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Showing 1 to 12 of 12 for “"G-quadruplex DNA"”.

  1. Development of nanobodies as tools to investigate G-quadruplex DNA secondary structures

    Guanine-rich sequences in DNA can fold into four-stranded alternative secondary structures called G-quadruplexes (G4). G4s are suggested to be involved in key genome functions such as transcription, genome stability and epigenetic regulation, together with numerous connections to cancer biology. …

    cambridge Repository record for Development of nanobodies as tools to investigate G-quadruplex DNA secondary structures (opens in a new tab)

  2. Interactions of small molecules with duplex DNA and lesion containing G-quadruplex DNA

    … to study their interactions with duplex DNA. The nickel complexes were found to selectively oxidize guanines in bulged DNA structures in the presence of oxidant and notably NiCR-2H oxidizes guanines more efficiently than NiCR. According to 1 H NMR studies, NiCR-2H binds strongly to the N7 …

    u-pacific Repository record for Interactions of small molecules with duplex DNA and lesion containing G-quadruplex DNA (opens in a new tab)

  3. Study of DNA damage on DNA G-quadruplexes and biophysical evaluation of the effects of modified bases (lesions) on their conformation and stability

    <p>Exposure of DNA to reactive oxygen species (ROS) results in the modified nucleobases (lesions) as well as strand scissions under physiological conditions. Due to its lowest oxidation potential (1.29 eV), guanine is the most easily oxidisable nucleobase. Furthermore, it has been observed that the …

    u-pacific Repository record for Study of DNA damage on DNA G-quadruplexes and biophysical evaluation of the effects of modified bases (lesions) on their conformation and stability (opens in a new tab)

  4. Synthesis and biophysical evaluation of thiazole orange derivatives as DNA binding ligands

    <p>Guanine-rich telomeric DNA at the end of chromosomes can form a unique DNA tertiary structure - G-quadruplex, which is known to inhibit the binding of telomerase to telomeric regions in cancer cells and thus regulate unrestricted cancer cell growth. Hence, G-quadruplex DNA has recently become a …

    u-pacific Repository record for Synthesis and biophysical evaluation of thiazole orange derivatives as DNA binding ligands (opens in a new tab)

  5. The synthesis of macrocyclic molecules related to telomestatin

    G-quadruplex DNA represents an attractive target for the development of anti-cancer therapeutic agents as it plays important roles in transcriptional regulation and the maintenance of telomeric length. Oxazole-containing macrocycles such as telomestatin are considered to be a promissing new class …

    laurentian Repository record for The synthesis of macrocyclic molecules related to telomestatin (opens in a new tab)

  6. NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS

    Traditional DNA-targeted anticancer agents, such as platinum-based therapies, have been a mainstay in the treatment of aggressive solid malignancies in the clinical setting. Unfortunately, due to multifactorial drug resistance and systemic toxicity the clinical efficacy of these drugs is severely …

    wfu Repository record for NOVEL APPROACHES FOR CONTROLLING TARGET SELECTIVITY AND PHARMACOLOGICAL PROPERTIES OF PLATINUM-INTERCALATOR-BASED ANTICANCER AGENTS (opens in a new tab)

  7. Characterization of inter-genomic and telomeric G-quadruplex structures through atomic force microscopy

    The G-quadruplex DNA structure, a secondary folding motif of DNA, is found throughout the genome. The dynamics of these structures has been seen to affect processes such as telomerase elongation and regulation of gene transcription. Typical investigation techniques require these structures to be …

    uiuc Repository record for Characterization of inter-genomic and telomeric G-quadruplex structures through atomic force microscopy (opens in a new tab)

  8. Evaluation of telomerase activity and telomerase inhibitors in Head and Neck cancer

    … evaluation of a series of small molecule G–quadruplex DNA binding agents as potential telomerase inhibitors. A total of 19 telomerase inhibitors were identified but of these, only 4 were specific inhibitors of telomerase. These compounds also caused toxicity to cell lines following a 2 hour …

    bradford Repository record for Evaluation of telomerase activity and telomerase inhibitors in Head and Neck cancer (opens in a new tab)

  9. Characterizing and targeting the genomic consequences of ATRX deficiency in glioma

    … glioma. Loss of ATRX gives rise to abnormal G-quadruplex DNA secondary structures at GC-rich sites of the genome, such as telomeric and pericentromeric regions, enhancing replication stress and genomic instability. These mutations are mutually exclusive with TERT promoter mutations, promoting …

    uthsc Repository record for Characterizing and targeting the genomic consequences of ATRX deficiency in glioma (opens in a new tab)

  10. The effect of replication impediments on differentiation

    … endoderm while replication was perturbed using DNA damaging agents, low dose hydroxyurea and G-quadruplex secondary structure stabilisation. DNA damage was induced both in the undifferentiated state and during differentiation. When damage was induced during differentiation, greater levels of …

    cambridge Repository record for The effect of replication impediments on differentiation (opens in a new tab)

  11. Vulnerability to G - Quadruplexes in BRCA2 - Null Medulloblastoma: A Protective Role for the PIF1 Helicase

    … with biallelic mutations in the essential DNA repair factor BRCA2 are highly predisposed to develop the most common pediatric brain cancer medulloblastoma (MB) before three years of age. Medulloblastoma is often the first malignancy in these children who have a high likelihood of developing …

    rockefeller Repository record for Vulnerability to G - Quadruplexes in BRCA2 - Null Medulloblastoma: A Protective Role for the PIF1 Helicase (opens in a new tab)