Sakurai Hidetoshi相关文献与解析，生知库

Embryonic lineage-specific iPSC-derived mesenchymal stem/stromal cells exhibit different morphologies and intrinsic functions.

胚胎谱系特异性 iPSC 衍生的间充质干/基质细胞表现出不同的形态和内在功能。

doi:10.1016/j.isci.2025.114482

Nguyen Linh, Motoike Souta, Zujur Denise, Yoshizawa Keiko, Takashima Yasuhiro, Uezumi Akiyoshi, Furuhashi Kazuhiro, Maruyama Shoichi, Jin Yonghui, Toguchida Junya, Sakurai Hidetoshi, Ikeya Makoto

Editorial: Induced pluripotent stem cells (iPSCs) for skeletal muscle diseases

社论：诱导多能干细胞（iPSCs）在骨骼肌疾病治疗中的应用

期刊:Frontiers in Cell and Developmental Biology

影响因子:4.3

doi:10.3389/fcell.2025.1556403

Sakurai, Hidetoshi; Suzuki, Masatoshi; Asakura, Atsushi

Early and non-destructive prediction of the differentiation efficiency of human induced pluripotent stem cells using imaging and machine learning.

利用成像和机器学习技术对人类诱导多能干细胞的分化效率进行早期无损预测

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-025-11108-5

Hojo Miki Arai, Tsuzuki Taku, Ozawa Yosuke, Araki Toshiyuki, Sakurai Hidetoshi

Combined rapamycin and mesenchymal stem/stromal cells derived from induced pluripotent stem cells-mediated delivery of ACVR2B-Fc fusion protein reduces heterotopic ossification in a mouse model of fibrodysplasia ossificans progressiva.

雷帕霉素与源自诱导多能干细胞的间充质干/基质细胞联合递送 ACVR2B-Fc 融合蛋白，可减少进行性骨化性纤维发育不良小鼠模型中的异位骨化

期刊:JBMR Plus

影响因子:2.4

doi:10.1093/jbmrpl/ziaf068

Gao Pan, Inada Yoshiko, LÃ³pez-Iniesta Maria JosÃ©, Zhao Chengzhu, Goto Megumi, Hotta Akitsu, Sakurai Hidetoshi, Ikeya Makoto

Establishment of quantitative and consistent in vitro skeletal muscle pathological models of myotonic dystrophy type 1 using patient-derived iPSCs

利用患者来源的诱导多能干细胞建立定量且一致的1型强直性肌营养不良症体外骨骼肌病理模型

期刊:Scientific Reports

影响因子:3.9

doi:10.1038/s41598-022-26614-z

Kawada, Ryu; Jonouchi, Tatsuya; Kagita, Akihiro; Sato, Masae; Hotta, Akitsu; Sakurai, Hidetoshi

A new immunodeficient Duchenne muscular dystrophy rat model to evaluate engraftment after human cell transplantation

一种新的免疫缺陷型杜氏肌营养不良症大鼠模型，用于评估人类细胞移植后的植入情况

期刊:Frontiers in Physiology

影响因子:3.4

doi:10.3389/fphys.2023.1094359

Sato, Masae; Goto, Megumi; Yamanouchi, Keitaro; Sakurai, Hidetoshi

Characterization of hiPSC-Derived Muscle Progenitors Reveals Distinctive Markers for Myogenic Cell Purification Toward Cell Therapy

hiPSC衍生肌肉祖细胞的表征揭示了肌源性细胞纯化的独特标记，有望用于细胞治疗

期刊:Stem Cell Reports

影响因子:5.1

doi:10.1016/j.stemcr.2021.03.004

Nalbandian, Minas; Zhao, Mingming; Sasaki-Honda, Mitsuru; Jonouchi, Tatsuya; Lucena-Cacace, Antonio; Mizusawa, Takuma; Yasuda, Masahiko; Yoshida, Yoshinori; Hotta, Akitsu; Sakurai, Hidetoshi

细胞生物学

发表日期：2021

文献求助收藏

Systemic Supplementation of Collagen VI by Neonatal Transplantation of iPSC-Derived MSCs Improves Histological Phenotype and Function of Col6-Deficient Model Mice

通过新生儿移植iPSC衍生的MSCs系统性补充胶原蛋白VI可改善Col6缺陷模型小鼠的组织学表型和功能

期刊:Frontiers in Cell and Developmental Biology

影响因子:4.3

doi:10.3389/fcell.2021.790341

Harada, Aya; Goto, Megumi; Kato, Atsuya; Takenaka-Ninagawa, Nana; Tanaka, Akito; Noguchi, Satoru; Ikeya, Makoto; Sakurai, Hidetoshi

多发性硬化症

发表日期：2021

文献求助收藏

Orai1-STIM1 Regulates Increased Ca(2+) Mobilization, Leading to Contractile Duchenne Muscular Dystrophy Phenotypes in Patient-Derived Induced Pluripotent Stem Cells

Orai1-STIM1 调节 Ca(2+) 动员增加，导致患者来源的诱导多能干细胞出现杜氏肌营养不良症的收缩表型

期刊:Biomedicines

影响因子:3.9

doi:10.3390/biomedicines9111589

Uchimura, Tomoya; Sakurai, Hidetoshi

Translation of expanded CGG repeats in LRP12 associated oculopharyngodistal myopathy

LRP12相关眼咽远端肌病中CGG重复序列扩增的翻译

Embryonic lineage-specific iPSC-derived mesenchymal stem/stromal cells exhibit different morphologies and intrinsic functions.

胚胎谱系特异性 iPSC 衍生的间充质干/基质细胞表现出不同的形态和内在功能。

Editorial: Induced pluripotent stem cells (iPSCs) for skeletal muscle diseases

社论：诱导多能干细胞（iPSCs）在骨骼肌疾病治疗中的应用

Early and non-destructive prediction of the differentiation efficiency of human induced pluripotent stem cells using imaging and machine learning.

利用成像和机器学习技术对人类诱导多能干细胞的分化效率进行早期无损预测

Combined rapamycin and mesenchymal stem/stromal cells derived from induced pluripotent stem cells-mediated delivery of ACVR2B-Fc fusion protein reduces heterotopic ossification in a mouse model of fibrodysplasia ossificans progressiva.

雷帕霉素与源自诱导多能干细胞的间充质干/基质细胞联合递送 ACVR2B-Fc 融合蛋白，可减少进行性骨化性纤维发育不良小鼠模型中的异位骨化

Establishment of quantitative and consistent in vitro skeletal muscle pathological models of myotonic dystrophy type 1 using patient-derived iPSCs

利用患者来源的诱导多能干细胞建立定量且一致的1型强直性肌营养不良症体外骨骼肌病理模型

A new immunodeficient Duchenne muscular dystrophy rat model to evaluate engraftment after human cell transplantation

一种新的免疫缺陷型杜氏肌营养不良症大鼠模型，用于评估人类细胞移植后的植入情况

Characterization of hiPSC-Derived Muscle Progenitors Reveals Distinctive Markers for Myogenic Cell Purification Toward Cell Therapy

hiPSC衍生肌肉祖细胞的表征揭示了肌源性细胞纯化的独特标记，有望用于细胞治疗

Systemic Supplementation of Collagen VI by Neonatal Transplantation of iPSC-Derived MSCs Improves Histological Phenotype and Function of Col6-Deficient Model Mice

通过新生儿移植iPSC衍生的MSCs系统性补充胶原蛋白VI可改善Col6缺陷模型小鼠的组织学表型和功能

Orai1-STIM1 Regulates Increased Ca(2+) Mobilization, Leading to Contractile Duchenne Muscular Dystrophy Phenotypes in Patient-Derived Induced Pluripotent Stem Cells

Orai1-STIM1 调节 Ca(2+) 动员增加，导致患者来源的诱导多能干细胞出现杜氏肌营养不良症的收缩表型