Measures of growth in children at risk for Huntington disease - Wikidata - wikimedia - TriplyDB

Measures of growth in children at risk for Huntington disease

Measures of growth in children at risk for Huntington disease

http://www.wikidata.org/entity/Q36149988

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Huntington's disease: the past, present, and future search for disease modifiers.Modeling Huntington's disease with induced pluripotent stem cells Dominant-Negative Effects of Adult-Onset Huntingtin Mutations Alter the Division of Human Embryonic Stem Cells-Derived Neural Cells A two years longitudinal study of a transgenic Huntington disease monkey.Regionally selective atrophy of subcortical structures in prodromal HD as revealed by statistical shape analysis.The dynamics of early-state transcriptional changes and aggregate formation in a Huntington's disease cell model Huntington's Disease as Neurodevelopmental Disorder: Altered Chromatin Regulation, Coding, and Non-Coding RNA Transcription.Abnormal Weight and Body Mass Index in Children with Juvenile Huntington's Disease.Managing juvenile Huntington's disease.Interregional compensatory mechanisms of motor functioning in progressing preclinical neurodegeneration Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells.Huntington disease: a single-gene degenerative disorder of the striatum.Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice.Juvenile Huntington disease in Argentina.Reduced motivation in the BACHD rat model of Huntington disease is dependent on the choice of food deprivation strategy Neurodegenerative disease: 'fifty shades of grey' in the Huntington disease gene.Differential diagnosis of Huntington's disease: what the clinician should know.Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: a population-based case-control cohort study of familial and sporadic amyotrophic lateral sclerosis.Effect of early embryonic deletion of huntingtin from pyramidal neurons on the development and long-term survival of neurons in cerebral cortex and striatum.Faulty neuronal determination and cell polarization are reverted by modulating HD early phenotypes.Overlap between age-at-onset and disease-progression determinants in Huntington disease.Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition Synaptic dysfunction in neurodegenerative and neurodevelopmental diseases: an overview of induced pluripotent stem-cell-based disease models

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Measures of growth in children at risk for Huntington disease

http://www.wikidata.org/entity/Q36149988

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2012年論文

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Measures of growth in children at risk for Huntington disease

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Measures of growth in children at risk for Huntington disease

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Measures of growth in children at risk for Huntington disease

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Measures of growth in children at risk for Huntington disease

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Measures of growth in children at risk for Huntington disease

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Measures of growth in children at risk for Huntington disease

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Jessica K Lee

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Kathy Mathews

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Leon Burmeister

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Peg Nopoulos

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P2860

Assumption-free estimation of heritability from genome-wide identity-by-descent sharing between full siblings

Expression of normal and mutant huntingtin in the developing brain

2000 CDC Growth Charts for the United States: methods and development

Dietary intake in adults at risk for Huntington disease: analysis of PHAROS research participants

N-terminal mutant huntingtin associates with mitochondria and impairs mitochondrial trafficking.

Early energy deficit in Huntington disease: identification of a plasma biomarker traceable during disease progression.

Increased metabolism in the R6/2 mouse model of Huntington's disease.

Impairment of developmental stem cell-mediated striatal neurogenesis and pluripotency genes in a knock-in model of Huntington's disease

Heritability of adult body height: a comparative study of twin cohorts in eight countries.

Smaller intracranial volume in prodromal Huntington's disease: evidence for abnormal neurodevelopment.

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Bradley L. Schlaggar

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22815549

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Huntington disease

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3414667

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