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P G Pentchev

Showing results (91-100 of 120) with videos related to

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Journal of Biomedical Optics|September 28, 2012
Infrared Spectroscopic Imaging of the Biochemical Modifications Induced in the Cerebellum of the Niemann-Pick type C MouseL H Kidder, P Colarusso, S A Stewart, et al.
Neurology|December 1, 1992
A clinical staging classification for type C Niemann-Pick diseaseJ J Higgins, M C Patterson, J M Dambrosia, et al.
Veterinary Pathology|July 1, 1984
A lysosomal storage disorder in the BALB/c mouse: bone marrow transplantationA D Boothe, H Weintroub, P G Pentchev, et al.
The Journal of Biological Chemistry|August 5, 1992
Deficiencies in sex-regulated expression and levels of two hepatic sterol carrier proteins in a murine model of Niemann-Pick type C diseaseC F Roff, A Pastuszyn, J F Strauss, et al.
Biochimica Et Biophysica Acta|February 22, 1994
The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterolP G Pentchev, R O Brady, E J Blanchette-Mackie, et al.
Journal of Medical Genetics|February 24, 2001
Genotype-phenotype relationship of Niemann-Pick disease type C: a possible correlation between clinical onset and levels of NPC1 protein in isolated skin fibroblastsT Yamamoto, H Ninomiya, M Matsumoto, et al.
Biochimica Et Biophysica Acta|November 28, 1989
Type C Niemann-Pick disease: dimethyl sulfoxide moderates abnormal LDL-cholesterol processing in mutant fibroblastsE J Blanchette Mackie, N K Dwyer, M T Vanier, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2001
Cessation of rapid late endosomal tubulovesicular trafficking in Niemann-Pick type C1 diseaseM Zhang, N K Dwyer, D C Love, et al.
Developmental Neuroscience|January 1, 1991
Type C Niemann-Pick disease: use of hydrophobic amines to study defective cholesterol transportC F Roff, E Goldin, M E Comly, et al.
Biochimica Et Biophysica Acta|September 8, 1980
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidaseP G Pentchev, A E Gal, A D Booth, et al.
Pageof 12

Showing results (91-100 of 120) with videos related to

Sort By:
Pageof 12
Journal of Biomedical Optics|September 28, 2012
Infrared Spectroscopic Imaging of the Biochemical Modifications Induced in the Cerebellum of the Niemann-Pick type C MouseL H Kidder, P Colarusso, S A Stewart, et al.
Neurology|December 1, 1992
A clinical staging classification for type C Niemann-Pick diseaseJ J Higgins, M C Patterson, J M Dambrosia, et al.
Veterinary Pathology|July 1, 1984
A lysosomal storage disorder in the BALB/c mouse: bone marrow transplantationA D Boothe, H Weintroub, P G Pentchev, et al.
The Journal of Biological Chemistry|August 5, 1992
Deficiencies in sex-regulated expression and levels of two hepatic sterol carrier proteins in a murine model of Niemann-Pick type C diseaseC F Roff, A Pastuszyn, J F Strauss, et al.
Biochimica Et Biophysica Acta|February 22, 1994
The Niemann-Pick C lesion and its relationship to the intracellular distribution and utilization of LDL cholesterolP G Pentchev, R O Brady, E J Blanchette-Mackie, et al.
Journal of Medical Genetics|February 24, 2001
Genotype-phenotype relationship of Niemann-Pick disease type C: a possible correlation between clinical onset and levels of NPC1 protein in isolated skin fibroblastsT Yamamoto, H Ninomiya, M Matsumoto, et al.
Biochimica Et Biophysica Acta|November 28, 1989
Type C Niemann-Pick disease: dimethyl sulfoxide moderates abnormal LDL-cholesterol processing in mutant fibroblastsE J Blanchette Mackie, N K Dwyer, M T Vanier, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 11, 2001
Cessation of rapid late endosomal tubulovesicular trafficking in Niemann-Pick type C1 diseaseM Zhang, N K Dwyer, D C Love, et al.
Developmental Neuroscience|January 1, 1991
Type C Niemann-Pick disease: use of hydrophobic amines to study defective cholesterol transportC F Roff, E Goldin, M E Comly, et al.
Biochimica Et Biophysica Acta|September 8, 1980
A lysosomal storage disorder in mice characterized by a dual deficiency of sphingomyelinase and glucocerebrosidaseP G Pentchev, A E Gal, A D Booth, et al.
Pageof 12