Paylor R - Search Results

1

Phenotypic characterization of Bbs4 null mice reveals age-dependent penetrance and variable expressivity.

Eichers ER, Abd-El-Barr MM, Paylor R, Lewis RA, Bi W, Lin X, Meehan TP, Stockton DW, Wu SM, Lindsay E, Justice MJ, Beales PL, Katsanis N, Lupski JR. Eichers ER, et al. Among authors: paylor r. Hum Genet. 2006 Sep;120(2):211-26. doi: 10.1007/s00439-006-0197-y. Epub 2006 Jun 23. Hum Genet. 2006. PMID: 16794820

2

Rai1 deficiency in mice causes learning impairment and motor dysfunction, whereas Rai1 heterozygous mice display minimal behavioral phenotypes.

Bi W, Yan J, Shi X, Yuva-Paylor LA, Antalffy BA, Goldman A, Yoo JW, Noebels JL, Armstrong DL, Paylor R, Lupski JR. Bi W, et al. Among authors: paylor r. Hum Mol Genet. 2007 Aug 1;16(15):1802-13. doi: 10.1093/hmg/ddm128. Epub 2007 May 21. Hum Mol Genet. 2007. PMID: 17517686

3

Enriched rearing improves behavioral responses of an animal model for CNV-based autistic-like traits.

Lacaria M, Spencer C, Gu W, Paylor R, Lupski JR. Lacaria M, et al. Among authors: paylor r. Hum Mol Genet. 2012 Jul 15;21(14):3083-96. doi: 10.1093/hmg/dds124. Epub 2012 Apr 5. Hum Mol Genet. 2012. PMID: 22492990 Free PMC article.

4

Behavioral characterization of mouse models for Smith-Magenis syndrome and dup(17)(p11.2p11.2).

Walz K, Spencer C, Kaasik K, Lee CC, Lupski JR, Paylor R. Walz K, et al. Among authors: paylor r. Hum Mol Genet. 2004 Feb 15;13(4):367-78. doi: 10.1093/hmg/ddh044. Epub 2004 Jan 6. Hum Mol Genet. 2004. PMID: 14709593

5

Mouse models of 22q11 deletion syndrome.

Paylor R, Lindsay E. Paylor R, et al. Biol Psychiatry. 2006 Jun 15;59(12):1172-9. doi: 10.1016/j.biopsych.2006.01.018. Epub 2006 Apr 17. Biol Psychiatry. 2006. PMID: 16616724 Review.

6

Mice deleted for the DiGeorge/velocardiofacial syndrome region show abnormal sensorimotor gating and learning and memory impairments.

Paylor R, McIlwain KL, McAninch R, Nellis A, Yuva-Paylor LA, Baldini A, Lindsay EA. Paylor R, et al. Hum Mol Genet. 2001 Nov 1;10(23):2645-50. doi: 10.1093/hmg/10.23.2645. Hum Mol Genet. 2001. PMID: 11726551

7

Rai1 duplication causes physical and behavioral phenotypes in a mouse model of dup(17)(p11.2p11.2).

Walz K, Paylor R, Yan J, Bi W, Lupski JR. Walz K, et al. Among authors: paylor r. J Clin Invest. 2006 Nov;116(11):3035-41. doi: 10.1172/JCI28953. Epub 2006 Oct 5. J Clin Invest. 2006. PMID: 17024248 Free PMC article.

8

Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: implications for 22q11 deletion syndrome.

Paylor R, Glaser B, Mupo A, Ataliotis P, Spencer C, Sobotka A, Sparks C, Choi CH, Oghalai J, Curran S, Murphy KC, Monks S, Williams N, O'Donovan MC, Owen MJ, Scambler PJ, Lindsay E. Paylor R, et al. Proc Natl Acad Sci U S A. 2006 May 16;103(20):7729-34. doi: 10.1073/pnas.0600206103. Epub 2006 May 9. Proc Natl Acad Sci U S A. 2006. PMID: 16684884 Free PMC article.

9

Exaggerated behavioral phenotypes in Fmr1/Fxr2 double knockout mice reveal a functional genetic interaction between Fragile X-related proteins.

Spencer CM, Serysheva E, Yuva-Paylor LA, Oostra BA, Nelson DL, Paylor R. Spencer CM, et al. Among authors: paylor r. Hum Mol Genet. 2006 Jun 15;15(12):1984-94. doi: 10.1093/hmg/ddl121. Epub 2006 May 4. Hum Mol Genet. 2006. PMID: 16675531

10

Abnormalities of social interactions and home-cage behavior in a mouse model of Rett syndrome.

Moretti P, Bouwknecht JA, Teague R, Paylor R, Zoghbi HY. Moretti P, et al. Among authors: paylor r. Hum Mol Genet. 2005 Jan 15;14(2):205-20. doi: 10.1093/hmg/ddi016. Epub 2004 Nov 17. Hum Mol Genet. 2005. PMID: 15548546

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