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Cancer Management and Research
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May 12, 2026
Hyperbaric Oxygen Reverses High-Glucose-Induced Stemness and Radioresistance in Non-Small Cell Lung Cancer Cells
Jui-Ying Lee, Chia-Li Chung, Tzu-Ting Tseng, et al.
Cell Proliferation
|
September 12, 2024
Kinesin-7 CENP-E mediates centrosome organization and spindle assembly to regulate chromosome alignment and genome stability
Jie Chen, Shan Wu, Jie-Jie He, et al.
World Journal of Pediatrics : WJP
|
March 7, 2018
Eight novel mutations of CBS gene in nine Chinese patients with classical homocystinuria
Dong-Xiao Li, Xi-Yuan Li, Hui Dong, et al.
Journal of Child Neurology
|
May 5, 2011
Analysis of the mitochondrial complex I-V enzyme activities of peripheral leukocytes in oxidative phosphorylation disorders
Yan-Yan Ma, Xue-Lin Zhang, Tong-Fei Wu, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
September 29, 2015
[Clinical analysis and follow-up study of cardiavascular system involvement in 10 children with methylmalonic aciduria combined with hyperhomocysteinemia]
Yan-Hua Qi, Jian-Guang Qi, Yu-Peng Liu, et al.
Journal of Colloid and Interface Science
|
July 24, 2025
Bovine serum albumin modified carbon dots and berberine composite promotes tumor mitochondrial dysfunction and apoptosis
He Feng, Yang-Jian Hong, Qi-Qi Zheng, et al.
Mitochondrial DNA
|
September 6, 2012
Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency
Yan Yan Ma, Tong Fei Wu, Yu Peng Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
May 15, 2010
Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus
Chih-Ping Chen, Yu-Peng Liu, Shaun-Pei Lin, et al.
Analytical Methods : Advancing Methods and Applications
|
September 1, 2025
High-efficiency chemiluminescent POCT assay for anti-Müllerian hormone: innovative development and application in polycystic ovary syndrome diagnosis
Yang Sun, Yun-Yun Zhang, Xiao-Tong Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 28, 2011
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction
Chih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, et al.
Page
of 19
Search research articles
Search
Showing results (111-120 of 187) with videos related to
Sort By:
Page
of 19
Cancer Management and Research
|
May 12, 2026
Hyperbaric Oxygen Reverses High-Glucose-Induced Stemness and Radioresistance in Non-Small Cell Lung Cancer Cells
Jui-Ying Lee, Chia-Li Chung, Tzu-Ting Tseng, et al.
Cell Proliferation
|
September 12, 2024
Kinesin-7 CENP-E mediates centrosome organization and spindle assembly to regulate chromosome alignment and genome stability
Jie Chen, Shan Wu, Jie-Jie He, et al.
World Journal of Pediatrics : WJP
|
March 7, 2018
Eight novel mutations of CBS gene in nine Chinese patients with classical homocystinuria
Dong-Xiao Li, Xi-Yuan Li, Hui Dong, et al.
Journal of Child Neurology
|
May 5, 2011
Analysis of the mitochondrial complex I-V enzyme activities of peripheral leukocytes in oxidative phosphorylation disorders
Yan-Yan Ma, Xue-Lin Zhang, Tong-Fei Wu, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics
|
September 29, 2015
[Clinical analysis and follow-up study of cardiavascular system involvement in 10 children with methylmalonic aciduria combined with hyperhomocysteinemia]
Yan-Hua Qi, Jian-Guang Qi, Yu-Peng Liu, et al.
Journal of Colloid and Interface Science
|
July 24, 2025
Bovine serum albumin modified carbon dots and berberine composite promotes tumor mitochondrial dysfunction and apoptosis
He Feng, Yang-Jian Hong, Qi-Qi Zheng, et al.
Mitochondrial DNA
|
September 6, 2012
Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency
Yan Yan Ma, Tong Fei Wu, Yu Peng Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
May 15, 2010
Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus
Chih-Ping Chen, Yu-Peng Liu, Shaun-Pei Lin, et al.
Analytical Methods : Advancing Methods and Applications
|
September 1, 2025
High-efficiency chemiluminescent POCT assay for anti-Müllerian hormone: innovative development and application in polycystic ovary syndrome diagnosis
Yang Sun, Yun-Yun Zhang, Xiao-Tong Liu, et al.
Taiwanese Journal of Obstetrics & Gynecology
|
October 28, 2011
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction
Chih-Ping Chen, Yi-Ning Su, Yi-Yung Chen, et al.
Page
of 19