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P G Pentchev

Showing results (81-90 of 120) with videos related to

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The Journal of Biological Chemistry|August 30, 1996
Intracellular trafficking of cholesterol monitored with a cyclodextrinE B Neufeld, A M Cooney, J Pitha, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 1, 1975
Pathogenesis of one variant of sea-blue histiocytosisD W Golde, E L Schneider, D F Bainton, et al.
Biochimica Et Biophysica Acta|September 24, 1981
Biliary excretion of glycolipid in induced or inherited glucosylceramide lipidosisP G Pentchev, A E Gal, R Wong, et al.
Experimental Cell Research|August 16, 2000
Determinants of NPC1 expression and action: key promoter regions, posttranscriptional control, and the importance of a "cysteine-rich" loopH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
The Journal of Biological Chemistry|July 27, 1999
Mutations in the leucine zipper motif and sterol-sensing domain inactivate the Niemann-Pick C1 glycoproteinH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
Developmental Biology|August 6, 2000
Cyclopamine inhibition of Sonic hedgehog signal transduction is not mediated through effects on cholesterol transportJ P Incardona, W Gaffield, Y Lange, et al.
American Journal of Human Genetics|October 16, 1999
Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotypeG Millat, C Marçais, M A Rafi, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Type C Niemann-Pick disease: documentation of abnormal LDL processing in lymphocytesC E Argoff, C R Kaneski, E J Blanchette-Mackie, et al.
DNA and Cell Biology|October 1, 1996
Molecular cloning of the mouse apolipoprotein D gene and its upregulated expression in Niemann-Pick disease type C mouse modelK Yoshida, E S Cleaveland, J W Nagle, et al.
The Journal of Biological Chemistry|December 15, 1986
Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblastsH S Kruth, M E Comly, J D Butler, et al.
Pageof 12

Showing results (81-90 of 120) with videos related to

Sort By:
Pageof 12
The Journal of Biological Chemistry|August 30, 1996
Intracellular trafficking of cholesterol monitored with a cyclodextrinE B Neufeld, A M Cooney, J Pitha, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|October 1, 1975
Pathogenesis of one variant of sea-blue histiocytosisD W Golde, E L Schneider, D F Bainton, et al.
Biochimica Et Biophysica Acta|September 24, 1981
Biliary excretion of glycolipid in induced or inherited glucosylceramide lipidosisP G Pentchev, A E Gal, R Wong, et al.
Experimental Cell Research|August 16, 2000
Determinants of NPC1 expression and action: key promoter regions, posttranscriptional control, and the importance of a "cysteine-rich" loopH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
The Journal of Biological Chemistry|July 27, 1999
Mutations in the leucine zipper motif and sterol-sensing domain inactivate the Niemann-Pick C1 glycoproteinH Watari, E J Blanchette-Mackie, N K Dwyer, et al.
Developmental Biology|August 6, 2000
Cyclopamine inhibition of Sonic hedgehog signal transduction is not mediated through effects on cholesterol transportJ P Incardona, W Gaffield, Y Lange, et al.
American Journal of Human Genetics|October 16, 1999
Niemann-Pick C1 disease: the I1061T substitution is a frequent mutant allele in patients of Western European descent and correlates with a classic juvenile phenotypeG Millat, C Marçais, M A Rafi, et al.
Biochemical and Biophysical Research Communications|August 31, 1990
Type C Niemann-Pick disease: documentation of abnormal LDL processing in lymphocytesC E Argoff, C R Kaneski, E J Blanchette-Mackie, et al.
DNA and Cell Biology|October 1, 1996
Molecular cloning of the mouse apolipoprotein D gene and its upregulated expression in Niemann-Pick disease type C mouse modelK Yoshida, E S Cleaveland, J W Nagle, et al.
The Journal of Biological Chemistry|December 15, 1986
Type C Niemann-Pick disease. Abnormal metabolism of low density lipoprotein in homozygous and heterozygous fibroblastsH S Kruth, M E Comly, J D Butler, et al.
Pageof 12