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

بواسطة Powers, Natalie R., Parvanov, Emil D., Baker, Christopher L., Walker, Michael, Petkov, Petko M., Paigen, Kenneth
الحاوية / القاعدة PLoS Genet (2016)

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

بواسطة Bhattacharyya, Tanmoy, Walker, Michael, Powers, Natalie R, Brunton, Catherine, Fine, Alexander D, Petkov, Petko M, Handel, Mary Ann
الحاوية / القاعدة Curr Biol (2019)

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

بواسطة Bhattacharyya, Tanmoy, Walker, Michael, Powers, Natalie R., Brunton, Catherine, Fine, Alexander D., Petkov, Petko M., Handel, Mary Ann
الحاوية / القاعدة Curr Biol (2021)

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

بواسطة Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
منشور في 2013

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

بواسطة Powers, Natalie R., Eicher, John D., Butter, Falk, Kong, Yong, Miller, Laura L., Ring, Susan M., Mann, Matthias, Gruen, Jeffrey R.
منشور في 2014

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

بواسطة Meng, Haiying, Powers, Natalie R., Tang, Ling, Cope, Natalie A., Zhang, Ping-Xia, Fuleihan, Ramsay, Gibson, Christopher, Page, Grier P., Gruen, Jeffrey R.
منشور في 2010

Associations of Prenatal Nicotine Exposure and the Dopamine Related Genes ANKK1 and DRD2 to Verbal Language

بواسطة Eicher, John D., Powers, Natalie R., Cho, Kelly, Miller, Laura L., Mueller, Kathryn L., Ring, Susan M., Tomblin, J. Bruce, Gruen, Jeffrey R.
منشور في 2013

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

بواسطة Powers, Natalie R., Dumont, Beth L., Emori, Chihiro, Lawal, Raman Akinyanju, Brunton, Catherine, Paigen, Kenneth, Handel, Mary Ann, Bolcun-Filas, Ewelina, Petkov, Petko M., Bhattacharyya, Tanmoy
الحاوية / القاعدة Sci Adv (2020)

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

بواسطة Powers, Natalie R, Eicher, John D, Miller, Laura L, Kong, Yong, Smith, Shelley D, Pennington, Bruce F, Willcutt, Erik G, Olson, Richard K, Ring, Susan M, Gruen, Jeffrey R
الحاوية / القاعدة J Med Genet (2016)

Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages

بواسطة DeMille, Mellissa M. C., Tang, Kevin, Mehta, Chintan M., Geissler, Christopher, Malins, Jeffrey G., Powers, Natalie R., Bowen, Beatrice M., Adams, Andrew K., Truong, Dongnhu T., Frijters, Jan C., Gruen, Jeffrey R.
الحاوية / القاعدة Proc Natl Acad Sci U S A (2018)

Tissue-Specific Trans Regulation of the Mouse Epigenome

بواسطة Baker, Christopher L., Walker, Michael, Arat, Seda, Ananda, Guruprasad, Petkova, Pavlina, Powers, Natalie R., Tian, Hui, Spruce, Catrina, Ji, Bo, Rausch, Dylan, Choi, Kwangbom, Petkov, Petko M., Carter, Gregory W., Paigen, Kenneth
الحاوية / القاعدة Genetics (2019)

Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQ

بواسطة Eicher, John D., Powers, Natalie R., Miller, Laura L., Mueller, Kathryn L., Mascheretti, Sara, Marino, Cecilia, Willcutt, Erik G., DeFries, John C., Olson, Richard K., Smith, Shelley D., Pennington, Bruce F., Tomblin, J. Bruce, Ring, Susan M., Gruen, Jeffrey R.
منشور في 2014