SWITCH: a dynamic CRISPR tool for genome engineering and metabolic pathway control for cell factory construction in Saccharomyces cerevisiae
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1475-2859
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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SWITCH: a dynamic CRISPR tool for genome engineering and metabolic pathway control for cell factory construction in Saccharomyces cerevisiae ; volume:16 ; number:1 ; day:8 ; month:2 ; year:2017 ; pages:1-12 ; date:12.2017
Microbial cell factories ; 16, Heft 1 (8.2.2017), 1-12, 12.2017
- Classification
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Biowissenschaften, Biologie
- Creator
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Vanegas, Katherina García
- Contributor
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Lehka, Beata Joanna
Mortensen, Uffe Hasbro
SpringerLink (Online service)
- DOI
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10.1186/s12934-017-0632-x
- URN
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urn:nbn:de:1111-2017030411234
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:02 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.
Associated
- Vanegas, Katherina García
- Lehka, Beata Joanna
- Mortensen, Uffe Hasbro
- SpringerLink (Online service)
Other Objects (12)
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Establishment of Saccharomyces cerevisiae as a cell factory for efficient de novo production of monogalactosyldiacylglycerol
Alpha-Terpineol production from an engineered Saccharomyces cerevisiae cell factory
Engineering Saccharomyces cerevisiae for targeted hydrolysis and fermentation of glucuronoxylan through CRISPR/Cas9 genome editing
Synthesizing ginsenoside Rh2 in Saccharomyces cerevisiae cell factory at high-efficiency
A copper switch for inducing CRISPR/Cas9-based transcriptional activation tightly regulates gene expression in Nicotiana benthamiana
CRISPR-Cas9 mediated gene deletions in lager yeast Saccharomyces pastorianus
Self-cloning CRISPR/Cpf1 facilitated genome editing in Saccharomyces cerevisiae
A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae
CrEdit: CRISPR mediated multi-loci gene integration in Saccharomyces cerevisiae
Erratum to: SWITCH: a dynamic CRISPR tool for genome engineering and metabolic pathway control for cell factory construction in Saccharomyces cerevisiae
An inducible CRISPR interference library for genetic interrogation of Saccharomyces cerevisiae biology
CRISPR-PCDup: a novel approach for simultaneous segmental chromosomal duplication in Saccharomyces cerevisiae
Establishment of Saccharomyces cerevisiae as a cell factory for efficient de novo production of monogalactosyldiacylglycerol
Alpha-Terpineol production from an engineered Saccharomyces cerevisiae cell factory
Engineering Saccharomyces cerevisiae for targeted hydrolysis and fermentation of glucuronoxylan through CRISPR/Cas9 genome editing
Synthesizing ginsenoside Rh2 in Saccharomyces cerevisiae cell factory at high-efficiency
A copper switch for inducing CRISPR/Cas9-based transcriptional activation tightly regulates gene expression in Nicotiana benthamiana
CRISPR-Cas9 mediated gene deletions in lager yeast Saccharomyces pastorianus
Self-cloning CRISPR/Cpf1 facilitated genome editing in Saccharomyces cerevisiae
A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae
CrEdit: CRISPR mediated multi-loci gene integration in Saccharomyces cerevisiae
Erratum to: SWITCH: a dynamic CRISPR tool for genome engineering and metabolic pathway control for cell factory construction in Saccharomyces cerevisiae
An inducible CRISPR interference library for genetic interrogation of Saccharomyces cerevisiae biology
CRISPR-PCDup: a novel approach for simultaneous segmental chromosomal duplication in Saccharomyces cerevisiae
Establishment of Saccharomyces cerevisiae as a cell factory for efficient de novo production of monogalactosyldiacylglycerol
Alpha-Terpineol production from an engineered Saccharomyces cerevisiae cell factory
Engineering Saccharomyces cerevisiae for targeted hydrolysis and fermentation of glucuronoxylan through CRISPR/Cas9 genome editing
Synthesizing ginsenoside Rh2 in Saccharomyces cerevisiae cell factory at high-efficiency
A copper switch for inducing CRISPR/Cas9-based transcriptional activation tightly regulates gene expression in Nicotiana benthamiana
CRISPR-Cas9 mediated gene deletions in lager yeast Saccharomyces pastorianus
Self-cloning CRISPR/Cpf1 facilitated genome editing in Saccharomyces cerevisiae
A gRNA-tRNA array for CRISPR-Cas9 based rapid multiplexed genome editing in Saccharomyces cerevisiae