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Showing 1 to 20 of 340 for “"oncogene"”.

  1. ONCOGENE-INDUCED ALTERED DNA REPLICATION DYNAMICS

    Oncogene Induced Senescence (OIS) is a tumor suppressive barrier that blocks cell cycle permanently. OIS results from a robust DNA damage response (DDR) activation due to oncogene-induced hyper-proliferation. By performing a whole genome analysis of DNA replication dynamics occurring upon oncogene

    milano Repository record for ONCOGENE-INDUCED ALTERED DNA REPLICATION DYNAMICS (opens in a new tab)

  2. Oncogene-induced remodelling of cellular networks

    … I introduce the concepts of evolution-driven oncogenesis, genetic and non-genetic heterogeneity and signal transduction pathways. In Chapter 2, I describe the characterisation of KRAS mutation-specific MAPK signalling. To do this, I generated an isogenic panel of cells stably expressing a FRET …

    cambridge Repository record for Oncogene-induced remodelling of cellular networks (opens in a new tab)

  3. Oncogene-Induced Signaling Heterogeneity in Lung Cancer

    … has identified 138 frequently occurring driver oncogenes and tumor suppressor genes in lung cancer. Currently, only 15 of these genes can be targeted therapeutically. Study of downstream signaling alterations of these oncogenes and tumor suppressor genes may identify novel therapeutic targets. …

    utswmed Repository record for Oncogene-Induced Signaling Heterogeneity in Lung Cancer (opens in a new tab)

  4. Molecular characterization of the putative oncogene myeov

    The myeov gene was identified using the tumorigenicity assay with DNA from a patient suffering a gastric carcinoma. The Myeov gene is localized at chromosome band 11q13, a frequent site for chromosomal rearrangements in various carcinomas and B-cell neoplasms. The gene was shown to be involved in …

    heid-diss Repository record for Molecular characterization of the putative oncogene myeov (opens in a new tab)

  5. Oncogene-induced reprogramming of heterotypic cellular interactions

    KRAS is a critical signalling hub that orchestrates fundamental cellular decisions such as cell survival, proliferation and differentiation. Activating mutations in KRAS are among the most frequently occurring oncogenic mutations driving cancers that are particularly refractory to therapy (e.g., …

    cambridge Repository record for Oncogene-induced reprogramming of heterotypic cellular interactions (opens in a new tab)

  6. Activation of the c-Ha-ras oncogene

    Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biology, 1984

    mit Repository record for Activation of the c-Ha-ras oncogene (opens in a new tab)

  7. Oncogene-driven post-transcriptional regulation in lung cancer

    Lung cancer is often caused by genetic mutations which alter the activity of proteins in the RAS family, with somatic mutation of the KRAS gene occurring in ~30% of lung adenocarcinoma tumors. A gene of the same family, RIT1, is mutated or amplified in 10-15% of lung adenocarcinomas. Although …

    washington Repository record for Oncogene-driven post-transcriptional regulation in lung cancer (opens in a new tab)

  8. Trim24 As An Oncogene In The Mammary Gland

    … cells, consistent with TRIM24 function as an oncogene. We hypothesize that TRIM24 acts as an oncogene in the mammary gland.</p> <p>To test this hypothesis, we generated transgenic mice, which in the presence of cre-recombinase, conditionally over-express mouse TRIM24 fused to a C-terminal FLAG …

    uthsc Repository record for Trim24 As An Oncogene In The Mammary Gland (opens in a new tab)

  9. Translational Regulation of the C-Jun Proto-Oncogene

    <p>The <em>v-jun</em> oncogene was originally isolated from the ASV17 virus in 1987. Ever since its isolation, extensive work has been done to understand the role of the v-jun oncogene in cell transformation. The c-Jun protein is a transcription factor which binds to the DNA target TGACTCA. The …

    odu Repository record for Translational Regulation of the C-Jun Proto-Oncogene (opens in a new tab)

  10. E2F1 induction following DNA damage and oncogene activation

    … pRb, is deregulated in most human cancers. Oncogenes have been shown to deregulate E2F1 through inhibition of pRB and deregulation of E2F1 is an event that occurs in most human cancers. The essential role of E2F1 in apoptosis is well documented and deregulated E2F1 can enhance drug induced …

    glasgow Repository record for E2F1 induction following DNA damage and oncogene activation (opens in a new tab)

  11. Proto-oncogene Regulation by Growth Factors in Bone Cells

    … molecular level, the expression of several proto-oncogenes was studied. IGF-I and IGF-II cause a rapid and transient induction of c-fos in MC3T3-E1 cells similar to that observed with other growth factors in other cell types. TGF-beta causes a similar rapid induction of c-fos which is slightly …

    loma-linda Repository record for Proto-oncogene Regulation by Growth Factors in Bone Cells (opens in a new tab)

  12. Identification and Characterization of TONSL as an Immortalizing Oncogene

    … findings reveal that TONSL is an immortalizing oncogene, capable of transforming primary breast epithelial cells in conjunction with defined oncogenes, resulting in Estrogen Receptor-positive breast adenocarcinomas. Furthermore, we observed that TONSL-amplified breast cancer cells are dependent …

    iupui Repository record for Identification and Characterization of TONSL as an Immortalizing Oncogene (opens in a new tab)

  13. Exploring the adaptive immune response to Oncogene-Induced-Senescence

    … transposons in mice, to model hepatocyte oncogene-induced senescence (OIS) combined with multiple downstream assays to interrogate four elements of adaptive senescence surveillance: functionality of T-helper subsets; their transcriptomic profile; antigen-reactivity; and adaptive …

    cambridge Repository record for Exploring the adaptive immune response to Oncogene-Induced-Senescence (opens in a new tab)

  14. Taspase1 is a Non-oncogene Mediator of Tumorigenesis and Maintenance

    The clinical success of oncogene-targeted therapies substantiates the continued reliance of certain cancers upon the continued function of apical oncogenes involved in its genesis--a phenomenon known as "oncogene addiction." Though this shift from non-targeted, cytotoxic therapies offers new hope …

    wustl Repository record for Taspase1 is a Non-oncogene Mediator of Tumorigenesis and Maintenance (opens in a new tab)

  15. Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance

    … the skin has exceptional capacity to tolerate oncogene hyperactivity. To date, we have made significant progress in understanding how homeostatic adult epidermis suppresses the expansion of individual clones derived from somatic mutations. However, the mechanisms behind oncogene tolerance …

    washington Repository record for Translational mechanisms of stem cell fate regulation in epidermal oncogene tolerance (opens in a new tab)

  16. Predictive Reporter System for Investigating Dose Dependency in Oncogene-Induced Senescence

    Oncogene-induced senescence (OIS) is a well-described autonomous tumour suppressor mechanism which removes cells harbouring oncogenic mutations from the proliferation pool. However, senescent cells remain metabolically active and express factors of the senescence-associated secretory phenotype …

    cambridge Repository record for Predictive Reporter System for Investigating Dose Dependency in Oncogene-Induced Senescence (opens in a new tab)

  17. A mouse model to study inducible oncogene cooperation <i>in vivo</i>

    … multiple changes occur in two kinds of genes: oncogenes and tumour suppressor genes.<br></br><br></br> Oncogene-products can be classified as growth factors, growth factor receptors, Ras oncoproteins, cytoplasmic protein kinases, transcription factors, anti-apoptotic proteins.<br></br><br></br> …

    the-open-u Repository record for A mouse model to study inducible oncogene cooperation <i>in vivo</i> (opens in a new tab)

  18. Studies on signaling pathways induced by FLT3, an important oncogene in AML

    FLT3, a receptor tyrosine kinase, is expressed in hematopoietic progenitor cells. FLT3-ITD (internal tandem duplication) and D835 mutations are found in approximately 30% and 7% of Acute Myeloid Leukemia (AML) patients respectively, and correlate with a poor prognosis, thus making the mutated …

    lund Repository record for Studies on signaling pathways induced by FLT3, an important oncogene in AML (opens in a new tab)

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