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Results: 1-8 |
Results: 8

Authors: Inaba, T Adachi, M Ida, A Fukushima, R Okinaga, K
Citation: T. Inaba et al., Segmental intestinal preservation and enteral nutrition help to maintain the intestinal function after a massive intestinal resection: Report of a case, SURG TODAY, 31(10), 2001, pp. 923-927

Authors: Haywood, MEK Vyse, TJ McDermott, A Thompson, EM Ida, A Walport, MJ Izui, S Morley, BJ
Citation: Mek. Haywood et al., Autoantigen glycoprotein 70 expression is regulated by a single locus, which acts as a checkpoint for pathogenic anti-glycoprotein 70 autoantibody production and hence for the corresponding development of severe nephritis, in lupus-prone BXSB mice, J IMMUNOL, 167(3), 2001, pp. 1728-1733

Authors: Ida, A Tsuji, Y Muranaka, J Kanazawa, R Nakata, Y Adachi, S Okamura, H Koyama, K
Citation: A. Ida et al., IL-18 in pregnancy; the elevation of IL-18 in maternal peripheral blood during labour and complicated pregnancies, J REPRO IMM, 47(1), 2000, pp. 65-74

Authors: Ida, A Todoroki, J Sanuki, H
Citation: A. Ida et al., Influence of numerical integration on convergence of eigenvalues in magnetohydrodynamics stability analysis, J PHYS JPN, 69(5), 2000, pp. 1259-1262

Authors: Iinuma, H Okinaga, K Adachi, M Suda, K Sekine, T Sakagawa, K Baba, Y Tamura, J Kumagai, H Ida, A
Citation: H. Iinuma et al., Detection of tumor cells in blood using CD45 magnetic cell separation followed by nested mutant allele-specific amplification of p53 and K-ras genes in patients with colorectal cancer, INT J CANC, 89(4), 2000, pp. 337-344

Authors: Sawai, H Komori, S Ida, A Henmi, T Bessho, T Koyama, K
Citation: H. Sawai et al., Prenatal diagnosis of thanatophoric dysplasia by mutational analysis of the fibroblast growth factor receptor 3 gene and a proposed correction of previously published PCR results, PRENAT DIAG, 19(1), 1999, pp. 21-24

Authors: Inai, Y Kurokawa, Y Ida, A Hirabayashi, T
Citation: Y. Inai et al., Effects of N-terminal L-amino acid residues on helical screw sense in achiral peptides, B CHEM S J, 72(1), 1999, pp. 55-61

Authors: Sawai, H Ida, A Nakata, Y Koyama, K
Citation: H. Sawai et al., Novel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasia, J HUM GENET, 43(4), 1998, pp. 259-261
Risultati: 1-8 |