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  2. MyoD - Wikipedia

    en.wikipedia.org/wiki/MyoD

    4654 17927 Ensembl ENSG00000129152 ENSMUSG00000009471 UniProt P15172 P10085 RefSeq (mRNA) NM_002478 NM_010866 RefSeq (protein) NP_002469 NP_034996 Location (UCSC) Chr 11: 17.72 – 17.72 Mb Chr 7: 46.03 – 46.03 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse MyoD, also known as myoblast determination protein 1, is a protein in animals that plays a major role in regulating muscle ...

  3. Myogenic regulatory factors - Wikipedia

    en.wikipedia.org/wiki/Myogenic_regulatory_factors

    Myogenic regulatory factors (MRF) are basic helix-loop-helix (bHLH) transcription factors that regulate myogenesis: MyoD, Myf5, myogenin, and MRF4. [1]These proteins contain a conserved basic DNA binding domain that binds the E box DNA motif. [2]

  4. MYO7A - Wikipedia

    en.wikipedia.org/wiki/MYO7A

    Myosin VIIA is protein that in humans is encoded by the MYO7A gene. [5] Myosin VIIA is a member of the unconventional myosin superfamily of proteins. [6] Myosins are actin binding molecular motors that use the enzymatic conversion of ATP - ADP + inorganic phosphate (Pi) to provide the energy for movement.

  5. Myogenin - Wikipedia

    en.wikipedia.org/wiki/Myogenin

    17928 Ensembl ENSG00000122180 ENSMUSG00000026459 UniProt P15173 P12979 RefSeq (mRNA) NM_002479 NM_031189 RefSeq (protein) NP_002470 NP_112466 Location (UCSC) Chr 1: 203.08 – 203.09 Mb Chr 1: 134.22 – 134.22 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Myogenin, is a transcriptional activator encoded by the MYOG gene. Myogenin is a muscle-specific basic-helix-loop-helix (bHLH ...

  6. Myotonic dystrophy - Wikipedia

    en.wikipedia.org/wiki/Myotonic_dystrophy

    Myotonic dystrophy (DM) is a type of muscular dystrophy, a group of genetic disorders that cause progressive muscle loss and weakness. [1] In DM, muscles are often unable to relax after contraction. [1]

  7. MYO15A - Wikipedia

    en.wikipedia.org/wiki/MYO15A

    17910 Ensembl ENSG00000091536 ENSMUSG00000042678 UniProt Q9UKN7 Q9QZZ4 RefSeq (mRNA) NM_016239 NM_001103171 NM_010862 NM_182698 RefSeq (protein) NP_057323 NP_001096641 NP_034992 NP_874357 Location (UCSC) Chr 17: 18.11 – 18.18 Mb Chr 11: 60.36 – 60.42 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Unconventional myosin-XV is a protein that in humans is encoded by the MYO15A gene ...

  8. MYO1G - Wikipedia

    en.wikipedia.org/wiki/MYO1G

    64005 246177 Ensembl ENSG00000136286 ENSMUSG00000020437 UniProt B0I1T2 Q5SUA5 RefSeq (mRNA) NM_033054 NM_178440 RefSeq (protein) NP_149043 NP_848534 Location (UCSC) Chr 7: 44.96 – 44.98 Mb Chr 11: 6.46 – 6.47 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Myosin IG, also known as myosin 1G and MYO1G, is a protein that in humans is encoded by the MYO1G gene. MYO1G is a member of ...

  9. Myopathy - Wikipedia

    en.wikipedia.org/wiki/Myopathy

    (G71.0) Dystrophies (or muscular dystrophies) are a subgroup of myopathies characterized by muscle degeneration and regeneration. Clinically, muscular dystrophies are typically progressive, because the muscles' ability to regenerate is eventually lost, leading to progressive weakness, often leading to use of a wheelchair, and eventually death, usually related to respiratory weakness.