Brilliant MH - Search Results

1

Predicting phenotype from genotype: normal pigmentation.

Valenzuela RK, Henderson MS, Walsh MH, Garrison NA, Kelch JT, Cohen-Barak O, Erickson DT, John Meaney F, Bruce Walsh J, Cheng KC, Ito S, Wakamatsu K, Frudakis T, Thomas M, Brilliant MH. Valenzuela RK, et al. Among authors: brilliant mh. J Forensic Sci. 2010 Mar 1;55(2):315-22. doi: 10.1111/j.1556-4029.2009.01317.x. Epub 2010 Feb 11. J Forensic Sci. 2010. PMID: 20158590 Free PMC article.

2

A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.

Yi Z, Garrison N, Cohen-Barak O, Karafet TM, King RA, Erickson RP, Hammer MF, Brilliant MH. Yi Z, et al. Among authors: brilliant mh. Am J Hum Genet. 2003 Jan;72(1):62-72. doi: 10.1086/345380. Epub 2002 Dec 5. Am J Hum Genet. 2003. PMID: 12469324 Free PMC article.

3

Albinism and disease causing pathogens in Tanzania: are alleles that are associated with OCA2 being maintained by balancing selection?

Tuli AM, Valenzuela RK, Kamugisha E, Brilliant MH. Tuli AM, et al. Among authors: brilliant mh. Med Hypotheses. 2012 Dec;79(6):875-8. doi: 10.1016/j.mehy.2012.09.013. Epub 2012 Oct 12. Med Hypotheses. 2012. PMID: 23063908 Free article.

4

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. Newton JM, et al. Among authors: brilliant mh. Am J Hum Genet. 2001 Nov;69(5):981-8. doi: 10.1086/324340. Epub 2001 Sep 26. Am J Hum Genet. 2001. PMID: 11574907 Free PMC article.

5

P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome.

Garrison NA, Yi Z, Cohen-Barak O, Huizing M, Hartnell LM, Gahl WA, Brilliant MH. Garrison NA, et al. Among authors: brilliant mh. J Med Genet. 2004 Jun;41(6):e86. doi: 10.1136/jmg.2003.014902. J Med Genet. 2004. PMID: 15173252 Free PMC article. No abstract available.

6

Sox6 directly silences epsilon globin expression in definitive erythropoiesis.

Yi Z, Cohen-Barak O, Hagiwara N, Kingsley PD, Fuchs DA, Erickson DT, Epner EM, Palis J, Brilliant MH. Yi Z, et al. Among authors: brilliant mh. PLoS Genet. 2006 Feb;2(2):e14. doi: 10.1371/journal.pgen.0020014. Epub 2006 Feb 3. PLoS Genet. 2006. PMID: 16462943 Free PMC article.

7

Stem cell transplantation demonstrates that Sox6 represses epsilon y globin expression in definitive erythropoiesis of adult mice.

Cohen-Barak O, Erickson DT, Badowski MS, Fuchs DA, Klassen CL, Harris DT, Brilliant MH. Cohen-Barak O, et al. Among authors: brilliant mh. Exp Hematol. 2007 Mar;35(3):358-67. doi: 10.1016/j.exphem.2006.11.009. Exp Hematol. 2007. PMID: 17309816 Free article.

8

Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death.

Hagiwara N, Klewer SE, Samson RA, Erickson DT, Lyon MF, Brilliant MH. Hagiwara N, et al. Among authors: brilliant mh. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4180-5. doi: 10.1073/pnas.97.8.4180. Proc Natl Acad Sci U S A. 2000. PMID: 10760285 Free PMC article.

9

Sox6 regulation of cardiac myocyte development.

Cohen-Barak O, Yi Z, Hagiwara N, Monzen K, Komuro I, Brilliant MH. Cohen-Barak O, et al. Among authors: brilliant mh. Nucleic Acids Res. 2003 Oct 15;31(20):5941-8. doi: 10.1093/nar/gkg807. Nucleic Acids Res. 2003. PMID: 14530442 Free PMC article.

10

Usefulness of alkaline hydrogen peroxide oxidation to analyze eumelanin and pheomelanin in various tissue samples: application to chemical analysis of human hair melanins.

Ito S, Nakanishi Y, Valenzuela RK, Brilliant MH, Kolbe L, Wakamatsu K. Ito S, et al. Among authors: brilliant mh. Pigment Cell Melanoma Res. 2011 Aug;24(4):605-13. doi: 10.1111/j.1755-148X.2011.00864.x. Epub 2011 May 17. Pigment Cell Melanoma Res. 2011. PMID: 21535429

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