Differential loss of striatal projection neurons in Huntington disease. - Wikidata - awgldk - TriplyDB

Differential loss of striatal projection neurons in Huntington disease.

Differential loss of striatal projection neurons in Huntington disease.

http://www.wikidata.org/entity/Q33637273

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Topical Review: Basal Ganglia: Functional Anatomy and Physiology. Part 1 Endoplasmic reticulum stress and Parkinson's disease: the role of HRD1 in averting apoptosis in neurodegenerative disease Activin A directs striatal projection neuron differentiation of human pluripotent stem cells Huntingtin in health and disease Conditional routing of information to the cortex: a model of the basal ganglia's role in cognitive coordination Age-dependent alterations of corticostriatal activity in the YAC128 mouse model of Huntington disease Complex trait analysis of the mouse striatum: independent QTLs modulate volume and neuron number.Subcellular Clearance and Accumulation of Huntington Disease Protein: A Mini-Review Current status of PET imaging in Huntington's disease Treatment of Huntington's disease.Modulation of the glutamatergic transmission by Dopamine: a focus on Parkinson, Huntington and Addiction diseases The neurobiological link between OCD and ADHD Dysregulation of cholesterol balance in the brain: contribution to neurodegenerative diseases Functional Differences Between Direct and Indirect Striatal Output Pathways in Huntington's Disease Genetics and neuropathology of Huntington's disease Maintenance of basal levels of autophagy in Huntington's disease mouse models displaying metabolic dysfunction Deep Brain Stimulation in Huntington's Disease-Preliminary Evidence on Pathophysiology, Efficacy and Safety The chicken or the egg: mitochondrial dysfunction as a cause or consequence of toxicity in Huntington's disease Striatal-enriched protein tyrosine phosphatase expression and activity in Huntington's disease: a STEP in the resistance to excitotoxicity Huntingtin and its role in neuronal degeneration Normal huntingtin function: an alternative approach to Huntington's disease Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's disease Cellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic mice Mutant huntingtin impairs axonal trafficking in mammalian neurons in vivo and in vitro Focal expression of mutant huntingtin in the songbird basal ganglia disrupts cortico-basal ganglia networks and vocal sequences Self-paced timing detects and tracks change in prodromal Huntington disease.Mouse models of Huntington's disease and methodological considerations for therapeutic trials.Motor tics evoked by striatal disinhibition in the rat.BDNF-TrkB signaling in striatopallidal neurons controls inhibition of locomotor behavior.Neuroimaging in Huntington's disease.Dysfunction of ventrolateral striatal dopamine receptor type 2-expressing medium spiny neurons impairs instrumental motivation.The expanded CAG repeat in the huntingtin gene as target for therapeutic RNA modulation throughout the HD mouse brain.Quantitative relationships between huntingtin levels, polyglutamine length, inclusion body formation, and neuronal death provide novel insight into huntington's disease molecular pathogenesis.Transcriptional dysregulation in striatal projection- and interneurons in a mouse model of Huntington's disease: neuronal selectivity and potential neuroprotective role of HAP1.Neurotransmitter distribution in the second trimester fetal human corpus striatum.Tiagabine is neuroprotective in the N171-82Q and R6/2 mouse models of Huntington's disease Dopamine D2 receptor stimulation potentiates PolyQ-Huntingtin-induced mouse striatal neuron dysfunctions via Rho/ROCK-II activation Protection from mitochondrial complex II inhibition in vitro and in vivo by Nrf2-mediated transcription.Restricted transgene expression in the brain with cell-type specific neuronal promoters.Seeking brain biomarkers for preventive therapy in Huntington disease.

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P2860

Differential loss of striatal projection neurons in Huntington disease.

http://www.wikidata.org/entity/Q33637273

description

1988 nî lūn-bûn

@nan

1988 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

1988 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

1988年の論文

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1988年論文

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1988年論文

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1988年論文

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1988年論文

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1988年論文

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1988年论文

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name

Differential loss of striatal projection neurons in Huntington disease.

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Differential loss of striatal projection neurons in Huntington disease.

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type

label

Differential loss of striatal projection neurons in Huntington disease.

@ast

Differential loss of striatal projection neurons in Huntington disease.

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prefLabel

Differential loss of striatal projection neurons in Huntington disease.

@ast

Differential loss of striatal projection neurons in Huntington disease.

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Differential loss of striatal projection neurons in Huntington disease.

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P2093

A B Young

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A Reiner

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C J D'Amato

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J B Penney

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K D Anderson

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R L Albin

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P2860

Evidence for degenerative and regenerative changes in neostriatal spiny neurons in Huntington's disease.

A polymorphic DNA marker genetically linked to Huntington's disease.

Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid.

Ramifications of the globus pallidus in the rat as indicated by patterns of immunohistochemistry.

Striatal inhomogeneities and basal ganglia function.

Huntington's disease. Pathogenesis and management.

Morphometric studies of the neuropathological changes in choreatic diseases.

Modulation of striatal enkephalinergic neurons by antipsychotic drugs.

Huntington's disease. A decade of progress.

Neurochemical alterations in Huntington's chorea: a study of post-mortem brain tissue.

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2456581

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corpus striatum

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