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Frontiers in Genetics|October 10, 2022
Evaluation of strategies for identification of infants with pathogenic glucose-6-phosphate dehydrogenase variants in ChinaZhongmin Xia, Xudong Wang, Huiming Ye, et al.Frontiers in Genetics|October 10, 2022
Effects of acupuncture treatment on microRNAs expression in ovarian tissues from Tripterygium glycoside-induced diminished ovarian reserve ratsGe Lu, Yao-Yao Zhu, Hong-Xiao Li, et al.Frontiers in Genetics|October 10, 2022
A novel marker based on necroptosis-related long non-coding RNA for forecasting prognostic in patients with clear cell renal cell carcinomaJinxing Lv, Qinghui Xu, Guoqing Wu, et al.Frontiers in Genetics|October 10, 2022
High Expression of ATP6V1C2 Predicts Unfavorable Overall Survival in Patients With Colon AdenocarcinomaGuanghua Li, Jiahua Huang, Sile Chen, et al.Frontiers in Genetics|October 10, 2022
Cuproptosis-related lncRNAs predict the clinical outcome and immune characteristics of hepatocellular carcinomaHongfei Zhu, Feifei Mao, Kang Wang, et al.Frontiers in Genetics|October 10, 2022
Keratinocyte-associated protein 3 plays a role in body weight and adiposity with differential effects in males and femalesAlexandria M Szalanczy, Emily Goff, Osborne Seshie, et al.Frontiers in Genetics|October 10, 2022
FN1 promotes prognosis and radioresistance in head and neck squamous cell carcinoma: From radioresistant HNSCC cell line to integrated bioinformatics methodsXiaojun Tang, Qinglai Tang, Xinming Yang, et al.Frontiers in Genetics|October 10, 2022
Impaired expression of serine/arginine protein kinase 2 (SRPK2) affects melanoma progressionMônica Maria Magalhães Caetano, Gabriela Alves Moreira, Maria Roméria da Silva, et al.Frontiers in Genetics|October 10, 2022
Integrated identification of key immune related genes and patterns of immune infiltration in calcified aortic valvular disease: A network based meta-analysisLi-Da Wu, Feng Xiao, Jin-Yu Sun, et al.Frontiers in Genetics|October 10, 2022
Systematic analysis of inheritance pattern determination in genes that cause rare neurodevelopmental diseasesSoojin Park, Se Song Jang, Seungbok Lee, et al.Pageof 1,586