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

Subcuticular symbionts of intertidal brittle stars: diversity, host specificity, and functional potential

潮间带海星皮下共生体:多样性、宿主特异性和功能潜力

Kawano, Keisuke; Morimura, Hiroyuki; Awano, Tatsuya; Kikuchi, Yoshitomo; Sawayama, Shigeki; Nakagawa, Satoshi

Titin fragment is a sensitive biomarker in Duchenne muscular dystrophy model mice carrying full-length human dystrophin gene on human artificial chromosome

肌联蛋白片段是携带人类人工染色体上全长人类肌营养不良蛋白基因的杜氏肌营养不良症模型小鼠的敏感生物标志物

Yosuke Hiramuki, Miwa Hosokawa, Kayo Osawa, Taku Shirakawa, Yasuhiro Watanabe, Ritsuko Hanajima, Hiroyuki Kugoh, Hiroyuki Awano, Masafumi Matsuo, Yasuhiro Kazuki

Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy

突变 SMN 蛋白的稳定性和寡聚化决定脊髓性肌萎缩症的临床严重程度

Emma Tabe Eko Niba, Hisahide Nishio, Yogik Onky Silvana Wijaya, Mawaddah Ar Rochmah, Toru Takarada, Atsuko Takeuchi, Tomokazu Kimizu, Kentaro Okamoto, Toshio Saito, Hiroyuki Awano, Yasuhiro Takeshima, Masakazu Shinohara

Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome

鉴定与 Dent 病 2 型和 Lowe 综合征之间的表型差异相关的新型 OCRL 亚型

Nana Sakakibara, Takeshi Ijuin, Tomoko Horinouchi, Tomohiko Yamamura, China Nagano, Eri Okada, Shinya Ishiko, Yuya Aoto, Rini Rossanti, Takeshi Ninchoji, Hiroyuki Awano, Hiroaki Nagase, Shogo Minamikawa, Ryojiro Tanaka, Takeshi Matsuyama, Koji Nagatani, Koichi Kamei, Kumiko Jinnouchi, Yasufumi Ohtsu

Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing

COL4A5 外显子最后的核苷酸替换导致异常剪接

Yuya Aoto, Tomoko Horinouchi, Tomohiko Yamamura, Atsushi Kondo, Sadayuki Nagai, Shinya Ishiko, Eri Okada, Rini Rossanti, Nana Sakakibara, China Nagano, Hiroyuki Awano, Hiroaki Nagase, Yuko Shima, Koichi Nakanishi, Masafumi Matsuo, Kazumoto Iijima, Kandai Nozu

Dystrophin Dp71 Subisoforms Localize to the Mitochondria of Human Cells

肌营养不良蛋白 Dp71 亚型定位于人类细胞的线粒体

Emma Tabe Eko Niba, Hiroyuki Awano, Tomoko Lee, Yasuhiro Takeshima, Masakazu Shinohara, Hisahide Nishio, Masafumi Matsuo

Intronic Alternative Polyadenylation in the Middle of the DMD Gene Produces Half-Size N-Terminal Dystrophin with a Potential Implication of ECG Abnormalities of DMD Patients

DMD 基因中部的内含子替代多聚腺苷酸化产生半尺寸的 N 端肌营养不良蛋白,可能与 DMD 患者的心电图异常有关

Abdul Qawee Mahyoob Rani, Tetsushi Yamamoto, Tatsuya Kawaguchi, Kazuhiro Maeta, Hiroyuki Awano, Hisahide Nishio, Masafumi Matsuo

In silico and in vitro analyses of the pathological relevance of the R258H mutation of hepatocyte nuclear factor 4α identified in maturity-onset diabetes of the young type 1

通过计算机模拟和体外分析在青少年 1 型糖尿病中发现的肝细胞核因子 4α R258H 突变的病理相关性

Kenji Sugawara, Kazuhiro Nomura, Yuko Okada, Aki Sugano, Masaaki Matsumoto, Toru Takarada, Atsuko Takeuchi, Hiroyuki Awano, Yushi Hirota, Hisahide Nishio, Yutaka Takaoka, Wataru Ogawa

Schwann cell-specific Dp116 is expressed in glioblastoma cells, revealing two novel DMD gene splicing patterns

雪旺细胞特异性 Dp116 在胶质母细胞瘤细胞中表达,揭示两种新的 DMD 基因剪接模式

Abdul Qawee Mahyoob Rani, Kazuhiro Maeta, Tatsuya Kawaguchi, Hiroyuki Awano, Masashi Nagai, Hisahide Nishio, Masafumi Matsuo

Detection of Dystrophin Dp71 in Human Skeletal Muscle Using an Automated Capillary Western Assay System

使用自动毛细管蛋白质印迹分析系统检测人类骨骼肌中的肌营养不良蛋白 Dp71

Tatsuya Kawaguchi, Emma Tabe Eko Niba, Abdul Qawee Mahyoob Rani, Yoshiyuki Onishi, Makoto Koizumi, Hiroyuki Awano, Masaaki Matsumoto, Masashi Nagai, Shinobu Yoshida, Sachiko Sakakibara, Naoyuki Maeda, Osamu Sato, Hisahide Nishio, Masafumi Matsuo