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Molecular Biosystems
|
January 12, 2007
Chemical genetics suggests a critical role for lysyl oxidase in zebrafish notochord morphogenesis
Carrie Anderson, Stephen J Bartlett, John M Gansner, et al.
The Journal of Pathology
|
February 3, 2015
X-linked spinal muscular atrophy in mice caused by autonomous loss of ATP7A in the motor neuron
Victoria L Hodgkinson, Jeffery M Dale, Michael L Garcia, et al.
The American Journal of Clinical Nutrition
|
July 10, 2007
Conflict of interest policy for Editors of The American Journal of Clinical Nutrition
Dennis M Bier, Steven A Abrams, Barbara A Bowman, et al.
American Journal of Physiology. Cell Physiology
|
August 14, 2015
Autonomous requirements of the Menkes disease protein in the nervous system
Victoria L Hodgkinson, Sha Zhu, Yanfang Wang, et al.
Molecular and Cellular Biology
|
February 16, 2010
Regulation of the copper chaperone CCS by XIAP-mediated ubiquitination
Graham F Brady, Stefanie Galbán, Xuwen Liu, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
October 7, 2014
Kinesin family member 6 (kif6) is necessary for spine development in zebrafish
Jillian G Buchan, Ryan S Gray, John M Gansner, et al.
Nature Neuroscience
|
March 13, 2002
Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading
Jamuna R Subramaniam, W Ernest Lyons, Jian Liu, et al.
Gastroenterology
|
October 9, 2007
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B
Prim de Bie, Bart van de Sluis, Ezra Burstein, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 25, 2018
Elesclomol restores mitochondrial function in genetic models of copper deficiency
Shivatheja Soma, Andrew J Latimer, Haarin Chun, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 49) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 49 results.
Molecular Biosystems
|
January 12, 2007
Chemical genetics suggests a critical role for lysyl oxidase in zebrafish notochord morphogenesis
Carrie Anderson, Stephen J Bartlett, John M Gansner, et al.
The Journal of Pathology
|
February 3, 2015
X-linked spinal muscular atrophy in mice caused by autonomous loss of ATP7A in the motor neuron
Victoria L Hodgkinson, Jeffery M Dale, Michael L Garcia, et al.
The American Journal of Clinical Nutrition
|
July 10, 2007
Conflict of interest policy for Editors of The American Journal of Clinical Nutrition
Dennis M Bier, Steven A Abrams, Barbara A Bowman, et al.
American Journal of Physiology. Cell Physiology
|
August 14, 2015
Autonomous requirements of the Menkes disease protein in the nervous system
Victoria L Hodgkinson, Sha Zhu, Yanfang Wang, et al.
Molecular and Cellular Biology
|
February 16, 2010
Regulation of the copper chaperone CCS by XIAP-mediated ubiquitination
Graham F Brady, Stefanie Galbán, Xuwen Liu, et al.
Developmental Dynamics : an Official Publication of the American Association of Anatomists
|
October 7, 2014
Kinesin family member 6 (kif6) is necessary for spine development in zebrafish
Jillian G Buchan, Ryan S Gray, John M Gansner, et al.
Nature Neuroscience
|
March 13, 2002
Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading
Jamuna R Subramaniam, W Ernest Lyons, Jian Liu, et al.
Gastroenterology
|
October 9, 2007
Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B
Prim de Bie, Bart van de Sluis, Ezra Burstein, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 25, 2018
Elesclomol restores mitochondrial function in genetic models of copper deficiency
Shivatheja Soma, Andrew J Latimer, Haarin Chun, et al.
Page
of 5