Further evidence for the role of IP(3)R(1) in regulating subsynaptic gene expression and neuromuscular transmission

Por Zhu, Haipeng, Gomez, Christopher M.
Publicado em 2012

Revelations from a bicistronic calcium channel gene

Por Du, Xiaofei, Semler, Bert L, Gomez, Christopher M
Publicado em 2014

Cerebrospinal Fluid Biomarkers in Spinocerebellar Ataxia: A Pilot Study

Por Brouillette, Ashley M., Öz, Gülin, Gomez, Christopher M.
Publicado no Dis Markers (2015)

Skeletal Muscle IP(3)R(1) Receptors Amplify Physiological and Pathological Synaptic Calcium Signals

Por Zhu, Haipeng, Bhattacharyya, Bula J., Lin, Hong, Gomez, Christopher M.
Publicado em 2011

Skeletal Muscle Calpain Acts through Nitric Oxide and Neural miRNAs to Regulate Acetylcholine Release in Motor Nerve Terminals

Por Zhu, Haipeng, Bhattacharyya, Bula J., Lin, Hong, Gomez, Christopher M.
Publicado em 2013

An miRNA-mediated therapy for SCA6 blocks IRES-driven translation of the CACNA1A second cistron

Por Miyazaki, Yu, Du, Xiaofei, Muramatsu, Shin-ichi, Gomez, Christopher M.
Publicado no Sci Transl Med (2016)

Dominant-Negative Suppression of Ca(v)2.1 Currents by α(1)2.1 Truncations Requires the Conserved Interaction Domain for β Subunits

Por Raike, Robert S., Kordasiewicz, Holly B., Thompson, Randall M., Gomez, Christopher M.
Publicado em 2006

Loss of Intrinsic Organization of Cerebellar Networks in Spinocerebellar Ataxia Type 1: Correlates with Disease Severity and Duration

Por Solodkin, Ana, Peri, Eitan, Chen, E. Elinor, Ben-Jacob, Eshel, Gomez, Christopher M.
Publicado em 2011

Mammalian polycistronic mRNAs and disease

Por Karginov, Timofey A., Hejazi Pastor, Daniel Parviz, Semler, Bert L., Gomez, Christopher M.
Publicado no Trends Genet (2016)

Distinct Neurochemical Profiles of Spinocerebellar Ataxias 1, 2, 6, and Cerebellar Multiple System Atrophy

Por Öz, Gülin, Iltis, Isabelle, Hutter, Diane, Thomas, William, Bushara, Khalaf O., Gomez, Christopher M.
Publicado em 2011

Polyglutamine length-dependent toxicity from α1ACT in Drosophila models of spinocerebellar ataxia type 6

Por Tsou, Wei-Ling, Qiblawi, Sultan H., Hosking, Ryan R., Gomez, Christopher M., Todi, Sokol V.
Publicado no Biol Open (2016)

Retinal Nerve Fibre Layer and Macular Thinning in Spinocerebellar Ataxia and Cerebellar Multisystem Atrophy

Por Pula, John H., Towle, Vernon L., Staszak, Victoria M., Cao, Dingcai, Bernard, Jacqueline T., Gomez, Christopher M.
Publicado em 2011

A second cistron in the CACNA1A gene encodes a transcription factor that mediates cerebellar development and SCA6

Por Du, Xiaofei, Wang, Jun, Zhu, Haipeng, Rinaldo, Lorenzo, Lamar, Kay-Marie, Palmenberg, Ann C., Hansel, Christian, Gomez, Christopher M.
Publicado em 2013

(1)H MR Spectroscopy in Friedreich's Ataxia and Ataxia with Oculomotor Apraxia Type 2

Por Iltis, Isabelle, Hutter, Diane, Bushara, Khalaf O., Clark, H. Brent, Gross, Myron, Eberly, Lynn E., Gomez, Christopher M., Öz, Gülin
Publicado em 2010

DnaJ-1 and karyopherin α3 suppress degeneration in a new Drosophila model of Spinocerebellar Ataxia Type 6

Por Tsou, Wei-Ling, Hosking, Ryan R., Burr, Aaron A., Sutton, Joanna R., Ouyang, Michelle, Du, Xiaofei, Gomez, Christopher M., Todi, Sokol V.
Publicado no Hum Mol Genet (2015)

NEUROCHEMICAL ALTERATIONS IN SPINOCEREBELLAR ATAXIA TYPE 1 AND THEIR CORRELATIONS WITH CLINICAL STATUS

Por Öz, Gülin, Hutter, Diane, Tkáč, Ivan, Clark, H. Brent, Gross, Myron D., Jiang, Hong, Eberly, Lynn E., Bushara, Khalaf O., Gomez, Christopher M.
Publicado em 2010

Calpain activation impairs neuromuscular transmission in a mouse model of the slow-channel myasthenic syndrome

Por Groshong, Jason S., Spencer, Melissa J., Bhattacharyya, Bula J., Kudryashova, Elena, Vohra, Bhupinder P.S., Zayas, Roberto, Wollmann, Robert L., Miller, Richard J., Gomez, Christopher M.
Publicado em 2007

Fluoxetine is neuroprotective in slow-channel congenital myasthenic syndrome

Por Zhu, Haipeng, Grajales-Reyes, E., Vázquez, Vivianette Alicea, Robinson, KaReisha, Pytel, Peter, Báez-Pagán, Carlos A, Lasalde-Dominicci, Jose A, Gomez, Christopher M
Publicado no Exp Neurol (2014)

Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)

Por Figueroa, Karla P., Waters, Michael F., Garibyan, Vartan, Bird, Thomas D., Gomez, Christopher M., Ranum, Laura P. W., Minassian, Natali A., Papazian, Diane M., Pulst, Stefan M.
Publicado em 2011

Novel β subunit mutation causes a slow-channel syndrome by enhancing activation and decreasing the rate of agonist dissociation

Por Navedo, Manuel F., Lasalde-Dominicci, José A., Báez-Pagán, Carlos A., Díaz-Pérez, Luzed, Rojas, Legier V., Maselli, Ricardo A., Staub, Julie, Schott, Kelly, Zayas, Roberto, Gomez, Christopher M.
Publicado no Mol Cell Neurosci (2006)