Search Results - "YOSHIURA, K"

Autosomal recessive cystinuria caused by genome-wide paternal uniparental isodisomy in a patient with Beckwith-Wiedemann syndrome by Ohtsuka, Y., Higashimoto, K., Sasaki, K., Jozaki, K., Yoshinaga, H., Okamoto, N., Takama, Y., Kubota, A., Nakayama, M., Yatsuki, H., Nishioka, K., Joh, K., Mukai, T., Yoshiura, K.-i., Soejima, H.

“…Approximately 20% of Beckwith–Wiedemann syndrome (BWS) cases are caused by mosaic paternal uniparental disomy of chromosome 11 (pUPD11). Although pUPD11 is…”
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64-channel photon-counting computed tomography using a new MPPC-CT system by Kiji, H., Maruhashi, T., Toyoda, T., Kataoka, J., Arimoto, M., Sato, D., Yoshiura, K., Kobayashi, S., Kawashima, H., Terazawa, S., Shiota, S., Ikeda, H.

“…X-ray computed tomography (CT) is a widely used diagnostic tool to visualize the interior of the human body. However, the exposure dose of conventional CT in a…”
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Performance demonstration of a novel photon-counting CT for preclinical application by Toyoda, T., Kataoka, J., Sagisaka, M., Arimoto, M., Sato, D., Yoshiura, K., Kawashima, H., Kobayashi, S., Kotoku, J., Terazawa, S., Shiota, S., Ueda, M.

“…Photon-counting computed tomography (PC-CT) has attracted attention over the last few years as the next-generation CT technique that solves the problems…”
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Surfactant protein C G100S mutation causes familial pulmonary fibrosis in Japanese kindred by ONO, S, TANAKA, T, SENBA, M, YASUNAMI, M, KUBO, Y, YOSHIDA, L. M, KUBO, H, ARIYOSHI, K, YOSHIURA, K, MORIMOTO, K, ISHIDA, M, KINOSHITA, A, FUKUOKA, J, TAKAKI, M, SAKAMOTO, N, ISHIMATSU, Y, KOHNO, S, HAYASHI, T

“…Several mutations in the surfactant protein C (SP-C) gene (SFTPC) have been reported as causing familial pulmonary fibrosis (FPF). However, the genetic…”
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Utility of a diffusion kurtosis model in the differential diagnosis of orofacial tumours by Panyarak, W., Chikui, T., Tokumori, K., Yamashita, Y., Kamitani, T., Togao, O., Yoshiura, K.

“…To compare the goodness of fit and correlations between diffusion kurtosis imaging (DKI) and a mono-exponential (ME) model, to compare the corrected apparent…”
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Detection of cell free placental DNA in maternal plasma: direct evidence from three cases of confined placental mosaicism by Masuzaki, H, Miura, K, Yoshiura, K-i, Yoshimura, S, Niikawa, N, Ishimaru, T

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Multifaceted array‐based keloidal gene expression profiling reveals specific MDFI upregulation in keloid lesions by Asai, M., Koike, Y., Kuwatsuka, Y., Yagi, Y., Kashiyama, K., Tanaka, K., Mishima, H., Yoshiura, K., Utani, A., Murota, H.

“…Summary Background Keloid lesions are characterized by mesenchymal cell proliferation and excessive extracellular matrix deposition. Previous microarray…”
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Characteristics of the peroxisome proliferator activated receptor γ (PPARγ) ligand induced apoptosis in colon cancer cells by Shimada, T, Kojima, K, Yoshiura, K, Hiraishi, H, Terano, A

“…Background: Involvement of peroxisome proliferator activated receptor γ (PPARγ) in the growth response of colon cancer cells has been suggested. Aims: To…”
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Clinical applications of analysis of plasma circulating complete hydatidiform mole pregnancy-associated miRNAs in gestational trophoblastic neoplasia: A preliminary investigation by Miura, K, Hasegawa, Y, Abe, S, Higashijima, A, Miura, S, Mishima, H, Kinoshita, A, Kaneuchi, M, Yoshiura, K, Masuzaki, H

“…Abstract The aim of this study was to investigate the clinical application of plasma complete hydatidiform mole pregnancy-associated microRNAs (CHM-miRNAs:…”
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Decreased cell-free but not exosomal miR-518b in maternal plasma is caused by amniocentesis by K., Miura, Higashijima, , A., Hasegawa, Y., Miura, S., Yoshiura, KI, Masuzaki, H.

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Circulating levels of maternal plasma cell-free pregnancy-associated placenta-specific microRNAs are associated with placental weight by Miura, K, Morisaki, S, Abe, S, Higashijima, A, Hasegawa, Y, Miura, S, Tateishi, S, Mishima, H, Yoshiura, K, Masuzaki, H

“…Abstract The aim of this study was to investigate the relationship between plasma concentration of cell-free pregnancy-associated placenta-specific microRNAs…”
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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 by Chikui, T, Kitamoto, E, Kami, Y, Kawano, S, Kobayashi, K, Kamitani, T, Obara, M, Yoshiura, K

“…To probe the utility of dynamic contrast-enhanced MRI (DCE-MRI) parameters in assessing the clinical characteristics of oral squamous cell carcinoma. A total…”
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Maternal uniparental isodisomy and heterodisomy on chromosome 6 encompassing a CUL7 gene mutation causing 3M syndrome by Sasaki, K, Okamoto, N, Kosaki, K, Yorifuji, T, Shimokawa, O, Mishima, H, Yoshiura, K-i, Harada, N

“…Sasaki K, Okamoto N, Kosaki K, Yorifuji T, Shimokawa O, Mishima H, Yoshiura K‐i, Harada N. Maternal uniparental isodisomy and heterodisomy on chromosome 6…”
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Evidence for association between a Toll-like receptor 4 gene polymorphism and moderate/severe periodontitis in the Japanese population by Fukusaki, T., Ohara, N., Hara, Y., Yoshimura, A., Yoshiura, K.

“…Background and Objective:  Chronic periodontitis is an inflammatory disease caused by bacteria in subgingival pockets. Because Toll‐like receptor 2 and…”
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A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family by Okubo, A, Miyoshi, O, Baba, K, Takagi, M, Tsukamoto, K, Kinoshita, A, Yoshiura, K, Kishino, T, Ohta, T, Niikawa, N, Matsumoto, N

“…Clinical re-evaluation of three members (III-4, IV-5, and IV-6) who were previously thought to be unaffected confirmed their disease. [...]penetrance in the…”
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A new method for displaying the lingual artery using high-resolution three-dimensional phase-contrast magnetic resonance angiography by Kami, Y.N, Chikui, T, Shiraishi, T, Inadomi, D, Nishioka, M, Yuasa, K, Yoshiura, K

“…Abstract The aim of this study was to display the lingual artery superimposed on the anatomical image and to confirm its course and relation to the adjacent…”
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Patched homologue 1 mutations in four Japanese families with basal cell nevus syndrome by Matsuzawa, N, Nagao, T, Shimozato, K, Niikawa, N, Yoshiura, K-i

“…Aim: To search for patched homologue 1 (PTCH1) mutations in four families with basal cell nevus syndrome (BCNS). Methods: Mutation analysis of PTCH1 in…”
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Silencing of the E-Cadherin Invasion-Suppressor Gene by CpG Methylation in Human Carcinomas by Yoshiura, Kenta, Kanai, Yae, Ochiai, Atsushi, Shimoyama, Yutaka, Sugimura, Takashi, Hirohashi, Setsuo

“…E-Cadherin, a cell adhesion molecule, which plays a key role in maintaining the epithelial phenotype, is regarded as an invasion-suppressor gene in light of…”
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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 by GOTO, T. K., YAMADA, T., YOSHIURA, K.

“…Summary  The purpose of this study was to investigate the difference in the occlusal force between deviated and non‐deviated sides of the mandible in adult…”
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A case of neonatal-onset autoinflammatory syndrome with a de novo PSMB9 mutation resembling Nakajo-Nishimura syndrome by Kinjo, N, Kanazawa, N, Mishima, H, Kinoshita, A, Yoshiura, K

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