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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2013 | 1 |
2014 | 1 |
2016 | 1 |
2018 | 1 |
2024 | 0 |
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Prickle1 stunts limb growth through alteration of cell polarity and gene expression.
Dev Dyn. 2013 Nov;242(11):1293-306. doi: 10.1002/dvdy.24025. Epub 2013 Sep 6.
Dev Dyn. 2013.
PMID: 23913870
Free PMC article.
Null and hypomorph Prickle1 alleles in mice phenocopy human Robinow syndrome and disrupt signaling downstream of Wnt5a.
Liu C, Lin C, Gao C, May-Simera H, Swaroop A, Li T.
Liu C, et al.
Biol Open. 2014 Sep 4;3(9):861-70. doi: 10.1242/bio.20148375.
Biol Open. 2014.
PMID: 25190059
Free PMC article.
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Prickle1 mutation causes planar cell polarity and directional cell migration defects associated with cardiac outflow tract anomalies and other structural birth defects.
Gibbs BC, Damerla RR, Vladar EK, Chatterjee B, Wan Y, Liu X, Cui C, Gabriel GC, Zahid M, Yagi H, Szabo-Rogers HL, Suyama KL, Axelrod JD, Lo CW.
Gibbs BC, et al.
Biol Open. 2016 Feb 16;5(3):323-35. doi: 10.1242/bio.015750.
Biol Open. 2016.
PMID: 26883626
Free PMC article.
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A Spatiotemporal Requirement for Prickle 1-Mediated PCP Signaling in Eyelid Morphogenesis and Homeostasis.
Guo D, Yuan Z, Ru J, Gu X, Zhang W, Mao F, Ouyang H, Wu K, Liu Y, Liu C.
Guo D, et al.
Invest Ophthalmol Vis Sci. 2018 Feb 1;59(2):952-966. doi: 10.1167/iovs.17-22947.
Invest Ophthalmol Vis Sci. 2018.
PMID: 29450535
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