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Human Mutation|August 14, 1999
Identification of a common PEX1 mutation in Zellweger syndromeC S Collins, S J GouldProceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum diseaseB V Geisbrecht, C S Collins, B E Reuber, et al.The Journal of School Health|April 14, 2000
A community pediatric prevention partnership: linking schools, providers, and tertiary care servicesK C Farrior, M K Engelke, C S Collins, et al.The American Journal of Clinical Nutrition|December 1, 1988
Red blood cell uptake of supplemental folate in patients on anticonvulsant drug therapyC S Collins, L B Bailey, S Hillier, et al.The Review of Scientific Instruments|July 10, 2021
Charge exchange recombination spectroscopy measurements of DIII-D poloidal rotation with poloidal asymmetry in angular rotationC Chrystal, S R Haskey, K H Burrell, et al.Computerized Medical Imaging and Graphics : the Official Journal of the Computerized Medical Imaging Society|September 1, 1994
Gradient echo imaging of the lumbar spineJ J Wasenko, A E Rosenbaum, S F Yu, et al.Molecular and Cellular Biology|September 26, 2000
The peroxisome biogenesis factors pex4p, pex22p, pex1p, and pex6p act in the terminal steps of peroxisomal matrix protein importC S Collins, J E Kalish, J C Morrell, et al.Journal of Spinal Disorders|December 1, 1996
Intrinsic cervical spinal cord deformation on MRI: "the distorted 'H' sign"I Ahmad, A E Rosenbaum, F S Yu, et al.The Review of Scientific Instruments|April 6, 2021
The imaging fast ion D-alpha diagnostic (IFIDA) on DIII-DC Marini, C S Collins, M A Van Zeeland, et al.The Review of Scientific Instruments|August 3, 2019
Diagnosis of fast ions produced by negative-ion neutral-beam injection with fast-ion deuterium-alpha spectroscopyC M Muscatello, W W Heidbrink, R L Boivin, et al.Pageof 2