Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

B C Paton

Showing results (51-60 of 70) with videos related to

Pageof 7
Sort By:
Human Genetics|September 1, 1993
Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage diseaseV Bradová, F Smíd, B Ulrich-Bott, et al.
The Journal of Surgical Research|July 1, 1974
The effect of pluronic F-68 on circulatory dynamics and renal and carotid artery flow during hemorrhagic shockF L Grover, D Amundsen, J L Warden, et al.
Archives of Surgery (Chicago, Ill. : 1960)|December 1, 1977
Pulmonary artery banding for ventricular septal defect with pulmonary hypertensionB C Paton, J R Stewart, J J Nora, et al.
Biological Chemistry Hoppe-Seyler|January 1, 1994
Further evidence that human lysosomal sialidase is not derived from prosaposin. Prosaposin biosynthesis and ganglioside sialidase studies in prosaposin- and sialidase-deficient fibroblast linesB C Paton, H R Schneider-Jakob, J Kopitz, et al.
Pediatric Cardiology|January 1, 1982
Infant coarctation of the aorta. Alternatives to subclavian flap repairD N Campbell, B C Paton, J W Wiggins, et al.
Lipids|November 26, 1999
Metabolism of trideuterated iso-lignoceric acid in rats in vivo and in human fibroblasts in cultureA Poulos, P C Stockham, D W Johnson, et al.
European Journal of Pediatrics|October 1, 1989
Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidosesK Harzer, B C Paton, A Poulos, et al.
FEBS Letters|December 31, 1997
Saposins (sap) A and C activate the degradation of galactosylceramide in living cellsK Harzer, B C Paton, H Christomanou, et al.
Chest|March 1, 1971
Advantages of the Beall valve prosthesisJ H Vogel, B C Paton, H R Overy, et al.
The Journal of Pediatrics|October 1, 1995
Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation groupA Poulos, J Christodoulou, C W Chow, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Human Genetics|September 1, 1993
Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage diseaseV Bradová, F Smíd, B Ulrich-Bott, et al.
The Journal of Surgical Research|July 1, 1974
The effect of pluronic F-68 on circulatory dynamics and renal and carotid artery flow during hemorrhagic shockF L Grover, D Amundsen, J L Warden, et al.
Archives of Surgery (Chicago, Ill. : 1960)|December 1, 1977
Pulmonary artery banding for ventricular septal defect with pulmonary hypertensionB C Paton, J R Stewart, J J Nora, et al.
Biological Chemistry Hoppe-Seyler|January 1, 1994
Further evidence that human lysosomal sialidase is not derived from prosaposin. Prosaposin biosynthesis and ganglioside sialidase studies in prosaposin- and sialidase-deficient fibroblast linesB C Paton, H R Schneider-Jakob, J Kopitz, et al.
Pediatric Cardiology|January 1, 1982
Infant coarctation of the aorta. Alternatives to subclavian flap repairD N Campbell, B C Paton, J W Wiggins, et al.
Lipids|November 26, 1999
Metabolism of trideuterated iso-lignoceric acid in rats in vivo and in human fibroblasts in cultureA Poulos, P C Stockham, D W Johnson, et al.
European Journal of Pediatrics|October 1, 1989
Sphingolipid activator protein deficiency in a 16-week-old atypical Gaucher disease patient and his fetal sibling: biochemical signs of combined sphingolipidosesK Harzer, B C Paton, A Poulos, et al.
FEBS Letters|December 31, 1997
Saposins (sap) A and C activate the degradation of galactosylceramide in living cellsK Harzer, B C Paton, H Christomanou, et al.
Chest|March 1, 1971
Advantages of the Beall valve prosthesisJ H Vogel, B C Paton, H R Overy, et al.
The Journal of Pediatrics|October 1, 1995
Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation groupA Poulos, J Christodoulou, C W Chow, et al.
Pageof 7