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

Neuromuscular electrical stimulation training induces myonuclear accretion and hypertrophy in mice without overt signs of muscle damage and regeneration

神经肌肉电刺激训练可诱导小鼠肌核增生和肥大,且无明显的肌肉损伤和再生迹象

Aurélie Fessard #, Aliki Zavoriti #, Natacha Boyer, Jules Guillemaud, Masoud Rahmati, Peggy Del Carmine, Christelle Gobet, Bénédicte Chazaud, Julien Gondin

Correction: A functional regulatory variant of MYH3 influences muscle fiber-type composition and intramuscular fat content in pigs

更正:MYH3 的一个功能性调控变体影响猪的肌肉纤维类型组成和肌内脂肪含量。

Cho, In-Cheol; Park, Hee-Bok; Ahn, Jin Seop; Han, Sang-Hyun; Lee, Jae-Bong; Lim, Hyun-Tae; Yoo, Chae-Kyoung; Jung, Eun-Ji; Kim, Dong-Hwan; Sun, Wu-Sheng; Ramayo-Caldas, Yuliaxis; Kim, Sang-Geum; Kang, Yong-Jun; Kim, Yoo-Kyung; Shin, Hyun-Sook; Seong, Pil-Nam; Hwang, In-Sul; Park, Beom-Young; Hwang, Seongsoo; Lee, Sung-Soo; Ryu, Youn-Chul; Lee, Jun-Heon; Ko, Moon-Suck; Lee, Kichoon; Andersson, Göran; Pérez-Enciso, Miguel; Lee, Jeong-Woong

Before scoliosis can be attributed to the variant c.326G>A in MYH3, its pathogenicity must be proven

在将脊柱侧弯归因于MYH3基因c.326G>A变异之前,必须先证实其致病性。

Finsterer, Josef

Reply to Before scoliosis can be attributed to the variant c.326G>A in MYH3, its pathogenicity must be proven

回复:在将脊柱侧弯归因于MYH3基因c.326G>A变异之前,必须先证明其致病性。

Maccarone, Maria Chiara; Paramento, Matilde; Passarotto, Edoardo; Contessa, Paola; Rubega, Maria; Formaggio, Emanuela; Masiero, Stefano

Novel heterozygous mutation in MYH3 causes contractures, pterygia, and spondylocarpostarsal fusion syndrome 1: A case report

MYH3基因中一种新的杂合突变导致挛缩、翼状胬肉和脊椎腕跖骨融合综合征1:病例报告

Zhu, Xuefen; Yao, Qiang

Tissue-resident skeletal muscle macrophages promote recovery from viral pneumonia-induced sarcopenia in normal aging

组织驻留骨骼肌巨噬细胞促进正常衰老过程中病毒性肺炎引起的肌肉减少症的恢复

Constance E Runyan, Lucy Luo, Lynn C Welch, Ziyan Lu, Fei Chen, Maxwell J Schleck, Radmila A Nafikova, Rogan A Grant, Raul Piseaux Aillon, Karolina J Senkow, Elsie G Bunyan, William T Plodzeen, Hiam Abdala-Valencia, Craig Weiss, Laura A Dada, Edward B Thorp, Jacob I Sznajder, Navdeep S Chandel, Alex

Vertebral Bone Density Abnormalities in Fetal Ultrasound: A Distinctive Clinical Sign of Spondylocarpotarsal Synostosis Syndrome MYH3-Related

胎儿超声检查中椎骨骨密度异常:脊椎腕跗骨融合综合征MYH3相关疾病的独特临床表现

Blasi, Immacolata; Pollazzon, Marzia; Caraffi, Stefano Giuseppe; Zuntini, Roberta; Comitini, Giuseppina; Bonasoni, Maria Paola; Daolio, Jessica; Unger, Sheila; Aguzzoli, Lorenzo; Superti-Furga, Andrea; Garavelli, Livia

Homozygous Pathogenic MYH3 Variants Associated With Arthrogryposis and Lingual Dystonia

纯合致病性MYH3变异与关节挛缩症和舌肌张力障碍相关

Mouraux, Charlotte; Fouquet, Claire; Durkin, Keith; Dideberg, Vinciane; Bulk, Saskia; Aktan, David; Artesi, Maria; Depierreux, Frédérique

Progressive cardiomyopathy with intercalated disc disorganization in a rat model of Becker dystrophy

贝克尔营养不良症大鼠模型中出现进行性心肌病,并伴有闰盘紊乱

Valentina Taglietti, Kaouthar Kefi, Busra Mirciloglu, Sultan Bastu, Jean-Daniel Masson, Iwona Bronisz-Budzyńska, Vassiliki Gouni, Carlotta Ferri, Alan Jorge, Christel Gentil, France Pietri-Rouxel, Edoardo Malfatti, Peggy Lafuste, Laurent Tiret #, Frederic Relaix #

Functional assessment of a novel biallelic MYH3 variation causing CPSKF1B (contractures, pterygia, and spondylocarpotarsal fusion syndrome1B)

对导致 CPSKF1B(挛缩、翼状胬肉和脊椎腕跗关节融合综合征 1B)的新型双等位基因 MYH3 变异进行功能评估

Qing-Bing He ,Cai-Hong Wu ,Dong-Lan Sun ,Jia-Yu Yuan ,Hua-Ying Hu ,Kai Yang ,Wen-Qi Chen ,You-Sheng Yan ,Guang-Yue Yin ,Jing Zhang ,Ya-Zhou Li