Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease. - Wikidata - awgldk - TriplyDB

Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease.

Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease.

http://www.wikidata.org/entity/Q42469950

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The importance of integrating basic and clinical research toward the development of new therapies for Huntington disease Early alterations of brain cellular energy homeostasis in Huntington disease models Role of cerebral cortex in the neuropathology of Huntington's disease Iron dysregulation in Huntington's disease Genetics and neuropathology of Huntington's disease The progeroid gene BubR1 regulates axon myelination and motor function.Decreased Lin7b expression in layer 5 pyramidal neurons may contribute to impaired corticostriatal connectivity in huntington disease.Functional connectivity of primary motor cortex is dependent on genetic burden in prodromal Huntington disease.Cerebral cortex structure in prodromal Huntington disease.A tale of two factors: what determines the rate of progression in Huntington's disease? A longitudinal MRI study.Cortical efferents lacking mutant huntingtin improve striatal neuronal activity and behavior in a conditional mouse model of Huntington's disease Basal Ganglia disorders associated with imbalances in the striatal striosome and matrix compartments.The Current Status of Neural Grafting in the Treatment of Huntington's Disease. A Review Impaired cortico-striatal functional connectivity in prodromal Huntington's Disease The Spectrum of Psychiatric Pathology in a Patient with Genetically Verified Huntington's Disease.Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington's Disease Depressive symptoms in prodromal Huntington's Disease correlate with Stroop-interference related functional connectivity in the ventromedial prefrontal cortex Assessment of cortical and striatal involvement in 523 Huntington disease brains.Consistent neurodegeneration and its association with clinical progression in Huntington's disease: a coordinate-based meta-analysis.Increased Olfactory Bulb BDNF Expression Does Not Rescue Deficits in Olfactory Neurogenesis in the Huntington's Disease R6/2 Mouse.MAP kinase phosphatase 1 (MKP-1/DUSP1) is neuroprotective in Huntington's disease via additive effects of JNK and p38 inhibition Striatal parvalbuminergic neurons are lost in Huntington's disease: implications for dystonia The pathogenesis of cingulate atrophy in behavioral variant frontotemporal dementia and Alzheimer's disease.Brain networks in Huntington disease.Milestones in huntington disease.Pathophysiology of Huntington's disease: time-dependent alterations in synaptic and receptor function.Stem cell-based therapy for Huntington's disease.Huntington's disease (HD): the neuropathology of a multisystem neurodegenerative disorder of the human brain.Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease.String Vessel Formation is Increased in the Brain of Parkinson Disease.Apraxia for differentiating Alzheimer's disease from subcortical vascular dementia and mild cognitive impairment.Alterations in mRNA 3' UTR Isoform Abundance Accompany Gene Expression Changes in Human Huntington's Disease Brains.Cortical interneuron loss and symptom heterogeneity in Huntington disease.Characterization of a rat model of Huntington's disease based on targeted expression of mutant huntingtin in the forebrain using adeno-associated viral vectors.Comparison of Huntington's disease CAG Repeat Length Stability in Human Motor Cortex and Cingulate Gyrus.Impaired ideomotor limb apraxia in cortical and subcortical dementia: a comparison of Alzheimer's and Huntington's disease.The structural involvement of the cingulate cortex in premanifest and early Huntington's disease.Selective loss of oxytocin and vasopressin in the hypothalamus in early Huntington disease: a case study.Disrupted vasculature and blood-brain barrier in Huntington disease.Distribution of the creatine transporter throughout the human brain reveals a spectrum of creatine transporter immunoreactivity.

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P2860

Cell loss in the motor and cingulate cortex correlates with symptomatology in Huntington's disease.

http://www.wikidata.org/entity/Q42469950

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2010 nî lūn-bûn

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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2010年论文

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name

Cell loss in the motor and cin ...... ology in Huntington's disease.

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Cell loss in the motor and cin ...... ology in Huntington's disease.

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Cell loss in the motor and cin ...... ology in Huntington's disease.

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Cell loss in the motor and cin ...... ology in Huntington's disease.

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Cell loss in the motor and cin ...... ology in Huntington's disease.

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Cell loss in the motor and cin ...... ology in Huntington's disease.

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Cell loss in the motor and cin ...... ology in Huntington's disease.

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Alissa L Nana

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Beth J Synek

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Doris C V Thu

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Dorothy E Oorschot

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Lynette J Tippett

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Richard L M Faull

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Virginia M Hogg

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P2860

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

Loss of huntingtin-mediated BDNF gene transcription in Huntington's disease

Early changes in Huntington's disease patient brains involve alterations in cytoskeletal and synaptic elements

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

Alterations in cortical excitation and inhibition in genetic mouse models of Huntington's disease.

The neuropathology of primary mood disorder.

Anterior cingulate dysfunction in geriatric depression.

Volumetric neuroimaging investigations in mood disorders: bipolar disorder versus major depressive disorder.

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

Immunohistochemical staining of post-mortem adult human brain sections.

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1094-1110

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10.1093/BRAIN/AWQ047

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Pt 4

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133

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Henry J. Waldvogel

Ruth Luthi-Carter

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2010-04-01T00:00:00Z

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43073103

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20375136

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Huntington disease