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Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome

Clinical genetics, 2015-09, Vol.88 (3), p.261-266

2015

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64-channel photon-counting computed tomography using a new MPPC-CT system

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2020-12, Vol.984, p.164610, Article 164610

2020

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Surfactant protein C G100S mutation causes familial pulmonary fibrosis in Japanese kindred

The European respiratory journal, 2011-10, Vol.38 (4), p.861-869

2011

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Utility of a diffusion kurtosis model in the differential diagnosis of orofacial tumours

Clinical radiology, 2020-07, Vol.75 (7), p.507-519

2020

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Performance demonstration of a novel photon-counting CT for preclinical application

Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment, 2022-10, Vol.1040, p.167181, Article 167181

2022

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Detection of cell free placental DNA in maternal plasma: direct evidence from three cases of confined placental mosaicism

Journal of medical genetics, 2004-04, Vol.41 (4), p.289-292

2004

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Multifaceted array‐based keloidal gene expression profiling reveals specific MDFI upregulation in keloid lesions

Clinical and experimental dermatology, 2021-10, Vol.46 (7), p.1255-1261

2021

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Clinical applications of analysis of plasma circulating complete hydatidiform mole pregnancy-associated miRNAs in gestational trophoblastic neoplasia: A preliminary investigation

Placenta (Eastbourne), 2014-09, Vol.35 (9), p.787-789

2014

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Decreased cell-free but not exosomal miR-518b in maternal plasma is caused by amniocentesis

Clinical and experimental obstetrics & gynecology, 2018-01, Vol.45 (6), p.875-879

2018

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Characteristics of the peroxisome proliferator activated receptor γ (PPARγ) ligand induced apoptosis in colon cancer cells

Gut, 2002-05, Vol.50 (5), p.658-664

2002

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Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome

Clinical genetics, 2011-11, Vol.80 (5), p.478-483

2011

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Dynamic contrast-enhanced MRI of oral squamous cell carcinoma: a preliminary study of the correlations between quantitative parameters and the clinical stage

British journal of radiology, 2015-06, Vol.88 (1050), p.20140814-20140814

2015

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Circulating levels of maternal plasma cell-free pregnancy-associated placenta-specific microRNAs are associated with placental weight

Placenta (Eastbourne), 2014-10, Vol.35 (10), p.848-851

2014

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Evidence for association between a Toll-like receptor 4 gene polymorphism and moderate/severe periodontitis in the Japanese population

Journal of periodontal research, 2007-12, Vol.42 (6), p.541-545

2007

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THU0371 Increased expression of inflammatory cytokines and chemokines in an autoinflammatory disorder, nakajo-nishimura syndrome

Annals of the rheumatic diseases, 2013-06, Vol.71 (Suppl 3), p.281-281

2013

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A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family

Journal of medical genetics, 2004-07, Vol.41 (7), p.e97-e97

2004

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Silencing of the E-Cadherin Invasion-Suppressor Gene by CpG Methylation in Human Carcinomas

Proceedings of the National Academy of Sciences - PNAS, 1995-08, Vol.92 (16), p.7416-7419

1995

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A new method for displaying the lingual artery using high-resolution three-dimensional phase-contrast magnetic resonance angiography

International journal of oral and maxillofacial surgery, 2013-11, Vol.42 (11), p.1494-1498

2013

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Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome

Journal of clinical pathology, 2006-10, Vol.59 (10), p.1084-1086

2006

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Occlusal pressure, contact area, force and the correlation with the morphology of the jaw-closing muscles in patients with skeletal mandibular asymmetry

Journal of oral rehabilitation, 2008-08, Vol.35 (8), p.594-603

2008

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Imaging findings of neurogenic tumours in the head and neck region

Dento-maxillo-facial radiology, 2012-01, Vol.41 (1), p.18-23

2012

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A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndrome

Pediatric rheumatology online journal, 2015-09, Vol.13 (Suppl 1), p.P183-P183, Article P183

2015

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CT analysis of the Stafne's bone defects of the mandible

Dento-maxillo-facial radiology, 2006-03, Vol.35 (2), p.95

2006

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Size and Orientation of Masticatory Muscles in Patients with Mandibular Laterognathism

Journal of dental research, 2006-06, Vol.85 (6), p.552-556

2006

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Evaluation of T 2 values and apparent diffusion coefficient of the masseter muscle by clenching

Dento-maxillo-facial radiology, 2011-01, Vol.40 (1), p.35-41

2011

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Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome

64-channel photon-counting computed tomography using a new MPPC-CT system

Surfactant protein C G100S mutation causes familial pulmonary fibrosis in Japanese kindred

Utility of a diffusion kurtosis model in the differential diagnosis of orofacial tumours

Performance demonstration of a novel photon-counting CT for preclinical application

Detection of cell free placental DNA in maternal plasma: direct evidence from three cases of confined placental mosaicism

Multifaceted array‐based keloidal gene expression profiling reveals specific MDFI upregulation in keloid lesions

Clinical applications of analysis of plasma circulating complete hydatidiform mole pregnancy-associated miRNAs in gestational trophoblastic neoplasia: A preliminary investigation

Decreased cell-free but not exosomal miR-518b in maternal plasma is caused by amniocentesis

Characteristics of the peroxisome proliferator activated receptor γ (PPARγ) ligand induced apoptosis in colon cancer cells

Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome

Dynamic contrast-enhanced MRI of oral squamous cell carcinoma: a preliminary study of the correlations between quantitative parameters and the clinical stage

Circulating levels of maternal plasma cell-free pregnancy-associated placenta-specific microRNAs are associated with placental weight

Evidence for association between a Toll-like receptor 4 gene polymorphism and moderate/severe periodontitis in the Japanese population

THU0371 Increased expression of inflammatory cytokines and chemokines in an autoinflammatory disorder, nakajo-nishimura syndrome

A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family

Silencing of the E-Cadherin Invasion-Suppressor Gene by CpG Methylation in Human Carcinomas

A new method for displaying the lingual artery using high-resolution three-dimensional phase-contrast magnetic resonance angiography

Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome

Occlusal pressure, contact area, force and the correlation with the morphology of the jaw-closing muscles in patients with skeletal mandibular asymmetry

Imaging findings of neurogenic tumours in the head and neck region

A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndrome

CT analysis of the Stafne's bone defects of the mandible

Size and Orientation of Masticatory Muscles in Patients with Mandibular Laterognathism

Evaluation of T 2 values and apparent diffusion coefficient of the masseter muscle by clenching

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