Cargando…

Correction: RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression

Detalles Bibliográficos
Autores principales:	Labadorf, Adam, Hoss, Andrew G., Lagomarsino, Valentina, Latourelle, Jeanne C., Hadzi, Tiffany C., Bregu, Joli, MacDonald, Marcy E., Gusella, James F., Chen, Jiang-Fan, Akbarian, Schahram, Weng, Zhiping, Myers, Richard H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2016
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959683/ https://www.ncbi.nlm.nih.gov/pubmed/27454300 http://dx.doi.org/10.1371/journal.pone.0160295

Ejemplares similares

RNA Sequence Analysis of Human Huntington Disease Brain Reveals an Extensive Increase in Inflammatory and Developmental Gene Expression
por: Labadorf, Adam, et al.
Publicado: (2015)

miR-10b-5p expression in Huntington’s disease brain relates to age of onset and the extent of striatal involvement
por: Hoss, Andrew G, et al.
Publicado: (2015)

MicroRNAs Located in the Hox Gene Clusters Are Implicated in Huntington's Disease Pathogenesis
por: Hoss, Andrew G., et al.
Publicado: (2014)

MicroRNAs in CSF as prodromal biomarkers for Huntington disease in the PREDICT-HD study
por: Reed, Eric R., et al.
Publicado: (2018)

The Role of H3K4me3 in Transcriptional Regulation Is Altered in Huntington’s Disease
por: Dong, Xianjun, et al.
Publicado: (2015)

The 4p16.3 Parkinson Disease Risk Locus Is Associated with GAK Expression and Genes Involved with the Synaptic Vesicle Membrane
por: Nagle, Michael W., et al.
Publicado: (2016)

microRNA Profiles in Parkinson's Disease Prefrontal Cortex
por: Hoss, Andrew G., et al.
Publicado: (2016)

Huntington's disease: the case for genetic modifiers
por: Gusella, James F, et al.
Publicado: (2009)

Novel microRNA discovery using small RNA sequencing in post-mortem human brain
por: Wake, Christian, et al.
Publicado: (2016)

Evaluation of Parkinson Disease Risk Variants as Expression-QTLs
por: Latourelle, Jeanne C., et al.
Publicado: (2012)

Genetic analysis of the GRIK2 modifier effect in Huntington's disease
por: Zeng, Wenqi, et al.
Publicado: (2006)

Evidence for a Pan-Neurodegenerative Disease Response in Huntington's and Parkinson's Disease Expression Profiles
por: Labadorf, Adam, et al.
Publicado: (2018)

Huntington’s Disease Pathogenesis: Two Sequential Components
por: Hong, Eun Pyo, et al.
Publicado: (2021)

Coordinated Cell Type–Specific Epigenetic Remodeling in Prefrontal Cortex Begins before Birth and Continues into Early Adulthood
por: Shulha, Hennady P., et al.
Publicado: (2013)

The caudate nucleus undergoes dramatic and unique transcriptional changes in human prodromal Huntington’s disease brain
por: Agus, Filisia, et al.
Publicado: (2019)

Integrative analyses of proteomics and RNA transcriptomics implicate mitochondrial processes, protein folding pathways and GWAS loci in Parkinson disease
por: Dumitriu, Alexandra, et al.
Publicado: (2016)

Gene Expression Profiles in Parkinson Disease Prefrontal Cortex Implicate FOXO1 and Genes under Its Transcriptional Regulation
por: Dumitriu, Alexandra, et al.
Publicado: (2012)

Evidence of Extensive Alternative Splicing in Post Mortem Human Brain HTT Transcription by mRNA Sequencing
por: Labadorf, Adam T., et al.
Publicado: (2015)

Timing and Impact of Psychiatric, Cognitive, and Motor Abnormalities in Huntington Disease
por: McAllister, Branduff, et al.
Publicado: (2021)

Hypomorphic mutation of the mouse Huntington’s disease gene orthologue
por: Murthy, Vidya, et al.
Publicado: (2019)

Epigenetic mechanisms in schizophrenia
por: Akbarian, Schahram
Publicado: (2014)

Metabolic disruption identified in the Huntington’s disease transgenic sheep model
por: Handley, Renee. R., et al.
Publicado: (2016)

Population-specific genetic modification of Huntington's disease in Venezuela
por: Chao, Michael J., et al.
Publicado: (2018)

Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain
por: Dumitriu, Alexandra, et al.
Publicado: (2012)

Haplotype analysis of the 4p16.3 region in Portuguese families with Huntington's disease
por: Ramos, Eliana Marisa, et al.
Publicado: (2015)

Use of the epigenetic toolbox to contextualize common variants associated with schizophrenia risk 
por: Rajarajan, Prashanth, et al.
Publicado: (2019)

The tRNA regulome in neurodevelopmental and neuropsychiatric disease
por: Blaze, Jennifer, et al.
Publicado: (2022)

Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington’s disease motor onset
por: Ramos, Eliana Marisa, et al.
Publicado: (2013)

Population stratification may bias analysis of PGC-1α as a modifier of age at Huntington disease motor onset
por: Ramos, Eliana Marisa, et al.
Publicado: (2012)

GAD1 mRNA Expression and DNA Methylation in Prefrontal Cortex of Subjects with Schizophrenia
por: Huang, Hsien-Sung, et al.
Publicado: (2007)

Huntington’s disease age at motor onset is modified by the tandem hexamer repeat in TCERG1
por: Lobanov, Sergey V., et al.
Publicado: (2022)

PMS1 as a target for splice modulation to prevent somatic CAG repeat expansion in Huntington’s disease
por: McLean, Zachariah L., et al.
Publicado: (2023)

Large-scale identification of clinical and genetic predictors of Parkinson’s disease motor progression in newly-diagnosed patients: a longitudinal cohort study and validation
por: Latourelle, Jeanne C., et al.
Publicado: (2017)

3D Genome Plasticity in Normal and Diseased Neurodevelopment
por: Plaza-Jennings, Amara, et al.
Publicado: (2022)

Reversal of a full-length mutant huntingtin neuronal cell phenotype by chemical inhibitors of polyglutamine-mediated aggregation
por: Wang, Jin, et al.
Publicado: (2005)

Promotion of somatic CAG repeat expansion by Fan1 knock-out in Huntington’s disease knock-in mice is blocked by Mlh1 knock-out
por: Loupe, Jacob M, et al.
Publicado: (2020)

Chromosome substitution strain assessment of a Huntington’s disease modifier locus
por: Ramos, Eliana Marisa, et al.
Publicado: (2015)

Risk of Parkinson's disease after tamoxifen treatment
por: Latourelle, Jeanne C, et al.
Publicado: (2010)

Estrogen-related and other disease diagnoses preceding Parkinson’s disease
por: Latourelle, Jeanne C, et al.
Publicado: (2010)

A Multi-Omic Huntington’s Disease Transgenic Sheep-Model Database for Investigating Disease Pathogenesis
por: Mears, Emily R., et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_4hidphajq42p65pt0f96ebe4fg