Piltz SG - Search Results

1

A Prox1 enhancer represses haematopoiesis in the lymphatic vasculature.

Kazenwadel J, Venugopal P, Oszmiana A, Toubia J, Arriola-Martinez L, Panara V, Piltz SG, Brown C, Ma W, Schreiber AW, Koltowska K, Taoudi S, Thomas PQ, Scott HS, Harvey NL. Kazenwadel J, et al. Among authors: piltz sg. Nature. 2023 Feb;614(7947):343-348. doi: 10.1038/s41586-022-05650-9. Epub 2023 Jan 25. Nature. 2023. PMID: 36697821

2

Deep sequencing analysis of the developing mouse brain reveals a novel microRNA.

Ling KH, Brautigan PJ, Hahn CN, Daish T, Rayner JR, Cheah PS, Raison JM, Piltz S, Mann JR, Mattiske DM, Thomas PQ, Adelson DL, Scott HS. Ling KH, et al. BMC Genomics. 2011 Apr 5;12:176. doi: 10.1186/1471-2164-12-176. BMC Genomics. 2011. PMID: 21466694 Free PMC article.

3

Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice.

Lee K, Tan J, Morris MB, Rizzoti K, Hughes J, Cheah PS, Felquer F, Liu X, Piltz S, Lovell-Badge R, Thomas PQ. Lee K, et al. PLoS One. 2012;7(1):e29041. doi: 10.1371/journal.pone.0029041. Epub 2012 Jan 26. PLoS One. 2012. PMID: 22291885 Free PMC article.

4

Mechanistic insight into the pathology of polyalanine expansion disorders revealed by a mouse model for X linked hypopituitarism.

Hughes J, Piltz S, Rogers N, McAninch D, Rowley L, Thomas P. Hughes J, et al. PLoS Genet. 2013;9(3):e1003290. doi: 10.1371/journal.pgen.1003290. Epub 2013 Mar 7. PLoS Genet. 2013. PMID: 23505376 Free PMC article.

5

Pcdh19 Loss-of-Function Increases Neuronal Migration In Vitro but is Dispensable for Brain Development in Mice.

Pederick DT, Homan CC, Jaehne EJ, Piltz SG, Haines BP, Baune BT, Jolly LA, Hughes JN, Gecz J, Thomas PQ. Pederick DT, et al. Among authors: piltz sg. Sci Rep. 2016 May 31;6:26765. doi: 10.1038/srep26765. Sci Rep. 2016. PMID: 27240640 Free PMC article.

6

Knockout of the epilepsy gene Depdc5 in mice causes severe embryonic dysmorphology with hyperactivity of mTORC1 signalling.

Hughes J, Dawson R, Tea M, McAninch D, Piltz S, Jackson D, Stewart L, Ricos MG, Dibbens LM, Harvey NL, Thomas P. Hughes J, et al. Sci Rep. 2017 Oct 3;7(1):12618. doi: 10.1038/s41598-017-12574-2. Sci Rep. 2017. PMID: 28974734 Free PMC article.

7

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.

8

PCDH19 regulation of neural progenitor cell differentiation suggests asynchrony of neurogenesis as a mechanism contributing to PCDH19 Girls Clustering Epilepsy.

Homan CC, Pederson S, To TH, Tan C, Piltz S, Corbett MA, Wolvetang E, Thomas PQ, Jolly LA, Gecz J. Homan CC, et al. Neurobiol Dis. 2018 Aug;116:106-119. doi: 10.1016/j.nbd.2018.05.004. Epub 2018 May 12. Neurobiol Dis. 2018. PMID: 29763708

9

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. 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.

10

Expanding the RNA-Guided Endonuclease Toolkit for Mouse Genome Editing.

Robertson L, Pederick D, Piltz S, White M, Nieto A, Ahladas M, Adikusuma F, Thomas PQ. Robertson L, et al. CRISPR J. 2018 Dec;1:431-439. doi: 10.1089/crispr.2018.0050. CRISPR J. 2018. PMID: 31021242

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