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American Journal of Medical Genetics|February 15, 1992
Niemann-Pick type-C disease: deficient intracellular transport of exogenously derived cholesterolC F Roff, E Goldin, M E Comly, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1985
A defect in cholesterol esterification in Niemann-Pick disease (type C) patientsP G Pentchev, M E Comly, H S Kruth, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|March 3, 2004
Differential trafficking of the Niemann-Pick C1 and 2 proteins highlights distinct roles in late endocytic lipid traffickingM Zhang, M Sun, N K Dwyer, et al.
Implementation Research and Practice|October 4, 2023
Therapist and supervisor perspectives about two train-the-trainer implementation strategies in schools: A qualitative studyGwendolyn M Lawson, Rachel Comly, Rinad S Beidas, 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.
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.
The American Journal of Gastroenterology|June 1, 1988
Cholesteryl ester storage disease: a patient with massive splenomegaly and splenic abscessR A Edelstein, M R Filling-Katz, P Pentchev, et al.
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