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Items: 1 to 20 of 46

1.

A classifier for the SNP-based inference of ancestry.

Frudakis T, Venkateswarlu K, Thomas MJ, Gaskin Z, Ginjupalli S, Gunturi S, Ponnuswamy V, Natarajan S, Nachimuthu PK.

J Forensic Sci. 2003 Jul;48(4):771-82. Erratum in: J Forensic Sci. 2004 Sep;49(5):1145-6.

PMID:
12877291
2.

Skin pigmentation, biogeographical ancestry and admixture mapping.

Shriver MD, Parra EJ, Dios S, Bonilla C, Norton H, Jovel C, Pfaff C, Jones C, Massac A, Cameron N, Baron A, Jackson T, Argyropoulos G, Jin L, Hoggart CJ, McKeigue PM, Kittles RA.

Hum Genet. 2003 Apr;112(4):387-99. Epub 2003 Feb 11.

PMID:
12579416
3.

P gene as an inherited biomarker of human eye color.

Rebbeck TR, Kanetsky PA, Walker AH, Holmes R, Halpern AC, Schuchter LM, Elder DE, Guerry D.

Cancer Epidemiol Biomarkers Prev. 2002 Aug;11(8):782-4.

4.

Human pigmentation genes: identification, structure and consequences of polymorphic variation.

Sturm RA, Teasdale RD, Box NF.

Gene. 2001 Oct 17;277(1-2):49-62. Review.

PMID:
11602344
5.

Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.

Newton JM, Cohen-Barak O, Hagiwara N, Gardner JM, Davisson MT, King RA, Brilliant MH.

Am J Hum Genet. 2001 Nov;69(5):981-8. Epub 2001 Sep 26.

6.
7.

Induction of tyrosinase gene transcription in human iris organ cultures exposed to latanoprost.

Lindsey JD, Jones HL, Hewitt EG, Angert M, Weinreb RN.

Arch Ophthalmol. 2001 Jun;119(6):853-60.

PMID:
11405836
8.

A new statistical method for haplotype reconstruction from population data.

Stephens M, Smith NJ, Donnelly P.

Am J Hum Genet. 2001 Apr;68(4):978-89. Epub 2001 Mar 9.

9.

Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation.

Flanagan N, Healy E, Ray A, Philips S, Todd C, Jackson IJ, Birch-Machin MA, Rees JL.

Hum Mol Genet. 2000 Oct 12;9(17):2531-7.

PMID:
11030758
10.

Empirical Bayes adjustments for multiple results in hypothesis-generating or surveillance studies.

Steenland K, Bray I, Greenland S, Boffetta P.

Cancer Epidemiol Biomarkers Prev. 2000 Sep;9(9):895-903.

11.

A mutation in Rab27a causes the vesicle transport defects observed in ashen mice.

Wilson SM, Yip R, Swing DA, O'Sullivan TN, Zhang Y, Novak EK, Swank RT, Russell LB, Copeland NG, Jenkins NA.

Proc Natl Acad Sci U S A. 2000 Jul 5;97(14):7933-8.

12.

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
13.
14.

Not just pretty eyes: Drosophila eye-colour mutations and lysosomal delivery.

Lloyd V, Ramaswami M, Krämer H.

Trends Cell Biol. 1998 Jul;8(7):257-9. Review.

PMID:
9714595
15.

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.

16.

Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.

Krude H, Biebermann H, Luck W, Horn R, Brabant G, Grüters A.

Nat Genet. 1998 Jun;19(2):155-7.

PMID:
9620771
17.

Altered expression of a novel adaptin leads to defective pigment granule biogenesis in the Drosophila eye color mutant garnet.

Ooi CE, Moreira JE, Dell'Angelica EC, Poy G, Wassarman DA, Bonifacino JS.

EMBO J. 1997 Aug 1;16(15):4508-18.

18.

Characterization of melanocyte stimulating hormone receptor variant alleles in twins with red hair.

Box NF, Wyeth JR, O'Gorman LE, Martin NG, Sturm RA.

Hum Mol Genet. 1997 Oct;6(11):1891-7.

PMID:
9302268
19.

Eye color changes past early childhood. The Louisville Twin Study.

Bito LZ, Matheny A, Cruickshanks KJ, Nondahl DM, Carino OB.

Arch Ophthalmol. 1997 May;115(5):659-63.

PMID:
9152135
20.

Identification of common polymorphisms in the coding sequence of the human MSH receptor (MCIR) with possible biological effects.

Koppula SV, Robbins LS, Lu D, Baack E, White CR Jr, Swanson NA, Cone RD.

Hum Mutat. 1997;9(1):30-6.

PMID:
8990005

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