Murray H. Brilliant
Affiliations: | Genetics | University of Arizona, Tucson, AZ |
Area:
Genetics, Medical and Forensic AnthropologyGoogle:
"Murray Brilliant"
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Publications
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| Tuli AM, Valenzuela RK, Kamugisha E, et al. (2012) Albinism and disease causing pathogens in Tanzania: are alleles that are associated with OCA2 being maintained by balancing selection? Medical Hypotheses. 79: 875-8 |
| Jiang YH, Pan Y, Zhu L, et al. (2010) Altered ultrasonic vocalization and impaired learning and memory in Angelman syndrome mouse model with a large maternal deletion from Ube3a to Gabrb3. Plos One. 5: e12278 |
| Valenzuela RK, Henderson MS, Walsh MH, et al. (2010) Predicting phenotype from genotype: normal pigmentation. Journal of Forensic Sciences. 55: 315-22 |
| Odeh H, Hunker KL, Belyantseva IA, et al. (2010) Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. American Journal of Human Genetics. 86: 148-60 |
| Carrasco A, Forbes EM, Jeambrun P, et al. (2009) A splice site mutation is the cause of the high prevalence of oculocutaneous albinism type 2 in the Kuna population. Pigment Cell & Melanoma Research. 22: 645-7 |
| Cohen-Barak O, Erickson DT, Badowski MS, et al. (2007) Stem cell transplantation demonstrates that Sox6 represses epsilon y globin expression in definitive erythropoiesis of adult mice. Experimental Hematology. 35: 358-67 |
| Yi Z, Cohen-Barak O, Hagiwara N, et al. (2006) Sox6 directly silences epsilon globin expression in definitive erythropoiesis. Plos Genetics. 2: e14 |
| Ikinciogullari A, Tekin M, Dogu F, et al. (2005) Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism. European Journal of Pediatrics. 164: 177-9 |
| Odeh H, Hagiwara N, Skynner M, et al. (2004) Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus. Audiology & Neuro-Otology. 9: 303-14 |
| Garrison NA, Yi Z, Cohen-Barak O, et al. (2004) P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome. Journal of Medical Genetics. 41: e86 |