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Results: 1-9 |
Results: 9

Authors: Iwawaki, T Hosoda, A Okuda, T Kamigori, Y Nomura-Furuwatari, C Kimata, Y Tsuru, A Kohno, K
Citation: T. Iwawaki et al., Translational control by the ER transmembrane kinase/ribonuclease IRE1 under ER stress, NAT CELL BI, 3(2), 2001, pp. 158-164

Authors: Kondoh, T Kamimura, N Tsuru, A Matsumoto, T Matsuzaka, T Moriuchi, H
Citation: T. Kondoh et al., A case of Schinzel-Giedion syndrome complicated with progressive severe gingival hyperplasia and progressive brain atrophy, PEDIATR INT, 43(2), 2001, pp. 181-184

Authors: Saito, M Iwawaki, T Taya, C Yonekawa, H Noda, M Inui, Y Mekada, E Kimata, Y Tsuru, A Kohno, K
Citation: M. Saito et al., Diphtheria toxin receptor-mediated conditional and targeted cell ablation in transgenic mice, NAT BIOTECH, 19(8), 2001, pp. 746-750

Authors: Matsuo, A Matsuzaka, T Tsuru, A Moriuchi, H Nakashita, Y Tanaka, S Baba, C Tomimasu, K
Citation: A. Matsuo et al., Epidemiological and clinical studies of West syndrome in Nagasaki Prefecture, Japan, BRAIN DEVEL, 23(7), 2001, pp. 575-579

Authors: Imamura, Y Kondoh, T Kamei, T Tsuru, A Shimasaki, Y Kinoshita, E Matsumoto, T Moriuchi, H
Citation: Y. Imamura et al., A case of achondroplasia with severe respiratory failure, profound developmental delay and hypercreatine phosphokinasemia, PEDIATR INT, 42(5), 2000, pp. 564-567

Authors: Kimata, Y Ooboki, K Nomura-Furuwatari, C Hosoda, A Tsuru, A Kohno, K
Citation: Y. Kimata et al., Identification of a novel mammalian endoplasmic reticulum-resident KDEL protein using an EST database motif search, GENE, 261(2), 2000, pp. 321-327

Authors: Tsuru, A Walker, RJ Kontinen, A Peltonen, P Hanski, E
Citation: A. Tsuru et al., Re-Os isotopic systematics of the 1.95 Ga Jormua Ophiolite Complex, northeastern Finland, CHEM GEOL, 164(1-2), 2000, pp. 123-141

Authors: Okamura, K Kimata, Y Higashio, H Tsuru, A Kohno, K
Citation: K. Okamura et al., Dissociation of Kar2p/BiP from an ER sensory molecule, Ire1p, triggers theunfolded protein response in yeast, BIOC BIOP R, 279(2), 2000, pp. 445-450

Authors: Kondoh, T Tsuru, A Matsumoto, T Matsuzaka, T Tsuji, Y
Citation: T. Kondoh et al., Autosomal dominant onychodystrophy and congenital sensorineural deafness, J HUM GENET, 44(1), 1999, pp. 60-62
Risultati: 1-9 |