Cargando…

Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1

Mostrar otras versiones (1)

Detalles Bibliográficos
Autores principales:	Coffin, Stephanie L., Durham, Mark A., Nitschke, Larissa, Xhako, Eder, Brown, Amanda M., Revelli, Jean-Pierre, Gonzalez, Esmeralda Villavicencio, Lin, Tao, Handler, Hillary P., Dai, Yanwan, Trostle, Alexander J., Wan, Ying-Wooi, Liu, Zhandong, Sillitoe, Roy V., Orr, Harry T., Zoghbi, Huda Y.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	2023
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10153637/ https://www.ncbi.nlm.nih.gov/pubmed/36924764 http://dx.doi.org/10.1016/j.neuron.2023.02.030

Ejemplares similares

Disruption of the ATXN1-CIC complex reveals the role of additional nuclear ATXN1 interactors in spinocerebellar ataxia type 1
por: Coffin, Stephanie L., et al.
Publicado: (2023)

Modulation of ATXN1 S776 phosphorylation reveals the importance of allele-specific targeting in SCA1
por: Nitschke, Larissa, et al.
Publicado: (2021)

miR760 regulates ATXN1 levels via interaction with its 5′ untranslated region
por: Nitschke, Larissa, et al.
Publicado: (2020)

Novel ATXN1/ATXN1L::NUTM2A fusions identified in aggressive infant sarcomas with gene expression and methylation patterns similar to CIC-rearranged sarcoma
por: Xu, Feng, et al.
Publicado: (2022)

Analysis of (CAG)(n) expansion in ATXN1, ATXN2 and ATXN3 in Chinese patients with multiple system atrophy
por: Zhou, X., et al.
Publicado: (2018)

Repeats expansions in ATXN2, NOP56, NIPA1 and ATXN1 are not associated with ALS in Africans
por: Nel, Melissa, et al.
Publicado: (2021)

Detection Methods and Status of CAT Interruption of ATXN1 in Korean Patients With Spinocerebellar Ataxia Type 1
por: Jang, Ja-Hyun, et al.
Publicado: (2022)

Reduction of mutant ATXN1 rescues premature death in a conditional SCA1 mouse model
por: Orengo, James P., et al.
Publicado: (2022)

Combined overexpression of ATXN1L and mutant ATXN1 knockdown by AAV rescue motor phenotypes and gene signatures in SCA1 mice
por: Carrell, Ellie M., et al.
Publicado: (2022)

A model for the dynamics of expanded CAG repeat alleles: ATXN2 and ATXN3 as prototypes
por: Sena, Lucas Schenatto, et al.
Publicado: (2023)

Co‐occurrence of ATXN3 and ATXN2 repeat expansions in Chinese ataxia patients with slow saccades
por: Wu, Chao, et al.
Publicado: (2019)

Region‐specific preservation of Purkinje cell morphology and motor behavior in the ATXN1[82Q] mouse model of spinocerebellar ataxia 1
por: White, Joshua J., et al.
Publicado: (2021)

14-3-3 Binding to Ataxin-1(ATXN1) Regulates Its Dephosphorylation at Ser-776 and Transport to the Nucleus
por: Lai, Shaojuan, et al.
Publicado: (2011)

Genetic Variance in the Spinocerebellar Ataxia Type 2 (ATXN2) Gene in Children with Severe Early Onset Obesity
por: Figueroa, Karla P., et al.
Publicado: (2009)

ATTCT and ATTCC repeat expansions in the ATXN10 gene affect disease penetrance of spinocerebellar ataxia type 10
por: Morato Torres, C. Alejandra, et al.
Publicado: (2022)

The complex structure of ATXN2 genetic variation
por: Pulst, Stefan M.
Publicado: (2018)

ATXN2 a culprit with multiple facets
por: Nkiliza, Aurore, et al.
Publicado: (2017)

Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population
por: Faruq, Mohammed, et al.
Publicado: (2015)

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways
por: Zeng, Li, et al.
Publicado: (2018)

The Truncated C-terminal Fragment of Mutant ATXN3 Disrupts Mitochondria Dynamics in Spinocerebellar Ataxia Type 3 Models
por: Hsu, Jung-Yu, et al.
Publicado: (2017)

Structural Analysis and Spatiotemporal Expression of Atxn1 Genes in Zebrafish Embryos and Larvae
por: Vauti, Franz, et al.
Publicado: (2021)

New alternative splicing variants of the ATXN2 transcript
por: Lastres-Becker, Isabel, et al.
Publicado: (2019)

Autophagy Promoted the Degradation of Mutant ATXN3 in Neurally Differentiated Spinocerebellar Ataxia-3 Human Induced Pluripotent Stem Cells
por: Ou, Zhanhui, et al.
Publicado: (2016)

A Novel Duplication in ATXN2 as Modifier for Spinocerebellar Ataxia 3 (SCA3) and C9ORF72‐ALS
por: Laffita‐Mesa, Jose Miguel, et al.
Publicado: (2020)

TRIM25 promotes Capicua degradation independently of ERK in the absence of ATXN1L
por: Wong, Derek, et al.
Publicado: (2020)

ATXN2 trinucleotide repeat length correlates with risk of ALS
por: Sproviero, William, et al.
Publicado: (2017)

Parkinson’s disease associated with pure ATXN10 repeat expansion
por: Schüle, Birgitt, et al.
Publicado: (2017)

Mid-Gestation lethality of Atxn2l-Ablated Mice
por: Key, Jana, et al.
Publicado: (2020)

ATXN3 promotes prostate cancer progression by stabilizing YAP
por: Wu, Longxiang, et al.
Publicado: (2023)

miRNA-Mediated Knockdown of ATXN3 Alleviates Molecular Disease Hallmarks in a Mouse Model for Spinocerebellar Ataxia Type 3
por: Nobre, Rui Jorge, et al.
Publicado: (2022)

ATXN1 N-terminal region explains the binding differences of wild-type and expanded forms
por: Rocha, Sara, et al.
Publicado: (2019)

Sphingolipid metabolism governs Purkinje cell patterned degeneration in Atxn1[82Q]/+ mice
por: Blot, François G. C., et al.
Publicado: (2021)

Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism
por: Casse, Fanny, et al.
Publicado: (2023)

ATXN3 controls DNA replication and transcription by regulating chromatin structure
por: Hernández‐Carralero, Esperanza, et al.
Publicado: (2023)

Brain tumor with an ATXN1-NUTM1 fusion gene expands the histologic spectrum of NUTM1-rearranged neoplasia
por: Siegfried, Aurore, et al.
Publicado: (2019)

UTteR control through miRs: fine-tuning ATXN1 levels to prevent ataxia
por: Xie, Mingyi, et al.
Publicado: (2020)

ATXN1 repeat expansions confer risk for amyotrophic lateral sclerosis and contribute to TDP-43 mislocalization
por: Tazelaar, Gijs H P, et al.
Publicado: (2020)

Internal Ribosome Entry Segment Activity of ATXN8 Opposite Strand RNA
por: Chen, I-Cheng, et al.
Publicado: (2013)

Noncoding repeat expansions for ALS in Japan are associated with the ATXN8OS gene
por: Hirano, Makito, et al.
Publicado: (2018)

Evaluation of Antisense Oligonucleotides Targeting ATXN3 in SCA3 Mouse Models
por: Moore, Lauren R., et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_kcsq6nv2es87q5ses2igaqev2u