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Medical Sciences Naruto, Takuya

Published Date (desc)
Next-generation sequencing for the diagnosis of patients with congenital multiple anomalies and / or intellectual disabilities
Author Suga, Kenichi/ Imoto, Issei/ Ito, Hiromichi/ Naruto, Takuya/ Goji, Aya/ Osumi, Keita/ Tokaji, Narumi/ Homma, Yukako/ Ono, Akemi/ Ichihara, Yuko/ Shono, Miki/ Mori, Tatsuo/ Urushihara, Maki/ Nakagawa, Ryuji/ Hayabuchi, Yasunobu/ Kagami, Shoji/
Content Type Journal Article
Journal Title The Journal of Medical Investigation
Volume 67
Issue 3-4
Published Date 2020-08
departments University Hospital Medical Sciences
Toll-Like Receptor 9 Plays a Pivotal Role in Angiotensin II–Induced Atherosclerosis
Author Fukuda, Daiju/ Nishimoto, Sachiko/ Aini, Kunduziayi/ Tanaka, Atsushi/ Nishiguchi, Tsuyoshi/ Kim-Kaneyama, Joo-ri/ Lei, Xiao-Feng/ Masuda, Kiyoshi/ Naruto, Takuya/ Tanaka, Kimie/ Higashikuni, Yasutomi/ Hirata, Yoichiro/ Yagi, Shusuke/ Kusunose, Kenya/ Yamada, Hirotsugu/ Soeki, Takeshi/ Imoto, Issei/ Akasaka, Takashi/ Shimabukuro, Michio/ Sata, Masataka/
Content Type Journal Article
Journal Title Journal of the American Heart Association
Volume 8
Issue 7
Published Date 2019-03-23
departments Medical Sciences University Hospital
KH-type splicing regulatory protein is involved in esophageal squamous cell carcinoma progression
Author Fujita, Yuji/ Masuda, Kiyoshi/ Hamada, Junichi/ Shoda, Katsutoshi/ Naruto, Takuya/ Hamada, Satoshi/ Miyakami, Yuko/ Kohmoto, Tomohiro/ Watanabe, Miki/ Takahashi, Rizu/ Tange, Shoichiro/ Saito, Masako/ Kudo, Yasusei/ Fujiwara, Hitoshi/ Ichikawa, Daisuke/ Tangoku, Akira/ Otsuji, Eigo/ Imoto, Issei/
Content Type Journal Article
Journal Title Oncotarget
Volume 8
Issue 60
Published Date 2017-09-15
departments Medical Sciences Oral Sciences
Novel CLCN7 compound heterozygous mutations in intermediate autosomal recessive osteopetrosis
Author Okamoto, Nana/ Kohmoto, Tomohiro/ Naruto, Takuya/ Masuda, Kiyoshi/ Komori, Takahide/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 4
Published Date 2017-08-17
departments Medical Sciences
The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via POLD1 mutation detection
Author Okada, Asami/ Kohmoto, Tomohiro/ Naruto, Takuya/ Yokota, Ichiro/ Kotani, Yumiko/ Shimada, Aki/ Miyamoto, Yoko/ Takahashi, Rizu/ Goji, Aya/ Masuda, Kiyoshi/ Kagami, Shoji/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 4
Published Date 2017-08-03
departments Medical Sciences University Hospital
Construction of a combinatorial pipeline using two somatic variant calling methods for whole exome sequence data of gastric cancer
Author Kohmoto, Tomohiro/ Masuda, Kiyoshi/ Naruto, Takuya/ Tange, Shoichiro/ Shoda, Katsutoshi/ Hamada, Junichi/ Saito, Masako/ Ichikawa, Daisuke/ Tajima, Atsushi/ Otsuji, Eigo/ Imoto, Issei/
Content Type Journal Article
Journal Title The Journal of Medical Investigation
Volume 64
Issue 3-4
Published Date 2017-08
departments Medical Sciences
Frequent silencing of RASSF1A by DNA methylation in thymic neuroendocrine tumours
Author Kajiura, Koichiro/ Takizawa, Hiromitsu/ Morimoto, Yuki/ Masuda, Kiyoshi/ Tsuboi, Mitsuhiro/ Kishibuchi, Reina/ Wusiman, Nuliamina/ Sawada, Toru/ Kawakita, Naoya/ Toba, Hiroaki/ Yoshida, Mitsuteru/ Kawakami, Yukikiyo/ Naruto, Takuya/ Imoto, Issei/ Tangoku, Akira/ Kondo, Kazuya/
Content Type Journal Article
Journal Title Lung Cancer
Volume 111
Published Date 2017-05-25
departments Medical Sciences University Hospital
A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements
Author Kohmoto, Tomohiro/ Okamoto, Nana/ Naruto, Takuya/ Murata, Chie/ Ouchi, Yuya/ Fujita, Naoko/ Inagaki, Hidehito/ Satomura, Shigeko/ Okamoto, Nobuhiko/ Saito, Masako/ Masuda, Kiyoshi/ Kurahashi, Hiroki/ Imoto, Issei/
Content Type Journal Article
Journal Title Molecular Cytogenetics
Volume 10
Published Date 2017-04-28
departments Medical Sciences
Targeted exome sequencing and chromosomal microarray for the molecular diagnosis of nevoid basal cell carcinoma syndrome
Author Matsudate, Yoshihiro/ Naruto, Takuya/ Hayashi, Yumiko/ Minami, Mitsuyoshi/ Tohyama, Mikiko/ Yokota, Kenji/ Yamada, Daisuke/ Imoto, Issei/ Kubo, Yoshiaki/
Content Type Thesis or Dissertation
Journal Title Journal of Dermatological Science
Volume 86
Issue 3
Published Date 2017-03-11
departments Medical Sciences
Genome-first approach diagnosed Cabezas syndrome via novel CUL4B mutation detection
Author Okamoto, Nobuhiko/ Watanabe, Miki/ Naruto, Takuya/ Matsuda, Keiko/ Kohmoto, Tomohiro/ Saito, Masako/ Masuda, Kiyoshi/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 4
Published Date 2017-01-19
departments Medical Sciences
Novel human mutation and CRISPR/Cas genome-edited mice reveal the importance of C-terminal domain of MSX1 in tooth and palate development
Author Mitsui, Silvia Naomi/ Yasue, Akihiro/ Masuda, Kiyoshi/ Naruto, Takuya/ Minegishi, Yoshiyuki/ Oyadomari, Seiichi/ Noji, Sumihare/ Imoto, Issei/ Tanaka, Eiji/
Content Type Journal Article
Journal Title Scientific Reports
Volume 6
Published Date 2016-12-05
departments University Hospital Medical Sciences Institute of Advanced Medical Sciences Oral Sciences Bioscience and Bioindustry
Frequent silencing of the candidate tumor suppressor TRIM 58 by promoter methylation in early-stage lung adenocarcinoma
Author Kajiura, Koichiro/ Masuda, Kiyoshi/ Naruto, Takuya/ Kohmoto, Tomohiro/ Watanabe, Miki/ Tsuboi, Mitsuhiro/ Takizawa, Hiromitsu/ Kondo, Kazuya/ Tangoku, Akira/ Imoto, Issei/
Content Type Thesis or Dissertation
Journal Title Oncotarget
Volume 8
Issue 2
Published Date 2016-12-01
departments Medical Sciences University Hospital
Exome-first approach identified a novel gloss deletion associated with Lowe syndrome
Author Watanabe, Miki/ Nakagawa, Ryuji/ Kohmoto, Tomohiro/ Naruto, Takuya/ Suga, Ken-ichi/ Goji, Aya/ Horikawa, Hideaki/ Masuda, Kiyoshi/ Kagami, Shoji/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 3
Published Date 2016-11-10
departments University Hospital Medical Sciences Technical Support Department
A novel missense mutation of COL5A2 in a patient with Ehlers–Danlos syndrome
Author Watanabe, Miki/ Nakagawa, Ryuji/ Naruto, Takuya/ Kohmoto, Tomohiro/ Suga, Ken-ichi/ Goji, Aya/ Kagami, Shoji/ Masuda, Kiyoshi/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 3
Published Date 2016-09-15
departments University Hospital Medical Sciences
Detection of 1p36 deletion by clinical exome-first diagnostic approach
Author Watanabe, Miki/ Hayabuchi, Yasunobu/ Ono, Akemi/ Naruto, Takuya/ Horikawa, Hideaki/ Kohmoto, Tomohiro/ Masuda, Kiyoshi/ Nakagawa, Ryuji/ Ito, Hiromichi/ Kagami, Shoji/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 3
Published Date 2016-05-12
departments Medical Sciences Technical Support Department University Hospital
A novel COL11A1 missense mutation in siblings with non-ocular Stickler syndrome
Author Kohmoto, Tomohiro/ Tsuji, Atsumi/ Morita, Kei-ichi/ Naruto, Takuya/ Masuda, Kiyoshi/ Kashimada, Kenichi/ Enomoto, Keisuke/ Morio, Tomohiro/ Harada, Hiroyuki/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 3
Published Date 2016-04-07
departments Medical Sciences
A novel frameshift mutation of CHD7 in a Japanese patient with CHARGE syndrome
Author Kohmoto, Tomohiro/ Shono, Miki/ Naruto, Takuya/ Watanabe, Miki/ Suga, Ken-ichi/ Nakagawa, Ryuji/ Kagami, Shoji/ Masuda, Kiyoshi/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 3
Published Date 2016-04-07
departments Medical Sciences University Hospital
Tumor-promoting function and prognostic significance of the RNA-binding protein T-cell intracellular antigen-1 in esophageal squamous cell carcinoma.
Author Hamada, Junichi/ Shoda, Katsutoshi/ Masuda, Kiyoshi/ Fujita, Yuji/ Naruto, Takuya/ Kohmoto, Tomohiro/ Miyakami, Yuko/ Watanabe, Miki/ Kudo, Yasusei/ Fujiwara, Hitoshi/ Ichikawa, Daisuke/ Otsuji, Eigo/ Imoto, Issei/
Content Type Journal Article
Journal Title Oncotarget
Volume 7
Issue 13
Published Date 2016-03-06
departments Medical Sciences Oral Sciences
Simultaneous Detection of Both Single Nucleotide Variations and Copy Number Alterations by Next-Generation Sequencing in Gorlin Syndrome
Author Morita, Kei-ichi/ Naruto, Takuya/ Tanimoto, Kousuke/ Yasukawa, Chisato/ Oikawa, Yu/ Masuda, Kiyoshi/ Imoto, Issei/ Inazawa, Johji/ Omura, Ken/ Harada, Hiroyuki/
Content Type Journal Article
Journal Title PLOS ONE
Volume 10
Issue 11
Published Date 2015-11-06
departments Medical Sciences
Deep intronic GPR143 mutation in a Japanese family with ocular albinism
Author Naruto, Takuya/ Okamoto, Nobuhiko/ Masuda, Kiyoshi/ Endo, Takao/ Hatsukawa, Yoshikazu/ Kohmoto, Tomohiro/ Imoto, Issei/
Content Type Journal Article
Journal Title Scientific Reports
Volume 5
Published Date 2015-06-10
departments Medical Sciences
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