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American Journal of Human Genetics|February 1, 1992
Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her childN G Larsson, H G Eiken, H Boman, et al.American Journal of Human Genetics|December 1, 1990
A termination mutant prevalent in Norwegian haplotype 7 phenylketonuria genesJ Apold, H G Eiken, E Odland, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Relative frequency, heterogeneity and geographic clustering of PKU mutations in NorwayH G Eiken, P M Knappskog, H Boman, et al.Human Genetics|February 1, 1994
394delTT: a Nordic cystic fibrosis mutationM Schwartz, M Anvret, M Claustres, et al.Journal of Molecular Medicine (Berlin, Germany)|February 24, 2001
Enhanced detection of mutations in BRCA1 exon 11 using restriction endonuclease fingerprinting-single-strand conformation polymorphismA Jugessur, P Frost, T I Andersen, et al.Basic Research in Cardiology|August 24, 2001
Monocyte chemoattractant protein-1 enhances and interleukin-10 suppresses the production of inflammatory cytokines in adult rat cardiomyocytesJ K Damås, P Aukrust, T Ueland, et al.Human Genetics|February 1, 1996
Mutations in the iduronate-2-sulfatase gene in five Norwegians with Hunter syndromeT C Olsen, H G Eiken, P M Knappskog, et al.Parasitology Research|May 10, 2017
Helminths of brown bears (Ursus arctos) in the Kola PeninsulaS V Bugmyrin, K F Tirronen, D V Panchenko, et al.Clinical and Experimental Immunology|October 23, 2002
Effects of interferon-alpha on gene expression of chemokines and members of the tumour necrosis factor superfamily in HIV-infected patientsE Stylianou, A Yndestad, L I Sikkeland, et al.The Biochemical Journal|March 1, 1995
Expression of recombinant human phenylalanine hydroxylase as fusion protein in Escherichia coli circumvents proteolytic degradation by host cell proteases. Isolation and characterization of the wild-type enzymeA Martinez, P M Knappskog, S Olafsdottir, et al.Pageof 4