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Cellular and Molecular Gastroenterology and Hepatology|December 13, 2021
Bile Acid-Mediated Activation of Brown Fat Protects From Alcohol-Induced Steatosis and Liver Injury in MiceMingjie Fan, Yangmeng Wang, Lihua Jin, et al.Frontiers in Genetics|March 21, 2022
MAP3K1 Variant Causes Hyperactivation of Wnt4/β-Catenin/FOXL2 Signaling Contributing to 46,XY Disorders/Differences of Sex DevelopmentHong Chen, Qingqing Chen, Yilin Zhu, et al.Journal of Colloid and Interface Science|November 23, 2006
Modeling synergistic adsorption of phenol/aniline mixtures in the aqueous phase onto porous polymer adsorbentsW M Zhang, Q J Zhang, B C Pan, et al.Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|April 5, 2022
[Short-term efficacy of venetoclax combined with azacitidine in acute myeloid leukemia: a single-institution experience]W J Yu, J S Jia, J Wang, et al.Zhonghua Zhong Liu Za Zhi [Chinese Journal of Oncology]|January 1, 1988
[In vivo metastasis of human tumor transplant in T and NK cell immune-deficient mice]B Q Wu, W G Fang, J Zheng, et al.Zhonghua Nei Ke Za Zhi|September 22, 2021
[Prognostic significance of DEK-NUP214 fusion gene in patients with acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation]M G Gao, Q Fu, Y Z Qin, et al.Proceedings of the National Academy of Sciences of the United States of America|February 28, 2019
Basolateral amygdala input to the medial prefrontal cortex controls obsessive-compulsive disorder-like checking behaviorTingting Sun, Zihua Song, Yanghua Tian, et al.Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi|January 7, 2019
[Clinical implication of minimal residue disease monitoring by WT1 gene detection and flow cytometry in myelodysplastic syndrome with allogeneic stem cell transplantation]X S Zhao, X D Mo, Y Hong, et al.Beijing Da Xue Xue Bao. Yi Xue Ban = Journal of Peking University. Health Sciences|December 22, 2017
[Clinical features and early treatment effects in intermediate risk and poor risk acute myeloid leukemia with EVI1 positive]W B Duan, L Z Gong, J S Jia, et al.Mitochondrion|September 10, 2018
Mitochondrial dysfunction caused by m.2336T>C mutation with hypertrophic cardiomyopathy in cybrid cell linesDan Li, Yaping Sun, Qianqian Zhuang, et al.Pageof 31