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J Ezaki

Showing results (1-10 of 25) with videos related to

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Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Batten disease]J Ezaki, E Kominami
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Batten disease (Neuronal ceroid lipofuscinoses)--accumulation of ATP synthase subunit c caused by the delay of lysosomal degradation]J Ezaki, E Kominami
Journal of Biochemistry|July 1, 1992
Purification and characterization of (Ca2+-Mg2+)-ATPase in rat liver lysosomal membranesJ Ezaki, M Himeno, K Kato
Journal of Inherited Metabolic Disease|January 1, 1993
Molecular basis of lysosomal accumulation of subunit c of mitochondrial ATP synthase in neuronal ceroid-lipofuscinosisJ Ezaki, L S Wolfe, E Kominami
Gerontology|January 1, 1995
Defect of proteolysis of mitochondrial ATP synthase subunit C in neuronal ceroid lipofuscinosisJ Ezaki, L S Wolfe, E Kominami
Neuropediatrics|February 1, 1997
Decreased lysosomal subunit c-degrading activity in fibroblasts from patients with late infantile neuronal ceroid lipofuscinosisJ Ezaki, L S Wolfe, E Kominami
Journal of Biochemistry|August 31, 2000
Tripeptidyl peptidase I, the late infantile neuronal ceroid lipofuscinosis gene product, initiates the lysosomal degradation of subunit c of ATP synthaseJ Ezaki, M Takeda-Ezaki, E Kominami
Neurochemical Research|November 1, 1995
New insight into lysosomal protein storage disease: delayed catabolism of ATP synthase subunit c in Batten diseaseE Kominami, J Ezaki, L S Wolfe
Journal of Neurochemistry|October 1, 1996
Specific delay in the degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis is derived from cellular proteolytic dysfunction rather than structural alteration of subunit cJ Ezaki, L S Wolfe, E Kominami
Journal of Neurochemistry|June 1, 1999
A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthaseJ Ezaki, I Tanida, N Kanehagi, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Ryoikibetsu Shokogun Shirizu|June 30, 1998
[Batten disease]J Ezaki, E Kominami
Nihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Batten disease (Neuronal ceroid lipofuscinoses)--accumulation of ATP synthase subunit c caused by the delay of lysosomal degradation]J Ezaki, E Kominami
Journal of Biochemistry|July 1, 1992
Purification and characterization of (Ca2+-Mg2+)-ATPase in rat liver lysosomal membranesJ Ezaki, M Himeno, K Kato
Journal of Inherited Metabolic Disease|January 1, 1993
Molecular basis of lysosomal accumulation of subunit c of mitochondrial ATP synthase in neuronal ceroid-lipofuscinosisJ Ezaki, L S Wolfe, E Kominami
Gerontology|January 1, 1995
Defect of proteolysis of mitochondrial ATP synthase subunit C in neuronal ceroid lipofuscinosisJ Ezaki, L S Wolfe, E Kominami
Neuropediatrics|February 1, 1997
Decreased lysosomal subunit c-degrading activity in fibroblasts from patients with late infantile neuronal ceroid lipofuscinosisJ Ezaki, L S Wolfe, E Kominami
Journal of Biochemistry|August 31, 2000
Tripeptidyl peptidase I, the late infantile neuronal ceroid lipofuscinosis gene product, initiates the lysosomal degradation of subunit c of ATP synthaseJ Ezaki, M Takeda-Ezaki, E Kominami
Neurochemical Research|November 1, 1995
New insight into lysosomal protein storage disease: delayed catabolism of ATP synthase subunit c in Batten diseaseE Kominami, J Ezaki, L S Wolfe
Journal of Neurochemistry|October 1, 1996
Specific delay in the degradation of mitochondrial ATP synthase subunit c in late infantile neuronal ceroid lipofuscinosis is derived from cellular proteolytic dysfunction rather than structural alteration of subunit cJ Ezaki, L S Wolfe, E Kominami
Journal of Neurochemistry|June 1, 1999
A lysosomal proteinase, the late infantile neuronal ceroid lipofuscinosis gene (CLN2) product, is essential for degradation of a hydrophobic protein, the subunit c of ATP synthaseJ Ezaki, I Tanida, N Kanehagi, et al.
Pageof 3