日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Genome sequencing provides high diagnostic yield and new etiological insights for intellectual disability and developmental delay

基因组测序能够提供高诊断率,并为智力障碍和发育迟缓的病因学研究提供新的见解。

Hamanaka, Kohei; Fujita, Atsushi; Miyatake, Satoko; Misawa, Kazuharu; Koshimizu, Eriko; Uchiyama, Yuri; Tsuchida, Naomi; Seyama, Rie; Sakamoto, Masamune; Iwama, Kazuhiro; Nishimura, Naoto; Utsuno, Yasuhiro; Fu, Li; Takizawa, Marina; Liang, Qiaowei; Itai, Toshiyuki; Saida, Ken; Ohori, Sachiko; Kameyama, Shinichi; Fukuda, Hiromi; Hayashi, Yukina; Inoue, Yuta; Goto, Tomohide; Ichikawa, Kazushi; Kuki, Ichiro; Fukuoka, Masataka; Kim, Kiyohiro; Shiohama, Tadashi; Shimoda, Konomi; Otsuka, Kosuke; Ueda, Yuki; Cho, Kazutoshi; Yuge, Kotaro; Tachi, Nobutada; Yoshida, Masaki; Daida, Atsuro; Hirasawa, Kyoko; Yanagishita, Tomoe; Yamamoto, Toshiyuki; Shirai, Kentaro; Mehr, Tammar Fixler; Fattal-Valevski, Aviva; Lev, Dorit; Yokoyama, Haruna; Iwabuchi, Emi; Saito, Yoshihiko; Miura, Masaki; Sugai, Kenji; Ishiyama, Akihiko; Sasaki, Masayuki; Watanabe, Yoshihiro; Takanashi, Jun-Ichi; Kim, Chong Ae; Yokochi, Kenji; Tohyama, Jun; Mori, Tatsuo; Izumi, Yuishin; Hasegawa, Yuiko; Okamoto, Nobuhiko; Ikeda, Takahiro; Osaka, Hitoshi; Kawai, Yosuke; Omae, Yosuke; Tokunaga, Katsushi; Kato, Mitsuhiro; Mizuguchi, Takeshi; Matsumoto, Naomichi

Multiplex Real-Time PCR-Based Newborn Screening for Severe Primary Immunodeficiency and Spinal Muscular Atrophy in Osaka, Japan: Our Results after 3 Years

日本大阪基于多重实时PCR技术的新生儿重症原发性免疫缺陷和脊髓性肌萎缩症筛查:3年后的结果

Kimizu, Tomokazu; Nozaki, Masatoshi; Okada, Yousuke; Sawada, Akihisa; Morisaki, Misaki; Fujita, Hiroshi; Irie, Akemi; Matsuda, Keiko; Hasegawa, Yuiko; Nishi, Eriko; Okamoto, Nobuhiko; Kawai, Masanobu; Imai, Kohsuke; Suzuki, Yasuhiro; Wada, Kazuko; Mitsuda, Nobuaki; Ida, Shinobu

Haploinsufficiency of NKX2-1 is likely to contribute to developmental delay involving 14q13 microdeletions

NKX2-1单倍体不足可能导致涉及14q13微缺失的发育迟缓。

Machida, Osamu; Sakamoto, Haruko; Yamamoto, Keiko Shimojima; Hasegawa, Yuiko; Nii, Satoi; Okada, Hidenori; Nishikawa, Kazuki; Sumimoto, Shin-Ichi; Nishi, Eriko; Okamoto, Nobuhiko; Yamamoto, Toshiyuki

Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome

116名日本努南综合征患者的遗传背景及人体测量参数的基因型-表型关系

Shoji, Yasuko; Hata, Ayaha; Maeyama, Takatoshi; Wada, Tamaki; Hasegawa, Yuiko; Nishi, Eriko; Ida, Shinobu; Etani, Yuri; Niihori, Tetsuya; Aoki, Yoko; Okamoto, Nobuhiko; Kawai, Masanobu

Breakpoints in complex chromosomal rearrangements correspond to transposase-accessible regions of DNA from mature sperm

复杂染色体重排中的断点对应于成熟精子DNA中转座酶可及的区域。

Sugimoto, Takeshi; Inagaki, Hidehito; Mariya, Tasuku; Kawamura, Rie; Taniguchi-Ikeda, Mariko; Mizuno, Seiji; Muramatsu, Yukako; Tsuge, Ikuya; Ohashi, Hirofumi; Saito, Nakamichi; Hasegawa, Yuiko; Ochi, Nobuhiko; Yamaguchi, Masatoshi; Murotsuki, Jun; Kurahashi, Hiroki

Interstitial deletions in the proximal regions of 6q: 12 original cases and a literature review

6q近端区域间质缺失:12例原始病例及文献综述

Machida, Osamu; Shimojima, Keiko Yamamoto; Shiihara, Takashi; Akamine, Satoshi; Kira, Ryutaro; Hasegawa, Yuiko; Nishi, Eriko; Okamoto, Nobuhiko; Nagata, Satoru; Yamamoto, Toshiyuki

Postnatal Arx transcriptional activity regulates functional properties of PV interneurons

出生后Arx转录活性调节PV中间神经元的功能特性

Joseph, Donald J; Von Deimling, Markus; Hasegawa, Yuiko; Cristancho, Ana G; Ahrens-Nicklas, Rebecca C; Rogers, Stephanie L; Risbud, Rashmi; McCoy, Almedia J; Marsh, Eric D

Promotion of axon regeneration by myelin-associated glycoprotein and Nogo through divergent signals downstream of Gi/G.

髓鞘相关糖蛋白和 Nogo 通过 Gi/G 下游的不同信号促进轴突再生

Hasegawa Yuiko, Fujitani Masashi, Hata Katsuhiko, Tohyama Masaya, Yamagishi Satoru, Yamashita Toshihide