Search Results - "Hara, Kaori"
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Incidence and clinical risk factors of Bednar's aphthae in Japanese newborns
Published in Pediatrics international (01-01-2023)“…Background The etiology of Bednar's aphthae remains unclear. Our aim was to investigate the incidence of, and factors associated with, Bednar's aphthae in a…”
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Association of Systemic Adverse Reactions and Serum SARS-CoV-2 Spike Protein Antibody Levels after Administration of BNT162b2 mRNA COVID-19 Vaccine
Published in Internal Medicine (01-11-2022)“…Objectives The influential factors for anti-severe acute respiratory syndrome coronavirus 2 spike protein antibody (S-ab) levels were assessed after the…”
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3
Compositional variations in spinel-hosted pargasite inclusions in the olivine-rich rock from the oceanic crust–mantle boundary zone
Published in Contributions to mineralogy and petrology (01-05-2016)“…The crust–mantle boundary zone of the oceanic lithosphere is composed mainly of olivine-rich rocks represented by dunite and troctolite. However, we still do…”
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Hybrid troctolites from mid-ocean ridges: inherited mantle in the lower crust
Published in Lithos (01-09-2015)“…Studies on olivine-rich troctolites from oceanic ridges propose that hybridized mantle rocks may locally constitute small portions of the lower oceanic crust…”
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Comparison of serum 25-hydroxyvitamin D levels between radioimmunoassay and liquid chromatography-tandem mass spectrometry in infants and postpartum women
Published in Journal of pediatric endocrinology & metabolism : JPEM (25-10-2018)“…Background Liquid chromatography-tandem mass spectrometry (LC-MS/MS) has become the gold standard for the measurement of serum 25-hydroxyvitamin D (25(OH)D)…”
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Seasonal variation in vitamin D status of Japanese infants starts to emerge at 2 months of age: a retrospective cohort study
Published in British journal of nutrition (14-06-2023)“…Vitamin D seasonality has been reported in adults and children, suggesting that sunlight exposure has effects on 25(OH)D production. While vitamin D deficiency…”
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A patient with Silver-Russell syndrome with multilocus imprinting disturbance, and Schimke immuno-osseous dysplasia unmasked by uniparental isodisomy of chromosome 2
Published in Journal of human genetics (01-11-2021)“…Silver-Russell syndrome (SRS) is a congenital disorder characterized by prenatal and postnatal growth failure and craniofacial features. Hypomethylation of the…”
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Urinary tract infection associated with bacteremia caused by vancomycin‐resistant enterococcus following continent urinary diversion
Published in Clinical case reports (01-01-2024)“…Key Clinical Message Even in a country where vancomycin–resistant enterococcus is rare, multidrug‐resistant organism precautions are necessary when admitting…”
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Clarithromycin suppresses IL-13-induced goblet cell metaplasia via the TMEM16A-dependent pathway in guinea pig airway epithelial cells
Published in Respiratory investigation (01-01-2019)“…Transmembrane protein 16A (TMEM16A) is associated with mucus secretion and ion transport in asthma. Clarithromycin (CAM) is reported to inhibit IL-13-induced…”
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Role of Imprinting Disorders in Short Children Born SGA and Silver-Russell Syndrome Spectrum
Published in The journal of clinical endocrinology and metabolism (08-03-2021)“…Abstract Background (Epi)genetic disorders associated with small-for-gestational-age with short stature (SGA-SS) include imprinting disorders (IDs)…”
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Local delivery of imatinib mesylate (STI571)-incorporated nanoparticle ex vivo suppresses vein graft neointima formation
Published in Circulation (New York, N.Y.) (30-09-2008)“…Clinical outcome of surgical revascularization using autologous vein graft is limited by vein graft failure attributable to neointima formation…”
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Particle size control of poly( dl-lactide-co-glycolide) nanospheres for sterile applications
Published in International journal of pharmaceutics (31-03-2009)“…Parameters affecting the particle sizes of poly(DL-lactide-co-glycolide) (PLGA) nanospheres produced by the Emulsion Solvent Diffusion (ESD) method were…”
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NIH3T3 cells overexpressing CD98 heavy chain resist early G1 arrest and apoptosis induced by serum starvation
Published in Cancer science (01-08-2012)“…CD98 is a heterodimeric glycoprotein of 125‐kDa, which consists of a 90‐kDa heavy chain (hc) subunit and 35‐kDa to 55‐kDa light chain (lc) subunits. It is…”
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The cut-off values of vitamin D deficiency in early infancy
Published in Pediatrics and neonatology (01-07-2022)“…Several cut-off points for 25-hydroxyvitamin D (25(OH)D) levels have been proposed to determine vitamin D deficiency or insufficiency. However, the level for…”
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Histological examination of PLGA nanospheres for intratracheal drug administration
Published in International journal of pharmaceutics (22-05-2008)“…Polylactide–glycolide (PLGA) nanospheres were reported as useful pulmonary drug delivery carriers for improving the pharmacological effect of drug. This paper…”
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Comprehensive molecular and clinical findings in 29 patients with multi-locus imprinting disturbance
Published in Clinical epigenetics (05-10-2024)“…Multi-locus imprinting disturbance (MLID) with methylation defects in various differentially methylated regions (DMRs) has recently been identified in…”
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Assisted reproductive technology represents a possible risk factor for development of epimutation-mediated imprinting disorders for mothers aged ≥ 30 years
Published in Clinical epigenetics (22-07-2020)“…Abstract Backgrounds The proportion of assisted reproductive technology (ART)-conceived livebirths of patients with imprinting disorders (IDs) is higher than…”
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Risk assessment of assisted reproductive technology and parental age at childbirth for the development of uniparental disomy-mediated imprinting disorders caused by aneuploid gametes
Published in Clinical epigenetics (06-05-2023)“…Our previous study suggested that assisted reproductive technology (ART) may be a possible risk factor for the development of epimutation-mediated imprinting…”
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Primary ciliary dyskinesia diagnosed on nasal mucosal biopsy in two newborns
Published in Pediatrics international (01-04-2014)“…Primary ciliary dyskinesia (PCD) is a genetic disease that causes abnormalities in ciliary structure and/or function. Ciliated cells line the upper and lower…”
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Genome-wide methylation analysis in Silver-Russell syndrome, Temple syndrome, and Prader-Willi syndrome
Published in Clinical epigenetics (22-10-2020)“…Imprinting disorders (IDs) show overlapping phenotypes, particularly in Silver-Russell syndrome (SRS), Temple syndrome (TS14), and Prader-Willi syndrome (PWS)…”
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