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Clinical Genetics
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April 5, 2019
Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome
Xue-Bi Cai, Kun-Chao Wu, Xiao Zhang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 3, 2018
Engineering the Direct Repeat Sequence of crRNA for Optimization of FnCpf1-Mediated Genome Editing in Human Cells
Li Lin, Xiubin He, Tianyuan Zhao, et al.
Iscience
|
September 8, 2023
Deep phenotyping of 11,880 highlanders reveals novel adaptive traits in native Tibetans
Yaoxi He, Wangshan Zheng, Yongbo Guo, et al.
Computers in Biology and Medicine
|
December 30, 2023
DeepGraFT: A novel semantic segmentation auxiliary ROI-based deep learning framework for effective fundus tessellation classification
Yinghao Yao, Jiaying Yang, Haojun Sun, et al.
Molecular Genetics and Metabolism
|
August 24, 2010
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation
Minglian Zhang, Xiangtian Zhou, Chengwu Li, et al.
The Plant Cell
|
March 29, 2018
TANDEM ZINC-FINGER/PLUS3 Is a Key Component of Phytochrome A Signaling
Shaoman Zhang, Cong Li, Yangyang Zhou, et al.
Biochemical and Biophysical Research Communications
|
August 10, 2010
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families
Juanjuan Zhang, Xiangtian Zhou, Jian Zhou, et al.
National Science Review
|
June 6, 2022
Diet high in branched-chain amino acid promotes PDAC development by USP1-mediated BCAT2 stabilization
Jin-Tao Li, Kai-Yue Li, Ying Su, et al.
Investigative Ophthalmology & Visual Science
|
October 14, 2016
The Role of Retinal Dopamine in C57BL/6 Mouse Refractive Development as Revealed by Intravitreal Administration of 6-Hydroxydopamine
Xiao-Hua Wu, Kang-Wei Qian, Guo-Zhong Xu, et al.
Yi Chuan = Hereditas
|
August 25, 2012
[The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families]
Hui-Hui Zhou, Xian-Ning Dai, Bei Lin, et al.
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of 75
Search research articles
Search
Showing results (661-670 of 746) with videos related to
Sort By:
Page
of 75
Clinical Genetics
|
April 5, 2019
Whole-exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod-cone dystrophy, cataract, and posterior staphyloma) syndrome
Xue-Bi Cai, Kun-Chao Wu, Xiao Zhang, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
October 3, 2018
Engineering the Direct Repeat Sequence of crRNA for Optimization of FnCpf1-Mediated Genome Editing in Human Cells
Li Lin, Xiubin He, Tianyuan Zhao, et al.
Iscience
|
September 8, 2023
Deep phenotyping of 11,880 highlanders reveals novel adaptive traits in native Tibetans
Yaoxi He, Wangshan Zheng, Yongbo Guo, et al.
Computers in Biology and Medicine
|
December 30, 2023
DeepGraFT: A novel semantic segmentation auxiliary ROI-based deep learning framework for effective fundus tessellation classification
Yinghao Yao, Jiaying Yang, Haojun Sun, et al.
Molecular Genetics and Metabolism
|
August 24, 2010
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation
Minglian Zhang, Xiangtian Zhou, Chengwu Li, et al.
The Plant Cell
|
March 29, 2018
TANDEM ZINC-FINGER/PLUS3 Is a Key Component of Phytochrome A Signaling
Shaoman Zhang, Cong Li, Yangyang Zhou, et al.
Biochemical and Biophysical Research Communications
|
August 10, 2010
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families
Juanjuan Zhang, Xiangtian Zhou, Jian Zhou, et al.
National Science Review
|
June 6, 2022
Diet high in branched-chain amino acid promotes PDAC development by USP1-mediated BCAT2 stabilization
Jin-Tao Li, Kai-Yue Li, Ying Su, et al.
Investigative Ophthalmology & Visual Science
|
October 14, 2016
The Role of Retinal Dopamine in C57BL/6 Mouse Refractive Development as Revealed by Intravitreal Administration of 6-Hydroxydopamine
Xiao-Hua Wu, Kang-Wei Qian, Guo-Zhong Xu, et al.
Yi Chuan = Hereditas
|
August 25, 2012
[The analysis of Leber's hereditary optic neuropathy associated with mitochondrial tRNAAla C5601T mutation in seven Han Chinese families]
Hui-Hui Zhou, Xian-Ning Dai, Bei Lin, et al.
Page
of 75