Picketts DJ - Search Results

1

Retinal interneuron survival requires non-cell-autonomous Atrx activity.

Lagali PS, Medina CF, Zhao BY, Yan K, Baker AN, Coupland SG, Tsilfidis C, Wallace VA, Picketts DJ. Lagali PS, et al. Among authors: picketts dj. Hum Mol Genet. 2016 Nov 1;25(21):4787-4803. doi: 10.1093/hmg/ddw306. Hum Mol Genet. 2016. PMID: 28173139

2

Personal journeys to and in human genetics and dysmorphology.

Schwartz CE, Aylsworth AS, Allanson J, Battaglia A, Carey JC, Curry CJ, Davies KE, Eichler EE, Graham JM Jr, Hall B, Hall JG, Holmes LB, Hoyme HE, Hunter A, Innis J, Johnson J, Keppler-Noreuil KM, Leroy JG, Moore C, Nelson DL, Neri G, Opitz JM, Picketts D, Raymond FL, Shalev SA, Stevenson RE, Stumpel CTRM, Sutherland G, Viskochil DH, Weaver DD, Zackai EH. Schwartz CE, et al. Am J Med Genet A. 2024 Jun;194(6):e63514. doi: 10.1002/ajmg.a.63514. Epub 2024 Feb 8. Am J Med Genet A. 2024. PMID: 38329159

3

Conditional Activation of c-MYC in Distinct Catecholaminergic Cells Drives Development of Neuroblastoma or Somatostatinoma.

Wang T, Liu L, Fang J, Jin H, Natarajan S, Sheppard H, Lu M, Turner G, Confer T, Johnson M, Steinberg J, Ha L, Yadak N, Jain R, Picketts DJ, Ma X, Murphy A, Davidoff AM, Glazer ES, Easton J, Chen X, Wang R, Yang J. Wang T, et al. Among authors: picketts dj. Cancer Res. 2024 Nov 12. doi: 10.1158/0008-5472.CAN-24-1142. Online ahead of print. Cancer Res. 2024. PMID: 39531507

4

ATRX encodes a novel member of the SNF2 family of proteins: mutations point to a common mechanism underlying the ATR-X syndrome.

Picketts DJ, Higgs DR, Bachoo S, Blake DJ, Quarrell OW, Gibbons RJ. Picketts DJ, et al. Hum Mol Genet. 1996 Dec;5(12):1899-907. doi: 10.1093/hmg/5.12.1899. Hum Mol Genet. 1996. PMID: 8968741

5

Cell cycle-dependent phosphorylation of the ATRX protein correlates with changes in nuclear matrix and chromatin association.

Bérubé NG, Smeenk CA, Picketts DJ. Bérubé NG, et al. Among authors: picketts dj. Hum Mol Genet. 2000 Mar 1;9(4):539-47. doi: 10.1093/hmg/9.4.539. Hum Mol Genet. 2000. PMID: 10699177

6

Neurodevelopmental defects resulting from ATRX overexpression in transgenic mice.

Bérubé NG, Jagla M, Smeenk C, De Repentigny Y, Kothary R, Picketts DJ. Bérubé NG, et al. Among authors: picketts dj. Hum Mol Genet. 2002 Feb 1;11(3):253-61. doi: 10.1093/hmg/11.3.253. Hum Mol Genet. 2002. PMID: 11823444

7

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.

Bérubé NG, Mangelsdorf M, Jagla M, Vanderluit J, Garrick D, Gibbons RJ, Higgs DR, Slack RS, Picketts DJ. Bérubé NG, et al. Among authors: picketts dj. J Clin Invest. 2005 Feb;115(2):258-67. doi: 10.1172/JCI22329. J Clin Invest. 2005. PMID: 15668733 Free PMC article.

8

Patient mutations alter ATRX targeting to PML nuclear bodies.

Bérubé NG, Healy J, Medina CF, Wu S, Hodgson T, Jagla M, Picketts DJ. Bérubé NG, et al. Among authors: picketts dj. Eur J Hum Genet. 2008 Feb;16(2):192-201. doi: 10.1038/sj.ejhg.5201943. Epub 2007 Oct 24. Eur J Hum Genet. 2008. PMID: 17957225

9

Characterization of novel isoforms and evaluation of SNF2L/SMARCA1 as a candidate gene for X-linked mental retardation in 12 families linked to Xq25-26.

Lazzaro MA, Todd MA, Lavigne P, Vallee D, De Maria A, Picketts DJ. Lazzaro MA, et al. Among authors: picketts dj. BMC Med Genet. 2008 Feb 26;9:11. doi: 10.1186/1471-2350-9-11. BMC Med Genet. 2008. PMID: 18302774 Free PMC article.

10

Altered visual function and interneuron survival in Atrx knockout mice: inference for the human syndrome.

Medina CF, Mazerolle C, Wang Y, Bérubé NG, Coupland S, Gibbons RJ, Wallace VA, Picketts DJ. Medina CF, et al. Among authors: picketts dj. Hum Mol Genet. 2009 Mar 1;18(5):966-77. doi: 10.1093/hmg/ddn424. Epub 2008 Dec 16. Hum Mol Genet. 2009. PMID: 19088125

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