DCDC2 抗体
(Doublecortin Domain Containing 2 (DCDC2))
This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013].
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Latest Publications for our DCDC2 抗体
: "Open-gate mutants of the mammalian proteasome show enhanced ubiquitin-conjugate degradation." in: Nature communications, Vol. 7, pp. 10963, (2016) (PubMed).: "Everolimus Stabilizes Podocyte Microtubules via Enhancing TUBB2B and DCDC2 Expression." in: PLoS ONE, Vol. 10, Issue 9, pp. e0137043, (2015) (PubMed).
: "Breakthroughs in the search for dyslexia candidate genes." in: Trends in molecular medicine, Vol. 12, Issue 7, pp. 333-41, (2006) (PubMed).
: "Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia." in: American journal of human genetics, Vol. 76, Issue 4, pp. 581-91, (2005) (PubMed).
Aliases for DCDC2 抗体
doublecortin domain containing 2 (DCDC2) 抗体doublecortin domain containing 2 (Dcdc2) 抗体
doublecortin domain containing 2B (dcdc2b) 抗体
DCDC2 抗体
DCDC2A 抗体
RU2 抗体
RU2S 抗体
zgc:123267 抗体
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