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  2. Keratin 14 - Wikipedia

    en.wikipedia.org/wiki/Keratin_14

    Keratin 14 was the first type I keratin sequence determined. [5] Keratin 14 is also known as cytokeratin-14 (CK-14) or keratin-14 (KRT14). In humans it is encoded by the KRT14 gene. [6] [7] [8] Keratin 14 is usually found as a heterodimer with type II keratin 5 and form the cytoskeleton of epithelial cells.

  3. Keratin - Wikipedia

    en.wikipedia.org/wiki/Keratin

    Keratin (/ ˈ k ɛr ə t ɪ n / [1] [2]) is one of a family of structural fibrous proteins also known as scleroproteins. It is the key structural material making up scales , hair , nails , feathers , horns , claws , hooves , and the outer layer of skin in vertebrates.

  4. List of keratins - Wikipedia

    en.wikipedia.org/wiki/List_of_keratins

    Human keratin pseudogenes. Protein name [3] Gene name [3] Other protein name: Other gene name: KRT121P: φhHbD, Kb31P KRT122P: φhHbC, Kb30P KRT123P: φhHbB, Kb29P ...

  5. Cytokeratin - Wikipedia

    en.wikipedia.org/wiki/Cytokeratin

    The term cytokeratin began to be used in the late 1970s, when the protein subunits of keratin intermediate filaments inside cells were first being identified and characterized. [2] In 2006 a new systematic nomenclature for mammalian keratins was created, and the proteins previously called cytokeratins are simply called keratins (human ...

  6. Keratinocyte - Wikipedia

    en.wikipedia.org/wiki/Keratinocyte

    A Civatte body (named after the French dermatologist Achille Civatte, 1877–1956) [36] is a damaged basal keratinocyte that has undergone apoptosis, and consist largely of keratin intermediate filaments, and are almost invariably covered with immunoglobulins, mainly IgM. [37]

  7. Naegeli–Franceschetti–Jadassohn syndrome - Wikipedia

    en.wikipedia.org/wiki/Naegeli–Franceschetti...

    NFJS is caused by mutations in the keratin 14 (KRT14) gene, located on chromosome 17q12-21. [3] [5] The disorder is inherited in an autosomal dominant manner, which means that the defective gene responsible for a disorder is located on an autosome (chromosome 17 is an autosome), and only one copy of the defective gene is sufficient to cause the disorder, when inherited from a parent who has ...

  8. Epidermolysis bullosa simplex - Wikipedia

    en.wikipedia.org/wiki/Epidermolysis_bullosa_simplex

    Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14. [1]: 598 [2] It is one of the major forms of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily. [3]

  9. Category:Keratins - Wikipedia

    en.wikipedia.org/wiki/Category:Keratins

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