Showing results (71-80 of 305) with videos related to
Sort By:
Pageof 31
Thrombosis and Haemostasis|April 30, 1986
Electroblot and immunoperoxidase staining for rapid screening of the abnormalities of the multimeric structure of von Willebrand factor in von Willebrand's diseaseR Lombardi, C Gelfi, P G Righetti, et al.Clinical Chemistry|May 1, 1987
Serum alkaline phosphatase isoenzymes in hepatobiliary disorders resolved by use of immobilized pH gradientsP Sorroche, A Bianchi-Bosisio, P K Sinha, et al.Rapid Communications in Mass Spectrometry : RCM|February 17, 2001
Investigating the reaction of a novel silica capillary coating compound with proteins/peptides by matrix-assisted laser desorption/ionisation time-of-flight mass spectrometryM Galvani, M Hamdan, P G Righetti, et al.Journal of Chromatography. A|July 7, 1995
CAG triplet analysis in families with androgen insensitivity syndrome by capillary electrophoresis in polymer networksC Gelfi, P G Righetti, F Leoncini, et al.Journal of Chromatography. A|September 16, 1999
General experimental aspects of the use of isoelectric buffers in capillary electrophoresisA Bossi, E Olivieri, L Castelletti, et al.Journal of Chromatography. A|July 26, 2000
Free solution mobility of DNA molecules containing variable numbers of cationic phosphoramidate internucleoside linkagesN C Stellwagen, S Magnusdottir, J M Dagle, et al.Analytical Chemistry|September 6, 2001
Protein analysis by capillary zone electrophoresis utilizing a trifunctional diamine for silica coatingC Gelfi, A ViganĂ², M Ripamonti, et al.Journal of Chromatography. B, Biomedical Applications|July 1, 1994
Capillary zone electrophoresis in polymer networks of polymerase chain reaction-amplified oligonucleotides: the case of congenital adrenal hyperplasiaC Gelfi, A Orsi, P G Righetti, et al.Electrophoresis|May 1, 1994
Capillary zone electrophoresis of polymerase chain reaction-amplified DNA fragments in polymer networks: the case of GATT microsatellites in cystic fibrosisC Gelfi, A Orsi, P G Righetti, et al.Clinical Chemistry|November 20, 1997
Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresisP Carrera, A M Barbieri, M Ferrari, et al.Pageof 31