339 related articles for article (PubMed ID: 11158380)
1. Global patterns of human DNA sequence variation in a 10-kb region on chromosome 1.
Yu N; Zhao Z; Fu YX; Sambuughin N; Ramsay M; Jenkins T; Leskinen E; Patthy L; Jorde LB; Kuromori T; Li WH
Mol Biol Evol; 2001 Feb; 18(2):214-22. PubMed ID: 11158380
[TBL] [Abstract][Full Text] [Related]
2. Worldwide DNA sequence variation in a 10-kilobase noncoding region on human chromosome 22.
Zhao Z; Jin L; Fu YX; Ramsay M; Jenkins T; Leskinen E; Pamilo P; Trexler M; Patthy L; Jorde LB; Ramos-Onsins S; Yu N; Li WH
Proc Natl Acad Sci U S A; 2000 Oct; 97(21):11354-8. PubMed ID: 11005839
[TBL] [Abstract][Full Text] [Related]
3. Nucleotide variation and haplotype diversity in a 10-kb noncoding region in three continental human populations.
Zhao Z; Yu N; Fu YX; Li WH
Genetics; 2006 Sep; 174(1):399-409. PubMed ID: 16783003
[TBL] [Abstract][Full Text] [Related]
4. Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees.
Chen FC; Li WH
Am J Hum Genet; 2001 Feb; 68(2):444-56. PubMed ID: 11170892
[TBL] [Abstract][Full Text] [Related]
5. Human DNA sequence variation in a 6.6-kb region containing the melanocortin 1 receptor promoter.
Makova KD; Ramsay M; Jenkins T; Li WH
Genetics; 2001 Jul; 158(3):1253-68. PubMed ID: 11454772
[TBL] [Abstract][Full Text] [Related]
6. Contrasting evolutionary histories of two introns of the duchenne muscular dystrophy gene, Dmd, in humans.
Nachman MW; Crowell SL
Genetics; 2000 Aug; 155(4):1855-64. PubMed ID: 10924480
[TBL] [Abstract][Full Text] [Related]
7. Sequence variation in ZFX introns in human populations.
Huang W; Fu YX; Chang BH; Gu X; Jorde LB; Li WH
Mol Biol Evol; 1998 Feb; 15(2):138-42. PubMed ID: 9491612
[TBL] [Abstract][Full Text] [Related]
8. Divergence of the genes on human chromosome 21 between human and other hominoids and variation of substitution rates among transcription units.
Shi J; Xi H; Wang Y; Zhang C; Jiang Z; Zhang K; Shen Y; Jin L; Zhang K; Yuan W; Wang Y; Lin J; Hua Q; Wang F; Xu S; Ren S; Xu S; Zhao G; Chen Z; Jin L; Huang W
Proc Natl Acad Sci U S A; 2003 Jul; 100(14):8331-6. PubMed ID: 12826612
[TBL] [Abstract][Full Text] [Related]
9. Evolution and the origins of man: clues from complete sequences of hominoid mitochondrial DNA.
Horai S
Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():146-54. PubMed ID: 8629095
[TBL] [Abstract][Full Text] [Related]
10. SSADH variation in primates: intra- and interspecific data on a gene with a potential role in human cognitive functions.
Blasi P; Palmerio F; Aiello A; Rocchi M; Malaspina P; Novelletto A
J Mol Evol; 2006 Jul; 63(1):54-68. PubMed ID: 16786440
[TBL] [Abstract][Full Text] [Related]
11. A comparison of TSPY genes from Y-chromosomal DNA of the great apes and humans: sequence, evolution, and phylogeny.
Kim HS; Takenaka O
Am J Phys Anthropol; 1996 Jul; 100(3):301-9. PubMed ID: 8798990
[TBL] [Abstract][Full Text] [Related]
12. DNA sequence variation in a non-coding region of low recombination on the human X chromosome.
Kaessmann H; Heissig F; von Haeseler A; Pääbo S
Nat Genet; 1999 May; 22(1):78-81. PubMed ID: 10319866
[TBL] [Abstract][Full Text] [Related]
13. Sequences from higher primates orthologous to the human Xp/Yp telomere junction region reveal gross rearrangements and high levels of divergence.
Baird DM; Royle NJ
Hum Mol Genet; 1997 Dec; 6(13):2291-9. PubMed ID: 9361036
[TBL] [Abstract][Full Text] [Related]
14. [The relationship among human, gorilla, chimpanzee and orangutan].
Ding B; Zhang YP; Ryder OA
Yi Chuan Xue Bao; 1999; 26(6):604-9. PubMed ID: 10876659
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Population genetic and phylogenetic evidence for positive selection on regulatory mutations at the factor VII locus in humans.
Hahn MW; Rockman MV; Soranzo N; Goldstein DB; Wray GA
Genetics; 2004 Jun; 167(2):867-77. PubMed ID: 15238535
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 10072600
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. The pattern of restriction enzyme-induced banding in the chromosomes of chimpanzee, gorilla, and orangutan and its evolutionary significance.
Bianchi NO; Bianchi MS; Cleaver JE; Wolff S
J Mol Evol; 1985; 22(4):323-33. PubMed ID: 3003371
[TBL] [Abstract][Full Text] [Related]
20. Nucleotide variation at Msn and Alas2, two genes flanking the centromere of the X chromosome in humans.
Nachman MW; D'Agostino SL; Tillquist CR; Mobasher Z; Hammer MF
Genetics; 2004 May; 167(1):423-37. PubMed ID: 15166166
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
