Cargando…

RNA Foci Formation in a Retinal Glial Model for Spinocerebellar Ataxia Type 7

Spinocerebellar ataxia type 7 (SCA7) is a neurodegenerative disorder characterized by cerebellar ataxia and retinopathy. SCA7 is caused by a CAG expansion in the ATXN7 gene, which results in an extended polyglutamine (polyQ) tract in the encoded protein, the ataxin-7. PolyQ expanded ataxin-7 elicits...

Descripción completa

Detalles Bibliográficos
Autores principales:	Suárez-Sánchez, Rocío, Ávila-Avilés, Rodolfo Daniel, Hernández-Hernández, J. Manuel, Sánchez-Celis, Daniel, Azotla-Vilchis, Cuauhtli N., Gómez-Macías, Enue R., Leyva-García, Norberto, Ortega, Arturo, Magaña, Jonathan J., Cisneros, Bulmaro, Hernández-Hernández, Oscar
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9861853/ https://www.ncbi.nlm.nih.gov/pubmed/36675972 http://dx.doi.org/10.3390/life13010023

Ejemplares similares

Transcriptome Analysis Reveals Altered Inflammatory Pathway in an Inducible Glial Cell Model of Myotonic Dystrophy Type 1
por: Azotla-Vilchis, Cuauhtli N., et al.
Publicado: (2021)

Genetic Distribution of Five Spinocerebellar Ataxia Microsatellite Loci in Mexican Native American Populations and Its Impact on Contemporary Mestizo Populations
por: Gómez, Rocío, et al.
Publicado: (2022)

New Perspectives of Gene Therapy on Polyglutamine Spinocerebellar Ataxias: From Molecular Targets to Novel Nanovectors
por: Borbolla-Jiménez, Fabiola V., et al.
Publicado: (2021)

Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7
por: Nambo-Venegas, Rafael, et al.
Publicado: (2020)

Antisense Oligonucleotides Reduce RNA Foci in Spinocerebellar Ataxia 36 Patient iPSCs
por: Matsuzono, Kosuke, et al.
Publicado: (2017)

Neural correlates of ataxia severity in spinocerebellar ataxia type 3/Machado-Joseph disease
por: Hernandez-Castillo, Carlos R., et al.
Publicado: (2017)

Spinocerebellar ataxia type 8 larger triplet expansion alters histone modification and induces RNA foci
por: Chen, I-Cheng, et al.
Publicado: (2009)

Deletion at ITPR1 Underlies Ataxia in Mice and Spinocerebellar Ataxia 15 in Humans
por: van de Leemput, Joyce, et al.
Publicado: (2007)

Unique degeneration signatures in the cerebellar cortex for spinocerebellar ataxias 2, 3, and 7
por: Hernandez-Castillo, Carlos R., et al.
Publicado: (2018)

An understanding of spinocerebellar ataxia
por: Ramachandra, N.B., et al.
Publicado: (2015)

Parkinsonism in Spinocerebellar Ataxia
por: Park, Hyeyoung, et al.
Publicado: (2015)

Spinocerebellar ataxia: an update
por: Sullivan, Roisin, et al.
Publicado: (2018)

Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias
por: Gan, Shi-Rui, et al.
Publicado: (2017)

Whole-brain connectivity analysis and classification of spinocerebellar ataxia type 7 by functional MRI
por: Hernandez-Castillo, Carlos R, et al.
Publicado: (2014)

Cell biology of spinocerebellar ataxia
por: Orr, Harry T.
Publicado: (2012)

Cognitive dysfunction in spinocerebellar ataxias
por: Teive, Helio Afonso Ghizoni, et al.
Publicado: (2009)

Neuroradiological Findings in the Spinocerebellar Ataxias
por: Meira, Alex Tiburtino, et al.
Publicado: (2019)

Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells
por: Rugerio-Martínez, Claudia Ivette, et al.
Publicado: (2022)

Quantitative evaluation of upper limb ataxia in spinocerebellar ataxias
por: Kishimoto, Yoshiyuki, et al.
Publicado: (2022)

Muscle Cramps Profile among Spinocerebellar Ataxias
por: Franklin, Gustavo Leite, et al.
Publicado: (2022)

Social and Cultural Elements Associated with Neurocognitive Dysfunctions in Spinocerebellar Ataxia Type 2 Patients
por: Mercadillo, Roberto Emmanuele, et al.
Publicado: (2015)

Spinocerebellar Ataxia 12 Patients have better Quality of Life than Spinocerebellar Ataxia 1 and 2
por: Dabla, Surekha, et al.
Publicado: (2022)

Endocannabinoid System in Spinocerebellar Ataxia Type-3 and Other Autosomal-Dominant Cerebellar Ataxias: Potential Role in Pathogenesis and Expected Relevance as Neuroprotective Targets
por: Gómez-Ruiz, María, et al.
Publicado: (2019)

Chromatin Landscape During Skeletal Muscle Differentiation
por: Hernández-Hernández, Oscar, et al.
Publicado: (2020)

Genetic and molecular aspects of spinocerebellar ataxias
por: Honti, Viktor, et al.
Publicado: (2005)

Decreasing fall risk in spinocerebellar ataxia
por: Santos de Oliveira, Laura Alice, et al.
Publicado: (2015)

Spinocerebellar ataxia-10 with paranoid schizophrenia
por: Trikamji, Bhavesh, et al.
Publicado: (2015)

Spinocerebellar Ataxia Type 31 with Blepharospasm
por: Itaya, Sakiko, et al.
Publicado: (2018)

Diagnosis of Spinocerebellar Ataxia in the West Indies
por: Yearwood, Ashley K., et al.
Publicado: (2018)

Nonmotor symptoms in spinocerebellar ataxias (SCAs)
por: Moro, Adriana, et al.
Publicado: (2019)

Aberrant Cerebellar Circuitry in the Spinocerebellar Ataxias
por: Robinson, Katherine J., et al.
Publicado: (2020)

Functionality and disease severity in spinocerebellar ataxias
por: da CRUZ, Geanison Castro, et al.
Publicado: (2022)

Temporal Dynamics of the Scale for the Assessment and Rating of Ataxia in Spinocerebellar Ataxias
por: Moulaire, Paul, et al.
Publicado: (2022)

Sensorimotor processing for balance in spinocerebellar ataxia type 6
por: Bunn, Lisa M., et al.
Publicado: (2015)

RNA Gain-of-Function in Spinocerebellar Ataxia Type 8
por: Daughters, Randy S., et al.
Publicado: (2009)

Altered striatal endocannabinoid signaling in a transgenic mouse model of spinocerebellar ataxia type-3
por: Rodríguez-Cueto, Carmen, et al.
Publicado: (2017)

Antisense oligonucleotide therapy for spinocerebellar ataxia type 2
por: Scoles, Daniel R., et al.
Publicado: (2017)

Prevalence of spinocerebellar ataxia 36 in a US population
por: Valera, Juliana M., et al.
Publicado: (2017)

Protein-protein interaction networks in the spinocerebellar ataxias
por: Rubinsztein, David C
Publicado: (2006)

Axonal inclusions in spinocerebellar ataxia type 3
por: Seidel, Kay, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_f9315s0ia6m5p9rnjvnftleogp