J Virol. 2003 Nov;77(21):11448-58.PMID: 14557630 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    Segmental duplications and copy-number variation in the human genome.

    Sharp AJ, Locke DP, McGrath SD, Cheng Z, Bailey JA, Vallente RU, Pertz LM, Clark RA, Schwartz S, Segraves R, Oseroff VV, Albertson DG, Pinkel D, Eichler EE.

    Am J Hum Genet. 2005 Jul;77(1):78-88. Epub 2005 May 25.PMID: 15918152 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    The sequence of the human genome.

    Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, Smith HO, Yandell M, Evans CA, Holt RA, Gocayne JD, Amanatides P, Ballew RM, Huson DH, Wortman JR, Zhang Q, Kodira CD, Zheng XH, Chen L, Skupski M, Subramanian G, Thomas PD, Zhang J, Gabor Miklos GL, Nelson C, Broder S, Clark AG, Nadeau J, McKusick VA, Zinder N, Levine AJ, Roberts RJ, Simon M, Slayman C, Hunkapiller M, Bolanos R, Delcher A, Dew I, Fasulo D, Flanigan M, Florea L, Halpern A, Hannenhalli S, Kravitz S, Levy S, Mobarry C, Reinert K, Remington K, Abu-Threideh J, Beasley E, Biddick K, Bonazzi V, Brandon R, Cargill M, Chandramouliswaran I, Charlab R, Chaturvedi K, Deng Z, Di Francesco V, Dunn P, Eilbeck K, Evangelista C, Gabrielian AE, Gan W, Ge W, Gong F, Gu Z, Guan P, Heiman TJ, Higgins ME, Ji RR, Ke Z, Ketchum KA, Lai Z, Lei Y, Li Z, Li J, Liang Y, Lin X, Lu F, Merkulov GV, Milshina N, Moore HM, Naik AK, Narayan VA, Neelam B, Nusskern D, Rusch DB, Salzberg S, Shao W, Shue B, Sun J, Wang Z, Wang A, Wang X, Wang J, Wei M, Wides R, Xiao C, Yan C, Yao A, Ye J, Zhan M, Zhang W, Zhang H, Zhao Q, Zheng L, Zhong F, Zhong W, Zhu S, Zhao S, Gilbert D, Baumhueter S, Spier G, Carter C, Cravchik A, Woodage T, Ali F, An H, Awe A, Baldwin D, Baden H, Barnstead M, Barrow I, Beeson K, Busam D, Carver A, Center A, Cheng ML, Curry L, Danaher S, Davenport L, Desilets R, Dietz S, Dodson K, Doup L, Ferriera S, Garg N, Gluecksmann A, Hart B, Haynes J, Haynes C, Heiner C, Hladun S, Hostin D, Houck J, Howland T, Ibegwam C, Johnson J, Kalush F, Kline L, Koduru S, Love A, Mann F, May D, McCawley S, McIntosh T, McMullen I, Moy M, Moy L, Murphy B, Nelson K, Pfannkoch C, Pratts E, Puri V, Qureshi H, Reardon M, Rodriguez R, Rogers YH, Romblad D, Ruhfel B, Scott R, Sitter C, Smallwood M, Stewart E, Strong R, Suh E, Thomas R, Tint NN, Tse S, Vech C, Wang G, Wetter J, Williams S, Williams M, Windsor S, Winn-Deen E, Wolfe K, Zaveri J, Zaveri K, Abril JF, Guigó R, Campbell MJ, Sjolander KV, Karlak B, Kejariwal A, Mi H, Lazareva B, Hatton T, Narechania A, Diemer K, Muruganujan A, Guo N, Sato S, Bafna V, Istrail S, Lippert R, Schwartz R, Walenz B, Yooseph S, Allen D, Basu A, Baxendale J, Blick L, Caminha M, Carnes-Stine J, Caulk P, Chiang YH, Coyne M, Dahlke C, Mays A, Dombroski M, Donnelly M, Ely D, Esparham S, Fosler C, Gire H, Glanowski S, Glasser K, Glodek A, Gorokhov M, Graham K, Gropman B, Harris M, Heil J, Henderson S, Hoover J, Jennings D, Jordan C, Jordan J, Kasha J, Kagan L, Kraft C, Levitsky A, Lewis M, Liu X, Lopez J, Ma D, Majoros W, McDaniel J, Murphy S, Newman M, Nguyen T, Nguyen N, Nodell M, Pan S, Peck J, Peterson M, Rowe W, Sanders R, Scott J, Simpson M, Smith T, Sprague A, Stockwell T, Turner R, Venter E, Wang M, Wen M, Wu D, Wu M, Xia A, Zandieh A, Zhu X.

    Science. 2001 Feb 16;291(5507):1304-51. Erratum in: Science 2001 Jun 5;292(5523):1838. PMID: 11181995 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 mb of mouse genome.

    Frazer KA, Wade CM, Hinds DA, Patil N, Cox DR, Daly MJ.

    Genome Res. 2004 Aug;14(8):1493-500.PMID: 15289472 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    Genome-wide assessments reveal extremely high levels of polymorphism of two active families of mouse endogenous retroviral elements.

    Zhang Y, Maksakova IA, Gagnier L, van de Lagemaat LN, Mager DL.

    PLoS Genet. 2008 Feb 29;4(2):e1000007.PMID: 18454193 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Reading between the LINEs: human genomic variation induced by LINE-1 retrotransposition.

    Sheen FM, Sherry ST, Risch GM, Robichaux M, Nasidze I, Stoneking M, Batzer MA, Swergold GD.

    Genome Res. 2000 Oct;10(10):1496-508.PMID: 11042149 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Genomic copy number and expression variation within the C57BL/6J inbred mouse strain.

    Watkins-Chow DE, Pavan WJ.

    Genome Res. 2008 Jan;18(1):60-6. Epub 2007 Nov 21.PMID: 18032724 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Recurrent DNA copy number variation in the laboratory mouse.

    Egan CM, Sridhar S, Wigler M, Hall IM.

    Nat Genet. 2007 Nov;39(11):1384-9. Epub 2007 Oct 28.PMID: 17965714 [PubMed - indexed for MEDLINE]Related articles

    16.

    Human copy number polymorphic genes.

    Bailey JA, Kidd JM, Eichler EE.

    Cytogenet Genome Res. 2008;123(1-4):234-43. Epub 2009 Mar 11.PMID: 19287160 [PubMed - indexed for MEDLINE]Related articles

    17.

    Shotgun sequence assembly and recent segmental duplications within the human genome.

    She X, Jiang Z, Clark RA, Liu G, Cheng Z, Tuzun E, Church DM, Sutton G, Halpern AL, Eichler EE.

    Nature. 2004 Oct 21;431(7011):927-30.PMID: 15496912 [PubMed - indexed for MEDLINE]Related articles

    18.

    Extensive variation between inbred mouse strains due to endogenous L1 retrotransposition.

    Akagi K, Li J, Stephens RM, Volfovsky N, Symer DE.

    Genome Res. 2008 Jun;18(6):869-80. Epub 2008 Apr 1.PMID: 18381897 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements.

    Armengol L, Pujana MA, Cheung J, Scherer SW, Estivill X.

    Hum Mol Genet. 2003 Sep 1;12(17):2201-8. Epub 2003 Jul 8.PMID: 12915466 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Complex patterns of copy number variation at sites of segmental duplications: an important category of structural variation in the human genome.

    Goidts V, Cooper DN, Armengol L, Schempp W, Conroy J, Estivill X, Nowak N, Hameister H, Kehrer-Sawatzki H.

    Hum Genet. 2006 Sep;120(2):270-84. Epub 2006 Jul 13.PMID: 16838144 [PubMed - indexed for MEDLINE]Related articles

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