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Veterinary Parasitology|January 30, 2021
Characterization of the complete mitochondrial genomes of Coronocyclus labiatus and Cylicodontophorus bicoronatus: Comparison with Strongylidae species and phylogenetic implicationYuan Gao, Xiao-Xu Wang, Xiao-Xiao Ma, et al.BMC Oral Health|March 5, 2025
From teeth to bone: dental caries has causal effects on osteoporosis and osteoporotic fractureGongzi Zhang, Juan Zheng, Ying Zhou, et al.Biochemical and Biophysical Research Communications|April 17, 2007
The mitochondrial tRNA(Ala) T5628C variant may have a modifying role in the phenotypic manifestation of the 12S rRNA C1494T mutation in a large Chinese family with hearing lossDongyi Han, Pu Dai, Qingwen Zhu, et al.Journal of Thrombosis and Haemostasis : JTH|July 20, 2023
Branched-chain amino acids promote thrombocytopoiesis by activating mTOR signalingHaojie Jiang, Lin Zhang, Mina Yang, et al.Molecular Genetics and Metabolism|July 15, 2010
Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutationXiangtian Zhou, Hongxing Zhang, Fuxin Zhao, et al.Human Genetics|April 21, 2005
Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing lossZhiyuan Li, Ronghua Li, Jianfu Chen, et al.Cell Research|April 18, 2006
Identification of AtENT3 as the main transporter for uridine uptake in Arabidopsis rootsKun Ling Chen, Min Xin Xu, Guang Yong Li, et al.Pharmacogenetics and Genomics|September 30, 2008
Mitochondrial tRNAThr G15927A mutation may modulate the phenotypic manifestation of ototoxic 12S rRNA A1555G mutation in four Chinese familiesXinjian Wang, Jianxin Lu, Yi Zhu, et al.JCI Insight|November 19, 2024
Mutation of CRYAB encoding a conserved mitochondrial chaperone and antiapoptotic protein causes hereditary optic atrophyChenghui Wang, Liyao Zhang, Zhipeng Nie, et al.Oxidative Medicine and Cellular Longevity|March 21, 2022
A Review of Bile Acid Metabolism and Signaling in Cognitive Dysfunction-Related DiseasesZe-Bin Weng, Yuan-Rong Chen, Jin-Tao Lv, et al.Pageof 37