Search Results - "Yoshimoto, Masaaki"
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Inhibitory Effects of Prior Low-dose X-irradiation on Cold-induced Brain Injury in Mouse
Published in Inflammation (01-02-2012)“…We examined the inhibitory effects of low-dose X-irradiation on mouse brain tissue with cold-induced injury by comparing tissue samples from three groups of…”
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Radon Inhalation Protects Mice from Carbon-Tetrachloride-Induced Hepatic and Renal Damage
Published in Inflammation (01-12-2011)“…We assessed whether radon inhalation provided protection from carbon tetrachloride (CCl 4 )-induced hepatic and renal damage in mice. Mice were subjected to…”
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Inhibitory Effects of Prior Low-dose X-irradiation on Ischemia-reperfusion Injury in Mouse Paw
Published in JOURNAL OF RADIATION RESEARCH (2007)“…We have reported that low-dose, unlike high-dose, irradiation enhanced antioxidation function and reduced oxidative damage. On the other hand,…”
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Basic Study on Active Changes in Biological Function of Mouse Liver Graft in Cold Storage after Low-Dose X-Irradiation
Published in Journal of Clinical Biochemistry and Nutrition (01-09-2009)“…We previously reported that low-dose X-irradiation alleviates ischemia-reperfusion injury such as mouse paw edema. In this study, we examined active changes in…”
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Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
Published in Endocrine Journal (2006)“…Deletions or mutations in the gene encoding the basolateral chloride channel CLC-Kb (CLCNKB) cause classic Bartter syndrome (MIM 602023), which is…”
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No Different Sensitivity in Terms of Whole-Body Irradiation between Normal and Acatalasemic Mice
Published in Journal of Clinical Biochemistry and Nutrition (01-07-2008)“…To elucidate the radiosensitivity of an acatalasemic mouse, we examined the time and dose-dependency in the survival rates, the lymphocytes and the intestinal…”
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Clinical Evaluation of Recombinant Human Growth Hormone in Noonan Syndrome
Published in ENDOCRINE JOURNAL (2004)“…The objective of this study was to investigate the effect of administration of recombinant human growth hormone (hGH) in patients with Noonan syndrome. hGH was…”
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Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
Published in ENDOCRINE JOURNAL (2006)“…Deletions or mutations in the gene encoding the basolateral chloride channel CLC-Kb (CLCNKB) cause classic Bartter syndrome (MIM 602023), which is…”
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Case with Small Testes Associated with Skeletal Dysplasia
Published in Clinical Pediatric Endocrinology (2001)“…We report an 18-year-old Japanese male with severe short stature and small testes. The endocrinological examination showed high plasma FSH value and normal…”
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Type 1 (Insulin-Dependent) Diabetes Mellitus with Coexisting Autoimmune Thyroid Disease in Japan
Published in Internal Medicine (1992)“…Type 1 diabetes mellitus is known to be a heterogenous disease which is frequently complicated with other autoimmune thyroid diseases (AITD). The present study…”
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Sequence of a Variant Thyroxine-Binding Globulin (TBG) in a Family with Partial TBG Deficiency in Japanese (TBG-PDJ)
Published in Endocrine Journal (1993)“…Thyroxine-binding globulin (TBG) is the major transport protein of thyroid hormones in human serum. In this communication, we present a sequence abnormality of…”
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Studies on possibility for alleviation of lifestyle diseases by low-dose irradiation or radon inhalation
Published in Radiation protection dosimetry (01-07-2011)“…Our previous studies showed the possibility that activation of the antioxidative function alleviates various oxidative damages, which are related to lifestyle…”
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Newly recognized syndrome of metaphyseal undermodeling, spondylar dysplasia, and overgrowth: Report of two adolescents and a child
Published in American journal of medical genetics. Part A (15-07-2004)“…We report on a previously undescribed syndrome characterized by generalized skeletal alterations and overgrowth in three unrelated individuals: a boy who died…”
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Mutations in intron 3 of GH-1 gene associated with isolated GH deficiency type II in three Japanese families
Published in Clinical endocrinology (Oxford) (01-09-1999)“…OBJECTIVE Isolated GH deficiency (IGHD) type II is a disorder inherited in an autosomal dominant manner. Three mutations at the donor splice site of intron 3…”
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A case of nemaline myopathy with abnormal mitochondria
Published in No to hattatsu (01-11-1984)Get more information
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Analysis of a non-functional HNF-1? (TCF1) mutation in Japanese subjects with familial type 1 diabetes
Published in Human mutation (01-10-2001)“…Mutations in the transcription factor hepatocyte nuclear factor-1± (HNF-1±; gene symbol TCF1) cause maturity-onset diabetes of the young type 3 (MODY3), a form…”
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Analysis of a non-functional HNF-1α (TCF1) mutation in Japanese subjects with familial type 1 diabetes
Published in Human mutation (01-10-2001)“…Mutations in the transcription factor hepatocyte nuclear factor‐1α (HNF‐1α; gene symbol TCF1) cause maturity‐onset diabetes of the young type 3 (MODY3), a form…”
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Complex glycerol kinase deficiency: molecular-genetic, cytogenetic, and clinical studies of five Japanese patients
Published in American journal of medical genetics (01-11-1988)“…Five male Japanese patients with complex glycerol kinase deficiency (CGKD) and their relatives were studied clinically, cytogenetically, and…”
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