Search Results - (Author, Cooperation:P. Wiesner)
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1Sui, P., Wiesner, D. L., Xu, J., Zhang, Y., Lee, J., Van Dyken, S., Lashua, A., Yu, C., Klein, B. S., Locksley, R. M., Deutsch, G., Sun, X.
American Association for the Advancement of Science (AAAS)
Published 2018Staff ViewPublication Date: 2018-06-08Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyGeosciencesComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Immunology, Medicine, Diseases, Online OnlyPublished by: -
2L. Fang ; S. H. Choi ; J. S. Baek ; C. Liu ; F. Almazan ; F. Ulrich ; P. Wiesner ; A. Taleb ; E. Deer ; J. Pattison ; J. Torres-Vazquez ; A. C. Li ; Y. I. Miller
Nature Publishing Group (NPG)
Published 2013Staff ViewPublication Date: 2013-05-31Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsKeywords: ATP-Binding Cassette Transporters/deficiency/genetics/metabolism ; Animals ; Biological Transport ; Blood Vessels/embryology ; Carrier Proteins/genetics/*metabolism/secretion ; Cholesterol/analysis/*metabolism ; Embryo, Nonmammalian/blood supply/metabolism ; Endothelial Cells/metabolism ; Human Umbilical Vein Endothelial Cells ; Humans ; Lipoproteins, HDL/metabolism ; Membrane Lipids/metabolism ; Membrane Microdomains/chemistry/metabolism ; Neovascularization, Physiologic/*physiology ; Protein Multimerization ; Signal Transduction ; Vascular Endothelial Growth Factor Receptor-2/chemistry/metabolism ; Zebrafish/embryology/*metabolism ; Zebrafish Proteins/deficiency/genetics/*metabolism/secretionPublished by: -
3Tötsch, M. ; Brömmelkamp, E. ; Stücker, A. ; Schmid, K. ; Böcker, W. ; Dockhorn-Dworniczak, B. ; Fille, M. ; Gross, R. ; Wiesner, P.
Springer
Published 1995Staff ViewISSN: 1432-2307Keywords: Automated laser fluorescence sequencer ; Partial digestion ; Restriction enzyme fragment length analysis ; Asymmetrically labelled fluorescence primer ; MycobacteriaSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Abstract An automated method for the restriction fragment length polymorphism (RFLP) analysis for the differentiation of mycobacteria to the species level is described. After polymerase chain reaction (PCR) amplification of a sequence of the gene encoding the 65-kDa surface antigen common to all mycobacteria the product was investigated by RFLP analysis. For accurate determination of fragment sizes the asymmetrically fluorescein-labelled PCR product was partially digested with restriction site enzymes BstEII and HaeIII. The fragments obtained were analysed electrophoretically using an automated laser fluorescence DNA sequencer. Determination of fragment sizes revealed a deviation of ±1 base pair (bp; 0.6%) when compared to expected sizes. The validity of this approach was confirmed by analysing mycobacterial DNA obtained from pure cultures of Mycobacterium (M.) tuberculosis and alcohol-fixed smears as well as paraffin-embedded sputa of patients with culture-proven tuberculosis. Additionally a diagnostic algorithm was established by investigation of cultured M. bovis, M. bovis bacille Calmette-Guérin, M. avium, M. intracellulare and M. fortuitum. The method allows the identification of restriction enzyme sites which are only 40 bp apart. Partial restriction enzyme digestion of asymmetrically fluorescence-labelled PCR products will presumably lead to the discovery of new restriction enzyme sites.Type of Medium: Electronic ResourceURL: