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Biochemistry|October 11, 1994
High-level expression of various apolipoprotein(a) isoforms by "transferrinfection": the role of kringle IV sequences in the extracellular association with low-density lipoproteinS Frank, K Krasznai, S Durovic, et al.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.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 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.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.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.Clinical Genetics|November 4, 2004
DHCR7 mutations and genotype-phenotype correlation in 37 Polish patients with Smith-Lemli-Opitz syndromeE Ciara, M J M Nowaczyk, M Witsch-Baumgartner, et al.Pageof 19