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Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1993
Cholesterol deprivation affects the fluorescence properties of a ceramide analog at the Golgi apparatus of living cells
O C Martin, M E Comly, E J Blanchette-Mackie, et al.
Clinical Genetics
|
May 1, 1988
Niemann-Pick disease group C: clinical variability and diagnosis based on defective cholesterol esterification. A collaborative study on 70 patients
M T Vanier, D A Wenger, M E Comly, et al.
Birth Defects Original Article Series
|
January 1, 1980
A lysosomal storage disorder in mice characterized by the accumulation of several sphingolipids
P G Pentchev, A E Gal, A D Boothe, et al.
Biochemical and Biophysical Research Communications
|
August 14, 1978
Studies of lysosomal function: I. Metabolism of some complex lipids by isolated hepatocytes and Kupffer cells
J A Barranger, P G Pentchev, F S Furbish, et al.
Neuroscience
|
April 20, 2000
Neuronal localization of sterol regulatory element binding protein-1 in the rodent and primate brain: a light and electron microscopic immunocytochemical study
W Y Ong, C Y Hu, Y P Soh, et al.
Journal of Neurochemistry
|
September 1, 1985
Neurological mutation characterized by dysmyelination in NCTR-Balb/C mouse with lysosomal lipid storage disease
H Weintraub, A Abramovici, U Sandbank, et al.
Neuroscience
|
September 24, 2004
Neuronal localization and association of Niemann Pick C2 protein (HE1/NPC2) with the postsynaptic density
W Y Ong, R K Sundaram, E Huang, et al.
Acta Neuropathologica
|
January 1, 1995
Neurofibrillary tangles in Niemann-Pick disease type C
K Suzuki, C C Parker, P G Pentchev, et al.
Neurology
|
January 1, 1992
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)
J J Higgins, M C Patterson, N M Papadopoulos, et al.
Brain Research
|
July 24, 1998
Neurochemical alterations in the cerebellum of a murine model of Niemann-Pick type C disease
G Yadid, I Sotnik-Barkai, C Tornatore, et al.
Page
of 12
Search research articles
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Showing results (61-70 of 120) with videos related to
Sort By:
Page
of 12
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1993
Cholesterol deprivation affects the fluorescence properties of a ceramide analog at the Golgi apparatus of living cells
O C Martin, M E Comly, E J Blanchette-Mackie, et al.
Clinical Genetics
|
May 1, 1988
Niemann-Pick disease group C: clinical variability and diagnosis based on defective cholesterol esterification. A collaborative study on 70 patients
M T Vanier, D A Wenger, M E Comly, et al.
Birth Defects Original Article Series
|
January 1, 1980
A lysosomal storage disorder in mice characterized by the accumulation of several sphingolipids
P G Pentchev, A E Gal, A D Boothe, et al.
Biochemical and Biophysical Research Communications
|
August 14, 1978
Studies of lysosomal function: I. Metabolism of some complex lipids by isolated hepatocytes and Kupffer cells
J A Barranger, P G Pentchev, F S Furbish, et al.
Neuroscience
|
April 20, 2000
Neuronal localization of sterol regulatory element binding protein-1 in the rodent and primate brain: a light and electron microscopic immunocytochemical study
W Y Ong, C Y Hu, Y P Soh, et al.
Journal of Neurochemistry
|
September 1, 1985
Neurological mutation characterized by dysmyelination in NCTR-Balb/C mouse with lysosomal lipid storage disease
H Weintraub, A Abramovici, U Sandbank, et al.
Neuroscience
|
September 24, 2004
Neuronal localization and association of Niemann Pick C2 protein (HE1/NPC2) with the postsynaptic density
W Y Ong, R K Sundaram, E Huang, et al.
Acta Neuropathologica
|
January 1, 1995
Neurofibrillary tangles in Niemann-Pick disease type C
K Suzuki, C C Parker, P G Pentchev, et al.
Neurology
|
January 1, 1992
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration (HARP syndrome)
J J Higgins, M C Patterson, N M Papadopoulos, et al.
Brain Research
|
July 24, 1998
Neurochemical alterations in the cerebellum of a murine model of Niemann-Pick type C disease
G Yadid, I Sotnik-Barkai, C Tornatore, et al.
Page
of 12