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

ACTN3 genotype influences masseter muscle characteristics and self-reported bruxism

ACTN3基因型影响咬肌特征和自我报告的磨牙症

Nicot, Romain; Raoul, Gwénaël; Vieira, Alexandre R; Ferri, Joël; Sciote, James J

TMJ related short-term outcomes comparing two different osteosynthesis techniques for bilateral sagittal split osteotomy

颞下颌关节相关短期疗效比较:双侧矢状劈开截骨术两种不同骨合成技术的比较

Roland-Billecart, T; Raoul, G; Kyheng, M; Sciote, J J; Ferri, J; Nicot, R

Temporomandibular Joint Dysplasia in Cranio-Maxillofacial Dysplasia: A Retrospective Study. Guideline Treatment Proposal

颞下颌关节发育不良合并颅颌面发育不良:一项回顾性研究及治疗指南建议

Ferri, Joël; Schlund, Matthias; Touzet-Roumazeille, Sandrine; Sciote, James J; Nicot, Romain

ENPP1 and ESR1 genotypes associated with subclassifications of craniofacial asymmetry and severity of temporomandibular disorders

ENPP1 和 ESR1 基因型与颅面不对称的亚型分类以及颞下颌关节紊乱的严重程度相关

Chung, Kay; Richards, Tabitha; Nicot, Romain; Vieira, Alexandre R; Cruz, Christiane V; Raoul, Gwénaël; Ferri, Joel; Sciote, James J

ENPP1 and ESR1 genotypes influence temporomandibular disorders development and surgical treatment response in dentofacial deformities

ENPP1 和 ESR1 基因型影响颞下颌关节紊乱的发生发展以及牙颌面畸形的手术治疗反应

Nicot, Romain; Vieira, Alexandre R; Raoul, Gwénaël; Delmotte, Constance; Duhamel, Alain; Ferri, Joël; Sciote, James J

Small-fiber polyneuropathy (SFPN), a common underlying diagnosis in syndromes involving unexplained chronic pain and multi-system symptoms

小纤维多发性神经病(SFPN)是涉及不明原因慢性疼痛和多系统症状的综合征中常见的潜在诊断。

Diatchenko, Luda; Scholz, Joachim; Tajerian, Maral; Alvarado, Sebastian; Millecamps, Magali; Szyf, Moshe; Stone, Laura S; Westlund, Karin N; McIlwrath, Sabrina L; Oz, Helieh S; Williams, David A; Kim, Yu Shin; Chu, Yuxia; Han, Liang; Park, Kyougsook; Li, Man; Li, Zhe; LaVinka, Pamela Colleen; Caterina, Michael J; Ren, Ke; Dubner, Ronald; Wei, Feng; Dong, Xinzhong; Barski, Artem; Cuddapah, Suresh; Kartashov, Andrey V; Imamichi, Hiromi; Yang, Wenjing; Peng, Weiqun; Lane, H Clifford; Zhao, Keji; Yoo, Seungyeul; Lee, Eunjee; Zhu, Jun; Gereau IV, Robert W; Cavallone, Laura F; Gersbach, Charles A; Goldman, David; ABD-Elsayed, Alaa; Kohan, Kevin; Zuo, Xiaozhuo; Cha, Meuonghoon; Ling, Jennifer; Gu, Jianguo; Levitt, Roy C; Zhuang, Gerald Z; Keeler, Benjamin; Grant, Jeff; Bianchi, Laura; Fu, Eugene S; Zhang, Yan Ping; Erasso, Diana M; Cui, Jian Guo; Wiltshire, Tim; Li, Qiongzhen; Hao, Shuanglin; Sarantopoulos, Konstantinos D; Candiotti, Keith; Smith, Shad B; Maixner, William; Diatchenko, Luda; Martin, Eden R; Chen, Yong; Wang, Fan; Liedtke, Wolfgang; Lötsch, Jörn; Ultsch, Alfred; Chen, Yong; Guilak, Farshid; Gereau IV, Robert W; Wang, Fan; Liedtke, Wolfgang; Harper, Daniel E; Pallazola, Vincent; Williams, David A; Harte, Steven; Clauw, Daniel J; Shtein, Roni M; King, Christopher; Ribeiro-Dasilva, Margarete; Fillingim, Roger; Wallet, Shannon; Godel, JH; Foley, BF; Nicot, R; Horton, MJ; Barton, ER; Ferri, J; Raoul, G; Vieira, AR; Sciote, JJ; Smith, Shad B; Bair, Eric; Xue, Wei; Slade, Gary D; Dubner, Ronald; Fillingim, Roger B; Greenspan, Joel D; Ohrbach, Richard; Knott, Charlie; Diatchenko, Luda; Maixner, William; Lang, Magdalena; Treister, Roi; Klein, Max; Oaklander, Anne Louise; Slade, Gary D; Ro, Jin Y; Chung, Man-Kyo; Lee, Jong S; Saloman, Jami L; Joseph, John; Schmidt, Brian L; Kim, Hyangin; McCabe, Michael F; Lim, Grewo; Chen, Lucy; Mao, Jianren; Nackley, Andrea G; Oaklander, Anne Louise; Downs, Heather; Herzog, Zeva Daniela; Klein, Max

Molecular motor MYO1C, acetyltransferase KAT6B and osteogenetic transcription factor RUNX2 expression in human masseter muscle contributes to development of malocclusion

人类咬肌中分子马达 MYO1C、乙酰转移酶 KAT6B 和成骨转录因子 RUNX2 的表达与咬合不正的发生发展有关

Desh, Heather; Gray, S Lauren; Horton, Michael J; Raoul, Gwenael; Rowlerson, Anthea M; Ferri, Joel; Vieira, Alexandre R; Sciote, James J

Nodal pathway genes are down-regulated in facial asymmetry

面部不对称中节点通路基因表达下调

Nicot, Romain; Hottenstein, Molly; Raoul, Gwenael; Ferri, Joel; Horton, Michael; Tobias, John W; Barton, Elisabeth; Gelé, Patrick; Sciote, James J

Epigenetic influence of KAT6B and HDAC4 in the development of skeletal malocclusion

KAT6B 和 HDAC4 对骨性错颌畸形发展的表观遗传影响

Ahrin Huh, Michael J Horton, Karen T Cuenco, Gwenael Raoul, Anthea M Rowlerson, Joel Ferri, James J Sciote

Cytochrome c oxidase deficiency in human posterior cricoarytenoid muscle

人类后环杓肌细胞色素c氧化酶缺乏症

Tellis, Cari M; Rosen, Clark; Close, John M; Horton, Michael; Yaruss, J Scott; Verdolini-Abbott, Katherine; Sciote, James J