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Journal of Ethnopharmacology
|
July 13, 2023
Modified Simiaowan prevents and treats gouty arthritis via the Nrf2/NLRP3 inflammasome signaling pathway
Dong-Er Qin, Wei Liang, Yun Yu, et al.
BMC Microbiology
|
October 22, 2025
Gut microbiota related steroid hormone biosynthesis provide novel insights into high-salt diet related renal injury vit gut-kidney axis
Tian-Hao Liu, Ting Xie, Yu-Sheng Yu, et al.
Translational Psychiatry
|
October 10, 2025
Viral infections and the risk of neurodegenerative diseases: a comprehensive meta-analysis and systematic review
Ru-Yin Liu, Kang-Fu Yin, Sheng-Yi He, et al.
Oncotarget
|
August 28, 2015
Rhodomycin A, a novel Src-targeted compound, can suppress lung cancer cell progression via modulating Src-related pathways
Yi-Hua Lai, Min-Hsuan Chen, Sih-Yin Lin, et al.
Genes, Chromosomes & Cancer
|
May 22, 2003
SOCS1 methylation in patients with newly diagnosed acute myeloid leukemia
Chien-Yuan Chen, Woei Tsay, Jih-Luh Tang, et al.
ACS Applied Materials & Interfaces
|
February 19, 2025
Boosting Sodium Storage in Pitch-Derived Hard Carbon via MgO Catalytic Preoxidation
Haizhou Liu, Shuhao Xiao, Zhou-Quan Lei, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 5, 2005
Characterization of CEBPA mutations in acute myeloid leukemia: most patients with CEBPA mutations have biallelic mutations and show a distinct immunophenotype of the leukemic cells
Liang-In Lin, Chien-Yuan Chen, Dong-Tsamn Lin, et al.
Brain & Development
|
May 1, 2022
Novel and recurrent ASPM mutations of founder effect in Chinese population
Mengting Li, Jingrong Luo, Qi Yang, et al.
Blood
|
December 18, 2015
Human STEAP3 mutations with no phenotypic red cell changes
Dun Liu, Sheng Yi, Xinhua Zhang, et al.
Molecular Genetics & Genomic Medicine
|
February 20, 2025
Unmasking a Recessive Allele by a Rare Interstitial Deletion at 10q26.13q26.2: Prenatal Diagnosis of MMP21 -Related Disorder and Further Refine INSYN2A Involvement in the Postnatal Cognitive Phenotype
Jiasun Su, Shujie Zhang, Wei Li, et al.
Page
of 47
Search research articles
Search
Showing results (411-420 of 461) with videos related to
Sort By:
Page
of 47
Journal of Ethnopharmacology
|
July 13, 2023
Modified Simiaowan prevents and treats gouty arthritis via the Nrf2/NLRP3 inflammasome signaling pathway
Dong-Er Qin, Wei Liang, Yun Yu, et al.
BMC Microbiology
|
October 22, 2025
Gut microbiota related steroid hormone biosynthesis provide novel insights into high-salt diet related renal injury vit gut-kidney axis
Tian-Hao Liu, Ting Xie, Yu-Sheng Yu, et al.
Translational Psychiatry
|
October 10, 2025
Viral infections and the risk of neurodegenerative diseases: a comprehensive meta-analysis and systematic review
Ru-Yin Liu, Kang-Fu Yin, Sheng-Yi He, et al.
Oncotarget
|
August 28, 2015
Rhodomycin A, a novel Src-targeted compound, can suppress lung cancer cell progression via modulating Src-related pathways
Yi-Hua Lai, Min-Hsuan Chen, Sih-Yin Lin, et al.
Genes, Chromosomes & Cancer
|
May 22, 2003
SOCS1 methylation in patients with newly diagnosed acute myeloid leukemia
Chien-Yuan Chen, Woei Tsay, Jih-Luh Tang, et al.
ACS Applied Materials & Interfaces
|
February 19, 2025
Boosting Sodium Storage in Pitch-Derived Hard Carbon via MgO Catalytic Preoxidation
Haizhou Liu, Shuhao Xiao, Zhou-Quan Lei, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 5, 2005
Characterization of CEBPA mutations in acute myeloid leukemia: most patients with CEBPA mutations have biallelic mutations and show a distinct immunophenotype of the leukemic cells
Liang-In Lin, Chien-Yuan Chen, Dong-Tsamn Lin, et al.
Brain & Development
|
May 1, 2022
Novel and recurrent ASPM mutations of founder effect in Chinese population
Mengting Li, Jingrong Luo, Qi Yang, et al.
Blood
|
December 18, 2015
Human STEAP3 mutations with no phenotypic red cell changes
Dun Liu, Sheng Yi, Xinhua Zhang, et al.
Molecular Genetics & Genomic Medicine
|
February 20, 2025
Unmasking a Recessive Allele by a Rare Interstitial Deletion at 10q26.13q26.2: Prenatal Diagnosis of MMP21 -Related Disorder and Further Refine INSYN2A Involvement in the Postnatal Cognitive Phenotype
Jiasun Su, Shujie Zhang, Wei Li, et al.
Page
of 47