Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Stefan Maeser"'
Autor:
Loredana-Mirela Lupu, Pascal Wiegand, Daria Holdschick, Delia Mihoc, Stefan Maeser, Stephan Rawer, Friedemann Völklein, Ebrahim Malek, Frederik Barka, Sascha Knauer, Christina Uth, Julia Hennermann, Wolfgang Kleinekofort, Andreas Hahn, Günes Barka, Michael Przybylski
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 23, p 12832 (2021)
Analytical methods for molecular characterization of diagnostic or therapeutic targets have recently gained high interest. This review summarizes the combination of mass spectrometry and surface plasmon resonance (SPR) biosensor analysis for identifi
Externí odkaz:
https://doaj.org/article/fca1a688335b424e9f454d6225b5d72c
Autor:
Sascha Knauer, Wolfgang Kleinekofort, Loredana-Mirela Lupu, Michael Przybylski, Frederik Barka, Pascal Wiegand, Günes Barka, Julia B. Hennermann, Daria Holdschick, Stephan Rawer, Ebrahim Malek, Stefan Maeser, Andreas Hahn, Delia Mihoc, Friedemann Völklein, Christina Uth
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 12832, p 12832 (2021)
International Journal of Molecular Sciences
International Journal of Molecular Sciences
Analytical methods for molecular characterization of diagnostic or therapeutic targets have recently gained high interest. This review summarizes the combination of mass spectrometry and surface plasmon resonance (SPR) biosensor analysis for identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b148d86900d23425f2fc4531ef0481c
https://www.mdpi.com/1422-0067/22/23/12832
https://www.mdpi.com/1422-0067/22/23/12832
Autor:
Michael Przybylski, Filippo M. Santorelli, Angela Schulz, Laura Ion, Alfried Kohlschütter, Stephan Rawer, Brindusa Alina Petre, Stefan Maeser, Alessandro Simonati
Neuronal ceroid lipofuscinoses (NCLs) are a group of neurodegenerative diseases predominantly in childhood that are characterized by psychomotor deterioration, epilepsy, and early death of patients. The NCLs analyzed in the present study are caused b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8e0520d50c29285f684b0220689cb0e
http://hdl.handle.net/11562/1032659
http://hdl.handle.net/11562/1032659
Autor:
Zdeněk Kukačka, Teodora Bavaro, Loredana Lupu, Sara Tengattini, Roberta Bernardini, Caterina Temporini, Hendrik Rusche, Enrica Calleri, Loredano Pollegioni, Michael Przybylski, Francesca Rinaldi, Luciano Piubelli, Stefan Maeser
Publikováno v:
Analytical and bioanalytical chemistry. 411(2)
Tuberculosis (TB) is the first cause of death from infectious diseases worldwide. Only a single anti-TB vaccine is currently available for clinical use, but its efficacy is not achieved with certainty. The aim of this work is to provide a basis for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b80d127a09743894876bf0ae8d9d31ca
https://pubmed.ncbi.nlm.nih.gov/30498982
https://pubmed.ncbi.nlm.nih.gov/30498982
Autor:
Lorenzo Altamore, Julia Hennermann, Hendrik Rusche, Fabio Borri, Marius Iurascu, Zdenek Kukacka, Michael Przybylski, Anna Maria Papini, Loredana Lupu, Mary Murphy, Stefan Maeser
Publikováno v:
ChemMedChem. 13(9)
α-Galactosidase (αGal) is a lysosomal enzyme that hydrolyses the terminal α-galactosyl moiety from glycosphingolipids. Mutations in the encoding genes for αGal lead to defective or misfolded enzyme, which results in substrate accumulation and sub
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b580312754d3c12afc8531adb42b118
https://pubmed.ncbi.nlm.nih.gov/29473701
https://pubmed.ncbi.nlm.nih.gov/29473701
Autor:
Michael Przybylski, Stephan Rawer, Jeff Bornheim, Stefan Maeser, Mary Murphy, Frederike Eggers, Adrian Moise
Publikováno v:
Journal of the American Society for Mass Spectrometry. 27(6)
Fabry disease (FD) is a rare metabolic disorder of a group of lysosomal storage diseases, caused by deficiency or reduced activity of the enzyme α-galactosidase. Human α-galactosidase A (hαGAL) hydrolyses the terminal α-galactosyl moiety from gly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f26620dd20fa04776432985fe7507ada
https://pubmed.ncbi.nlm.nih.gov/27112153
https://pubmed.ncbi.nlm.nih.gov/27112153
Autor:
Irene Toldo, Sara Rossato, Stefano Sartori, Michael Przybylski, Francesco Pezzini, Stefano Doccini, Stefan Maeser, Filippo M. Santorelli, Francesca Moro, Alessandro Simonati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d3785f811102ec9e5f8d9fc0bb15b68
http://hdl.handle.net/11562/942957
http://hdl.handle.net/11562/942957
Publikováno v:
Nucleic Acids Research. 18:6215-6222
The repAC operon of plasmid RSF1010 consists of the genes for proteins E, F, RepA (DNA helicase), and RepC (origin-binding initiator protein) and is transcriptionally initiated by a promoter called P4. We have studied the expression of the repAC oper
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::caecbce00947e36927ab6a6b6835b556
https://doi.org/10.1093/nar/18.21.6215
https://doi.org/10.1093/nar/18.21.6215
Autor:
Stefan Maeser, Regine Kahmann
Publikováno v:
Moleculargeneral genetics : MGG. 230(1-2)
A mutant Gin recombinase of the phage Mu DNA inversion system was successfully expressed in Arabidopsis thaliana and tobacco protoplasts. Site-specific recombination was monitored both physically and biologically with the help of a recombination assa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9a355b7d7406c4909563f18c20bf043
https://pubmed.ncbi.nlm.nih.gov/1836050
https://pubmed.ncbi.nlm.nih.gov/1836050