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Neurology. Genetics
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November 14, 2024
Disease Progression of GNE Myopathy and Its Relationship With Genotype: A Retrospective, Observational Study in Chinese Patients
Haozhe Sun, Fuze Zheng, Jiaxi Yu, et al.
Clinical Genetics
|
March 31, 2020
Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy
Qi Wang, Zhenxian Hu, Xingzhi Chang, et al.
Bioorganic & Medicinal Chemistry
|
March 10, 2022
Synthesis and biological evaluation of 7H-pyrrolo [2,3-d] pyrimidine derivatives as potential p21-activated kinase 4 (PAK4) inhibitors
Cong Wang, Jiawei Xia, Yan Lei, et al.
Plos One
|
April 14, 2017
Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing
Meng Yu, Yiming Zheng, Suqin Jin, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
June 20, 2022
Clinicopathological features in two families with MARS-related Charcot-Marie-Tooth disease
Zhixing Ma, He Lv, Hongwei Zhang, et al.
Journal of Hazardous Materials
|
September 16, 2021
N-doped three-dimensional needle-like CoS<sub>2</sub> bridge connection Co<sub>3</sub>O<sub>4</sub> core-shell structure as high-efficiency room temperature NO<sub>2</sub> gas sensor
Xue Bai, Zhuo Liu, He Lv, et al.
International Journal of Molecular Sciences
|
June 26, 2026
Physiological and Proteomic Insights into Melatonin-Mediated Regulation of Copper Toxicity in the Crayfish <i>Procambarus clarkii</i>
Zaihang Yu, Xinyu Li, Le Zhang, et al.
World Journal of Stem Cells
|
November 3, 2025
Sclerostin-silenced human umbilical cord mesenchymal stem cells ameliorate bone metabolism in steroid-induced femoral head necrosis
He Lv, Cai-Fang Zheng, Xing-Yu Chen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 12, 2024
Multiomics analysis reveals serine catabolism as a potential therapeutic target for MELAS
Tongling Liufu, Xutong Zhao, Meng Yu, et al.
Journal of Human Genetics
|
August 19, 2011
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Danhua Zhao, Daojun Hong, Wei Zhang, et al.
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of 17
Search research articles
Search
Showing results (111-120 of 167) with videos related to
Sort By:
Page
of 17
Neurology. Genetics
|
November 14, 2024
Disease Progression of GNE Myopathy and Its Relationship With Genotype: A Retrospective, Observational Study in Chinese Patients
Haozhe Sun, Fuze Zheng, Jiaxi Yu, et al.
Clinical Genetics
|
March 31, 2020
Mutational and clinical spectrum in a cohort of Chinese patients with hereditary nemaline myopathy
Qi Wang, Zhenxian Hu, Xingzhi Chang, et al.
Bioorganic & Medicinal Chemistry
|
March 10, 2022
Synthesis and biological evaluation of 7H-pyrrolo [2,3-d] pyrimidine derivatives as potential p21-activated kinase 4 (PAK4) inhibitors
Cong Wang, Jiawei Xia, Yan Lei, et al.
Plos One
|
April 14, 2017
Mutational spectrum of Chinese LGMD patients by targeted next-generation sequencing
Meng Yu, Yiming Zheng, Suqin Jin, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
June 20, 2022
Clinicopathological features in two families with MARS-related Charcot-Marie-Tooth disease
Zhixing Ma, He Lv, Hongwei Zhang, et al.
Journal of Hazardous Materials
|
September 16, 2021
N-doped three-dimensional needle-like CoS<sub>2</sub> bridge connection Co<sub>3</sub>O<sub>4</sub> core-shell structure as high-efficiency room temperature NO<sub>2</sub> gas sensor
Xue Bai, Zhuo Liu, He Lv, et al.
International Journal of Molecular Sciences
|
June 26, 2026
Physiological and Proteomic Insights into Melatonin-Mediated Regulation of Copper Toxicity in the Crayfish <i>Procambarus clarkii</i>
Zaihang Yu, Xinyu Li, Le Zhang, et al.
World Journal of Stem Cells
|
November 3, 2025
Sclerostin-silenced human umbilical cord mesenchymal stem cells ameliorate bone metabolism in steroid-induced femoral head necrosis
He Lv, Cai-Fang Zheng, Xing-Yu Chen, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
June 12, 2024
Multiomics analysis reveals serine catabolism as a potential therapeutic target for MELAS
Tongling Liufu, Xutong Zhao, Meng Yu, et al.
Journal of Human Genetics
|
August 19, 2011
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes
Danhua Zhao, Daojun Hong, Wei Zhang, et al.
Page
of 17