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  2. Telomere - Wikipedia

    en.wikipedia.org/wiki/Telomere

    Telomeres form large loop structures called telomere loops, or T-loops. Here, the single-stranded DNA curls around in a long circle, stabilized by telomere-binding proteins. [26] At the very end of the T-loop, the single-stranded telomere DNA is held onto a region of double-stranded DNA by the telomere strand disrupting the double-helical DNA ...

  3. Telomere-binding protein - Wikipedia

    en.wikipedia.org/wiki/Telomere-binding_protein

    Telomere-binding proteins function to generate a T-loop, which is a specialized loop structure to cap the telomeric ends. Telomerase activity is regulated by protection of telomeres 1 (POT1). [9] They serve as a protective safeguard against premature degradation as the telomere ends are no longer hidden from damage detection.

  4. Telomeric repeat-binding factor 2 - Wikipedia

    en.wikipedia.org/wiki/Telomeric_repeat-binding...

    To prevent the cellular DNA repair machinery from mistakenly identifying telomeres as chromosome breaks, t-loops are formed in which the 3’ TTAGGG overhang of the telomere loops back into the DNA duplex. TERF2 promotes t-loop formation by preferentially binding to a telomeric double-stranded DNA duplex containing a 3’ TTAGGG single-stranded ...

  5. Shelterin - Wikipedia

    en.wikipedia.org/wiki/Shelterin

    Shelterin (also called telosome) is a protein complex known to protect telomeres in many eukaryotes from DNA repair mechanisms, as well as to regulate telomerase activity. In mammals and other vertebrates, telomeric DNA consists of repeating double-stranded 5'-TTAGGG-3' (G-strand) sequences (2-15 kilobases in humans) along with the 3'-AATCCC-5' (C-strand) complement, ending with a 50-400 ...

  6. Telomerase - Wikipedia

    en.wikipedia.org/wiki/Telomerase

    The existence of a compensatory mechanism for telomere shortening was first found by Soviet biologist Alexey Olovnikov in 1973, [4] who also suggested the telomere hypothesis of aging and the telomere's connections to cancer and perhaps some neurodegenerative diseases.

  7. Flow-FISH - Wikipedia

    en.wikipedia.org/wiki/Flow-FISH

    Flow-FISH was first published in 1998 by Rufer et al. [11] as a modification of another technique for analyzing telomere length, Q-FISH, that employs peptide nucleic acid probes [12] of a 3'-CCCTAACCCTAACCCTAA-5' sequence labeled with a fluorescin fluorophore to stain telomeric repeats on prepared metaphase spreads of cells that have been treated with colcemid, hypotonic shock, and fixation to ...

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  9. G-quadruplex - Wikipedia

    en.wikipedia.org/wiki/G-quadruplex

    The potential positive and negative roles of quadruplexes in telomere replication and function remains controversial. T-loops and G-quadruplexes are described as the two tertiary DNA structures that protect telomere ends and regulate telomere length. [49]

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