A comprehensive review of spinocerebellar ataxia type 2 in Cuba. - Wikidata - wikimedia - TriplyDB

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

http://www.wikidata.org/entity/Q37852582

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Motor Dysfunctions and Neuropathology in Mouse Models of Spinocerebellar Ataxia Type 2: A Comprehensive Review Progression of brain atrophy in spinocerebellar ataxia type 2: a longitudinal tensor-based morphometry study.Neurogenetics in Peru: clinical, scientific and ethical perspectives.Ayurvedic approach in the management of spinocerebellar ataxia-2.De novo mutations in ataxin-2 gene and ALS risk.Couples at risk for spinocerebellar ataxia type 2: the Cuban prenatal diagnosis experience.Oxidative stress as a cofactor in spinocerebellar ataxia type 2.Spinocerebellar ataxia type 2: clinical presentation, molecular mechanisms, and therapeutic perspectives.NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2.Prodromal spinocerebellar ataxia type 2: Prospects for early interventions and ethical challenges.The Cuban program for predictive testing of SCA2: 11 years and 768 individuals to learn from.Atxn2 Knockout and CAG42-Knock-in Cerebellum Shows Similarly Dysregulated Expression in Calcium Homeostasis Pathway.Functional connectivity changes related to cognitive and motor performance in spinocerebellar ataxia type 2.The Multiple Faces of Spinocerebellar Ataxia type 2.Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches.Comprehensive study of early features in spinocerebellar ataxia 2: delineating the prodromal stage of the disease.Spinocerebellar ataxia type 2 neurodegeneration differentially affects error-based and strategic-based visuomotor learning.Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.Pattern of Peripheral Nerve Involvement in Spinocerebellar Ataxia Type 2: a Neurophysiological Assessment.Recessive spinocerebellar ataxia with paroxysmal cough attacks: a report of five cases.Lisuride reduces involuntary periodic leg movements in spinocerebellar ataxia type 2 patients.Infantile childhood onset of spinocerebellar ataxia type 2.Large normal and intermediate alleles in the context of SCA2 prenatal diagnosis.Spinocerebellar ataxia type 2: Measures of saccade changes improve power for clinical trials.Current molecular insight to reveal the dynamics of CAG repeating units in spinocerebellar ataxia.Cuban Adolescents Requesting Presymptomatic Testing for Spinocerebellar Ataxia Type 2

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A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

http://www.wikidata.org/entity/Q37852582

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on June 2011

@en

vedecký článok

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vetenskaplig artikel

@sv

videnskabelig artikel

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vědecký článek

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name

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

@en

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

@nl

type

label

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

@en

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

@nl

prefLabel

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

@en

A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

@nl

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S12311-011-0265-2

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A comprehensive review of spinocerebellar ataxia type 2 in Cuba.

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José Miguel Laffita-Mesa

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Julio Cesar García-Rodríguez

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Luis Enrique Almaguer-Mederos

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Luis Velázquez-Pérez

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Roberto Rodríguez-Labrada

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Tania Cruz-Mariño

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P2860

A novel protein with RNA-binding motifs interacts with ataxin-2

Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human

Ataxin-2 and its Drosophila homolog, ATX2, physically assemble with polyribosomes

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules

Ataxin-2 and huntingtin interact with endophilin-A complexes to function in plastin-associated pathways

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations

Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23-24.1

Generation and characterization of Sca2 (ataxin-2) knockout mice

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s12311-011-0265-2

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184-198

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scholarly article

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10.1007/S12311-011-0265-2

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2

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10

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2011-06-01T00:00:00Z

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