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Hans R Waterham

Showing results (1-10 of 223) with videos related to

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FEBS Letters|August 1, 2006
Defects of cholesterol biosynthesisHans R Waterham
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Transfection of Primary Human Skin Fibroblasts for Peroxisomal StudiesJanet Koster, Hans R Waterham
Frontiers in Immunology|September 20, 2021
Compromised Protein Prenylation as Pathogenic Mechanism in Mevalonate Kinase DeficiencyFrouwkje A Politiek, Hans R Waterham
Biochimica Et Biophysica Acta|August 9, 2012
Genetics and molecular basis of human peroxisome biogenesis disordersHans R Waterham, Merel S Ebberink
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 9, 2012
Mutational spectrum of Smith-Lemli-Opitz syndromeHans R Waterham, Raoul C M Hennekam
Biochimica Et Biophysica Acta|June 16, 2012
Metabolic functions and biogenesis of peroxisomes in health and diseaseHans R Waterham, Ronald J A Wanders
Annual Review of Biochemistry|June 8, 2006
Biochemistry of mammalian peroxisomes revisitedRonald J A Wanders, Hans R Waterham
Biochimica Et Biophysica Acta|October 24, 2006
Peroxisomal disorders: the single peroxisomal enzyme deficienciesRonald J A Wanders, Hans R Waterham
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2023
Applying CRISPR-Cas9 Genome Editing to Study Genes Involved in Peroxisome Biogenesis or Peroxisomal FunctionsSerhii Chornyi, Janet Koster, Hans R Waterham
Journal of Lipid Research|March 29, 2023
The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesisSerhii Chornyi, Rob Ofman, Janet Koster, et al.
Pageof 23

Showing results (1-10 of 223) with videos related to

Sort By:
Pageof 23
FEBS Letters|August 1, 2006
Defects of cholesterol biosynthesisHans R Waterham
Methods in Molecular Biology (Clifton, N.J.)|April 15, 2017
Transfection of Primary Human Skin Fibroblasts for Peroxisomal StudiesJanet Koster, Hans R Waterham
Frontiers in Immunology|September 20, 2021
Compromised Protein Prenylation as Pathogenic Mechanism in Mevalonate Kinase DeficiencyFrouwkje A Politiek, Hans R Waterham
Biochimica Et Biophysica Acta|August 9, 2012
Genetics and molecular basis of human peroxisome biogenesis disordersHans R Waterham, Merel S Ebberink
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 9, 2012
Mutational spectrum of Smith-Lemli-Opitz syndromeHans R Waterham, Raoul C M Hennekam
Biochimica Et Biophysica Acta|June 16, 2012
Metabolic functions and biogenesis of peroxisomes in health and diseaseHans R Waterham, Ronald J A Wanders
Annual Review of Biochemistry|June 8, 2006
Biochemistry of mammalian peroxisomes revisitedRonald J A Wanders, Hans R Waterham
Biochimica Et Biophysica Acta|October 24, 2006
Peroxisomal disorders: the single peroxisomal enzyme deficienciesRonald J A Wanders, Hans R Waterham
Methods in Molecular Biology (Clifton, N.J.)|March 23, 2023
Applying CRISPR-Cas9 Genome Editing to Study Genes Involved in Peroxisome Biogenesis or Peroxisomal FunctionsSerhii Chornyi, Janet Koster, Hans R Waterham
Journal of Lipid Research|March 29, 2023
The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesisSerhii Chornyi, Rob Ofman, Janet Koster, et al.
Pageof 23