Search Results - "Takada‐Watanabe, Aki"
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R3hdml regulates satellite cell proliferation and differentiation
Published in EMBO reports (05-11-2019)“…In this study, we identified a previously uncharacterized skeletal satellite cell‐secreted protein, R3h domain containing‐like (R3hdml). Expression of R3hdml…”
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Sex differences in symptom presentation and their impact on diagnostic accuracy in Werner syndrome
Published in Geriatrics & gerontology international (01-01-2024)“…Aim Whether sex differences exist in hereditary progeroid syndromes remains unclear. In this study, we investigated sex differences in patients with Werner…”
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Case of sarcomatoid carcinoma occurring in a patient with Werner syndrome
Published in Journal of dermatology (01-11-2016)Get full text
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R3hdml regulates satellite cell proliferation and differentiation
Published in EMBO reports (05-11-2019)Get full text
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A case of Werner syndrome without metabolic abnormality: Implications for the early pathophysiology
Published in Geriatrics & gerontology international (01-01-2012)“…Werner syndrome (WS) is an autosomal recessive progeroid disorder caused by mutations in the WRN DNA helicase. It is characterized by the graying and loss of…”
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Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner Syndrome
Published in Journal of the American Geriatrics Society (JAGS) (01-08-2017)“…Objectives To determine recent trends in mutation patterns in the WRN gene, which cause Werner syndrome (WS), a rare, inheritable progeroid syndrome in Japan…”
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Fibroblasts from different body parts exhibit distinct phenotypes in adult progeria Werner syndrome
Published in Aging (Albany, NY.) (24-02-2021)“…Werner syndrome (WS), also known as adult progeria, is characterized by accelerated aging symptoms from a young age. Patients with WS experience painful…”
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Insulinoma with suspected mutant somatostatin receptor expression according to histological examination
Published in Clinical case reports (01-11-2024)“…Key Clinical Message This case highlights the possibility of an insulinoma expressing an aberrant form of SSTRs resulting in a discrepancy between the…”
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Generation of disease-specific and CRISPR/Cas9-mediated gene-corrected iPS cells from a patient with adult progeria Werner syndrome
Published in Stem cell research (01-05-2021)“…Adult progeria Werner syndrome (WS), a rare autosomal recessive disorder, is characterized by accelerated aging symptoms after puberty. The causative gene,…”
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Senescence-associated inflammation and inhibition of adipogenesis in subcutaneous fat in Werner syndrome
Published in Aging (Albany, NY.) (15-10-2023)“…Werner syndrome (WS) is a hereditary premature aging disorder characterized by visceral fat accumulation and subcutaneous lipoatrophy, resulting in severe…”
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A novel podocyte protein, R3h domain containing-like, inhibits TGF-β-induced p38 MAPK and regulates the structure of podocytes and glomerular basement membrane
Published in Journal of molecular medicine (Berlin, Germany) (01-06-2021)“…Not only in kidney glomerular physiological function but also glomerular pathology especially in diabetic condition, glomerular podocytes play pivotal roles…”
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Case of sarcomatoid carcinoma occurring in a patient with Werner syndrome
Published in The Journal of dermatology (01-11-2016)Get full text
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