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

G Utermann

Showing results (181-190 of 208) with videos related to

Pageof 21
Sort By:
Human Genetics|January 1, 1982
Apolipoprotein AIMarburg: studies on two kindreds with a mutant of human apolipoprotein AIG Utermann, A Steinmetz, R Paetzold, et al.
The Journal of Biological Chemistry|January 15, 1990
Abetalipoproteinemia with an ApoB-100-lipoprotein(a) glycoprotein complex in plasma. Indication for an assembly defectH J Menzel, H Dieplinger, C Lackner, et al.
Human Genetics|November 9, 2000
Mutation analysis in glycogen storage disease type 1 non-aA R Janecke, M Lindner, M Erdel, et al.
British Journal of Cancer|September 25, 1999
Switch from antagonist to agonist of the androgen receptor bicalutamide is associated with prostate tumour progression in a new model systemZ Culig, J Hoffmann, M Erdel, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Dopamine D4 receptor polymorphism and idiopathic Parkinson's diseaseM F Kronenberg, H J Menzel, G Ebersbach, et al.
European Journal of Immunology|February 13, 2001
T cell expressed PKCtheta demonstrates cell-type selective functionB Bauer, N Krumböck, N Ghaffari-Tabrizi, et al.
Human Mutation|March 19, 2005
Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and ItalyM Witsch-Baumgartner, P Clayton, N Clusellas, et al.
Atherosclerosis|July 17, 1999
Lipoprotein(a) plasma concentrations after renal transplantation: a prospective evaluation after 4 years of follow-upL Kerschdorfer, P König, U Neyer, et al.
Genomics|December 15, 1996
Chromosomal localization of the genes (CLNS1A and CLNS1B) coding for the swelling-dependent chloride channel IClnU O Nagl, M Erdel, A Schmarda, et al.
Journal of Medical Genetics|August 3, 2004
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndromeM Witsch-Baumgartner, M Gruber, H G Kraft, et al.
Pageof 21

Showing results (181-190 of 208) with videos related to

Sort By:
Pageof 21
Human Genetics|January 1, 1982
Apolipoprotein AIMarburg: studies on two kindreds with a mutant of human apolipoprotein AIG Utermann, A Steinmetz, R Paetzold, et al.
The Journal of Biological Chemistry|January 15, 1990
Abetalipoproteinemia with an ApoB-100-lipoprotein(a) glycoprotein complex in plasma. Indication for an assembly defectH J Menzel, H Dieplinger, C Lackner, et al.
Human Genetics|November 9, 2000
Mutation analysis in glycogen storage disease type 1 non-aA R Janecke, M Lindner, M Erdel, et al.
British Journal of Cancer|September 25, 1999
Switch from antagonist to agonist of the androgen receptor bicalutamide is associated with prostate tumour progression in a new model systemZ Culig, J Hoffmann, M Erdel, et al.
European Journal of Human Genetics : EJHG|May 11, 1999
Dopamine D4 receptor polymorphism and idiopathic Parkinson's diseaseM F Kronenberg, H J Menzel, G Ebersbach, et al.
European Journal of Immunology|February 13, 2001
T cell expressed PKCtheta demonstrates cell-type selective functionB Bauer, N Krumböck, N Ghaffari-Tabrizi, et al.
Human Mutation|March 19, 2005
Identification of 14 novel mutations in DHCR7 causing the Smith-Lemli-Opitz syndrome and delineation of the DHCR7 mutational spectra in Spain and ItalyM Witsch-Baumgartner, P Clayton, N Clusellas, et al.
Atherosclerosis|July 17, 1999
Lipoprotein(a) plasma concentrations after renal transplantation: a prospective evaluation after 4 years of follow-upL Kerschdorfer, P König, U Neyer, et al.
Genomics|December 15, 1996
Chromosomal localization of the genes (CLNS1A and CLNS1B) coding for the swelling-dependent chloride channel IClnU O Nagl, M Erdel, A Schmarda, et al.
Journal of Medical Genetics|August 3, 2004
Maternal apo E genotype is a modifier of the Smith-Lemli-Opitz syndromeM Witsch-Baumgartner, M Gruber, H G Kraft, et al.
Pageof 21