Zanhua Yi, Ph.D. - Publications
Affiliations: | 2005 | University of Arizona, Tucson, AZ |
Area:
Genetics, Molecular Biology, PathologyYear | Citation | Score | |||
---|---|---|---|---|---|
2006 | Yi Z, Cohen-Barak O, Hagiwara N, Kingsley PD, Fuchs DA, Erickson DT, Epner EM, Palis J, Brilliant MH. Sox6 directly silences epsilon globin expression in definitive erythropoiesis. Plos Genetics. 2: e14. PMID 16462943 DOI: 10.1371/Journal.Pgen.0020014 | 0.474 | |||
2005 | Ikinciogullari A, Tekin M, Dogu F, Reisli I, Tanir G, Yi Z, Garrison N, Brilliant MH, Babacan E. Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism. European Journal of Pediatrics. 164: 177-9. PMID 15565285 DOI: 10.1007/S00431-004-1582-Y | 0.424 | |||
2004 | Garrison NA, Yi Z, Cohen-Barak O, Huizing M, Hartnell LM, Gahl WA, Brilliant MH. P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome. Journal of Medical Genetics. 41: e86. PMID 15173252 DOI: 10.1136/Jmg.2003.014902 | 0.466 | |||
2003 | Cohen-Barak O, Yi Z, Hagiwara N, Monzen K, Komuro I, Brilliant MH. Sox6 regulation of cardiac myocyte development. Nucleic Acids Research. 31: 5941-8. PMID 14530442 DOI: 10.1093/Nar/Gkg807 | 0.478 | |||
2003 | Yi Z, Garrison N, Cohen-Barak O, Karafet TM, King RA, Erickson RP, Hammer MF, Brilliant MH. A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population. American Journal of Human Genetics. 72: 62-72. PMID 12469324 DOI: 10.1086/345380 | 0.466 | |||
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