Actinin-associated LIM Protein: Identification of a Domain Interaction between PDZ and Spectrin-like Repeat Motifs

Por Xia, Houhui, Winokur, Sara T., Kuo, Wen-Lin, Altherr, Michael R., Bredt, David S.
Publicado em 1997

RNAPol-ChIP Analysis of Transcription from FSHD-Linked Tandem Repeats and Satellite DNA

Por Alexiadis, Vassilios, Ballestas, Mary E., Sanchez, Cecilia, Winokur, Sara, Vedanarayanan, Vettaikorumakankav, Warren, Mary, Ehrlich, Melanie
Publicado em 2006

Gene Selection for Multiclass Prediction by Weighted Fisher Criterion

Por Xuan, Jianhua, Wang, Yue, Dong, Yibin, Feng, Yuanjian, Wang, Bin, Khan, Javed, Bakay, Maria, Wang, Zuyi, Pachman, Lauren, Winokur, Sara, Chen, Yi-Wen, Clarke, Robert, Hoffman, Eric
Publicado em 2007

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei

Por Masny, Peter S, Chan, On Ying A, de Greef, Jessica C, Bengtsson, Ulla, Ehrlich, Melanie, Tawil, Rabi, Lock, Leslie F, Hewitt, Jane E, Stocksdale, Jennifer, Martin, Jorge H, van der Maarel, Silvere M, Winokur, Sara T
Publicado em 2010

DUX4, a candidate gene of facioscapulohumeral muscular dystrophy, encodes a transcriptional activator of PITX1

Por Dixit, Manjusha, Ansseau, Eugénie, Tassin, Alexandra, Winokur, Sara, Shi, Rongye, Qian, Hong, Sauvage, Sébastien, Mattéotti, Christel, van Acker, Anne M., Leo, Oberdan, Figlewicz, Denise, Barro, Marietta, Laoudj-Chenivesse, Dalila, Belayew, Alexandra, Coppée, Frédérique, Chen, Yi-Wen
Publicado em 2007

RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

Por Snider, Lauren, Asawachaicharn, Amy, Tyler, Ashlee E., Geng, Linda N., Petek, Lisa M., Maves, Lisa, Miller, Daniel G., Lemmers, Richard J.L.F., Winokur, Sara T., Tawil, Rabi, van der Maarel, Silvère M., Filippova, Galina N., Tapscott, Stephen J.
Publicado em 2009

Specific Loss of Histone H3 Lysine 9 Trimethylation and HP1γ/Cohesin Binding at D4Z4 Repeats Is Associated with Facioscapulohumeral Dystrophy (FSHD)

Por Zeng, Weihua, de Greef, Jessica C., Chen, Yen-Yun, Chien, Richard, Kong, Xiangduo, Gregson, Heather C., Winokur, Sara T., Pyle, April, Robertson, Keith D., Schmiesing, John A., Kimonis, Virginia E., Balog, Judit, Frants, Rune R., Ball, Alexander R., Lock, Leslie F., Donovan, Peter J., van der Maarel, Silvère M., Yokomori, Kyoko
Publicado em 2009

Induced Pluripotent Stem Cells from Patients with Huntington’s Disease Show CAG Repeat Expansion Associated Phenotypes

Por Mattis, Virginia B, Svendsen, Soshana P, Ebert, Allison, Svendsen, Clive N, King, Alvin R, Casale, Malcolm, Winokur, Sara T, Batugedara, Gayani, Vawter, Marquis, Donovan, Peter J, Lock, Leslie F, Thompson, Leslie M, Zhu, Yu, Fossale, Elisa, Singh Atwal, Ranjit, Gillis, Tammy, Mysore, Jayalakshmi, Li, Jian-hong, Seong, IhnSik, Shen, Yiping, Chen, Xiaoli, Wheeler, Vanessa C, MacDonald, Marcy E, Gusella, James F, Akimov, Sergey, Arbez, Nicolas, Juopperi, Tarja, Ratovitski, Tamara, Chiang, Jason H, Kim, Woon Roung, Chighladze, Eka, Watkin, Erin, Zhong, Chun, Makri, Georgia, Cole, Robert N, Margolis, Russell L, Song, Hongjun, Ming, Guoli, Ross, Christopher A, Kaye, Julia A, Daub, Aaron, Sharma, Punita, Mason, Amanda R, Finkbeiner, Steven, Yu, Junying, Thomson, James A, Rushton, David, Brazier, Stephen P, Battersby, Alysia A, Redfern, Amanda, Tseng, Hsui-Er, Harrison, Alexander W, Kemp, Paul J, Allen, Nicholas D, Onorati, Marco, Castiglioni, Valentina, Cattaneo, Elena, Arjomand, Jamshid
Publicado em 2012