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  2. Imoto, Issei

Imoto, Issei

ID (desc)
Effects of Wnt10a and Wnt10b Double Mutations on Tooth Development
Author Yoshinaga, Kaoru/ Yasue, Akihiro/ Mitsui, Silvia Naomi/ Minegishi, Yoshiyuki/ Oyadomari, Seiichi/ Imoto, Issei/ Tanaka, Eiji/
Content Type Thesis or Dissertation
Journal Title Genes
Volume 14
Issue 2
Published Date 2023-01-28
departments University Hospital Oral Sciences Institute of Advanced Medical Sciences Medical Sciences
JRAB/MICAL-L2 undergoes liquid–liquid phase separation to form tubular recycling endosomes
Author Sakane, Ayuko/ Yano, Taka-aki/ Uchihashi, Takayuki/ Horikawa, Kazuki/ Hara, Yusuke/ Imoto, Issei/ Kurisu, Shusaku/ Yamada, Hiroshi/ Takei, Kohji/ Sasaki, Takuya/
Content Type Journal Article
Journal Title Communications Biology
Volume 4
Published Date 2021-05-11
departments Medical Sciences Institute of Post-LED Photonics Advanced Research Promotion Center
Visualization and unsupervised clustering of emphysema progression using t-SNE analysis of longitudinal CT images and SNPs
Author Suzuki, Hidenobu/ Matsuhiro, Mikio/ Kawata, Yoshiki/ Imoto, Issei/ Nakano, Yasutaka/ Kusumoto, Masahiko/ Kaneko, Masahiro/ Niki, Noboru/
Content Type Journal Article
Journal Title Proceedings of SPIE
Volume 12033
Published Date 2022-04-04
departments Science and Technology Medical Sciences
Association analysis of SNPs with CT image-based phenotype of emphysema progression in heavy smokers
Author Suzuki, Hidenobu/ Matsuhiro, Mikio/ Kawata, Yoshiki/ Niki, Noboru/ Imoto, Issei/ Nakano, Yasutaka/ Kusumoto, Masahiko/ Kaneko, Masahiro/
Content Type Journal Article
Journal Title Proceedings of SPIE
Volume 11314
Published Date 2020-03-16
departments Science and Technology Medical Sciences
Functionally confirmed compound heterozygous ADAM17 missense loss-of-function variants cause neonatal inflammatory skin and bowel disease 1
Author Imoto, Issei/ Saito, Masako/ Suga, Kenichi/ Kohmoto, Tomohiro/ Otsu, Masanobu/ Horiuchi, Keisuke/ Nakayama, Hironao/ Higashiyama, Shigeki/ Sugimoto, Mayumi/ Sasaki, Ayumi/ Homma, Yukako/ Shono, Miki/ Nakagawa, Ryuji/ Hayabuchi, Yasunobu/ Tange, Shoichiro/ Kagami, Shoji/ Masuda, Kiyoshi/
Content Type Journal Article
Journal Title Scientific Reports
Volume 11
Published Date 2021-05-05
departments Medical Sciences University Hospital
Molecular diagnosis of an infant with TSC2/PKD1 contiguous gene syndrome
Author Osumi, Keita/ Suga, Kenichi/ Ono, Akemi/ Goji, Aya/ Mori, Tatsuo/ Kinoshita, Yukiko/ Sugano, Mikio/ Toda, Yoshihiro/ Urushihara, Maki/ Nakagawa, Ryuji/ Hayabuchi, Yasunobu/ Imoto, Issei/ Kagami, Shoji/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 7
Published Date 2020-07-16
departments University Hospital Medical Sciences
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
Genome-wide association study of semen volume, sperm concentration, testis size, and plasma inhibin B levels
Author Sato, Youichi/ Tajima, Atsushi/ Kiguchi, Misaki/ Kogusuri, Suzu/ Fujii, Aki/ Sato, Takehiro/ Nozawa, Shiari/ Yoshiike, Miki/ Mieno, Makiko/ Kojo, Kosuke/ Uchida, Masahiro/ Tsuchiya, Haruki/ Yamasaki, Kazumitu/ Imoto, Issei/ Iwamoto, Teruaki/
Content Type Journal Article
Journal Title Journal of Human Genetics
Volume 65
Issue 8
Published Date 2020-04-27
departments Pharmaceutical Sciences Medical Sciences
Genome-Wide Association Study to Identify a New Susceptibility Locus for Central Serous Chorioretinopathy in the Japanese Population
Author Miki, Akiko/ Sakurada, Yoichi/ Tanaka, Koji/ Semba, Kentaro/ Mitamura, Yoshinori/ Yuzawa, Mitsuko/ Tajima, Atsushi/ Nakatochi, Masahiro/ Yamamoto, Ken/ Matsuo, Keitaro/ Imoto, Issei/ Honda, Shigeru/
Content Type Journal Article
Journal Title Investigative Ophthalmology & Visual Science
Volume 59
Issue 13
Published Date 2018-11
departments Medical Sciences
A novel PTCH1 mutation in a patient with Gorlin syndrome
Author Okamoto, Nana/ Naruto, Takuya/ Kohmoto, Tomohiro/ Komori, Takahide/ Imoto, Issei/
Content Type Journal Article
Journal Title Human Genome Variation
Volume 1
Published Date 2014-11-13
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
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
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 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
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
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
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
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
Overexpression of SMYD2 contributes to malignant outcome in gastric cancer
Author Komatsu, S/ Ichikawa, D/ Hirajima, S/ Nagata, H/ Nishimura, Y/ Kawaguchi, T/ Miyamae, M/ Okajima, W/ Ohashi, T/ Konishi, H/ Shiozaki, A/ Fujiwara, H/ Okamoto, K/ Tsuda, H/ Imoto, Issei/ Inazawa, J/ Otsuji, E/
Content Type Journal Article
Journal Title British Journal of Cancer
Volume 112
Issue 2
Published Date 2014-10-16
departments Medical Sciences
The C-terminal region including the MH6 domain of Msx1 regulates skeletal development
Author Ichihara, Aki/ Yasue, Akihiro/ Mitsui, Silvia Naomi/ Arai, Daishi/ Minegishi, Yoshiyuki/ Oyadomari, Seiichi/ Imoto, Issei/ Tanaka, Eiji/
Content Type Thesis or Dissertation
Journal Title Biochemical and Biophysical Research Communications
Volume 526
Issue 1
Published Date 2020-03-16
departments University Hospital Oral Sciences Institute of Advanced Medical Sciences Medical Sciences
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