Hochschulschrift
Mechanism of HPV8 mediated silencing of Syntenin-2 gene expression and modulation of nuclear phospholipid metabolism
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Dimensions
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21 cm
- Extent
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110 Blätter
- Language
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Englisch
- Notes
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Illustrationen
Universität zu Köln, Dissertation, 2017
- Classification
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Biowissenschaften, Biologie
- Keyword
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Histologie
Cytologie
- Table of contents
- Rights
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Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Last update
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11.06.2025, 2:04 PM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
Time of origin
- 2017
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Neurochemical aspects of phospholipid metabolism : [proceedings of the International Meeting on Neurochemical Aspects of Phospholipid Metabolism, May 26 - 28, 1988, Perugia, Italy]
Investigation of the mechanism of the specific phospholipid enrichment in the bile
Proteolytic regulation of mitochondrial phospholipid metabolism by the i-AAA protease Yme1
Calorimetric and molecular acoustic study of phospholipid sterol and phospholipid peptide interactions
The Effect of Dexamethasone, Adrenergic and Cholinergic Receptor Agonists on Phospholipid Metabolism in Human Osteoarthritic Synoviocytes
Atp23 and Mdn35 perform antagonistic functions in mitochondrial phospholipid metabolism
Investigations on the mechanism of Host-Induced Gene Silencing of the fungal CYP51 genes in the Fusarium Arabidopsis pathosystem
Tracking Epistemic Violence, Tracking Practices of Silencing
Regulation of heterochromatic gene silencing in mouse
Rewiring of neuronal networks during synaptic silencing
Optogenetic silencing of Parvalbumin-expressing hippocampal interneurons
Silencing and counter-silencing of the Lsr2-like protein CgpS in Corynebacterium glutamicum
Neurochemical aspects of phospholipid metabolism : [proceedings of the International Meeting on Neurochemical Aspects of Phospholipid Metabolism, May 26 - 28, 1988, Perugia, Italy]
Investigation of the mechanism of the specific phospholipid enrichment in the bile
Proteolytic regulation of mitochondrial phospholipid metabolism by the i-AAA protease Yme1
Calorimetric and molecular acoustic study of phospholipid sterol and phospholipid peptide interactions
The Effect of Dexamethasone, Adrenergic and Cholinergic Receptor Agonists on Phospholipid Metabolism in Human Osteoarthritic Synoviocytes
Atp23 and Mdn35 perform antagonistic functions in mitochondrial phospholipid metabolism
Investigations on the mechanism of Host-Induced Gene Silencing of the fungal CYP51 genes in the Fusarium Arabidopsis pathosystem
Tracking Epistemic Violence, Tracking Practices of Silencing
Regulation of heterochromatic gene silencing in mouse
Rewiring of neuronal networks during synaptic silencing
Optogenetic silencing of Parvalbumin-expressing hippocampal interneurons
Silencing and counter-silencing of the Lsr2-like protein CgpS in Corynebacterium glutamicum
Neurochemical aspects of phospholipid metabolism : [proceedings of the International Meeting on Neurochemical Aspects of Phospholipid Metabolism, May 26 - 28, 1988, Perugia, Italy]
Investigation of the mechanism of the specific phospholipid enrichment in the bile
Proteolytic regulation of mitochondrial phospholipid metabolism by the i-AAA protease Yme1
Calorimetric and molecular acoustic study of phospholipid sterol and phospholipid peptide interactions
The Effect of Dexamethasone, Adrenergic and Cholinergic Receptor Agonists on Phospholipid Metabolism in Human Osteoarthritic Synoviocytes
Atp23 and Mdn35 perform antagonistic functions in mitochondrial phospholipid metabolism
Investigations on the mechanism of Host-Induced Gene Silencing of the fungal CYP51 genes in the Fusarium Arabidopsis pathosystem
Tracking Epistemic Violence, Tracking Practices of Silencing
Regulation of heterochromatic gene silencing in mouse
Rewiring of neuronal networks during synaptic silencing
Optogenetic silencing of Parvalbumin-expressing hippocampal interneurons