Monografie
Analysis of the role of N-terminal acetylation of newly synthesized proteins in Saccharomyces cerevisiae
- Sprache
-
Englisch
- Identifier
-
1181792215
Thema
Proteins; Proteolysis; Proteins--Synthesis; Saccharomyces cerevisiae; Acetylation; protein synthesis; Hochschulschrift
Beteiligte Personen und Organisationen
- DOI
-
10.11588/heidok.00024223
- URN
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
26.01.2023, 13:54 MEZ
Objekttyp
- Monografie
Beteiligte
Ähnliche Objekte (12)
Analysis of the role of N-terminal acetylation of newly synthesized proteins in Saccharomyces cerevisiae
Dynamic Control of Translation During Adult Neurogenesis
Identification of novel substrates of the Insoluble Protein Deposit (IPOD) in the yeast S. cerevisiae
Strukturelle und funktionelle Charakterisierung von Protein-O-Mannosyltransferasen der Bäckerhefe Saccharomyces cerevisiae
Interaktion des humanen Tight-junction-Proteins ZO-1 mit dem Ras-Effektor AF6 und Untersuchungen am Zellwandprotein Aga2 von Saccharomyces cerevisiae
In-cell structural biology of protein synthesis in Mycoplasma pneumoniae
Untersuchungen zur Wahrnehmung und zur Aufnahme von Riboflavin in Saccharomyces cerevisiae
Biochemical analysis of essential components involved in mitochondrial and cytosolic iron-sulfur protein biogenesis in Saccharomyces cerevisiae
Physiological role and funcion of Nα-terminal acetylation in Saccharomyces cerevisiae
The case for membrane-associated RNA-binding proteins in Saccharomyces cerevisiae
Quantitative and Structural Description of Molecular Crowding Using In-Cell Cryo-Electron Tomography
Untersuchungen zur Biogenese von Eisen-Schwefel-Proteinen und zur Eisenhomeostase am Modellorganismus Saccharomyces cerevisiae
Analysis of the role of N-terminal acetylation of newly synthesized proteins in Saccharomyces cerevisiae
Dynamic Control of Translation During Adult Neurogenesis
Identification of novel substrates of the Insoluble Protein Deposit (IPOD) in the yeast S. cerevisiae
Strukturelle und funktionelle Charakterisierung von Protein-O-Mannosyltransferasen der Bäckerhefe Saccharomyces cerevisiae
Interaktion des humanen Tight-junction-Proteins ZO-1 mit dem Ras-Effektor AF6 und Untersuchungen am Zellwandprotein Aga2 von Saccharomyces cerevisiae
In-cell structural biology of protein synthesis in Mycoplasma pneumoniae
Untersuchungen zur Wahrnehmung und zur Aufnahme von Riboflavin in Saccharomyces cerevisiae
Biochemical analysis of essential components involved in mitochondrial and cytosolic iron-sulfur protein biogenesis in Saccharomyces cerevisiae
Physiological role and funcion of Nα-terminal acetylation in Saccharomyces cerevisiae
The case for membrane-associated RNA-binding proteins in Saccharomyces cerevisiae
Quantitative and Structural Description of Molecular Crowding Using In-Cell Cryo-Electron Tomography
Untersuchungen zur Biogenese von Eisen-Schwefel-Proteinen und zur Eisenhomeostase am Modellorganismus Saccharomyces cerevisiae
Analysis of the role of N-terminal acetylation of newly synthesized proteins in Saccharomyces cerevisiae
Dynamic Control of Translation During Adult Neurogenesis
Identification of novel substrates of the Insoluble Protein Deposit (IPOD) in the yeast S. cerevisiae
Strukturelle und funktionelle Charakterisierung von Protein-O-Mannosyltransferasen der Bäckerhefe Saccharomyces cerevisiae
Interaktion des humanen Tight-junction-Proteins ZO-1 mit dem Ras-Effektor AF6 und Untersuchungen am Zellwandprotein Aga2 von Saccharomyces cerevisiae
In-cell structural biology of protein synthesis in Mycoplasma pneumoniae
Untersuchungen zur Wahrnehmung und zur Aufnahme von Riboflavin in Saccharomyces cerevisiae
Biochemical analysis of essential components involved in mitochondrial and cytosolic iron-sulfur protein biogenesis in Saccharomyces cerevisiae
Physiological role and funcion of Nα-terminal acetylation in Saccharomyces cerevisiae
The case for membrane-associated RNA-binding proteins in Saccharomyces cerevisiae
Quantitative and Structural Description of Molecular Crowding Using In-Cell Cryo-Electron Tomography