62 related articles for article (PubMed ID: 11827455)
1. Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28.
Aradhya S; Woffendin H; Bonnen P; Heiss NS; Yamagata T; Esposito T; Bardaro T; Poustka A; D'Urso M; Kenwrick S; Nelson DL
Genomics; 2002 Jan; 79(1):31-40. PubMed ID: 11827455
[TBL] [Abstract][Full Text] [Related]
2. A transcript map of a 2-Mb BAC contig in the proximal portion of the mouse X chromosome and regional mapping of the scurfy mutation.
Means GD; Toy DY; Baum PR; Derry JM
Genomics; 2000 May; 65(3):213-23. PubMed ID: 10857745
[TBL] [Abstract][Full Text] [Related]
3. Physical and transcript map of the hereditary prostate cancer region at xq27.
Stephan DA; Howell GR; Teslovich TM; Coffey AJ; Smith L; Bailey-Wilson JE; Malechek L; Gildea D; Smith JR; Gillanders EM; Schleutker J; Hu P; Steingruber HE; Dhami P; Robbins CM; Makalowska I; Carpten JD; Sood R; Mumm S; Reinbold R; Bonner TI; Baffoe-Bonnie A; Bubendorf L; Heiskanen M; Kallioneimi OP; Baxevanis AD; Joseph SS; Zucchi I; Burk RD; Isaacs W; Ross MT; Trent JM
Genomics; 2002 Jan; 79(1):41-50. PubMed ID: 11827456
[TBL] [Abstract][Full Text] [Related]
4. A short pseudoautosomal region in laboratory mice.
Perry J; Palmer S; Gabriel A; Ashworth A
Genome Res; 2001 Nov; 11(11):1826-32. PubMed ID: 11691846
[TBL] [Abstract][Full Text] [Related]
5. Polymorphic segmental duplications at 8p23.1 challenge the determination of individual defensin gene repertoires and the assembly of a contiguous human reference sequence.
Taudien S; Galgoczy P; Huse K; Reichwald K; Schilhabel M; Szafranski K; Shimizu A; Asakawa S; Frankish A; Loncarevic IF; Shimizu N; Siddiqui R; Platzer M
BMC Genomics; 2004 Dec; 5(1):92. PubMed ID: 15588320
[TBL] [Abstract][Full Text] [Related]
6. Characterization of the human Xq21.3/Yp11 homology block and conservation of organization in primates.
Sargent CA; Boucher CA; Blanco P; Chalmers IJ; Highet L; Hall N; Ross N; Crow T; Affara NA
Genomics; 2001 Apr; 73(1):77-85. PubMed ID: 11352568
[TBL] [Abstract][Full Text] [Related]
7. Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region.
Cruts M; Rademakers R; Gijselinck I; van der Zee J; Dermaut B; de Pooter T; de Rijk P; Del-Favero J; van Broeckhoven C
Hum Mol Genet; 2005 Jul; 14(13):1753-62. PubMed ID: 15888485
[TBL] [Abstract][Full Text] [Related]
8. Comparative cytogenetics of human chromosome 3q21.3 reveals a hot spot for ectopic recombination in hominoid evolution.
Yue Y; Grossmann B; Ferguson-Smith M; Yang F; Haaf T
Genomics; 2005 Jan; 85(1):36-47. PubMed ID: 15607420
[TBL] [Abstract][Full Text] [Related]
9. Alport syndrome. Molecular genetic aspects.
Hertz JM
Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
[TBL] [Abstract][Full Text] [Related]
10. Duplication of a gene-rich cluster between 16p11.1 and Xq28: a novel pericentromeric-directed mechanism for paralogous genome evolution.
Eichler EE; Lu F; Shen Y; Antonacci R; Jurecic V; Doggett NA; Moyzis RK; Baldini A; Gibbs RA; Nelson DL
Hum Mol Genet; 1996 Jul; 5(7):899-912. PubMed ID: 8817324
[TBL] [Abstract][Full Text] [Related]
11. Integrated pseudogene annotation for human chromosome 22: evidence for transcription.
Zheng D; Zhang Z; Harrison PM; Karro J; Carriero N; Gerstein M
J Mol Biol; 2005 May; 349(1):27-45. PubMed ID: 15876366
[TBL] [Abstract][Full Text] [Related]
12. Co-duplication of olfactory receptor and MHC class I genes in the mouse major histocompatibility complex.
Amadou C; Younger RM; Sims S; Matthews LH; Rogers J; Kumanovics A; Ziegler A; Beck S; Lindahl KF
Hum Mol Genet; 2003 Nov; 12(22):3025-40. PubMed ID: 14506126
[TBL] [Abstract][Full Text] [Related]
13. A physical map of the highly heterozygous Populus genome: integration with the genome sequence and genetic map and analysis of haplotype variation.
Kelleher CT; Chiu R; Shin H; Bosdet IE; Krzywinski MI; Fjell CD; Wilkin J; Yin T; DiFazio SP; Ali J; Asano JK; Chan S; Cloutier A; Girn N; Leach S; Lee D; Mathewson CA; Olson T; O'connor K; Prabhu AL; Smailus DE; Stott JM; Tsai M; Wye NH; Yang GS; Zhuang J; Holt RA; Putnam NH; Vrebalov J; Giovannoni JJ; Grimwood J; Schmutz J; Rokhsar D; Jones SJ; Marra MA; Tuskan GA; Bohlmann J; Ellis BE; Ritland K; Douglas CJ; Schein JE
Plant J; 2007 Jun; 50(6):1063-78. PubMed ID: 17488239
[TBL] [Abstract][Full Text] [Related]
14. High-resolution combined linkage physical map of short tandem repeat loci on human chromosome band Xq28 for indirect haemophilia A carrier detection.
Machado FB; Medina-Acosta E
Haemophilia; 2009 Jan; 15(1):297-308. PubMed ID: 18752533
[TBL] [Abstract][Full Text] [Related]
15. An integrated physical and gene map of the 3.5-Mb chromosome 3p21.3 (AP20) region implicated in major human epithelial malignancies.
Protopopov A; Kashuba V; Zabarovska VI; Muravenko OV; Lerman MI; Klein G; Zabarovsky ER
Cancer Res; 2003 Jan; 63(2):404-12. PubMed ID: 12543795
[TBL] [Abstract][Full Text] [Related]
16. PKLR- GBA region shows almost complete linkage disequilibrium over 70 kb in a set of worldwide populations.
Mateu E; Pérez-Lezaun A; Martínez-Arias R; Andrés A; Vallés M; Bertranpetit J; Calafell F
Hum Genet; 2002 Jun; 110(6):532-44. PubMed ID: 12107439
[TBL] [Abstract][Full Text] [Related]
17. Physical and transcript map of a 2-Mb region in Xp22.1 containing candidate genes for X-linked mental retardation and short stature.
Zhang S; Krahe R
Genomics; 2002 Mar; 79(3):274-7. PubMed ID: 11863356
[TBL] [Abstract][Full Text] [Related]
18. Nonneutral evolution of the transcribed pseudogene Makorin1-p1 in mice.
Podlaha O; Zhang J
Mol Biol Evol; 2004 Dec; 21(12):2202-9. PubMed ID: 15306660
[TBL] [Abstract][Full Text] [Related]
19. Not all isolates are equal: linkage disequilibrium analysis on Xq13.3 reveals different patterns in Sardinian sub-populations.
Angius A; Bebbere D; Petretto E; Falchi M; Forabosco P; Maestrale B; Casu G; Persico I; Melis PM; Pirastu M
Hum Genet; 2002 Jul; 111(1):9-15. PubMed ID: 12136230
[TBL] [Abstract][Full Text] [Related]
20. A transposable element-mediated gene divergence that directly produces a novel type bovine Bcnt protein including the endonuclease domain of RTE-1.
Iwashita S; Osada N; Itoh T; Sezaki M; Oshima K; Hashimoto E; Kitagawa-Arita Y; Takahashi I; Masui T; Hashimoto K; Makalowski W
Mol Biol Evol; 2003 Sep; 20(9):1556-63. PubMed ID: 12832649
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]