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Experimental and Therapeutic Medicine|July 9, 2025
Genetic and clinical insights into acute kidney injury in maturity-onset diabetes of the young caused by the ABCC8 c.2500C>T mutation: Potential risk factors associated with SGLT2 inhibitorsJing Zou, Xiang Chen, Hong-Ping Yu, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|February 15, 2020
A Phase II Trial of 5-Day Neoadjuvant Radiotherapy for Patients with High-Risk Primary Soft Tissue SarcomaAnusha Kalbasi, Mitchell Kamrava, Fang-I Chu, et al.Nature Communications|December 2, 2025
CIP2A mediates mitotic recruitment of SLX4/MUS81/XPF to resolve replication stress-induced DNA lesionsLauren de Haan, Sietse J Dijt, Alejandro García-López, et al.Medical Physics|July 15, 2025
TrackRAD2025 challenge dataset: real-time tumor tracking for MRI-guided radiotherapyYiling Wang, Elia Lombardo, Adrian Thummerer, et al.Medscience|February 24, 2026
Differential genetic analysis of ectrodactyly in a Fanconi anemia pedigree with FANCA mutationsJian-Hui Zhang, Zi-Yan Xu, Hong-Ping Yu, et al.Gene|September 25, 2025
Genetic analysis of a family with skeletal muscle ion channelopathy and hereditary spastic paraplegia type 7 caused by SCN4A and SPG7 double mutationsHong-Ping Yu, Zi-Yan Xu, Meng-Qian Wu, et al.Clinical Medicine (London, England)|August 8, 2026
Association Between Dietary Magnesium Intake and All-Cause Mortality in Patients with Chronic Kidney Disease: Insights from NHANES 1999-2018Zi-Yan Xu, Jing Zou, Li-Jun Xie, et al.The Lancet. Oncology|May 31, 2024
Addressing challenges in low-income and middle-income countries through novel radiotherapy research opportunitiesMay Abdel-Wahab, C Norman Coleman, Jesper Grau Eriksen, et al.Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences|March 17, 2026
Phosphoproteomics elucidates the functional impact of the PTPN11 p.Asn308Ser variant in a Noonan syndrome pedigreeWei-Jing Xu, Li-Jun Xie, Wen-Jun Chen, et al.Gene|August 1, 2026
Clinical and genetic analysis of Liver-Predominant ornithine transcarbamylase deficiency caused by a novel de novo OTC sequence variant in a female childAn-Kang Zhu, Shi-Ni Cai, Chun-Hui Hu, et al.Pageof 38