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Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1.
Oishi S, Zalucki O, Vega MS, Harkins D, Harvey TJ, Kasherman M, Davila RA, Hale L, White M, Piltz S, Thomas P, Burne THJ, Harris L, Piper M. Oishi S, et al. Among authors: piltz s. Genes Brain Behav. 2020 Apr;19(4):e12637. doi: 10.1111/gbb.12637. Epub 2020 Jan 14. Genes Brain Behav. 2020. PMID: 31909872 Free article.
Abnormal Cell Sorting Underlies the Unique X-Linked Inheritance of PCDH19 Epilepsy.
Pederick DT, Richards KL, Piltz SG, Kumar R, Mincheva-Tasheva S, Mandelstam SA, Dale RC, Scheffer IE, Gecz J, Petrou S, Hughes JN, Thomas PQ. Pederick DT, et al. Among authors: piltz sg. Neuron. 2018 Jan 3;97(1):59-66.e5. doi: 10.1016/j.neuron.2017.12.005. Neuron. 2018. PMID: 29301106 Free article.
Large deletions induced by Cas9 cleavage.
Adikusuma F, Piltz S, Corbett MA, Turvey M, McColl SR, Helbig KJ, Beard MR, Hughes J, Pomerantz RT, Thomas PQ. Adikusuma F, et al. Among authors: piltz s. Nature. 2018 Aug;560(7717):E8-E9. doi: 10.1038/s41586-018-0380-z. Epub 2018 Aug 8. Nature. 2018. PMID: 30089922 No abstract available.
78 results