Hochschulschrift
Global regulators of fungal secondary metabolism: molecular genetic characterization of Velvet in the β-lactam [beta-lactam] producer Acremonium chrysogenum
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
Bochum, Univ., Diss., 2007
- Keyword
-
Genexpression
Genregulation
Repression
Biosynthese
Anabolismus
Deuteromycetes
- Creator
- URN
-
urn:nbn:de:hbz:294-19649
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:56 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
Other Objects (12)
![Valclavam - ein antifungisches β-Lactam [Beta-Lactam], Fermentation, Isolierung, Biogenese und biologische Wirkung](/assets/placeholder/searchResultMediaNoDigitisedMedia.png)
Valclavam - ein antifungisches β-Lactam [Beta-Lactam], Fermentation, Isolierung, Biogenese und biologische Wirkung
Molecular biotechnology of fungal β-lactam [beta-lactam] antibiotics and related peptide synthetases
β-lactam antibiotic concentrations during continuous renal replacement therapy
Molecular modeling studies of lipase-catalyzed β-lactam polymerization
In-vitro-Aktivität von SCH 29482, einem neuen β-Lactam Antibiotikum [Beta-Lactam-Antibiotikum] und Thienamycin
Staphylococcus aureus functional amyloids catalyze degradation of β-lactam antibiotics
Time-resolved β-lactam cleavage by L1 metallo-β-lactamase
Aziridine and β-Lactam Synthesis by Amination and Carbonylation Reactions
Visible Light-Mediated β-Lactam Synthesis from Acryl Amide Precursors
Outer membrane vesicles from β-lactam-resistant Escherichia coli enable the survival of β-lactam-susceptible E. coli in the presence of β-lactam antibiotics
A Natural Deep Eutectic Solvent Formulated to Stabilize β-Lactam Antibiotics
Pitfalls in the Immunochemical Determination of β-Lactam Antibiotics in Water
Valclavam - ein antifungisches β-Lactam [Beta-Lactam], Fermentation, Isolierung, Biogenese und biologische Wirkung
Molecular biotechnology of fungal β-lactam [beta-lactam] antibiotics and related peptide synthetases
β-lactam antibiotic concentrations during continuous renal replacement therapy
Molecular modeling studies of lipase-catalyzed β-lactam polymerization
In-vitro-Aktivität von SCH 29482, einem neuen β-Lactam Antibiotikum [Beta-Lactam-Antibiotikum] und Thienamycin
Staphylococcus aureus functional amyloids catalyze degradation of β-lactam antibiotics
Time-resolved β-lactam cleavage by L1 metallo-β-lactamase
Aziridine and β-Lactam Synthesis by Amination and Carbonylation Reactions
Visible Light-Mediated β-Lactam Synthesis from Acryl Amide Precursors
Outer membrane vesicles from β-lactam-resistant Escherichia coli enable the survival of β-lactam-susceptible E. coli in the presence of β-lactam antibiotics
A Natural Deep Eutectic Solvent Formulated to Stabilize β-Lactam Antibiotics
Pitfalls in the Immunochemical Determination of β-Lactam Antibiotics in Water
Valclavam - ein antifungisches β-Lactam [Beta-Lactam], Fermentation, Isolierung, Biogenese und biologische Wirkung
Molecular biotechnology of fungal β-lactam [beta-lactam] antibiotics and related peptide synthetases
β-lactam antibiotic concentrations during continuous renal replacement therapy
Molecular modeling studies of lipase-catalyzed β-lactam polymerization
In-vitro-Aktivität von SCH 29482, einem neuen β-Lactam Antibiotikum [Beta-Lactam-Antibiotikum] und Thienamycin
Staphylococcus aureus functional amyloids catalyze degradation of β-lactam antibiotics
Time-resolved β-lactam cleavage by L1 metallo-β-lactamase
Aziridine and β-Lactam Synthesis by Amination and Carbonylation Reactions
Visible Light-Mediated β-Lactam Synthesis from Acryl Amide Precursors
Outer membrane vesicles from β-lactam-resistant Escherichia coli enable the survival of β-lactam-susceptible E. coli in the presence of β-lactam antibiotics
A Natural Deep Eutectic Solvent Formulated to Stabilize β-Lactam Antibiotics