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Items: 1 to 20 of 36

1.

Minisatellite mutational processes reduce F(st) estimates.

Flint J, Bond J, Rees DC, Boyce AJ, Roberts-Thomson JM, Excoffier L, Clegg JB, Beaumont MA, Nichols RA, Harding RM.

Hum Genet. 1999 Dec;105(6):567-76.

PMID:
10647891
2.

Genomic views of human history.

Owens K, King MC.

Science. 1999 Oct 15;286(5439):451-3.

PMID:
10521333
3.
4.

Loss of function mutations of the human melanocortin 1 receptor are common and are associated with red hair.

Schiöth HB, Phillips SR, Rudzish R, Birch-Machin MA, Wikberg JE, Rees JL.

Biochem Biophys Res Commun. 1999 Jul 5;260(2):488-91.

PMID:
10403794
5.

Characterization of single-nucleotide polymorphisms in coding regions of human genes.

Cargill M, Altshuler D, Ireland J, Sklar P, Ardlie K, Patil N, Shaw N, Lane CR, Lim EP, Kalyanaraman N, Nemesh J, Ziaugra L, Friedland L, Rolfe A, Warrington J, Lipshutz R, Daley GQ, Lander ES.

Nat Genet. 1999 Jul;22(3):231-8. Erratum in: Nat Genet 1999 Nov;23(3):373.

PMID:
10391209
6.

Molecular analysis of a new splice variant of the human melanocortin-1 receptor.

Tan CP, McKee KK, Weinberg DH, MacNeil T, Palyha OC, Feighner SD, Hreniuk DL, Van Der Ploeg LH, MacNeil DJ, Howard AD.

FEBS Lett. 1999 May 21;451(2):137-41.

8.

Pigmentation, melanocortins and red hair.

Rees JL, Flanagan N.

QJM. 1999 Mar;92(3):125-31. No abstract available.

PMID:
10326071
9.

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.

PMID:
10319866
10.

High polymorphism at the human melanocortin 1 receptor locus.

Rana BK, Hewett-Emmett D, Jin L, Chang BH, Sambuughin N, Lin M, Watkins S, Bamshad M, Jorde LB, Ramsay M, Jenkins T, Li WH.

Genetics. 1999 Apr;151(4):1547-57.

11.

X chromosome evidence for ancient human histories.

Harris EE, Hey J.

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):3320-4.

12.

More on the X files.

Harding RM.

Proc Natl Acad Sci U S A. 1999 Mar 16;96(6):2582-4. No abstract available.

13.

High genomic deleterious mutation rates in hominids.

Eyre-Walker A, Keightley PD.

Nature. 1999 Jan 28;397(6717):344-7.

PMID:
9950425
14.

Melanocortin receptors and antagonists regulate pigmentation and body weight.

Jordan SA, Jackson IJ.

Bioessays. 1998 Aug;20(8):603-6. Review.

PMID:
9780833
15.

Genetic structure of the ancestral population of modern humans.

Zietkiewicz E, Yotova V, Jarnik M, Korab-Laskowska M, Kidd KK, Modiano D, Scozzari R, Stoneking M, Tishkoff S, Batzer M, Labuda D.

J Mol Evol. 1998 Aug;47(2):146-55.

PMID:
9694663
16.

Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase.

Clark AG, Weiss KM, Nickerson DA, Taylor SL, Buchanan A, Stengård J, Salomaa V, Vartiainen E, Perola M, Boerwinkle E, Sing CF.

Am J Hum Genet. 1998 Aug;63(2):595-612.

17.

Melanocortin 1 receptor variants in an Irish population.

Smith R, Healy E, Siddiqui S, Flanagan N, Steijlen PM, Rosdahl I, Jacques JP, Rogers S, Turner R, Jackson IJ, Birch-Machin MA, Rees JL.

J Invest Dermatol. 1998 Jul;111(1):119-22.

18.

Using mitochondrial and nuclear DNA markers to reconstruct human evolution.

Jorde LB, Bamshad M, Rogers AR.

Bioessays. 1998 Feb;20(2):126-36. Review.

PMID:
9631658
19.

Human pigmentation phenotype: a point mutation generates nonfunctional MSH receptor.

Frändberg PA, Doufexis M, Kapas S, Chhájlani V.

Biochem Biophys Res Commun. 1998 Apr 17;245(2):490-2.

PMID:
9571181
20.

Heterogeneity of microsatellite mutations within and between loci, and implications for human demographic histories.

Di Rienzo A, Donnelly P, Toomajian C, Sisk B, Hill A, Petzl-Erler ML, Haines GK, Barch DH.

Genetics. 1998 Mar;148(3):1269-84.

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