Gao, L Y, Guo, S, McLaughlin, B, Morisaki, H, Engel, J N, Brown, Eric J
Initiation and maintenance of infection by mycobacteria in susceptible hosts are not well understood. A screen of Mycobacterium marinum transposon mutant library led to isolation of eight mutants...
Sevoflurane preconditions stunned myocardium in septic but not healthy isolated rat hearts (2002)
Serita, R., Morisaki, H., Ai, K., Morita, Y., Innami, Y., Satoh, T., ...
Background. Recent evidence indicates that sevoflurane treatment before prolonged ischaemia reduces infarct size in normal hearts, mimicking ischaemic preconditioning. We examined whether exposure to...
Leucocyte distribution during sevoflurane anaesthesia (1998)
Morisaki, H., Aoyama, Y., Shimada, M., Ochiai, R., Takeda, J.
MORISAKI, H., TANAKA, T., ISHIMURA, Y., TAKEDA, J., SEKIGUCHI, H., NAGANO, M.
Inhibitory effects of diazepam and flunitrazepam on the superoxide anion (O2−) -generating system in granulocytes were examined for their clinical relevance. When the effects of commercial...
Molecular basis of AMP deaminase deficiency in skeletal muscle.
Morisaki, T, Gross, M, Morisaki, H, Pongratz, D, Zöllner, N, Holmes, E W
AMP deaminase (AMPD; EC 3.5.4.6) is encoded by a multigene family in mammals. The AMPD1 gene is expressed at high levels in skeletal muscle, where this enzyme is thought to play an important role in...
Mouse U2af1-rs1 is a neomorphic imprinted gene.
Nabetani, A, Hatada, I, Morisaki, H, Oshimura, M, Mukai, T
The mouse U2af1-rs1 gene is an endogenous imprinted gene on the proximal region of chromosome 11. This gene is transcribed exclusively from the unmethylated paternal allele, while the methylated...
Alternative splicing: a mechanism for phenotypic rescue of a common inherited defect.
Morisaki, H, Morisaki, T, Newby, L K, Holmes, E W
Approximately 2% of Caucasians and African-Americans are homozygous for a nonsense mutation in exon 2 of the AMPD1 (AMP deaminase) gene. These individuals have a high grade deficiency of AMPD...
Hisatome, I, Kurata, Y, Sasaki, N, Morisaki, T, Morisaki, H, Tanaka, Y, ...
Divalent mercury (Hg(2+)) blocked human skeletal Na(+) channels (hSkM1) in a stable dose-dependent manner (K(d) = 0.96 microM) in the absence of reducing agent. Dithiothreitol (DTT) significantly...
Molecular basis of AMP deaminase deficiency in skeletal muscle.
Morisaki, T, Gross, M, Morisaki, H, Pongratz, D, Zöllner, N, Holmes, E W
AMP deaminase (AMPD; EC 3.5.4.6) is encoded by a multigene family in mammals. The AMPD1 gene is expressed at high levels in skeletal muscle, where this enzyme is thought to play an important role in...
Mouse U2af1-rs1 is a neomorphic imprinted gene.
Nabetani, A, Hatada, I, Morisaki, H, Oshimura, M, Mukai, T
The mouse U2af1-rs1 gene is an endogenous imprinted gene on the proximal region of chromosome 11. This gene is transcribed exclusively from the unmethylated paternal allele, while the methylated...
Alternative splicing: a mechanism for phenotypic rescue of a common inherited defect.
Morisaki, H, Morisaki, T, Newby, L K, Holmes, E W
Approximately 2% of Caucasians and African-Americans are homozygous for a nonsense mutation in exon 2 of the AMPD1 (AMP deaminase) gene. These individuals have a high grade deficiency of AMPD...
Hisatome, I, Kurata, Y, Sasaki, N, Morisaki, T, Morisaki, H, Tanaka, Y, ...
Divalent mercury (Hg(2+)) blocked human skeletal Na(+) channels (hSkM1) in a stable dose-dependent manner (K(d) = 0.96 microM) in the absence of reducing agent. Dithiothreitol (DTT) significantly...