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Proceedings of the National Academy of Sciences of the United States of America
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June 24, 2005
Enhancing calstabin binding to ryanodine receptors improves cardiac and skeletal muscle function in heart failure
Xander H T Wehrens, Stephan E Lehnart, Steven Reiken, et al.
Food & Function
|
March 6, 2020
Carnosine ameliorates age-related dementia via improving mitochondrial dysfunction in SAMP8 mice
Zhao Dai, Xin-Yi Lu, Wen-Li Zhu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 26, 2006
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria
Han-Xiang Deng, Yong Shi, Yoshiaki Furukawa, et al.
Journal of the American Chemical Society
|
November 16, 2020
Regulating Surface Termination for Efficient Inverted Perovskite Solar Cells with Greater Than 23% Efficiency
Fengzhu Li, Xiang Deng, Feng Qi, et al.
Journal of Ethnopharmacology
|
January 4, 2011
The effects of Boehmeria nivea (L.) Gaud. on embryonic development: in vivo and in vitro studies
Xiao Ying Tian, Min Xu, Bin Deng, et al.
Nature Genetics
|
December 29, 2009
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4
Han-Xiang Deng, Christopher J Klein, Jianhua Yan, et al.
Physical Review Letters
|
June 26, 2026
Efficient Implementation of a Single-Qutrit Gate Set via Coherent Control
Xiang-Min Yu, Xiang Deng, Wen Zheng, et al.
Plos One
|
April 25, 2012
Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology
Justin Y Kwan, Suh Young Jeong, Peter Van Gelderen, et al.
Archives of Neurology
|
November 16, 2011
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis
Faisal Fecto, Jianhua Yan, S Pavan Vemula, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2
George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
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Search research articles
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Showing results (191-200 of 220) with videos related to
Sort By:
Page
of 22
Proceedings of the National Academy of Sciences of the United States of America
|
June 24, 2005
Enhancing calstabin binding to ryanodine receptors improves cardiac and skeletal muscle function in heart failure
Xander H T Wehrens, Stephan E Lehnart, Steven Reiken, et al.
Food & Function
|
March 6, 2020
Carnosine ameliorates age-related dementia via improving mitochondrial dysfunction in SAMP8 mice
Zhao Dai, Xin-Yi Lu, Wen-Li Zhu, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 26, 2006
Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria
Han-Xiang Deng, Yong Shi, Yoshiaki Furukawa, et al.
Journal of the American Chemical Society
|
November 16, 2020
Regulating Surface Termination for Efficient Inverted Perovskite Solar Cells with Greater Than 23% Efficiency
Fengzhu Li, Xiang Deng, Feng Qi, et al.
Journal of Ethnopharmacology
|
January 4, 2011
The effects of Boehmeria nivea (L.) Gaud. on embryonic development: in vivo and in vitro studies
Xiao Ying Tian, Min Xu, Bin Deng, et al.
Nature Genetics
|
December 29, 2009
Scapuloperoneal spinal muscular atrophy and CMT2C are allelic disorders caused by alterations in TRPV4
Han-Xiang Deng, Christopher J Klein, Jianhua Yan, et al.
Physical Review Letters
|
June 26, 2026
Efficient Implementation of a Single-Qutrit Gate Set via Coherent Control
Xiang-Min Yu, Xiang Deng, Wen Zheng, et al.
Plos One
|
April 25, 2012
Iron accumulation in deep cortical layers accounts for MRI signal abnormalities in ALS: correlating 7 tesla MRI and pathology
Justin Y Kwan, Suh Young Jeong, Peter Van Gelderen, et al.
Archives of Neurology
|
November 16, 2011
SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis
Faisal Fecto, Jianhua Yan, S Pavan Vemula, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 24, 2014
Dendritic spinopathy in transgenic mice expressing ALS/dementia-linked mutant UBQLN2
George H Gorrie, Faisal Fecto, Daniel Radzicki, et al.
Page
of 22