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Biochemical and Biophysical Research Communications
|
October 7, 2006
Relationship between glycogen accumulation and the laforin dual specificity phosphatase
Wei Wang, Gretchen E Parker, Alexander V Skurat, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 30, 2006
Autophagy and mistargeting of therapeutic enzyme in skeletal muscle in Pompe disease
Tokiko Fukuda, Meghan Ahearn, Ashley Roberts, et al.
Molecular Cell
|
April 2, 2003
Targeted disruption of pyrin, the FMF protein, causes heightened sensitivity to endotoxin and a defect in macrophage apoptosis
Jae Jin Chae, Hirsh D Komarow, Jun Cheng, et al.
Annals of Neurology
|
March 15, 2006
Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease
Tokiko Fukuda, Lindsay Ewan, Martina Bauer, et al.
Transgenic Research
|
May 13, 2003
Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout mice
Nina Raben, Kanneboyina Nagaraju, Alicia Lee, et al.
The Journal of Biological Chemistry
|
September 24, 2004
Conjugation of mannose 6-phosphate-containing oligosaccharides to acid alpha-glucosidase improves the clearance of glycogen in pompe mice
Yunxiang Zhu, Xuemei Li, Josephine Kyazike, et al.
The American Journal of Pathology
|
February 16, 2008
Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B
Kanneboyina Nagaraju, Rashmi Rawat, Edina Veszelovszky, et al.
Arthritis and Rheumatism
|
August 1, 2007
Novel conformation of histidyl-transfer RNA synthetase in the lung: the target tissue in Jo-1 autoantibody-associated myositis
Stuart M Levine, Nina Raben, Dan Xie, et al.
The Biochemical Journal
|
April 21, 2005
Carbohydrate-remodelled acid alpha-glucosidase with higher affinity for the cation-independent mannose 6-phosphate receptor demonstrates improved delivery to muscles of Pompe mice
Yunxiang Zhu, Xuemei Li, Alison McVie-Wylie, et al.
Molecular Genetics and Metabolism
|
August 31, 2010
Differences in the predominance of lysosomal and autophagic pathologies between infants and adults with Pompe disease: implications for therapy
Nina Raben, Evelyn Ralston, Yin-Hsiu Chien, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 72) with videos related to
Sort By:
Page
of 8
Biochemical and Biophysical Research Communications
|
October 7, 2006
Relationship between glycogen accumulation and the laforin dual specificity phosphatase
Wei Wang, Gretchen E Parker, Alexander V Skurat, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
September 30, 2006
Autophagy and mistargeting of therapeutic enzyme in skeletal muscle in Pompe disease
Tokiko Fukuda, Meghan Ahearn, Ashley Roberts, et al.
Molecular Cell
|
April 2, 2003
Targeted disruption of pyrin, the FMF protein, causes heightened sensitivity to endotoxin and a defect in macrophage apoptosis
Jae Jin Chae, Hirsh D Komarow, Jun Cheng, et al.
Annals of Neurology
|
March 15, 2006
Dysfunction of endocytic and autophagic pathways in a lysosomal storage disease
Tokiko Fukuda, Lindsay Ewan, Martina Bauer, et al.
Transgenic Research
|
May 13, 2003
Induction of tolerance to a recombinant human enzyme, acid alpha-glucosidase, in enzyme deficient knockout mice
Nina Raben, Kanneboyina Nagaraju, Alicia Lee, et al.
The Journal of Biological Chemistry
|
September 24, 2004
Conjugation of mannose 6-phosphate-containing oligosaccharides to acid alpha-glucosidase improves the clearance of glycogen in pompe mice
Yunxiang Zhu, Xuemei Li, Josephine Kyazike, et al.
The American Journal of Pathology
|
February 16, 2008
Dysferlin deficiency enhances monocyte phagocytosis: a model for the inflammatory onset of limb-girdle muscular dystrophy 2B
Kanneboyina Nagaraju, Rashmi Rawat, Edina Veszelovszky, et al.
Arthritis and Rheumatism
|
August 1, 2007
Novel conformation of histidyl-transfer RNA synthetase in the lung: the target tissue in Jo-1 autoantibody-associated myositis
Stuart M Levine, Nina Raben, Dan Xie, et al.
The Biochemical Journal
|
April 21, 2005
Carbohydrate-remodelled acid alpha-glucosidase with higher affinity for the cation-independent mannose 6-phosphate receptor demonstrates improved delivery to muscles of Pompe mice
Yunxiang Zhu, Xuemei Li, Alison McVie-Wylie, et al.
Molecular Genetics and Metabolism
|
August 31, 2010
Differences in the predominance of lysosomal and autophagic pathologies between infants and adults with Pompe disease: implications for therapy
Nina Raben, Evelyn Ralston, Yin-Hsiu Chien, et al.
Page
of 8