Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells. (Q39335116)

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English	Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells.	scientific article

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scholarly article

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4 February 2020

Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells (English)

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Huntington's disease

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human embryonic stem cell

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based on heuristic

inferred from title

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Anselme Perrier

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Marc Peschanski

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Marc Peschanski

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Fany Bourgois-Rocha

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Fany Bourgois-Rocha

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Nathalie Lefort

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Nathalie Lefort

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Aurore Bugi

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Caroline Bonnefond

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Caroline Bonnefond

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author name string

Maxime Feyeux

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Amanda Redfern

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Peter Giles

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Sophie Aubert

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Marta Ruiz

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Lesley Jones

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publication date

7 June 2012

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Human Molecular Genetics

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21

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17

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3883-3895

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4 February 2020

Human pluripotent stem cells for disease modelling and drug screening

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Modelling pathogenesis and treatment of familial dysautonomia using patient-specific iPSCs.

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21 January 2018

A human iPSC model of Hutchinson Gilford Progeria reveals vascular smooth muscle and mesenchymal stem cell defects

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Induced pluripotent stem cells from a spinal muscular atrophy patient

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21 January 2018

Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome

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21 January 2018

Targeted disruption of the Huntington's disease gene results in embryonic lethality and behavioral and morphological changes in heterozygotes

1 reference

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21 January 2018

Huntingtin is required for mitotic spindle orientation and mammalian neurogenesis

1 reference

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21 January 2018

Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

1 reference

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21 January 2018

Huntington's disease: from molecular pathogenesis to clinical treatment

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21 January 2018

Molecular mechanisms and potential therapeutical targets in Huntington's disease

1 reference

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21 January 2018

Transcriptional signatures in Huntington's disease

1 reference

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21 January 2018

Transcriptional abnormalities in Huntington disease

1 reference

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21 January 2018

Human embryonic stem cell lines with genetic disorders

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Derivation of human embryonic stem cell lines from embryos obtained after IVF and after PGD for monogenic disorders.

1 reference

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21 January 2018

High-efficiency derivation of human embryonic stem cell lines following pre-implantation genetic diagnosis.

1 reference

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21 January 2018

Derivation of Huntington's disease-affected human embryonic stem cell lines

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Regional and cellular gene expression changes in human Huntington's disease brain

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Impaired PGC-1alpha function in muscle in Huntington's disease.

1 reference

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21 January 2018

Impairment of PGC-1alpha expression, neuropathology and hepatic steatosis in a transgenic mouse model of Huntington's disease following chronic energy deprivation

1 reference

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21 January 2018

Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset

1 reference

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21 January 2018

Mutant huntingtin's effects on striatal gene expression in mice recapitulate changes observed in human Huntington's disease brain and do not differ with mutant huntingtin length or wild-type huntingtin dosage

1 reference

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21 January 2018

Analysis of potential transcriptomic biomarkers for Huntington's disease in peripheral blood

1 reference

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21 January 2018

Cross-platform comparison of microarray data using order restricted inference

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Population-specific expression analysis (PSEA) reveals molecular changes in diseased brain

1 reference

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21 January 2018

Transcriptional changes in Huntington disease identified using genome-wide expression profiling and cross-platform analysis

1 reference

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21 January 2018

Longitudinal analysis of gene expression and behaviour in the HdhQ150 mouse model of Huntington's disease

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Genome-wide expression profiling of human blood reveals biomarkers for Huntington's disease.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Dysregulation of gene expression in primary neuron models of Huntington's disease shows that polyglutamine-related effects on the striatal transcriptome may not be dependent on brain circuitry.

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Molecular markers of early Parkinson's disease based on gene expression in blood

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21 January 2018

Polyglutamine expansions cause decreased CRE-mediated transcription and early gene expression changes prior to cell death in an inducible cell model of Huntington's disease

1 reference

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21 January 2018

Early transcriptional profiles in huntingtin-inducible striatal cells by microarray analyses

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Modulation of polyglutamine-induced cell death by genes identified by expression profiling

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDS216

21 January 2018

Decreased cAMP response element-mediated transcription: an early event in exon 1 and full-length cell models of Huntington's disease that contributes to polyglutamine pathogenesis

1 reference

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21 January 2018

Mutant huntingtin alters MAPK signaling pathways in PC12 and striatal cells: ERK1/2 protects against mutant huntingtin-associated toxicity.

1 reference

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21 January 2018

Transcriptional profiling of Alzheimer blood mononuclear cells by microarray

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21 January 2018

HD CAG-correlated gene expression changes support a simple dominant gain of function

1 reference

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21 January 2018

Peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC-1 alpha): transcriptional coactivator and metabolic regulator

1 reference

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21 January 2018

Transcriptional repression of PGC-1alpha by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration.

1 reference

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21 January 2018

Huntingtin interacting proteins are genetic modifiers of neurodegeneration

1 reference

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21 January 2018

Mitochondria in Huntington's disease

1 reference

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21 January 2018

A computational screen for regulators of oxidative phosphorylation implicates SLIRP in mitochondrial RNA homeostasis

1 reference

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21 January 2018

Neuroprotective role of Sirt1 in mammalian models of Huntington's disease through activation of multiple Sirt1 targets

1 reference

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21 January 2018

Sirt1 mediates neuroprotection from mutant huntingtin by activation of the TORC1 and CREB transcriptional pathway

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Identification and characterization of proteins interacting with SIRT1 and SIRT3: implications in the anti-aging and metabolic effects of sirtuins

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Akt is altered in an animal model of Huntington's disease and in patients

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21 January 2018

Identification of novel cell migration-promoting genes by a functional genetic screen

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Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules

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Protein inhibitor of neuronal nitric oxide synthase interacts with protein kinase A inhibitors

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Phosphorylation of the SSBP2 and ABL proteins by the ZNF198-FGFR1 fusion kinase seen in atypical myeloproliferative disorders as revealed by phosphopeptide-specific MS.

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Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms

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Identifiers

10.1093/HMG/DDS216

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4 February 2020

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4 February 2020

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