MYO5A 抗体
(Myosin VA (MYO5A))
This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008].
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Latest Publications for our MYO5A 抗体
: "The Actin-Based Motor Myosin Vb Is Crucial to Maintain Epidermal Barrier Integrity." in: The Journal of investigative dermatology, (2019) (PubMed).
: "The C7orf43/TRAPPC14 component links the TRAPPII complex to Rabin8 for preciliary vesicle tethering at the mother centriole during ciliogenesis." in: The Journal of biological chemistry, Vol. 294, Issue 42, pp. 15418-15434, (2019) (PubMed).
: "Myosin Va cooperates with PKA RIalpha to mediate maintenance of the endplate in vivo." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 5, pp. 2031-6, (2010) (PubMed).
: "Genetic susceptibility to distinct bladder cancer subphenotypes." in: European urology, Vol. 57, Issue 2, pp. 283-92, (2010) (PubMed).
: "Cyclic AMP promotes a peripheral distribution of melanosomes and stimulates melanophilin/Slac2-a and actin association." in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology, Vol. 18, Issue 9, pp. 989-91, (2004) (PubMed).
: "Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)." in: The Journal of clinical investigation, Vol. 112, Issue 3, pp. 450-6, (2003) (PubMed).
: "Interactions of human Myosin Va isoforms, endogenously expressed in human melanocytes, are tightly regulated by the tail domain." in: The Journal of investigative dermatology, Vol. 120, Issue 3, pp. 465-75, (2003) (PubMed).
: "The C7orf43/TRAPPC14 component links the TRAPPII complex to Rabin8 for preciliary vesicle tethering at the mother centriole during ciliogenesis." in: The Journal of biological chemistry, Vol. 294, Issue 42, pp. 15418-15434, (2019) (PubMed).
: "Myosin Va cooperates with PKA RIalpha to mediate maintenance of the endplate in vivo." in: Proceedings of the National Academy of Sciences of the United States of America, Vol. 107, Issue 5, pp. 2031-6, (2010) (PubMed).
: "Genetic susceptibility to distinct bladder cancer subphenotypes." in: European urology, Vol. 57, Issue 2, pp. 283-92, (2010) (PubMed).
: "Cyclic AMP promotes a peripheral distribution of melanosomes and stimulates melanophilin/Slac2-a and actin association." in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology, Vol. 18, Issue 9, pp. 989-91, (2004) (PubMed).
: "Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)." in: The Journal of clinical investigation, Vol. 112, Issue 3, pp. 450-6, (2003) (PubMed).
: "Interactions of human Myosin Va isoforms, endogenously expressed in human melanocytes, are tightly regulated by the tail domain." in: The Journal of investigative dermatology, Vol. 120, Issue 3, pp. 465-75, (2003) (PubMed).
Aliases for MYO5A 抗体
myosin VA L homeolog (myo5a.L) 抗体myosin VAa (myo5aa) 抗体
myosin VA (MYO5A) 抗体
myosin va (PY04789) 抗体
myosin VA (Myo5a) 抗体
9630007J19Rik 抗体
AI413174 抗体
AI661011 抗体
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MyoVA 抗体
myoxin) 抗体
MYR12 抗体
non-muscle 抗体
Sev-1 抗体
si:dkey-266j9.1 抗体
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