Search Results - "Ishii, Norie"
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Endoscopic management of a traumatic disruption of the bulbous urethra using a thin trocar puncture
Published in International journal of urology (01-04-2001)“…A case is reported in which complete disruption of the bulbous urethra resulted in a straddled‐type injury, which was managed by endoscopic realignment with a…”
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Wobble modification defect in tRNA disturbs codon-anticodon interaction in a mitochondrial disease
Published in The EMBO journal (03-09-2001)“…We previously showed that in mitochondrial tRNALys with an A8344G mutation responsible for myoclonus epilepsy associated with ragged‐red fibers (MERRF), a…”
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Wobble modification deficiency in mutant tRNAs in patients with mitochondrial diseases
Published in FEBS letters (23-05-2005)“…Point mutations in mitochondrial (mt) tRNA genes are associated with a variety of human mitochondrial diseases. We have shown previously that mt tRNA Leu(UUR)…”
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Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA(Lys) with the MERRF encephalomyopathy pathogenic mutation
Published in FEBS letters (11-02-2000)“…A mitochondrial tRNA(Lys) gene mutation at nucleotide position 8344 is responsible for the myoclonus epilepsy associated with ragged-red fibers (MERRF)…”
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Transduction of the anti-apoptotic PTD-FNK protein improves the efficiency of transplantation of bone marrow mononuclear cells
Published in Journal of molecular and cellular cardiology (01-03-2007)“…Abstract Since most transplanted cells rapidly die in an ischemic environment by hypoxia and hyponutrition, it is crucial to know how to protect transplanted…”
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Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNA Lys with the MERRF encephalomyopathy pathogenic mutation
Published in FEBS letters (11-02-2000)“…A mitochondrial tRNA Lys gene mutation at nucleotide position 8344 is responsible for the myoclonus epilepsy associated with ragged‐red fibers (MERRF) subgroup…”
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Defect in modification at the anticodon wobble nucleotide of mitochondrial tRNALys with the MERRF encephalomyopathy pathogenic mutation
Published in FEBS letters (11-02-2000)“…A mitochondrial tRNALys gene mutation at nucleotide position 8344 is responsible for the myoclonus epilepsy associated with ragged-red fibers (MERRF) subgroup…”
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Acetylcholine supersensitivity in the rat heart produced by neonatal sympathectomy
Published in Canadian journal of physiology and pharmacology (01-07-1985)“…Effects of neonatal sympathectomy with antiserum to nerve growth factor or 6-hydroxydopamine on the acetylcholine sensitivity of the rat left atria were…”
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