Sox6, Jack of all trades: A versatile regulatory protein in vertebrate development

Por Hagiwara, Nobuko
Publicado em 2011

Application of active learning modalities to achieve medical genetics competencies and their learning outcome assessments

Por Hagiwara, Nobuko
Publicado no Adv Med Educ Pract (2017)

Genome-wide mapping of Sox6 binding sites in skeletal muscle reveals both direct and indirect regulation of muscle terminal differentiation by Sox6

Por An, Chung-Il, Dong, Yao, Hagiwara, Nobuko
Publicado em 2011

Trip12, a HECT domain E3 ubiquitin ligase, targets Sox6 for proteasomal degradation and affects fiber type-specific gene expression in muscle cells

Por An, Chung-Il, Ganio, Edward, Hagiwara, Nobuko
Publicado em 2013

Transcriptome Dynamics and Potential Roles of Sox6 in the Postnatal Heart

Por An, Chung-Il, Ichihashi, Yasunori, Peng, Jie, Sinha, Neelima R., Hagiwara, Nobuko
Publicado no PLoS One (2016)

Sox6 regulation of cardiac myocyte development

Por Cohen-Barak, Orit, Yi, Zanhua, Hagiwara, Nobuko, Monzen, Koshiro, Komuro, Issei, Brilliant, Murray H.
Publicado em 2003

Sox6 is a candidate gene for p(100H) myopathy, heart block, and sudden neonatal death

Por Hagiwara, Nobuko, Klewer, Scott E., Samson, Ricardo A., Erickson, Drew T., Lyon, Mary F., Brilliant, Murray H.
Publicado em 2000

Mutations in the Human Orthologue of the Mouse underwhite Gene (uw) Underlie a New Form of Oculocutaneous Albinism, OCA4

Por Newton, J. M., Cohen-Barak, Orit, Hagiwara, Nobuko, Gardner, John M., Davisson, Muriel T., King, Richard A., Brilliant, Murray H.
Publicado em 2001

Expression of Sox genes in tooth development

Por KAWASAKI, KATSUSHIGE, KAWASAKI, MAIKO, WATANABE, MOMOKO, IDRUS, ERIK, NAGAI, TAKAHIRO, OOMMEN, SHELLY, MAEDA, TAKEYASU, HAGIWARA, NOBUKO, QUE, JIANWEN, SHARPE, PAUL T., OHAZAMA, ATSUSHI
Publicado no Int J Dev Biol (2015)

Sox6 Directly Silences Epsilon Globin Expression in Definitive Erythropoiesis

Por Yi, Zanhua, Cohen-Barak, Orit, Hagiwara, Nobuko, Kingsley, Paul D, Fuchs, Deborah A, Erickson, Drew T, Epner, Elliot M, Palis, James, Brilliant, Murray H
Publicado em 2006

The mouse pale ear (ep) mutation is the homologue of human Hermansky–Pudlak syndrome

Por Gardner, John M., Wildenberg, Scott C., Keiper, Natalie M., Novak, Edward K., Rusiniak, Michael E., Swank, Richard T., Puri, Neelu, Finger, Joshua N., Hagiwara, Nobuko, Lehman, Anne L., Gales, Tracy L., Bayer, Manfred E., King, Richard A., Brilliant, Murray H.
Publicado em 1997

Mice devoid of γ-aminobutyrate type A receptor β3 subunit have epilepsy, cleft palate, and hypersensitive behavior

Por Homanics, Gregg E., DeLorey, Timothy M., Firestone, Leonard L., Quinlan, Joseph J., Handforth, Adrian, Harrison, Neil L., Krasowski, Matthew D., Rick, Caroline E. M., Korpi, Esa R., Mäkelä, Riikka, Brilliant, Murray H., Hagiwara, Nobuko, Ferguson, Carolyn, Snyder, Kimberly, Olsen, Richard W.
Publicado em 1997

Mutations in Grxcr1 Are The Basis for Inner Ear Dysfunction in the Pirouette Mouse

Por Odeh, Hana, Hunker, Kristina L., Belyantseva, Inna A., Azaiez, Hela, Avenarius, Matthew R., Zheng, Lili, Peters, Linda M., Gagnon, Leona H., Hagiwara, Nobuko, Skynner, Michael J., Brilliant, Murray H., Allen, Nicholas D., Riazuddin, Saima, Johnson, Kenneth R., Raphael, Yehoash, Najmabadi, Hossein, Friedman, Thomas B., Bartles, James R., Smith, Richard J.H., Kohrman, David C.
Publicado em 2010