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Results: 1-7 |
Results: 7
Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene (vol 26, pg 237, 2000)
Authors: Akama, TO
Citation: To. Akama, Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene (vol 26, pg 237, 2000), NAT GENET, 27(1), 2001, pp. 125-125
Human ITCH is a coregulator of the hematopoietic transcription factor NF-E2
Authors: Chen, X Wen, SC Fukuda, MN Gavva, NR Hsu, DW Akama, TO Yang-Feng, T Shen, CKJ
Citation: X. Chen et al., Human ITCH is a coregulator of the hematopoietic transcription factor NF-E2, GENOMICS, 73(2), 2001, pp. 238-241
Human corneal GlcNAc 6-O-sulfotransferase and mouse intestinal GlcNAc 6-O-sulfotransferase both produce keratan sulfate
Authors: Akama, TO Nakayama, J Nishida, K Hiraoka, N Suzuki, M McAuliffe, J Hindsgaul, O Fukuda, M Fukuda, MN
Citation: To. Akama et al., Human corneal GlcNAc 6-O-sulfotransferase and mouse intestinal GlcNAc 6-O-sulfotransferase both produce keratan sulfate, J BIOL CHEM, 276(19), 2001, pp. 16271-16278
Overexpression of the Golgi-localized enzyme alpha-mannosidase IIx in Chinese hamster ovary cells results in the conversion of hexamannosyl-N-acetylchitobiose to tetramannosyl-N-acetylchitobiose in the N-glycan-processing pathway
Authors: Oh-eda, M Nakagawa, H Akama, TO Lowitz, K Misago, M Moremen, KW Fukuda, MN
Citation: M. Oh-eda et al., Overexpression of the Golgi-localized enzyme alpha-mannosidase IIx in Chinese hamster ovary cells results in the conversion of hexamannosyl-N-acetylchitobiose to tetramannosyl-N-acetylchitobiose in the N-glycan-processing pathway, EUR J BIOCH, 268(5), 2001, pp. 1280-1288
Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland
Authors: Liu, NP Dew-Knight, S Rayner, M Jonasson, F Akama, TO Fukuda, MN Bao, WJ Gilbert, JR Vance, JM Klintworth, GK
Citation: Np. Liu et al., Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland, MOL VIS, 6(33), 2000, pp. 261-264
Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene
Authors: Akama, TO Nishida, K Nakayama, J Watanabe, H Ozaki, K Nakamura, T Dota, A Kawasaki, S Inoue, Y Maeda, N Yamamoto, S Fujiwara, T Thonar, EJMA Shimomura, Y Kinoshita, S Tanigami, A Fukuda, MN
Citation: To. Akama et al., Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene, NAT GENET, 26(2), 2000, pp. 237-241
Molecular cloning and expression of two distinct human chondroitin 4-O-sulfotransferases that belong to the HNK-1 sulfotransferase gene family
Authors: Hiraoka, N Nakagawa, H Ong, E Akama, TO Fukuda, MN Fukuda, M
Citation: N. Hiraoka et al., Molecular cloning and expression of two distinct human chondroitin 4-O-sulfotransferases that belong to the HNK-1 sulfotransferase gene family, J BIOL CHEM, 275(26), 2000, pp. 20188-20196
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