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Human Mutation|June 22, 2000
Fanconi anemia A due to a novel frameshift mutation in hotspot motifs: lack of FANCA proteinG Balta, J P de Winter, H Kayserili, et al.Electrophoresis|January 1, 1991
Electrophoretic characterization of posttranslational modifications of human parotid salivary alpha-amylaseR A Bank, E H Hettema, F Arwert, et al.Annals of Human Biology|May 1, 1986
ABH secretion polymorphism in Icelanders, Aland Islanders, Finns, Finnish Lapps, Komi and Greenland Eskimos: a review and new dataA W Eriksson, K Partanen, R R Frants, et al.Human Genetics|January 1, 1982
Evidence of duplication of the human salivary amylase geneJ C Pronk, R R Frants, W Jansen, et al.Nephron|January 1, 1989
Tubular handling of pepsinogen A and C in man: evidence for two distinct tubular reabsorption mechanisms for low molecular weight proteins in manR W ten Kate, G Pals, A J Donker, et al.FEBS Letters|September 26, 1988
Identification of a Glu greater than Lys substitution in the activation segment of human pepsinogen A-3 and -5 isozymogens by peptide mapping using endoproteinase Lys-CR A Bank, B C Crusius, T Zwiers, et al.Scandinavian Journal of Clinical and Laboratory Investigation|November 1, 1985
Purification of the pepsinogen A isozymogens by means of high resolution ion-exchange chromatography. Evidence for post-translational modificationsJ Défize, G Pals, J C Pronk, et al.Human Heredity|January 1, 1984
Salivary protein polymorphism in Kenya: evidence for a new AMY1 alleleJ C Pronk, W J Jansen, A Pronk, et al.Progress in Clinical and Biological Research|January 1, 1985
Serum pepsinogen I levels in relation to pepsinogen phenotypesG Pals, I Biemond, J Défize, et al.Human Genetics|May 1, 1992
Variation in gene copy number and polymorphism of the human salivary amylase isoenzyme system in CaucasiansR A Bank, E H Hettema, M A Muijs, et al.Pageof 7