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Items: 1 to 20 of 222

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Breakpoint analysis of the pericentric inversion distinguishing human chromosome 4 from the homologous chromosome in the chimpanzee (Pan troglodytes).

Kehrer-Sawatzki H, Sandig C, Chuzhanova N, Goidts V, Szamalek JM, Tänzer S, Müller S, Platzer M, Cooper DN, Hameister H.

Hum Mutat. 2005 Jan;25(1):45-55.

PMID:
15580561
5.

Conservation of pericentromeric duplications of a 200-kb part of the human 21q22.1 region in primates.

Orti R, Potier MC, Maunoury C, Prieur M, Créau N, Delabar JM.

Cytogenet Cell Genet. 1998;83(3-4):262-5.

PMID:
10072600
6.

Distinct retroelement classes define evolutionary breakpoints demarcating sites of evolutionary novelty.

Longo MS, Carone DM; NISC Comparative Sequencing Program, Green ED, O'Neill MJ, O'Neill RJ.

BMC Genomics. 2009 Jul 24;10:334. doi: 10.1186/1471-2164-10-334.

7.

The evolutionary origin of human subtelomeric homologies--or where the ends begin.

Martin CL, Wong A, Gross A, Chung J, Fantes JA, Ledbetter DH.

Am J Hum Genet. 2002 Apr;70(4):972-84. Epub 2002 Mar 1.

8.

[Tandem and interspersed repeats contribute to the mosaic structure of segmented duplications in the human genome].

Oparina NIu, Lakrua ME, Rychkov AA, Mashkova TD.

Mol Biol (Mosk). 2003 Mar-Apr;37(2):228-33. Russian.

PMID:
12723470
9.

Generation and annotation of the DNA sequences of human chromosomes 2 and 4.

Hillier LW, Graves TA, Fulton RS, Fulton LA, Pepin KH, Minx P, Wagner-McPherson C, Layman D, Wylie K, Sekhon M, Becker MC, Fewell GA, Delehaunty KD, Miner TL, Nash WE, Kremitzki C, Oddy L, Du H, Sun H, Bradshaw-Cordum H, Ali J, Carter J, Cordes M, Harris A, Isak A, van Brunt A, Nguyen C, Du F, Courtney L, Kalicki J, Ozersky P, Abbott S, Armstrong J, Belter EA, Caruso L, Cedroni M, Cotton M, Davidson T, Desai A, Elliott G, Erb T, Fronick C, Gaige T, Haakenson W, Haglund K, Holmes A, Harkins R, Kim K, Kruchowski SS, Strong CM, Grewal N, Goyea E, Hou S, Levy A, Martinka S, Mead K, McLellan MD, Meyer R, Randall-Maher J, Tomlinson C, Dauphin-Kohlberg S, Kozlowicz-Reilly A, Shah N, Swearengen-Shahid S, Snider J, Strong JT, Thompson J, Yoakum M, Leonard S, Pearman C, Trani L, Radionenko M, Waligorski JE, Wang C, Rock SM, Tin-Wollam AM, Maupin R, Latreille P, Wendl MC, Yang SP, Pohl C, Wallis JW, Spieth J, Bieri TA, Berkowicz N, Nelson JO, Osborne J, Ding L, Meyer R, Sabo A, Shotland Y, Sinha P, Wohldmann PE, Cook LL, Hickenbotham MT, Eldred J, Williams D, Jones TA, She X, Ciccarelli FD, Izaurralde E, Taylor J, Schmutz J, Myers RM, Cox DR, Huang X, McPherson JD, Mardis ER, Clifton SW, Warren WC, Chinwalla AT, Eddy SR, Marra MA, Ovcharenko I, Furey TS, Miller W, Eichler EE, Bork P, Suyama M, Torrents D, Waterston RH, Wilson RK.

Nature. 2005 Apr 7;434(7034):724-31.

PMID:
15815621
10.

The evolution of MHC diversity by segmental duplication and transposition of retroelements.

Kulski JK, Gaudieri S, Bellgard M, Balmer L, Giles K, Inoko H, Dawkins RL.

J Mol Evol. 1997 Dec;45(6):599-609. Erratum in: J Mol Evol 1998 Jun;46(6):734.

PMID:
9419237
11.

Ancestrally-duplicated paraHOX gene clusters in humans.

Coulier F, Burtey S, Chaffanet M, Birg F, Birnbaum D.

Int J Oncol. 2000 Sep;17(3):439-44.

PMID:
10938381
12.

Analyses of cross species polymerase chain reaction products to infer the ancestral state of human polymorphisms.

Iyengar S, Seaman M, Deinard AS, Rosenbaum HC, Sirugo G, Castiglione CM, Kidd JR, Kidd KK.

DNA Seq. 1998;8(5):317-27.

PMID:
10993602
13.

Synteny comparison between apes and human using fine-mapping of the genome.

de Pontbriand A, Wang XP, Cavaloc Y, Mattei MG, Galibert F.

Genomics. 2002 Oct;80(4):395-401.

PMID:
12376093
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Genomic structure and paralogous regions of the inversion breakpoint occurring between human chromosome 3p12.3 and orangutan chromosome 2.

Yue Y, Grossmann B, Tsend-Ayush E, Grützner F, Ferguson-Smith MA, Yang F, Haaf T.

Cytogenet Genome Res. 2005;108(1-3):98-105.

PMID:
15545721
17.

FRA2B is distinct from inverted telomere repeat arrays at 2q13.

IJdo JW, Baldini A, Wells RA, Ward DC, Reeders ST.

Genomics. 1992 Apr;12(4):833-5.

PMID:
1572659
18.

Recent human-specific spreading of a subtelomeric domain.

Monfouilloux S, Avet-Loiseau H, Amarger V, Balazs I, Pourcel C, Vergnaud G.

Genomics. 1998 Jul 15;51(2):165-76.

PMID:
9722938
19.

Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions.

Jenne DE, Tinschert S, Reimann H, Lasinger W, Thiel G, Hameister H, Kehrer-Sawatzki H.

Am J Hum Genet. 2001 Sep;69(3):516-27. Epub 2001 Jul 20.

20.

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