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

Glutathione Synthesis via the Cystine/Glutamate Transporter Promotes the Formation of Tertiary Lymphoid Structures in the Kidney

胱氨酸/谷氨酸转运蛋白介导的谷胱甘肽合成促进肾脏中三级淋巴结构的形成

Arai, Hiroyuki; Sugiura, Yuki; Yamamoto, Shinya; Yoshikawa, Takahisa; Matsuoka, Yuta; Maeda, Rae; Neyama, Hiroyuki; Kamimatsuse, Ryo; Goto, Shima; Taniguchi, Keisuke; Toriu, Naoya; Kondo, Makiko; Sato, Yuki; Fukuma, Shingo; Yanagita, Motoko

Rare heterozygous de novo variants in RAPGEF2 are associated with a neurodevelopmental disorder

RAPGEF2基因中罕见的杂合新生变异与神经发育障碍相关。

Bereshneh, Ali H; Wilson, Kirkland A; Pan, Xueyang; Hannan, Shabab B; Cooper, Megan A; Diaz, Jullianne; Leon, Eyby; Moses, Tiana M; Azamian, Mahshid S; Scott, Daryl A; Billie Au, Ping Yee; Appendino, Juan Pablo; Scheffer, Ingrid E; Kaspi, Antony; Bahlo, Melanie; Hildebrand, Michael S; Morgan, Angela T; Ekure, Ekanem; Shulman, Joshua M; Hildebrandt, Friedhelm; Posey, Jennifer E; Kruszka, Paul; Vilain, Eric; Yamamoto, Shinya; Kanca, Oguz; Berger, Seth; Bellen, Hugo J

Translating multi-omics into healthcare: requisites for scalable and equitable implementation

将多组学转化为医疗保健:可扩展和公平实施的必要条件

Tumiene, Birute; Adams, David R; Allaway, Robert; Barrero, Maria J; Chan, Chun-Hung; Faundes, Víctor; Fear, Vanessa S; Glezer, Polina; Fuchs, Claudia; Groza, Tudor; Houwink, Elisa J F; Jamuar, Saumya Shekhar; Letinturier, Mary Catherine V; Lomash, Richa Madan; Puri, Ratna Dua; Reichardt, Juergen K V; Mehrian-Shai, Ruty; van der Westhuizen, Francois H; Varshney, Gaurav K; Yamamoto, Shinya; Baynam, Gareth

Resolving SLC6A1 variable expressivity with deep clinical phenotyping and Drosophila models

利用深度临床表型分析和果蝇模型解析SLC6A1基因表达变异性

Jay, Kristy L; Gogate, Nikhita; Hall, Paige I; Ezell, Kimberly M; Andrews, Jonathan C; Jangam, Sharayu V; Pan, Hongling; Pham, Kelvin; German, Ryan; Gomez, Vanessa; Jellinek-Russo, Emily; Storch, Eric A; Yamamoto, Shinya; Kanca, Oguz; Bellen, Hugo J; Dierick, Herman A; Cogan, Joy D; Phillips, John A; Hamid, Rizwan; Cassini, Thomas; Rives, Lynette; Pruthi, Sumit; Chen, Hua-Chang; Posey, Jennifer E; Wangler, Michael F

Organ-Specific Clinicopathological Features That Are Associated With Post-Relapse Survival of Metastatic Breast Cancer in Japanese Women: A Multicenter Cohort Study

与日本女性转移性乳腺癌复发后生存相关的器官特异性临床病理特征:一项多中心队列研究

Koyama, Yoichi; Horimoto, Yoshiya; Yamada, Akimitsu; Narui, Kazutaka; Yamamoto, Shinya; Kaise, Hiroshi; Yamada, Kimito; Ishikawa, Takashi

A Rare Case of Eosinophilic Granulomatosis with Polyangiitis Following Development of Central Diabetes Insipidus: A Case Report and Literature Review

一例罕见的中枢性尿崩症后并发嗜酸性肉芽肿性血管炎的病例报告及文献复习

Kosaka, Tatsuaki; Yamamoto, Shinya; Yasugi, Naoko; Sugioka, Sayaka; Hakata, Takuro; Saito, Rintaro; Hiwa, Ryosuke; Koyasu, Sho; Teramoto, Yuki; Yanagita, Motoko

A case of chronic Campylobacter fetus infection-related glomerulonephritis, mimicking systemic autoimmune diseases

一例慢性弯曲杆菌胎儿感染相关性肾小球肾炎,其临床表现酷似系统性自身免疫性疾病

Matsumoto, Minami; Kitai, Yuichiro; Yamamoto, Shinya; Iwashige, Yohei; Muro, Koji; Kato, Yukiko; Tsuchido, Yasuhiro; Shinohara, Koh; Tsuda, Yusuke; Murakami, Kosaku; Kaneko, Keiichi; Nakata, Hirosuke; Matsubara, Takeshi; Yokoi, Hideki; Ito, Isao; Minamiguchi, Sachiko; Oda, Takashi; Nagao, Miki; Yanagita, Motoko

From Diagnostic Challenge to Clinical Success: Rapid Multiplex PCR Identification of Cryptosporidium in HIV-Associated Refractory Diarrhea: A Case Report

从诊断挑战到临床成功:快速多重PCR鉴定HIV相关难治性腹泻中的隐孢子虫:病例报告

Kono, Yudai; Arase, Mayu; Ukai, Kohei; Soneda, Keiko; Yamamoto, Shinya; Ikeuchi, Kazuhiko; Adachi, Eisuke; Nomura, Yusuke; Higurashi, Yoshimi; Izumiyama, Shinji; Honjo, Kazuki; Miyakawa, Yu; Ihara, Sozaburo; Abe, Hiroyuki; Fujishiro, Mitsuhiro; Okugawa, Shu; Tsutsumi, Takeya

NLGN3 autism variants have distinct functional impact on synapses and sleep behavior in Drosophila

NLGN3自闭症变异体对果蝇的突触和睡眠行为具有不同的功能影响

Townsley, Rebekah E; Andrews, Jonathan C; Srivastav, Saurabh; Jangam, Sharayu V; Hannan, Shabab B; Kanca, Oguz; Yamamoto, Shinya; Wangler, Michael F

De novo and inherited variants in DDX39B cause a novel neurodevelopmental syndrome

DDX39B基因的新生突变和遗传突变会导致一种新的神经发育综合征。

Booth, Kevin T A; Jangam, Sharayu V; Chui, Martin M C; Treat, Kayla; Graziani, Lorenzo; Soldano, Alessia; Ruan, Yao; Wan-Hei Hui, Jeffrey; White, Kerry; Christensen, Celanie K; Lynnes, Ty; Yamamoto, Shinya; Kanca, Oguz; Tsang, Mandy H Y; Lynch, Sally A; Mullegama, Sureni V; Baptista, Julia; Iancu, Daniela; Joss, Shelagh K; Wong, Sandra Y Y; Mak, Christopher C Y; Kwong, Anna K Y; Bellen, Hugo J; Conboy, Erin; Sanges, Remo; Leung, Anskar Yu-Hung; Wangler, Michael F; Chung, Brian H Y; Vetrini, Francesco