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Hans R Waterham

Showing results (61-70 of 223) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Clinical and Laboratory Diagnosis of Peroxisomal DisordersRonald J A Wanders, Femke C C Klouwer, Sacha Ferdinandusse, et al.
Pflugers Archiv : European Journal of Physiology|October 14, 2006
The peroxisomal ABC transporter familyRonald J A Wanders, Wouter F Visser, Carlo W T van Roermund, et al.
Biochemical and Biophysical Research Communications|April 10, 2007
Demonstration of bile acid transport across the mammalian peroxisomal membraneWouter F Visser, Carlo W T van Roermund, Lodewijk Ijlst, et al.
Molecular Genetics and Metabolism|February 20, 2004
Human mevalonate pyrophosphate decarboxylase is localized in the cytosolSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 27, 2010
Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophySacha Ferdinandusse, Simon Barker, Katherine Lachlan, et al.
American Journal of Medical Genetics. Part A|December 6, 2011
Abnormal facial appearance, body asymmetry, limb deformities, and internal malformationsGrétel Oudesluijs, Marleen E H Simon, Rianne H J Burggraaf, et al.
Molecular Genetics and Metabolism|June 2, 2017
Identification and diagnostic value of phytanoyl- and pristanoyl-carnitine in plasma from patients with peroxisomal disordersKatharina Herzog, Henk van Lenthe, Ronald J A Wanders, et al.
Journal of Lipid Research|January 17, 2002
Absence of functional peroxisomes does not lead to deficiency of enzymes involved in cholesterol biosynthesisSietske Hogenboom, Gerrit Jan Romeijn, Sander M Houten, et al.
Journal of Lipid Research|January 20, 2004
Phosphomevalonate kinase is a cytosolic protein in humansSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.
Biochemical Society Transactions|October 31, 2015
Peroxisomal ABC transporters: functions and mechanismAlison Baker, David J Carrier, Theresia Schaedler, et al.
Pageof 23

Showing results (61-70 of 223) with videos related to

Sort By:
Pageof 23
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Clinical and Laboratory Diagnosis of Peroxisomal DisordersRonald J A Wanders, Femke C C Klouwer, Sacha Ferdinandusse, et al.
Pflugers Archiv : European Journal of Physiology|October 14, 2006
The peroxisomal ABC transporter familyRonald J A Wanders, Wouter F Visser, Carlo W T van Roermund, et al.
Biochemical and Biophysical Research Communications|April 10, 2007
Demonstration of bile acid transport across the mammalian peroxisomal membraneWouter F Visser, Carlo W T van Roermund, Lodewijk Ijlst, et al.
Molecular Genetics and Metabolism|February 20, 2004
Human mevalonate pyrophosphate decarboxylase is localized in the cytosolSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|February 27, 2010
Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophySacha Ferdinandusse, Simon Barker, Katherine Lachlan, et al.
American Journal of Medical Genetics. Part A|December 6, 2011
Abnormal facial appearance, body asymmetry, limb deformities, and internal malformationsGrétel Oudesluijs, Marleen E H Simon, Rianne H J Burggraaf, et al.
Molecular Genetics and Metabolism|June 2, 2017
Identification and diagnostic value of phytanoyl- and pristanoyl-carnitine in plasma from patients with peroxisomal disordersKatharina Herzog, Henk van Lenthe, Ronald J A Wanders, et al.
Journal of Lipid Research|January 17, 2002
Absence of functional peroxisomes does not lead to deficiency of enzymes involved in cholesterol biosynthesisSietske Hogenboom, Gerrit Jan Romeijn, Sander M Houten, et al.
Journal of Lipid Research|January 20, 2004
Phosphomevalonate kinase is a cytosolic protein in humansSietske Hogenboom, John J M Tuyp, Marc Espeel, et al.
Biochemical Society Transactions|October 31, 2015
Peroxisomal ABC transporters: functions and mechanismAlison Baker, David J Carrier, Theresia Schaedler, et al.
Pageof 23