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Annual Review of Cell and Developmental Biology
|
June 15, 2016
TFEB and TFE3: Linking Lysosomes to Cellular Adaptation to Stress
Nina Raben, Rosa Puertollano
Biomolecules
|
September 23, 2020
Pompe Disease: New Developments in an Old Lysosomal Storage Disorder
Naresh K Meena, Nina Raben
Ebiomedicine
|
December 20, 2020
Impaired autophagy: The collateral damage of lysosomal storage disorders
Rachel Myerowitz, Rosa Puertollano, Nina Raben
The Journal of Biological Chemistry
|
June 18, 2002
The human acid alpha-glucosidase gene is a novel target of the Notch-1/Hes-1 signaling pathway
Bo Yan, Nina Raben, Paul Plotz
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
August 18, 2018
Pompe Disease: From Basic Science to Therapy
Lara Kohler, Rosa Puertollano, Nina Raben
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
November 21, 2008
Therapeutic approaches in glycogen storage disease type II/Pompe Disease
Benedikt Schoser, Victoria Hill, Nina Raben
Journal of Biomedical Optics
|
February 5, 2013
Quantitative evaluation of skeletal muscle defects in second harmonic generation images
Wenhua Liu, Nina Raben, Evelyn Ralston
Biochemical and Biophysical Research Communications
|
February 22, 2002
Hes-1, a known transcriptional repressor, acts as a transcriptional activator for the human acid alpha-glucosidase gene in human fibroblast cells
Bo Yan, Nina Raben, Paul H Plotz
Current Molecular Medicine
|
April 13, 2002
Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease)
Nina Raben, Paul Plotz, Barry J Byrne
Frontiers in Aging Neuroscience
|
September 4, 2014
Pompe disease: from pathophysiology to therapy and back again
Jeong-A Lim, Lishu Li, Nina Raben
Page
of 8
Search research articles
Search
Showing results (1-10 of 72) with videos related to
Sort By:
Page
of 8
Annual Review of Cell and Developmental Biology
|
June 15, 2016
TFEB and TFE3: Linking Lysosomes to Cellular Adaptation to Stress
Nina Raben, Rosa Puertollano
Biomolecules
|
September 23, 2020
Pompe Disease: New Developments in an Old Lysosomal Storage Disorder
Naresh K Meena, Nina Raben
Ebiomedicine
|
December 20, 2020
Impaired autophagy: The collateral damage of lysosomal storage disorders
Rachel Myerowitz, Rosa Puertollano, Nina Raben
The Journal of Biological Chemistry
|
June 18, 2002
The human acid alpha-glucosidase gene is a novel target of the Notch-1/Hes-1 signaling pathway
Bo Yan, Nina Raben, Paul Plotz
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
August 18, 2018
Pompe Disease: From Basic Science to Therapy
Lara Kohler, Rosa Puertollano, Nina Raben
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
November 21, 2008
Therapeutic approaches in glycogen storage disease type II/Pompe Disease
Benedikt Schoser, Victoria Hill, Nina Raben
Journal of Biomedical Optics
|
February 5, 2013
Quantitative evaluation of skeletal muscle defects in second harmonic generation images
Wenhua Liu, Nina Raben, Evelyn Ralston
Biochemical and Biophysical Research Communications
|
February 22, 2002
Hes-1, a known transcriptional repressor, acts as a transcriptional activator for the human acid alpha-glucosidase gene in human fibroblast cells
Bo Yan, Nina Raben, Paul H Plotz
Current Molecular Medicine
|
April 13, 2002
Acid alpha-glucosidase deficiency (glycogenosis type II, Pompe disease)
Nina Raben, Paul Plotz, Barry J Byrne
Frontiers in Aging Neuroscience
|
September 4, 2014
Pompe disease: from pathophysiology to therapy and back again
Jeong-A Lim, Lishu Li, Nina Raben
Page
of 8