Vangl1 抗体
(Vang-Like 1 (Vangl1))
This gene encodes a member of the tretraspanin family. The encoded protein may be involved in mediating intestinal trefoil factor induced wound healing in the intestinal mucosa. Mutations in this gene are associated with neural tube defects. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010].
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Latest Publications for our Vangl1 抗体
: "Observing planar cell polarity in multiciliated mouse airway epithelial cells." in: Methods in cell biology, Vol. 127, pp. 37-54, (2015) (PubMed).: "Flattop regulates basal body docking and positioning in mono- and multiciliated cells." in: eLife, Vol. 3, (2014) (PubMed).
: "Postnatal refinement of auditory hair cell planar polarity deficits occurs in the absence of Vangl2." in: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 33, Issue 35, pp. 14001-16, (2013) (PubMed).
: "Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary cilia." in: Cell death and differentiation, Vol. 20, Issue 1, pp. 130-8, (2012) (PubMed).
Aliases for Vangl1 抗体
VANGL planar cell polarity protein 1 (Vangl1) 抗体VANGL planar cell polarity protein 1 (vangl1) 抗体
VANGL planar cell polarity protein 1 (VANGL1) 抗体
vang-like 1 (van gogh, Drosophila) (Vangl1) 抗体
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