302 related articles for article (PubMed ID: 19165922)
1. Evolutionary toggling of the MAPT 17q21.31 inversion region.
Zody MC; Jiang Z; Fung HC; Antonacci F; Hillier LW; Cardone MF; Graves TA; Kidd JM; Cheng Z; Abouelleil A; Chen L; Wallis J; Glasscock J; Wilson RK; Reily AD; Duckworth J; Ventura M; Hardy J; Warren WC; Eichler EE
Nat Genet; 2008 Sep; 40(9):1076-83. PubMed ID: 19165922
[TBL] [Abstract][Full Text] [Related]
2. Recurrent inversion events at 17q21.31 microdeletion locus are linked to the MAPT H2 haplotype.
Rao PN; Li W; Vissers LE; Veltman JA; Ophoff RA
Cytogenet Genome Res; 2010; 129(4):275-9. PubMed ID: 20606400
[TBL] [Abstract][Full Text] [Related]
3. Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner.
de Jong S; Chepelev I; Janson E; Strengman E; van den Berg LH; Veldink JH; Ophoff RA
BMC Genomics; 2012 Sep; 13():458. PubMed ID: 22950410
[TBL] [Abstract][Full Text] [Related]
4. Using the neanderthal and denisova genetic data to understand the common MAPT 17q21 inversion in modern humans.
Setó-Salvia N; Sánchez-Quinto F; Carbonell E; Lorenzo C; Comas D; Clarimón J
Hum Biol; 2012 Dec; 84(6):633-40. PubMed ID: 23959642
[TBL] [Abstract][Full Text] [Related]
5. Independent intrachromosomal recombination events underlie the pericentric inversions of chimpanzee and gorilla chromosomes homologous to human chromosome 16.
Goidts V; Szamalek JM; de Jong PJ; Cooper DN; Chuzhanova N; Hameister H; Kehrer-Sawatzki H
Genome Res; 2005 Sep; 15(9):1232-42. PubMed ID: 16140991
[TBL] [Abstract][Full Text] [Related]
6. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees.
Nickerson E; Nelson DL
Genomics; 1998 Jun; 50(3):368-72. PubMed ID: 9676431
[TBL] [Abstract][Full Text] [Related]
7. Tau gene (MAPT) sequence variation among primates.
Holzer M; Craxton M; Jakes R; Arendt T; Goedert M
Gene; 2004 Oct; 341():313-22. PubMed ID: 15474313
[TBL] [Abstract][Full Text] [Related]
8. Structural diversity and African origin of the 17q21.31 inversion polymorphism.
Steinberg KM; Antonacci F; Sudmant PH; Kidd JM; Campbell CD; Vives L; Malig M; Scheinfeldt L; Beggs W; Ibrahim M; Lema G; Nyambo TB; Omar SA; Bodo JM; Froment A; Donnelly MP; Kidd KK; Tishkoff SA; Eichler EE
Nat Genet; 2012 Jul; 44(8):872-80. PubMed ID: 22751100
[TBL] [Abstract][Full Text] [Related]
9. Primate segmental duplication creates novel promoters for the LRRC37 gene family within the 17q21.31 inversion polymorphism region.
Bekpen C; Tastekin I; Siswara P; Akdis CA; Eichler EE
Genome Res; 2012 Jun; 22(6):1050-8. PubMed ID: 22419166
[TBL] [Abstract][Full Text] [Related]
10. Nucleotide sequence comparison of a chromosome rearrangement on human chromosome 12 and the corresponding ape chromosomes.
Shimada MK; Kim CG; Kitano T; Ferrell RE; Kohara Y; Saitou N
Cytogenet Genome Res; 2005; 108(1-3):83-90. PubMed ID: 15545719
[TBL] [Abstract][Full Text] [Related]
11. Breakpoint analysis of the pericentric inversion between chimpanzee chromosome 10 and the homologous chromosome 12 in humans.
Kehrer-Sawatzki H; Sandig CA; Goidts V; Hameister H
Cytogenet Genome Res; 2005; 108(1-3):91-7. PubMed ID: 15545720
[TBL] [Abstract][Full Text] [Related]
12. Refinement of a chimpanzee pericentric inversion breakpoint to a segmental duplication cluster.
Locke DP; Archidiacono N; Misceo D; Cardone MF; Deschamps S; Roe B; Rocchi M; Eichler EE
Genome Biol; 2003; 4(8):R50. PubMed ID: 12914658
[TBL] [Abstract][Full Text] [Related]
13. 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. PubMed ID: 15580561
[TBL] [Abstract][Full Text] [Related]
14. 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. PubMed ID: 15545721
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. The origin, global distribution, and functional impact of the human 8p23 inversion polymorphism.
Salm MP; Horswell SD; Hutchison CE; Speedy HE; Yang X; Liang L; Schadt EE; Cookson WO; Wierzbicki AS; Naoumova RP; Shoulders CC
Genome Res; 2012 Jun; 22(6):1144-53. PubMed ID: 22399572
[TBL] [Abstract][Full Text] [Related]
17. Characterization of six human disease-associated inversion polymorphisms.
Antonacci F; Kidd JM; Marques-Bonet T; Ventura M; Siswara P; Jiang Z; Eichler EE
Hum Mol Genet; 2009 Jul; 18(14):2555-66. PubMed ID: 19383631
[TBL] [Abstract][Full Text] [Related]
18. The ZNF75 zinc finger gene subfamily: isolation and mapping of the four members in humans and great apes.
Villa A; Strina D; Frattini A; Faranda S; Macchi P; Finelli P; Bozzi F; Susani L; Archidiacono N; Rocchi M; Vezzoni P
Genomics; 1996 Jul; 35(2):312-20. PubMed ID: 8661144
[TBL] [Abstract][Full Text] [Related]
19. Molecular characterization of the pericentric inversion of chimpanzee chromosome 11 homologous to human chromosome 9.
Kehrer-Sawatzki H; Szamalek JM; Tänzer S; Platzer M; Hameister H
Genomics; 2005 May; 85(5):542-50. PubMed ID: 15820305
[TBL] [Abstract][Full Text] [Related]
20. Structural haplotypes and recent evolution of the human 17q21.31 region.
Boettger LM; Handsaker RE; Zody MC; McCarroll SA
Nat Genet; 2012 Jul; 44(8):881-5. PubMed ID: 22751096
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]