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Showing 1 to 13 of 13 for “"COS7"”.

  1. Identifizierung regulatorischer Proteindomänen der zytolytischen Eigenschaften des humanen P2X7-Rezeptors

    … valdidate the developed method, I investigated COS7-cells expressing the wildtype-P2X7-cDNA and 264.7-RAW-macrophages which expresses an endogenous P2X7-receptor. Furthermore I investigated the previous published E496A-Polymorphismem. According to the literature the activation of transfected …

    aachen Repository record for Identifizierung regulatorischer Proteindomänen der zytolytischen Eigenschaften des humanen P2X7-Rezeptors (opens in a new tab)

  2. Identifikation und Charakterisierung von Interaktionspartnern des Zystennierenproteins DZIP1L

    … studies in transiently transfected COS7-, HEK293- and mIMCD-3- cells have been performed for validation of the interaction of DZIP1L with EEF1G, NAGK and PSAP. All three identified binding partners are involved in SMAD-/TGF-ß- signaling. NAGK and PSAP are known to directly interact …

    aachen Repository record for Identifikation und Charakterisierung von Interaktionspartnern des Zystennierenproteins DZIP1L (opens in a new tab)

  3. QUANTIFYING OLIGOMERIC STATES OF PROTEINS IN-CELL VIA SINGLE-MOLECULE SUPER-RESOLUTION MICROSCOPY

    … PA-JF549, and acceptor fluorophore, JF646, in COS7 cells. Analyzing the FRET contribution on donor's intensity distributions allows us to estimate the dimerization of SOD1 proteins in cells. To apply our methods to a system that can provide physiologically relevant information, we further used …

    houston Repository record for QUANTIFYING OLIGOMERIC STATES OF PROTEINS IN-CELL VIA SINGLE-MOLECULE SUPER-RESOLUTION MICROSCOPY (opens in a new tab)

  4. Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy

    … polymorphism (SNP) in transfection studies in COS7 fibroblasts and, partially, in C2C12 myoblasts. The EGFP or DsRed2 tagged lamins were exogenously expressed either individually or both A-types together and examined by light and electron microscopy. The protein mobility of lamin A mutants was …

    wurz-thes Repository record for Lamin A and lamin C are differentially dysfunctional in autosomal dominant Emery-Dreifuss muscular dystrophy (opens in a new tab)

  5. An Alternative View of the Templates and Functions of RNA Polymerase II

    … RNA also modulates HDV replication in vivo, in COS7 and HeLa cells. The correlation between the effects of secondary structure alterations on the efficiency of pol II transcription in vitro and HDV replication in vivo suggests that the observed RNA-templated pol II transcription in vitro …

    rockefeller Repository record for An Alternative View of the Templates and Functions of RNA Polymerase II (opens in a new tab)

  6. Pathologie und Pathogenität eines viralen Strukturproteins : Faltung und pathogene Effekte von mutierten TMV -Hüllproteinen in pflanzlichen und tierischen Zellen

    … transient in Säugerzellen (Neuro2a und Cos7) transfiziert und die Zustandsformen der TMV-HPs und die Reaktion der Zelle darauf untersucht. Die Bedeutung der Prolinreste (P) im TMV-HP für seine Stabilität wurde durch den Austausch von P gegen Leucin (PnL) an den acht möglichen Positionen …

    bielefeld Repository record for Pathologie und Pathogenität eines viralen Strukturproteins : Faltung und pathogene Effekte von mutierten TMV -Hüllproteinen in pflanzlichen und tierischen Zellen (opens in a new tab)

  7. Morphological Remodeling of the Endoplasmic Reticulum During Mitosis and Its Influence on the Integrity of the Spindle Apparatus

    … subclasses we overexpressed each fly Reep in Cos7 cells, resulting in varied phenotypes with ReepB appearing to remodel ER tubules more readily. We then turn back to fly embryos to elucidate the mechanism behind <em>ReepB</em> spindle disruption. Together these data suggest that ReepA and …

    denver Repository record for Morphological Remodeling of the Endoplasmic Reticulum During Mitosis and Its Influence on the Integrity of the Spindle Apparatus (opens in a new tab)

  8. Microelectrode Array Modeling of Genetic Neurological Disorders in the Era of Next Generation Sequencing

    … We first investigate ATP1A3 mutations in COS7 cells and observe no clear differences. We next evaluate the effect of two mutations that cause the most severe ATP1A3-associated disorder, Alternating Hemiplegia of Childhood (AHC), on network dynamics. We show that mutant cultures demonstrate …

    duke Repository record for Microelectrode Array Modeling of Genetic Neurological Disorders in the Era of Next Generation Sequencing (opens in a new tab)

  9. Untersuchung zu (epi)genetischen Veränderungen auf Chromosom 11p15 und ihre funktionelle Relevanz bei Patienten mit Silver-Russell-Syndrom

    … out expression analyses in cultured HEK293- and Cos7-cells after transfection with constructs containing the different variants. An altered splicing of the H19 mRNA in comparison to wild-type construct could be found in two of the three patients (SR81K; SR93K), therefore indicating a relevance of …

    aachen Repository record for Untersuchung zu (epi)genetischen Veränderungen auf Chromosom 11p15 und ihre funktionelle Relevanz bei Patienten mit Silver-Russell-Syndrom (opens in a new tab)

  10. Molecular and Biochemical Investigations into VMD2, the gene associated with Best Disease

    … These included the establishment of an in vitro COS7 heterologous expression assay, the generation of numerous VMD2 mutations by site-directed mutagenesis as well as the development of bestrophin-specific antibodies. Surprisingly, membrane fractionation/Western blot experiments revealed no …

    wurz-thes Repository record for Molecular and Biochemical Investigations into VMD2, the gene associated with Best Disease (opens in a new tab)

  11. Funktion des Wind-Proteins in Drosophila melanogaster bei Faltung und/ oder Transport des sekretorischen Proteins Pipe

    Wind ist ein ER luminales Protein der Protein Disulfid Isomerase-Familie, welches seine Bedeutung in der Dorsoventral-Entwicklung von Drosophila hat. Es ist für die korrekte Lokalisation eines weiteren Proteins Pipe, einem Golgi-Transmembranprotein, verantwortlich. In Zusammenarbeit mit der Abt. f. …

    goettingen Repository record for Funktion des Wind-Proteins in Drosophila melanogaster bei Faltung und/ oder Transport des sekretorischen Proteins Pipe (opens in a new tab)