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

circRNA: A New Biomarker and Therapeutic Target for Esophageal Cancer

环状RNA：食管癌的新型生物标志物和治疗靶点

期刊:Biomedicines
影响因子:3.9
doi:10.3390/biomedicines10071643
Shoda, Katsutoshi; Kuwano, Yuki; Ichikawa, Daisuke; Masuda, Kiyoshi
食管癌
肿瘤
肿瘤免疫
发表日期：2022
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The plant nuclear lamina proteins NMCP1 and NMCP2 form a filamentous network with lateral filament associations

植物核纤层蛋白NMCP1和NMCP2形成具有侧向丝状关联的丝状网络。

期刊:Journal of Experimental Botany
影响因子:5.7
doi:10.1093/jxb/erab243
Masuda, Kiyoshi; Hikida, Riku; Fujino, Kaien
发表日期：2021
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Significance of Circular FAT1 as a Prognostic Factor and Tumor Suppressor for Esophageal Squamous Cell Carcinoma

环状FAT1作为食管鳞状细胞癌预后因子和肿瘤抑制因子的意义

期刊:Annals of Surgical Oncology
影响因子:3.5
doi:10.1245/s10434-021-10089-9
Takaki, Wataru; Konishi, Hirotaka; Shoda, Katsutoshi; Arita, Tomohiro; Kataoka, Satoshi; Shibamoto, Jun; Furuke, Hirotaka; Takabatake, Kazuya; Shimizu, Hiroki; Komatsu, Shuhei; Shiozaki, Atsushi; Fujiwara, Hitoshi; Masuda, Kiyoshi; Otsuji, Eigo
细胞生物学
肿瘤
肿瘤免疫
FAT1
发表日期：2021
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Evolutionary history and structure of nuclear matrix constituent proteins, the plant analogues of lamins

核基质组成蛋白（层粘蛋白的植物同源物）的进化历史和结构

期刊:Journal of Experimental Botany
影响因子:5.7
doi:10.1093/jxb/erz102
Ciska, Malgorzata; Hikida, Riku; Masuda, Kiyoshi; Moreno Díaz de la Espina, Susana
发表日期：2019
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Novel compound heterozygous CDH23 variants in a patient with Usher syndrome type I

Usher综合征I型患者中发现新的CDH23复合杂合变异

期刊:Human Genome Variation
影响因子:1.3
doi:10.1038/s41439-019-0037-y
Okano, Satomi; Makita, Yoshio; Katada, Akihiro; Harabuchi, Yasuaki; Kohmoto, Tomohiro; Naruto, Takuya; Masuda, Kiyoshi; Imoto, Issei
CDH2
发表日期：2019
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Primary microcephaly caused by novel compound heterozygous mutations in ASPM

由ASPM基因新型复合杂合突变引起的原发性小头畸形

期刊:Human Genome Variation
影响因子:1.3
doi:10.1038/hgv.2018.15
Okamoto, Nobuhiko; Kohmoto, Tomohiro; Naruto, Takuya; Masuda, Kiyoshi; Imoto, Issei
ASPM
发表日期：2018
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A putative MYB35 ortholog is a candidate for the sex-determining genes in Asparagus officinalis

推测的MYB35直系同源基因是芦笋（Asparagus officinalis）性别决定基因的候选基因。

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/srep41497
Tsugama, Daisuke; Matsuyama, Kohei; Ide, Mayui; Hayashi, Masato; Fujino, Kaien; Masuda, Kiyoshi
发表日期：2017
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A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements

1q42.12-qter区域同时存在重复、三重复和单亲二体性的病例支持微同源介导的断裂诱导复制模型，用于解释复制重排。

期刊:Molecular Cytogenetics
影响因子:1.4
doi:10.1186/s13039-017-0316-6
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
发表日期：2017
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Genome-first approach diagnosed Cabezas syndrome via novel CUL4B mutation detection

采用基因组优先的方法，通过检测新的CUL4B突变诊断出卡贝萨斯综合征。

期刊:Human Genome Variation
影响因子:1.3
doi:10.1038/hgv.2016.45
Okamoto, Nobuhiko; Watanabe, Miki; Naruto, Takuya; Matsuda, Keiko; Kohmoto, Tomohiro; Saito, Masako; Masuda, Kiyoshi; Imoto, Issei
CUL4B
发表日期：2017
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The first Japanese patient with mandibular hypoplasia, deafness, progeroid features and lipodystrophy diagnosed via POLD1 mutation detection

首例通过POLD1基因突变检测确诊的下颌发育不全、耳聋、早衰样特征和脂肪营养不良的日本患者

期刊:Human Genome Variation
影响因子:1.3
doi:10.1038/hgv.2017.31
Okada, Asami; Kohmoto, Tomohiro; Naruto, Takuya; Yokota, Ichiro; Kotani, Yumiko; Shimada, Aki; Miyamoto, Yoko; Takahashi, Rizu; Goji, Aya; Masuda, Kiyoshi; Kagami, Shoji; Imoto, Issei
发育与干细胞
发表日期：2017
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