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

par Hagiwara, Nobuko
Publié 2011

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

par Hagiwara, Nobuko
Publié dans 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

par An, Chung-Il, Dong, Yao, Hagiwara, Nobuko
Publié 2011

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

par An, Chung-Il, Ganio, Edward, Hagiwara, Nobuko
Publié 2013

Transcriptome Dynamics and Potential Roles of Sox6 in the Postnatal Heart

par An, Chung-Il, Ichihashi, Yasunori, Peng, Jie, Sinha, Neelima R., Hagiwara, Nobuko
Publié dans PLoS One (2016)

Sox6 regulation of cardiac myocyte development

par Cohen-Barak, Orit, Yi, Zanhua, Hagiwara, Nobuko, Monzen, Koshiro, Komuro, Issei, Brilliant, Murray H.
Publié 2003

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

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

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

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

Expression of Sox genes in tooth development

par KAWASAKI, KATSUSHIGE, KAWASAKI, MAIKO, WATANABE, MOMOKO, IDRUS, ERIK, NAGAI, TAKAHIRO, OOMMEN, SHELLY, MAEDA, TAKEYASU, HAGIWARA, NOBUKO, QUE, JIANWEN, SHARPE, PAUL T., OHAZAMA, ATSUSHI
Publié dans Int J Dev Biol (2015)

Sox6 Directly Silences Epsilon Globin Expression in Definitive Erythropoiesis

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

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

par 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.
Publié 1997

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

par 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.
Publié 1997

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

par 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.
Publié 2010