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Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency.
Hum Mol Genet. 2015 Sep 15;24(18):5250-9. doi: 10.1093/hmg/ddv245. Epub 2015 Jun 29.
Hum Mol Genet. 2015.
PMID: 26123493
Rare copy number variation in cerebral palsy.
McMichael G, Girirajan S, Moreno-De-Luca A, Gecz J, Shard C, Nguyen LS, Nicholl J, Gibson C, Haan E, Eichler E, Martin CL, MacLennan A.
McMichael G, et al. Among authors: shard c.
Eur J Hum Genet. 2014 Jan;22(1):40-5. doi: 10.1038/ejhg.2013.93. Epub 2013 May 22.
Eur J Hum Genet. 2014.
PMID: 23695280
Free PMC article.
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Emerging biomaterials and technologies to control stem cell fate and patterning in engineered 3D tissues and organoids.
Farahani M, Carthew J, Bhowmik S, Shard C, Nunez-Nescolarde A, Gomez GA, Cadarso VJ, Combes AN, Frith JE.
Farahani M, et al. Among authors: shard c.
Biointerphases. 2022 Nov 7;17(6):060801. doi: 10.1116/6.0002034.
Biointerphases. 2022.
PMID: 36344295
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Tissue-wide coordination of epithelium-to-neural stem cell transition in the Drosophila optic lobe requires Neuralized.
Shard C, Luna-Escalante J, Schweisguth F.
Shard C, et al.
J Cell Biol. 2020 Nov 2;219(11):e202005035. doi: 10.1083/jcb.202005035.
J Cell Biol. 2020.
PMID: 32946560
Free PMC article.
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