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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 2, 2022
[Genetic analysis of a patient with Papillorenal syndrome due to variant of PAX2 gene]
Xuechao Zhao, Yuting Zheng, Ning Liu, et al.
Nanoscale
|
January 3, 2024
Recent development of manganese dioxide-based materials as zinc-ion battery cathode
Shaofeng Jia, Le Li, Yue Shi, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
March 28, 2025
QIM25-232: Extracellular Vesicles Evade the Antiangiogenic Effect of Bevacizumab in Ovarian Cancer
Zhuoye Chen, Conghui Wang, Mingxia Xu, et al.
JACS Au
|
September 29, 2023
Photocontrolled Reversibly Chiral-Ordered Assembly Based on Cucurbituril
Guoxing Liu, Changming Tian, Xinhui Fan, et al.
The Science of the Total Environment
|
January 3, 2022
Phosphorous partitioning in sediments by particle size distribution in shallow lakes: From its mechanisms and patterns to its ecological implications
Peiyao Deng, Qitao Yi, Jin Zhang, et al.
Experimental Cell Research
|
June 27, 2020
Microenvironment remodeled by tumor and stromal cells elevates fibroblast-derived COL1A1 and facilitates ovarian cancer metastasis
Mingyue Li, Jiaying Wang, Conghui Wang, et al.
Molecular Cytogenetics
|
January 1, 2020
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
Ganye Zhao, Peng Dai, Shanshan Gao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
January 25, 2022
[The value of re-sampling for patients who had failed non-invasive prenatal testing due to low cell-free fetal DNA fraction]
Ganye Zhao, Peng Dai, Shanshan Gao, et al.
Iscience
|
May 1, 2023
Effects of lysate/tissue storage at -80°C on subsequently extracted EVs of epithelial ovarian cancer tissue origins
Shizhen Shen, Zhangjin Shen, Conghui Wang, et al.
European Journal of Medical Genetics
|
July 14, 2020
Identification of two novel SMN1 point mutations associated with a very severe SMA-I phenotype
Xuechao Zhao, Yanhong Wang, Shiyue Mei, et al.
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Showing results (61-70 of 161) with videos related to
Sort By:
Page
of 17
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 2, 2022
[Genetic analysis of a patient with Papillorenal syndrome due to variant of PAX2 gene]
Xuechao Zhao, Yuting Zheng, Ning Liu, et al.
Nanoscale
|
January 3, 2024
Recent development of manganese dioxide-based materials as zinc-ion battery cathode
Shaofeng Jia, Le Li, Yue Shi, et al.
Journal of the National Comprehensive Cancer Network : JNCCN
|
March 28, 2025
QIM25-232: Extracellular Vesicles Evade the Antiangiogenic Effect of Bevacizumab in Ovarian Cancer
Zhuoye Chen, Conghui Wang, Mingxia Xu, et al.
JACS Au
|
September 29, 2023
Photocontrolled Reversibly Chiral-Ordered Assembly Based on Cucurbituril
Guoxing Liu, Changming Tian, Xinhui Fan, et al.
The Science of the Total Environment
|
January 3, 2022
Phosphorous partitioning in sediments by particle size distribution in shallow lakes: From its mechanisms and patterns to its ecological implications
Peiyao Deng, Qitao Yi, Jin Zhang, et al.
Experimental Cell Research
|
June 27, 2020
Microenvironment remodeled by tumor and stromal cells elevates fibroblast-derived COL1A1 and facilitates ovarian cancer metastasis
Mingyue Li, Jiaying Wang, Conghui Wang, et al.
Molecular Cytogenetics
|
January 1, 2020
A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing
Ganye Zhao, Peng Dai, Shanshan Gao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
January 25, 2022
[The value of re-sampling for patients who had failed non-invasive prenatal testing due to low cell-free fetal DNA fraction]
Ganye Zhao, Peng Dai, Shanshan Gao, et al.
Iscience
|
May 1, 2023
Effects of lysate/tissue storage at -80°C on subsequently extracted EVs of epithelial ovarian cancer tissue origins
Shizhen Shen, Zhangjin Shen, Conghui Wang, et al.
European Journal of Medical Genetics
|
July 14, 2020
Identification of two novel SMN1 point mutations associated with a very severe SMA-I phenotype
Xuechao Zhao, Yanhong Wang, Shiyue Mei, et al.
Page
of 17