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Handbook of Clinical Neurology
|
April 30, 2013
Inborn errors of copper metabolism
Stephen G Kaler
The Journal of Clinical Investigation
|
June 21, 2016
Microbial peptide de-coppers mitochondria: implications for Wilson disease
Stephen G Kaler
Annals of the New York Academy of Sciences
|
April 17, 2014
Translational research investigations on ATP7A: an important human copper ATPase
Stephen G Kaler
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|
October 5, 2014
Neurodevelopment and brain growth in classic Menkes disease is influenced by age and symptomatology at initiation of copper treatment
Stephen G Kaler
Nature Reviews. Neurology
|
January 12, 2011
ATP7A-related copper transport diseases-emerging concepts and future trends
Stephen G Kaler
Annals of the New York Academy of Sciences
|
June 27, 2008
Diseases of poverty with high mortality in infants and children: malaria, measles, lower respiratory infections, and diarrheal illnesses
Stephen G Kaler
The American Journal of Clinical Nutrition
|
September 10, 2008
Role of copper in human neurological disorders
Vishal Desai, Stephen G Kaler
The Journal of Biological Chemistry
|
March 31, 2018
Interaction between the AAA ATPase p97/VCP and a concealed UBX domain in the copper transporter ATP7A is associated with motor neuron degeneration
Ling Yi, Stephen G Kaler
Human Molecular Genetics
|
January 10, 2015
Direct interactions of adaptor protein complexes 1 and 2 with the copper transporter ATP7A mediate its anterograde and retrograde trafficking
Ling Yi, Stephen G Kaler
Advances in Pharmacology (San Diego, Calif.)
|
September 24, 2013
Catecholamine metabolites affected by the copper-dependent enzyme dopamine-beta-hydroxylase provide sensitive biomarkers for early diagnosis of menkes disease and viral-mediated ATP7A gene therapy
Stephen G Kaler, Courtney S Holmes
Page
of 7
Search research articles
Search
Showing results (1-10 of 65) with videos related to
Sort By:
Page
of 7
Handbook of Clinical Neurology
|
April 30, 2013
Inborn errors of copper metabolism
Stephen G Kaler
The Journal of Clinical Investigation
|
June 21, 2016
Microbial peptide de-coppers mitochondria: implications for Wilson disease
Stephen G Kaler
Annals of the New York Academy of Sciences
|
April 17, 2014
Translational research investigations on ATP7A: an important human copper ATPase
Stephen G Kaler
Journal of Trace Elements in Medicine and Biology : Organ of the Society for Minerals and Trace Elements (GMS)
|
October 5, 2014
Neurodevelopment and brain growth in classic Menkes disease is influenced by age and symptomatology at initiation of copper treatment
Stephen G Kaler
Nature Reviews. Neurology
|
January 12, 2011
ATP7A-related copper transport diseases-emerging concepts and future trends
Stephen G Kaler
Annals of the New York Academy of Sciences
|
June 27, 2008
Diseases of poverty with high mortality in infants and children: malaria, measles, lower respiratory infections, and diarrheal illnesses
Stephen G Kaler
The American Journal of Clinical Nutrition
|
September 10, 2008
Role of copper in human neurological disorders
Vishal Desai, Stephen G Kaler
The Journal of Biological Chemistry
|
March 31, 2018
Interaction between the AAA ATPase p97/VCP and a concealed UBX domain in the copper transporter ATP7A is associated with motor neuron degeneration
Ling Yi, Stephen G Kaler
Human Molecular Genetics
|
January 10, 2015
Direct interactions of adaptor protein complexes 1 and 2 with the copper transporter ATP7A mediate its anterograde and retrograde trafficking
Ling Yi, Stephen G Kaler
Advances in Pharmacology (San Diego, Calif.)
|
September 24, 2013
Catecholamine metabolites affected by the copper-dependent enzyme dopamine-beta-hydroxylase provide sensitive biomarkers for early diagnosis of menkes disease and viral-mediated ATP7A gene therapy
Stephen G Kaler, Courtney S Holmes
Page
of 7