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

Evaluation of the knowledge, perception, and practice of nurses regarding sarcopenia: a descriptive study

护士对肌少症的知识、认知和实践评价:一项描述性研究

Taani, Murad H; Skuble, Heather; Antwi-Boasiako, Charles; Wangler, Dawn M; Kerby, Christopher J; Kawafha, Mariam M; AlAbidi, Suzan; Andargeery, Shaherah Yousef

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

International Forum on Visceral Myopathy 2024: Advances in the Knowledge of the Disease

2024年内脏肌病国际论坛:疾病知识进展

Barbara, Pascal De Santa; Ceccherini, Isabella; Heuckeroth, Robert O; Di Lorenzo, Carlo; Alves, Maria M; Beyder, Arthur; Borrelli, Osvaldo; Cacopardo, Ludovica; Ceron, Rachel; Chen, Jihong; Chiappori, Federica; Contessa, Antonio; De Giorgio, Roberto; Diamanti, Antonella; Faticato, Maria Grazia; Faure, Sandrine; Hashmi, Sohaib K; Huizinga, Jan D; Kapur, Raj P; Lambe, Cecile; Lancon, Laurence; McManigal, Ryan; Mousa, Hayat; Palmitelli, Alessandro; Perreaux, Victor; Prato, Alessio Pini; Pitto, Michela; Proietti, Elisa; Rendu, John; Rybak, Anna; Sanders, Kenton M; Sardar, Sabah; Stanghellini, Vincenzo; Tambucci, Renato; Thapar, Nikhil; Vanden Berghe, Pieter; Vassalli, Massimo; Wang, Qianqian; Wangler, Michael; Wolfson, Sharon; Zada, Almira; Zhou, Jiliang; Viti, Federica

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

Diffuse traumatic brain injury induced stimulator of interferons (STING) signaling in microglia drives cortical neuroinflammation, neuronal dysfunction, and impaired cognition.

弥漫性创伤性脑损伤诱导小胶质细胞中干扰素刺激因子(STING)信号传导,导致皮质神经炎症、神经元功能障碍和认知功能受损

Packer Jonathan M, Giammo Samantha G, Wangler Lynde M, Davis Amara C, Bray Chelsea E, Godbout Jonathan P

Phosphorylation-dependent activation of the bHLH transcription factor ICE1/SCRM promotes polarization of the Arabidopsis zygote

磷酸化依赖的bHLH转录因子ICE1 / SCRM激活促进拟南芥合子的极化

Houming Chen, Feng Xiong, Alexa-Maria Wangler, Torren Bischoff, Kai Wang, Yingjing Miao, Daniel Slane, Rebecca Schwab, Thomas Laux, Martin Bayer

De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms

CDKL1 和 CDKL2 的新生变异与神经发育症状相关

Bereshneh, Ali H; Andrews, Jonathan C; Eberl, Daniel F; Bademci, Guney; Borja, Nicholas A; Bivona, Stephanie; Chung, Wendy K; Yamamoto, Shinya; Wangler, Michael F; McKee, Shane; Tekin, Mustafa; Bellen, Hugo J; Kanca, Oguz

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function.

PLCG1 的杂合变异会影响听力、视力、心脏和免疫功能

Ma Mengqi, Zheng Yiming, Deng Mingxi, Lu Shenzhao, Pan Xueyang, Luo Xi, Etoundi Michelle, Li-Kroeger David, Worley Kim C, Burrage Lindsay C, Blieden Lauren S, Allworth Aimee, Chen Wei-Liang, Merla Giuseppe, Mandriani Barbara, Otten Catherine E, Blanc Pierre, Rosenfeld Jill A, Dutta Debdeep, Yamamoto Shinya, Wangler Michael F, Glass Ian A, Chen Jingheng, Blue Elizabeth, Prontera Paolo, Rosain Jeremie, Marlin Sandrine, Lalani Seema R, Bellen Hugo J

De novo variants in RYBP are associated with a severe neurodevelopmental disorder and congenital anomalies

RYBP基因的新生突变与严重的神经发育障碍和先天性异常有关。

Weisz-Hubshman, Monika; Burrage, Lindsay C; Jangam, Sharayu V; Rosenfeld, Jill A; von Hardenberg, Sandra; Bergmann, Anke; Richter, Manuela Friederike; Rydzanicz, Malgorzata; Ploski, Rafal; Stembalska, Agnieszka; Chung, Wendy K; Hernan, Rebecca R; Lim, Foong Y; Brunet, Theresa; Syrbe, Steffen; Keren, Boris; Heide, Solveig; Murdock, David R; Dai, Hongzheng; Xia, Fan; Ketkar, Shamika; Dawson, Brian; Narayanan, Vinodh; Graves, Hillary K; Wangler, Michael F; Bacino, Carlos; Lee, Brendan