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Molecular Genetics and Genomics : MGG|May 22, 2013
Novel POMGnT1 mutations cause muscle-eye-brain disease in Chinese patientsHui Jiao, Hiroshi Manya, Shuo Wang, et al.Chinese Medical Journal|September 15, 2005
Clinicopathological, immunohistochemical, and ultrastructural study of 13 cases of melanotic schwannomaHong-ying Zhang, Guang-hua Yang, Hui-jiao Chen, et al.Sichuan Da Xue Xue Bao. Yi Xue Ban = Journal of Sichuan University. Medical Science Edition|December 3, 2004
[Interobserver reproducibility in the pathologic diagnosis of borderline ductal proliferative breast diseases]Bing Wei, Hong Bu, Cai-rong Zhu, et al.Zhonghua Bing Li Xue Za Zhi = Chinese Journal of Pathology|June 9, 2005
[HER2 expression and its prognostic implication in lymph node negative breast carcinoma: a Meta-analysis]Hua Guo, Bing Wei, Hong-ying Zhang, et al.World Journal of Gastroenterology|September 22, 2010
Infantile hepatic hemangioendothelioma: a clinicopathologic study in a Chinese populationZhang Zhang, Hui-Jiao Chen, Wen-Juan Yang, et al.Medical Science Monitor : International Medical Journal of Experimental and Clinical Research|February 8, 2020
SHOX CNE9/10 Knockout in U2OS Osteosarcoma Cells and Its Effects on Cell Growth and ApoptosisXue-Jiao Xu, Shi-Jie Xin, Hui-Ying Mao, et al.Journal of Cellular and Molecular Medicine|January 26, 2016
Interleukin-1B 31 C>T polymorphism combined with Helicobacter pylori-modified gastric cancer susceptibility: evidence from 37 studiesHua-Yong Ying, Bei-Wei Yu, Zong Yang, et al.Human Molecular Genetics|December 10, 2021
Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse modelJia Wang, Jinli Bai, Shijia OuYang, et al.Journal of Human Genetics|May 20, 2016
Analysis of phenotype, enzyme activity and genotype of Chinese patients with POMT1 mutationHaipo Yang, Hiroshi Manya, Kazuhiro Kobayashi, et al.Neuromuscular Disorders : NMD|April 6, 2023
Novel Alu-mediated deletions of the SMN1 gene were identified by ultra-long read sequencing technology in patients with spinal muscular atrophyJinli Bai, Yujin Qu, Shijia OuYang, et al.Pageof 16