Marina Kniazeva - Research Associate
MCDB
(303) 735-4688
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Porter B347
Kniazeva M, Crawford QT, Seiber M, Wang CY, Han M, "Monomethyl branched-chain fatty acids play an essential role in Caenorhabditis elegans development." PLoS biology 2 (2004): E257
Kniazeva M, Sieber M, McCauley S, Zhang K, Watts JL, Han M, "Suppression of the ELO-2 FA elongation activity results in alterations of the fatty acid composition and multiple physiological defects, including abnormal ultradian rhythms, in Caenorhabditis elegans." Genetics 163 (2003): 159-69
Kniazeva M, Traboulsi EI, Yu Z, Stefko ST, Gorin MB, Shugart YY, O'Connell JR, Blaschak CJ, Cutting G, Han M, Zhang K, "A new locus for dominant drusen and macular degeneration maps to chromosome 6q14." American journal of ophthalmology 130 (2000): 197-202
Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K, "Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease." Ophthalmic genetics 20 (1999): 71-81
Kniazeva M, Chiang MF, Morgan B, Anduze AL, Zack DJ, Han M, Zhang K, "A new locus for autosomal dominant stargardt-like disease maps to chromosome 4." American journal of human genetics 64 (1999): 1394-9
Kniazeva M, Sieber M, McCauley S, Zhang K, Watts JL, Han M, "Suppression of the ELO-2 FA elongation activity results in alterations of the fatty acid composition and multiple physiological defects, including abnormal ultradian rhythms, in Caenorhabditis elegans." Genetics 163 (2003): 159-69
Kniazeva M, Traboulsi EI, Yu Z, Stefko ST, Gorin MB, Shugart YY, O'Connell JR, Blaschak CJ, Cutting G, Han M, Zhang K, "A new locus for dominant drusen and macular degeneration maps to chromosome 6q14." American journal of ophthalmology 130 (2000): 197-202
Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K, "Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease." Ophthalmic genetics 20 (1999): 71-81
Kniazeva M, Chiang MF, Morgan B, Anduze AL, Zack DJ, Han M, Zhang K, "A new locus for autosomal dominant stargardt-like disease maps to chromosome 4." American journal of human genetics 64 (1999): 1394-9
