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Human Molecular Genetics|May 1, 1993
Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutationsA Wedell, H LuthmanNucleic Acids Research|March 11, 1983
High efficiency polyoma DNA transfection of chloroquine treated cellsH Luthman, G MagnussonHuman Genetics|April 1, 1993
Steroid 21-hydroxylase (P450c21): a new allele and spread of mutations through the pseudogeneA Wedell, H LuthmanLakartidningen|August 25, 1993
[Physiopathology of mitochondria. From Luft's disease to aging and diabetes]R Luft, H LuthmanActa Pharmacologica Et Toxicologica|January 1, 1985
Cytochrome P-450-dependent fragmentation of DNA in reconstituted membranesH Luthman, M Ingelman-SundbergHuman Genetics|February 1, 1994
A steroid 21-hydroxylase allele concomitantly carrying four disease-causing mutations is not uncommon in the swedish populationA Wedell, X Chun, H LuthmanNucleic Acids Research|October 11, 1984
Inhibition of polyoma DNA synthesis by base pair substitutions at the replication originH Luthman, M Osterlund, G MagnussonThe Journal of Clinical Endocrinology and Metabolism|March 1, 1994
Insulin receptor ribonucleic acid levels and alternative splicing in human liver, muscle, and adipose tissue: tissue specificity and relation to insulin actionS Norgren, P Arner, H LuthmanHuman Genetics|July 1, 1994
Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiencyA Wedell, B Stengler, H LuthmanMutation Research|January 1, 1989
Induced recombination between duplicated neo genes stably integrated in the genome of CHO cellsD Hellgren, H Luthman, B LambertPageof 9