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J C Heikoop

Showing results (11-20 of 19) with videos related to

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Biochimica Et Biophysica Acta|March 24, 1993
Subcellular fractionation of cultured normal human melanocytes: new insights into the relationship of melanosomes with lysosomes and peroxisomesN P Smit, C W van Roermund, H M Aerts, et al.
European Journal of Cell Biology|April 1, 1992
Turnover of peroxisomal vesicles by autophagic proteolysis in cultured fibroblasts from Zellweger patientsJ C Heikoop, M van den Berg, A Strijland, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Protein truncation test (PTT) to rapidly screen the DMD gene for translation terminating mutationsP A Roest, R G Roberts, A C van der Tuijn, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 30, 1999
Random mutagenesis and screening of complex glycoproteins: expression of human gonadotropins in Dictyostelium discoideumM H Linskens, P D Grootenhuis, M Blaauw, et al.
Nucleic Acids Research|April 25, 2000
Optimizing heterologous expression in dictyostelium: importance of 5' codon adaptationE B Vervoort, A van Ravestein, N N van Peij, et al.
Biochimica Et Biophysica Acta|July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblastsJ C Heikoop, M Van den Berg, A Strijland, et al.
The Journal of Clinical Investigation|July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzymeJ C Heikoop, C W van Roermund, W W Just, et al.
European Journal of Biochemistry|August 17, 1990
Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolaseS Van Weely, J M Aerts, M B Van Leeuwen, et al.
Ultrastructural Pathology|November 1, 1993
Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctataM Espeel, J C Heikoop, J A Smeitink, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Biochimica Et Biophysica Acta|March 24, 1993
Subcellular fractionation of cultured normal human melanocytes: new insights into the relationship of melanosomes with lysosomes and peroxisomesN P Smit, C W van Roermund, H M Aerts, et al.
European Journal of Cell Biology|April 1, 1992
Turnover of peroxisomal vesicles by autophagic proteolysis in cultured fibroblasts from Zellweger patientsJ C Heikoop, M van den Berg, A Strijland, et al.
Neuromuscular Disorders : NMD|September 1, 1993
Protein truncation test (PTT) to rapidly screen the DMD gene for translation terminating mutationsP A Roest, R G Roberts, A C van der Tuijn, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 30, 1999
Random mutagenesis and screening of complex glycoproteins: expression of human gonadotropins in Dictyostelium discoideumM H Linskens, P D Grootenhuis, M Blaauw, et al.
Nucleic Acids Research|April 25, 2000
Optimizing heterologous expression in dictyostelium: importance of 5' codon adaptationE B Vervoort, A van Ravestein, N N van Peij, et al.
Biochimica Et Biophysica Acta|July 26, 1991
Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in rhizomelic chondrodysplasia punctata fibroblastsJ C Heikoop, M Van den Berg, A Strijland, et al.
The Journal of Clinical Investigation|July 1, 1990
Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzymeJ C Heikoop, C W van Roermund, W W Just, et al.
European Journal of Biochemistry|August 17, 1990
Function of oligosaccharide modification in glucocerebrosidase, a membrane-associated lysosomal hydrolaseS Van Weely, J M Aerts, M B Van Leeuwen, et al.
Ultrastructural Pathology|November 1, 1993
Cytoplasmic catalase and ghostlike peroxisomes in the liver from a child with atypical chondrodysplasia punctataM Espeel, J C Heikoop, J A Smeitink, et al.
Pageof 2