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

W Just

Showing results (111-120 of 125) with videos related to

Pageof 13
Sort By:
Human Molecular Genetics|July 23, 2003
Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in miceClaus Rodemer, Thanh-Phuong Thai, Britta Brugger, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 8, 1998
Functional characterization of the human biglycan 5'-flanking DNA and binding of the transcription factor c-KroxA M Heegaard, P Gehron Robey, W Vogel, et al.
FEBS Letters|January 22, 2013
Localization of Rab proteins to peroxisomes: a proteomics and immunofluorescence studyThomas Gronemeyer, Sebastian Wiese, Sören Grinhagens, et al.
American Journal of Medical Genetics|October 23, 1995
Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndromeI Kennerknecht, P von Saurma, R Brenner, 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.
Plos One|November 17, 2010
RhoA regulates peroxisome association to microtubules and the actin cytoskeletonLukas Schollenberger, Thomas Gronemeyer, Christoph M Huber, et al.
Human Genetics|July 1, 1995
The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous geneC Geerkens, U Vetter, W Just, et al.
American Journal of Human Genetics|June 1, 1997
Characterization of FMR1 promoter elements by in vivo-footprinting analysisS Schwemmle, E de Graaff, H Deissler, et al.
Human Genetics|January 1, 1996
Xp-duplications with and without sex reversalA Baumstark, G Barbi, M Djalali, et al.
Pageof 13

Showing results (111-120 of 125) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|July 23, 2003
Inactivation of ether lipid biosynthesis causes male infertility, defects in eye development and optic nerve hypoplasia in miceClaus Rodemer, Thanh-Phuong Thai, Britta Brugger, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|January 8, 1998
Functional characterization of the human biglycan 5'-flanking DNA and binding of the transcription factor c-KroxA M Heegaard, P Gehron Robey, W Vogel, et al.
FEBS Letters|January 22, 2013
Localization of Rab proteins to peroxisomes: a proteomics and immunofluorescence studyThomas Gronemeyer, Sebastian Wiese, Sören Grinhagens, et al.
American Journal of Medical Genetics|October 23, 1995
Agonadism in two sisters with XY gonosomal constitution, mental retardation, short stature, severely retarded bone age, and multiple extragenital malformations: a new autosomal recessive syndromeI Kennerknecht, P von Saurma, R Brenner, 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.
Plos One|November 17, 2010
RhoA regulates peroxisome association to microtubules and the actin cytoskeletonLukas Schollenberger, Thomas Gronemeyer, Christoph M Huber, et al.
Human Genetics|July 1, 1995
The X-chromosomal human biglycan gene BGN is subject to X inactivation but is transcribed like an X-Y homologous geneC Geerkens, U Vetter, W Just, et al.
American Journal of Human Genetics|June 1, 1997
Characterization of FMR1 promoter elements by in vivo-footprinting analysisS Schwemmle, E de Graaff, H Deissler, et al.
Human Genetics|January 1, 1996
Xp-duplications with and without sex reversalA Baumstark, G Barbi, M Djalali, et al.
Pageof 13