Transgenic Models of Spinocerebellar Ataxia Type 10: Modeling a Repeat Expansion Disorder

Por McFarland, Karen N., Ashizawa, Tetsuo
Publicado em 2012

A case report of SPG11 mutations in a Chinese ARHSP-TCC family

Por Zhang, Linwei, McFarland, Karen N., Jiao, Jinsong, Jiao, Yujuan
Publicado no BMC Neurol (2016)

Purkinje Cell Loss is the Major Brain Pathology of Spinocerebellar Ataxia Type 10

Por Xia, Guangbin, McFarland, Karen N., Wang, Kang, Sarkar, Partha S., Yachnis, Anthony T., Ashizawa, Tetsuo
Publicado em 2013

SPG7 and Impaired Emotional Communication

Por Zhang, Linwei, McFarland, Karen N., Subramony, S.H., Heilman, Kenneth M., Ashizawa, Tetsuo
Publicado no Cerebellum (2017)

Inheritance patterns of ATCCT repeat interruptions in spinocerebellar ataxia type 10 (SCA10) expansions

Por Landrian, Ivette, McFarland, Karen N., Liu, Jilin, Mulligan, Connie J., Rasmussen, Astrid, Ashizawa, Tetsuo
Publicado no PLoS One (2017)

SMRT Sequencing of Long Tandem Nucleotide Repeats in SCA10 Reveals Unique Insight of Repeat Expansion Structure

Por McFarland, Karen N., Liu, Jilin, Landrian, Ivette, Godiska, Ronald, Shanker, Savita, Yu, Fahong, Farmerie, William G., Ashizawa, Tetsuo
Publicado no PLoS One (2015)

Characterization of harpy/Rca1/emi1 mutants: Patterning in the absence of cell division

Por Riley, Bruce B., Sweet, Elly M., Heck, Rebecca, Evans, Adrienne, McFarland, Karen N., Warga, Rachel M., Kane, Donald A.
Publicado em 2010

Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease

Por Leonardi, Luca, Marcotulli, Christian, McFarland, Karen N., Tessa, Alessandra, DiFabio, Roberto, Santorelli, Filippo M, Pierelli, Francesco, Ashizawa, Tetsuo, Casali, Carlo
Publicado no J Neurol (2014)

Expansion of the Spinocerebellar Ataxia Type 10 (SCA10) Repeat in a Patient with Sioux Native American Ancestry

Por Bushara, Khalaf, Bower, Matthew, Liu, Jilin, McFarland, Karen N., Landrian, Ivette, Hutter, Diane, Teive, Hélio A. G., Rasmussen, Astrid, Mulligan, Connie J., Ashizawa, Tetsuo
Publicado em 2013

MeCP2: a novel Huntingtin interactor

Por McFarland, Karen N., Huizenga, Megan N., Darnell, Shayna B., Sangrey, Gavin R., Berezovska, Oksana, Cha, Jang-Ho J., Outeiro, Tiago F., Sadri-Vakili, Ghazaleh
Publicado em 2014

Spinocerebellar ataxia type 10 in Chinese Han

Por Wang, Kang, McFarland, Karen N., Liu, Jilin, Zeng, Desmond, Landrian, Ivette, Xia, Guangbin, Hao, Ying, Jin, Miao, Mulligan, Connie J., Gu, Weihong, Ashizawa, Tetsuo
Publicado no Neurol Genet (2015)

Repeat interruptions in spinocerebellar ataxia type 10 expansions are strongly associated with epileptic seizures

Por McFarland, Karen N., Liu, Jilin, Landrian, Ivette, Zeng, Desmond, Raskin, Salmo, Moscovich, Mariana, Gatto, Emilia M., Ochoa, Adriana, Teive, Hélio A. G., Rasmussen, Astrid, Ashizawa, Tetsuo
Publicado em 2013

Huntingtin Modulates Transcription, Occupies Gene Promoters In Vivo, and Binds Directly to DNA in a Polyglutamine-Dependent Manner

Por Benn, Caroline L., Sun, Tingting, Sadri-Vakili, Ghazaleh, McFarland, Karen N., DiRocco, Derek P., Yohrling, George J., Clark, Timothy W., Bouzou, Bérengère, Cha, Jang-Ho J.
Publicado em 2008

Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability

Por McFarland, Karen N, Liu, Jilin, Landrian, Ivette, Gao, Rui, Sarkar, Partha S, Raskin, Salmo, Moscovich, Mariana, Gatto, Emilia M, Teive, Hélio A G, Ochoa, Adriana, Rasmussen, Astrid, Ashizawa, Tetsuo
Publicado em 2013

Genome-Wide Histone Acetylation Is Altered in a Transgenic Mouse Model of Huntington's Disease

Por McFarland, Karen N., Das, Sudeshna, Sun, Ting Ting, Leyfer, Dmitri, Xia, Eva, Sangrey, Gavin R., Kuhn, Alexandre, Luthi-Carter, Ruth, Clark, Timothy W., Sadri-Vakili, Ghazaleh, Cha, Jang-Ho J.
Publicado em 2012

Parkinson’s disease associated with pure ATXN10 repeat expansion

Por Schüle, Birgitt, McFarland, Karen N., Lee, Kelsey, Tsai, Yu-Chih, Nguyen, Khanh-Dung, Sun, Chao, Liu, Mei, Byrne, Christie, Gopi, Ramesh, Huang, Neng, Langston, J. William, Clark, Tyson, Gil, Francisco Javier Jiménez, Ashizawa, Tetsudo
Publicado no NPJ Parkinsons Dis (2017)