Structural basis of protein complex formation and reconfiguration by polyglutamine disease protein Ataxin-1 and Capicua

Por Kim, Eunji, Lu, Hsiang-Chih, Zoghbi, Huda Y., Song, Ji-Joon
Publicado em 2013

Calvarial Langerhans cell histiocytosis in an Adult: Typical imaging findings in an atypical age group

Por Samara, Amjad, Nepute, Jordan, Lu, Hsiang-Chih, Perrin, Richard J., Eldaya, Rami W.
Publicado no Radiol Case Rep (2019)

In vivo evolution of biopsy‐proven inflammatory demyelination quantified by R2t* mapping

Por Xiang, Biao, Wen, Jie, Lu, Hsiang‐Chih, Schmidt, Robert E., Yablonskiy, Dmitriy A., Cross, Anne H.
Publicado no Ann Clin Transl Neurol (2020)

Aberrant ATRX protein expression is associated with poor overall survival in NF1-MPNST

Por Lu, Hsiang-Chih, Eulo, Vanessa, Apicelli, Anthony J., Pekmezci, Melike, Tao, Yu, Luo, Jingqin, Hirbe, Angela C., Dahiya, Sonika
Publicado no Oncotarget (2018)

Loss of Capicua alters early T cell development and predisposes mice to T cell lymphoblastic leukemia/lymphoma

Por Tan, Qiumin, Brunetti, Lorenzo, Rousseaux, Maxime W. C., Lu, Hsiang-Chih, Wan, Ying-Wooi, Revelli, Jean-Pierre, Liu, Zhandong, Goodell, Margaret A., Zoghbi, Huda Y.
Publicado no Proc Natl Acad Sci U S A (2018)

Drosophila Tempura, a Novel Protein Prenyltransferase α Subunit, Regulates Notch Signaling Via Rab1 and Rab11

Por Charng, Wu-Lin, Yamamoto, Shinya, Jaiswal, Manish, Bayat, Vafa, Xiong, Bo, Zhang, Ke, Sandoval, Hector, David, Gabriela, Gibbs, Stephen, Lu, Hsiang-Chih, Chen, Kuchuan, Giagtzoglou, Nikos, Bellen, Hugo J.
Publicado em 2014

Extensive cryptic splicing upon loss of RBM17 and TDP43 in neurodegeneration models

Por Tan, Qiumin, Yalamanchili, Hari Krishna, Park, Jeehye, De Maio, Antonia, Lu, Hsiang-Chih, Wan, Ying-Wooi, White, Joshua J., Bondar, Vitaliy V., Sayegh, Layal S., Liu, Xiuyun, Gao, Yan, Sillitoe, Roy V., Orr, Harry T., Liu, Zhandong, Zoghbi, Huda Y.
Publicado no Hum Mol Genet (2016)

ATXN1-CIC Complex Is the Primary Driver of Cerebellar Pathology in Spinocerebellar Ataxia Type 1 through a Gain-of-Function Mechanism

Por Rousseaux, Maxime W.C., Tschumperlin, Tyler, Lu, Hsiang-Chih, Lackey, Elizabeth P., Bondar, Vitaliy V., Wan, Ying-Wooi, Tan, Qiumin, Adamski, Carolyn J., Friedrich, Jillian, Twaroski, Kirk, Chen, Weili, Tolar, Jakub, Henzler, Christine, Sharma, Ajay, Bajić, Aleksandar, Lin, Tao, Duvick, Lisa, Liu, Zhandong, Sillitoe, Roy V., Zoghbi, Huda Y., Orr, Harry T.
Publicado no Neuron (2018)

Genetic screens reveal RAS/MAPK/MSK1 modulate ataxin 1 protein levels and toxicity in SCA1

Por Park, Jeehye, Al-Ramahi, Ismael, Tan, Qiumin, Mollema, Nissa, Diaz-Garcia, Javier R., Gallego-Flores, Tatiana, Lu, Hsiang-Chih, Lagalwar, Sarita, Duvick, Lisa, Kang, Hyojin, Lee, Yoontae, Jafar-Nejad, Paymaan, Sayegh, Layal S., Richman, Ronald, Liu, Xiuyun, Gao, Yan, Shaw, Chad A., Arthur, J. Simon C., Orr, Harry T., Westbrook, Thomas F., Botas, Juan, Zoghbi, Huda Y.
Publicado em 2013

Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans

Por Lu, Hsiang-Chih, Tan, Qiumin, Rousseaux, Maxime WC, Wang, Wei, Kim, Ji-Yoen, Richman, Ronald, Wan, Ying-Wooi, Yeh, Szu-Ying, Patel, Jay M, Liu, Xiuyun, Lin, Tao, Lee, Yoontae, Fryer, John D, Han, Jing, Chahrour, Maria, Finnell, Richard H, Lei, Yunping, Zurita-Jimenez, Maria E, Ahimaz, Priyanka, Anyane-Yeboa, Kwame, Van Maldergem, Lionel, Lehalle, Daphne, Jean-Marcais, Nolwenn, Mosca-Boidron, Anne-Laure, Thevenon, Julien, Cousin, Margot A, Bro, Della E, Lanpher, Brendan C, Klee, Eric W, Alexander, Nora, Bainbridge, Matthew N, Orr, Harry T, Sillitoe, Roy V, Ljungberg, M. Cecilia, Liu, Zhandong, Schaaf, Christian P, Zoghbi, Huda Y
Publicado no Nat Genet (2017)