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Brain : a Journal of Neurology
|
March 22, 2021
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy
Hai-Lin Dong, Yin Ma, Hao Yu, et al.
Neurobiology of Aging
|
January 2, 2019
Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing
Bin Jiang, Jiong Zhou, Hong-Lei Li, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
April 22, 2024
Hybrid Membrane-Coated Nanoparticles for Precise Targeting and Synergistic Therapy in Alzheimer's Disease
Rong-Rong Lin, Lu-Lu Jin, Yan-Yan Xue, et al.
Stress (Amsterdam, Netherlands)
|
October 5, 2016
The RNA-editing deaminase ADAR is involved in stress resistance of Artemia diapause embryos
Li Dai, Xue-Chen Liu, Sen Ye, et al.
Peptides
|
February 9, 2017
Molecular characterization and functional analyses of a diapause hormone receptor-like gene in parthenogenetic Artemia
Hui-Li Ye, Dong-Rui Li, Jin-Shu Yang, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
|
March 15, 2014
NRP-1 expression in bladder cancer and its implications for tumor progression
Wen Cheng, Dian Fu, Zhi-Feng Wei, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
January 15, 2025
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia
Qiao Wei, Wenlu Fan, Hong-Fu Li, et al.
BMC Biology
|
March 5, 2016
An La-related protein controls cell cycle arrest by nuclear retrograde transport of tRNAs during diapause formation in Artemia
Dian-Fu Chen, Cheng Lin, Hong-Liang Wang, et al.
Cancer Cell International
|
June 10, 2022
KCNN4 may weaken anti-tumor immune response via raising Tregs and diminishing resting mast cells in clear cell renal cell carcinoma
Yankang Cui, Tianyi Shen, Feng Xu, et al.
Research (Washington, D.C.)
|
December 12, 2024
Single-Nucleus RNA Sequencing Reveals the Spatiotemporal Dynamics of Disease-Associated Microglia in Amyotrophic Lateral Sclerosis
Lu-Xi Chen, Mei-Di Zhang, Hai-Feng Xu, et al.
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of 9
Search research articles
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Showing results (71-80 of 81) with videos related to
Sort By:
Page
of 9
Brain : a Journal of Neurology
|
March 22, 2021
Bi-allelic loss of function variants in COX20 gene cause autosomal recessive sensory neuronopathy
Hai-Lin Dong, Yin Ma, Hao Yu, et al.
Neurobiology of Aging
|
January 2, 2019
Mutation screening in Chinese patients with familial Alzheimer's disease by whole-exome sequencing
Bin Jiang, Jiong Zhou, Hong-Lei Li, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)
|
April 22, 2024
Hybrid Membrane-Coated Nanoparticles for Precise Targeting and Synergistic Therapy in Alzheimer's Disease
Rong-Rong Lin, Lu-Lu Jin, Yan-Yan Xue, et al.
Stress (Amsterdam, Netherlands)
|
October 5, 2016
The RNA-editing deaminase ADAR is involved in stress resistance of Artemia diapause embryos
Li Dai, Xue-Chen Liu, Sen Ye, et al.
Peptides
|
February 9, 2017
Molecular characterization and functional analyses of a diapause hormone receptor-like gene in parthenogenetic Artemia
Hui-Li Ye, Dong-Rui Li, Jin-Shu Yang, et al.
Tumour Biology : the Journal of the International Society for Oncodevelopmental Biology and Medicine
|
March 15, 2014
NRP-1 expression in bladder cancer and its implications for tumor progression
Wen Cheng, Dian Fu, Zhi-Feng Wei, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao
|
January 15, 2025
Biallelic variants in SREBF2 cause autosomal recessive spastic paraplegia
Qiao Wei, Wenlu Fan, Hong-Fu Li, et al.
BMC Biology
|
March 5, 2016
An La-related protein controls cell cycle arrest by nuclear retrograde transport of tRNAs during diapause formation in Artemia
Dian-Fu Chen, Cheng Lin, Hong-Liang Wang, et al.
Cancer Cell International
|
June 10, 2022
KCNN4 may weaken anti-tumor immune response via raising Tregs and diminishing resting mast cells in clear cell renal cell carcinoma
Yankang Cui, Tianyi Shen, Feng Xu, et al.
Research (Washington, D.C.)
|
December 12, 2024
Single-Nucleus RNA Sequencing Reveals the Spatiotemporal Dynamics of Disease-Associated Microglia in Amyotrophic Lateral Sclerosis
Lu-Xi Chen, Mei-Di Zhang, Hai-Feng Xu, et al.
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of 9