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

J Loeffen

Showing results (1-10 of 17) with videos related to

Pageof 2
Sort By:
Journal of Inherited Metabolic Disease|September 10, 2005
Fumarase deficiency presenting with periventricular cystsJ Loeffen, R Smeets, T Voit, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
Cloning of the human mitochondrial 51 kDa subunit (NDUFV1) reveals a 100% antisense homology of its 3'UTR with the 5'UTR of the gamma-interferon inducible protein (IP-30) precursor: is this a link between mitochondrial myopathy and inflammation?M Schuelke, J Loeffen, E Mariman, et al.
Human Genetics|December 22, 1998
The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patientsR Triepels, L van den Heuvel, J Loeffen, et al.
Human Genetics|June 1, 2000
Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patientsR Triepels, J Smeitink, J Loeffen, et al.
Biochemical and Biophysical Research Communications|July 2, 1998
cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completedJ Loeffen, L van den Heuvel, R Smeets, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patientsJ Loeffen, R Smeets, J Smeitink, et al.
Scandinavian Journal of Medicine & Science in Sports|May 7, 2015
A one-season prospective study of injuries and illness in elite junior tennisB M Pluim, F G J Loeffen, B Clarsen, et al.
Human Genetics|October 6, 1998
Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex IJ Smeitink, J Loeffen, R Smeets, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathologyR Triepels, J Smeitink, J Loeffen, et al.
International Journal of Public Health|May 27, 2010
Health care utilisation and problems in accessing health care of female undocumented immigrants in the NetherlandsMarianne A Schoevers, Maartje J Loeffen, Maria E van den Muijsenbergh, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|September 10, 2005
Fumarase deficiency presenting with periventricular cystsJ Loeffen, R Smeets, T Voit, et al.
Biochemical and Biophysical Research Communications|May 8, 1998
Cloning of the human mitochondrial 51 kDa subunit (NDUFV1) reveals a 100% antisense homology of its 3'UTR with the 5'UTR of the gamma-interferon inducible protein (IP-30) precursor: is this a link between mitochondrial myopathy and inflammation?M Schuelke, J Loeffen, E Mariman, et al.
Human Genetics|December 22, 1998
The nuclear-encoded human NADH:ubiquinone oxidoreductase NDUFA8 subunit: cDNA cloning, chromosomal localization, tissue distribution, and mutation detection in complex-I-deficient patientsR Triepels, L van den Heuvel, J Loeffen, et al.
Human Genetics|June 1, 2000
Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patientsR Triepels, J Smeitink, J Loeffen, et al.
Biochemical and Biophysical Research Communications|July 2, 1998
cDNA sequence and chromosomal localization of the remaining three human nuclear encoded iron sulphur protein (IP) subunits of complex I: the human IP fraction is completedJ Loeffen, L van den Heuvel, R Smeets, et al.
Journal of Inherited Metabolic Disease|March 10, 1999
The human NADH: ubiquinone oxidoreductase NDUFS5 (15 kDa) subunit: cDNA cloning, chromosomal localization, tissue distribution and the absence of mutations in isolated complex I-deficient patientsJ Loeffen, R Smeets, J Smeitink, et al.
Scandinavian Journal of Medicine & Science in Sports|May 7, 2015
A one-season prospective study of injuries and illness in elite junior tennisB M Pluim, F G J Loeffen, B Clarsen, et al.
Human Genetics|October 6, 1998
Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex IJ Smeitink, J Loeffen, R Smeets, et al.
Journal of Inherited Metabolic Disease|May 11, 1999
The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathologyR Triepels, J Smeitink, J Loeffen, et al.
International Journal of Public Health|May 27, 2010
Health care utilisation and problems in accessing health care of female undocumented immigrants in the NetherlandsMarianne A Schoevers, Maartje J Loeffen, Maria E van den Muijsenbergh, et al.
Pageof 2