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International Archives of Occupational and Environmental Health|January 1, 1984
Cytogenetic effects of paraoxon and methyl-parathion on cultured human lymphocytes: SCE, clastogenic activity and cell cycle delayS Singh, B Lehmann-Grube, H W GoeddeHuman Heredity|January 1, 1982
Isoelectric focusing studies of human red cell PGM1 in Japanese, with special reference to the characterization of PGM17I Nishigaki, H G Benkmann, H W GoeddePraktische Anasthesie, Wiederbelebung Und Intensivtherapie|October 1, 1976
[Succinyldicholin sensitivity resulting from genetically determined serumcholinesterase variants]H W Goedde, H Münsch, H G BenkmannClinical Genetics|September 1, 1986
delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiencyM Doss, H G Benkmann, H W GoeddeJournal of Clinical Chemistry and Clinical Biochemistry. Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|June 1, 1977
A simplified micromethod for the determination of the acetylator phenotypeJ J Hoo, L Hussein, H W GoeddeBiochemical Genetics|October 1, 1981
High-resolution protein mapping of human fibroblasts and hair root cells: a standardized reproducible procedure considering the effect of cell culture parametersS Singh, I Willers, J Klose, et al.Clinical Genetics|September 1, 1981
High resolution protein mapping in fibroblast cell lines and hair roots from patients with genetic diseaseI Willers, S Singh, H W Goedde, et al.Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 1, 1993
Characterisation of human tumour cell lines using antibodies to intermediate filamentsC Moorthi, I Willers, B Ressler, et al.Journal of Inherited Metabolic Disease|January 1, 1981
Analysis of inborn errors of metabolism and other genetic defects in human fibroblasts using two-dimensional polypeptide mappingS Singh, I Willers, H W Goedde, et al.Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|January 1, 1991
Growth studies on fibroblasts of patients with autosomal recessive Friedreich's ataxiaI Willers, A Koeppen, S Singh, et al.Pageof 18