PNKD 抗体
(Paroxysmal Nonkinesigenic Dyskinesia (PNKD))
This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010].
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Latest Publications for our PNKD 抗体
: "Detrusor induction of miR-132/212 following bladder outlet obstruction: association with MeCP2 repression and cell viability." in: PLoS ONE, Vol. 10, Issue 1, pp. e0116784, (2015) (PubMed).: "Myofibrillogenesis regulator-1 overexpression is associated with poor prognosis of gastric cancer patients." in: World journal of gastroenterology, Vol. 18, Issue 38, pp. 5434-41, (2012) (PubMed).
Aliases for PNKD 抗体
paroxysmal nonkinesigenic dyskinesia (PNKD) 抗体paroxysmal nonkinesiogenic dyskinesia (Pnkd) 抗体
2210013N15Rik 抗体
2810403H05Rik 抗体
AI854243 抗体
BRP17 抗体
Brp17 抗体
DYT8 抗体
FPD1 抗体
KIPP1184 抗体
MNCb-5687 抗体
MR-1 抗体
MR1 抗体
PDC 抗体
PKND1 抗体
TAHCCP2 抗体
Tahccp2 抗体
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