Powers NR - Search Results

1

Prdm9 and meiotic cohesin proteins cooperatively promote DNA double-strand break formation in mammalian spermatocytes.

Bhattacharyya T, Walker M, Powers NR, Brunton C, Fine AD, Petkov PM, Handel MA. Bhattacharyya T, et al. Among authors: powers nr. Curr Biol. 2021 Mar 22;31(6):1351. doi: 10.1016/j.cub.2021.03.002. Curr Biol. 2021. PMID: 33756132 Free PMC article. No abstract available.

2

Prdm9 and Meiotic Cohesin Proteins Cooperatively Promote DNA Double-Strand Break Formation in Mammalian Spermatocytes.

Bhattacharyya T, Walker M, Powers NR, Brunton C, Fine AD, Petkov PM, Handel MA. Bhattacharyya T, et al. Among authors: powers nr. Curr Biol. 2019 Mar 18;29(6):1002-1018.e7. doi: 10.1016/j.cub.2019.02.007. Epub 2019 Mar 7. Curr Biol. 2019. PMID: 30853435 Free PMC article.

3

Sexual dimorphism in the meiotic requirement for PRDM9: A mammalian evolutionary safeguard.

Powers NR, Dumont BL, Emori C, Lawal RA, Brunton C, Paigen K, Handel MA, Bolcun-Filas E, Petkov PM, Bhattacharyya T. Powers NR, et al. Sci Adv. 2020 Oct 23;6(43):eabb6606. doi: 10.1126/sciadv.abb6606. Print 2020 Oct. Sci Adv. 2020. PMID: 33097538 Free PMC article.

4

The Meiotic Recombination Activator PRDM9 Trimethylates Both H3K36 and H3K4 at Recombination Hotspots In Vivo.

Powers NR, Parvanov ED, Baker CL, Walker M, Petkov PM, Paigen K. Powers NR, et al. PLoS Genet. 2016 Jun 30;12(6):e1006146. doi: 10.1371/journal.pgen.1006146. eCollection 2016 Jun. PLoS Genet. 2016. PMID: 27362481 Free PMC article.

5

Affinity-seq detects genome-wide PRDM9 binding sites and reveals the impact of prior chromatin modifications on mammalian recombination hotspot usage.

Walker M, Billings T, Baker CL, Powers N, Tian H, Saxl RL, Choi K, Hibbs MA, Carter GW, Handel MA, Paigen K, Petkov PM. Walker M, et al. Epigenetics Chromatin. 2015 Sep 7;8:31. doi: 10.1186/s13072-015-0024-6. eCollection 2015. Epigenetics Chromatin. 2015. PMID: 26351520 Free PMC article.

6

Differential effects of two catalytic mutations on full-length PRDM9 and its isolated PR/SET domain reveal a case of pseudomodularity.

Powers NR, Billings T, Paigen K, Petkov PM. Powers NR, et al. Genetics. 2021 Dec 10;219(4):iyab172. doi: 10.1093/genetics/iyab172. Genetics. 2021. PMID: 34747456 Free PMC article.

7

Tissue-Specific Trans Regulation of the Mouse Epigenome.

Baker CL, Walker M, Arat S, Ananda G, Petkova P, Powers NR, Tian H, Spruce C, Ji B, Rausch D, Choi K, Petkov PM, Carter GW, Paigen K. Baker CL, et al. Among authors: powers nr. Genetics. 2019 Mar;211(3):831-845. doi: 10.1534/genetics.118.301697. Epub 2018 Dec 28. Genetics. 2019. PMID: 30593494 Free PMC article.

8

The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.

Powers NR, Eicher JD, Miller LL, Kong Y, Smith SD, Pennington BF, Willcutt EG, Olson RK, Ring SM, Gruen JR. Powers NR, et al. J Med Genet. 2016 Mar;53(3):163-71. doi: 10.1136/jmedgenet-2015-103418. Epub 2015 Dec 11. J Med Genet. 2016. PMID: 26660103 Free PMC article.

9

Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.

Powers NR, Eicher JD, Butter F, Kong Y, Miller LL, Ring SM, Mann M, Gruen JR. Powers NR, et al. Am J Hum Genet. 2013 Jul 11;93(1):19-28. doi: 10.1016/j.ajhg.2013.05.008. Epub 2013 Jun 6. Am J Hum Genet. 2013. PMID: 23746548 Free PMC article.

10

A dyslexia-associated variant in DCDC2 changes gene expression.

Meng H, Powers NR, Tang L, Cope NA, Zhang PX, Fuleihan R, Gibson C, Page GP, Gruen JR. Meng H, et al. Among authors: powers nr. Behav Genet. 2011 Jan;41(1):58-66. doi: 10.1007/s10519-010-9408-3. Epub 2010 Nov 2. Behav Genet. 2011. PMID: 21042874 Free PMC article.

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