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Dose-Response : a Publication of International Hormesis Society
|
January 6, 2022
Active Enhancer Assessment by H3K27ac ChIP-seq Reveals Claudin-1 as a Biomarker for Radiation Resistance in Colorectal Cancer
Zu-Xuan Chen, He-Qing Huang, Jia-Ying Wen, et al.
Acta Pharmacologica Sinica
|
January 19, 2016
Sulforaphane prevents rat cardiomyocytes from hypoxia/reoxygenation injury in vitro via activating SIRT1 and subsequently inhibiting ER stress
Yun-peng Li, Shu-lin Wang, Bei Liu, et al.
Thyroid : Official Journal of the American Thyroid Association
|
January 6, 2024
Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling
Hai-Yang Zhang, Feng-Yao Wu, Cao-Xu Zhang, et al.
Biomedical and Environmental Sciences : BES
|
June 21, 2019
Next-generation Sequencing Study of Pathogens in Serum from Patients with Febrile Jaundice in Sierra Leone
Yi Zhang, Fei Ye, Lian Xu Xia, et al.
Nanotechnology
|
November 22, 2017
Formation and magnetic properties of InFeP:Ag nanorods fabricated with noble metal Ag using an ion milling method
Jae Min Sohn, Hyungsang Kim, Hyunsik Im, et al.
European Journal of Endocrinology
|
February 2, 2011
A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiency
Jie Qiao, Bing Han, Bing-Li Liu, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research
|
July 21, 2023
Prediction of overall survival after radical gastrectomy using nomograms created by tumor markers
Li-Xiang Zhang, Zi-Yi Cao, Hao-Hao Li, et al.
Clinical Endocrinology
|
June 11, 2009
Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency
Jie Qiao, Xia Chen, Chun-Lin Zuo, et al.
Molecular and Cellular Endocrinology
|
February 24, 2020
The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism
Rui-Jia Zhang, Feng Sun, Feng Chen, et al.
The Journal of Infection
|
June 18, 2026
Convergent neutralizing antibodies to SARS-CoV-2 variants over 2.5 years after BA.5/BF.7 breakthrough infection
Meng Kong, Hui-Xia Gao, Xue-Dong Song, et al.
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of 90
Search research articles
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Showing results (801-810 of 898) with videos related to
Sort By:
Page
of 90
Dose-Response : a Publication of International Hormesis Society
|
January 6, 2022
Active Enhancer Assessment by H3K27ac ChIP-seq Reveals Claudin-1 as a Biomarker for Radiation Resistance in Colorectal Cancer
Zu-Xuan Chen, He-Qing Huang, Jia-Ying Wen, et al.
Acta Pharmacologica Sinica
|
January 19, 2016
Sulforaphane prevents rat cardiomyocytes from hypoxia/reoxygenation injury in vitro via activating SIRT1 and subsequently inhibiting ER stress
Yun-peng Li, Shu-lin Wang, Bei Liu, et al.
Thyroid : Official Journal of the American Thyroid Association
|
January 6, 2024
Contactin 6, A Novel Causative Gene for Congenital Hypothyroidism, Mediates Thyroid Hormone Biosynthesis Through Notch Signaling
Hai-Yang Zhang, Feng-Yao Wu, Cao-Xu Zhang, et al.
Biomedical and Environmental Sciences : BES
|
June 21, 2019
Next-generation Sequencing Study of Pathogens in Serum from Patients with Febrile Jaundice in Sierra Leone
Yi Zhang, Fei Ye, Lian Xu Xia, et al.
Nanotechnology
|
November 22, 2017
Formation and magnetic properties of InFeP:Ag nanorods fabricated with noble metal Ag using an ion milling method
Jae Min Sohn, Hyungsang Kim, Hyunsik Im, et al.
European Journal of Endocrinology
|
February 2, 2011
A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiency
Jie Qiao, Bing Han, Bing-Li Liu, et al.
Journal of Investigative Medicine : the Official Publication of the American Federation for Clinical Research
|
July 21, 2023
Prediction of overall survival after radical gastrectomy using nomograms created by tumor markers
Li-Xiang Zhang, Zi-Yi Cao, Hao-Hao Li, et al.
Clinical Endocrinology
|
June 11, 2009
Identification of steroid biosynthetic defects in genotype-proven heterozygous individuals for 17alpha-hydroxylase/17,20-lyase deficiency
Jie Qiao, Xia Chen, Chun-Lin Zuo, et al.
Molecular and Cellular Endocrinology
|
February 24, 2020
The TPO mutation screening and genotype-phenotype analysis in 230 Chinese patients with congenital hypothyroidism
Rui-Jia Zhang, Feng Sun, Feng Chen, et al.
The Journal of Infection
|
June 18, 2026
Convergent neutralizing antibodies to SARS-CoV-2 variants over 2.5 years after BA.5/BF.7 breakthrough infection
Meng Kong, Hui-Xia Gao, Xue-Dong Song, et al.
Page
of 90