about
Ubiquitin-proteasome system involvement in Huntington's diseaseAnticipation in Huntington's disease is inherited through the male line but may originate in the female.3-Hydroxyanthranilate oxygenase activity is increased in the brains of Huntington disease victimsHomozygosity for Waardenburg syndromeHuntington's disease: the past, present, and future search for disease modifiers.Genetics and neuropathology of Huntington's diseaseCloning of the alpha-adducin gene from the Huntington's disease candidate region of chromosome 4 by exon amplificationHuntingtin: alive and well and working in middle managementNormal huntingtin function: an alternative approach to Huntington's diseaseShaping the role of mitochondria in the pathogenesis of Huntington's diseaseCellular localization and development of neuronal intranuclear inclusions in striatal and cortical neurons in R6/2 transgenic miceA Huntington's disease CAG expansion at the murine Hdh locus is unstable and associated with behavioural abnormalities in miceHuntingtin is required for neurogenesis and is not impaired by the Huntington's disease CAG expansionTemporal separation of aggregation and ubiquitination during early inclusion formation in transgenic mice carrying the Huntington's disease mutationThe molecular basis of genetic dominanceImpaired TrkB receptor signaling underlies corticostriatal dysfunction in Huntington's diseaseAblation of huntingtin in adult neurons is nondeleterious but its depletion in young mice causes acute pancreatitis.CAG repeat expansion in Huntington disease determines age at onset in a fully dominant fashion.Complex patterns of linkage disequilibrium in the Huntington disease region.Genomic imprinting: review and relevance to human diseases.Wild-type huntingtin ameliorates striatal neuronal atrophy but does not prevent other abnormalities in the YAC128 mouse model of Huntington disease.Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?Patterns of inheritance of the symptoms of Huntington's disease suggestive of an effect of genomic imprinting.The value of the study of natural history in genetic disorders and congenital anomaly syndromes.Considerations in using linkage analysis as a presymptomatic test for Huntington's diseaseAre there multiple pathways in the pathogenesis of Huntington's disease?Huntington disease models and human neuropathology: similarities and differencesA yeast artificial chromosome telomere clone spanning a possible location of the Huntington disease geneOf mice and men: solving the molecular mysteries of Huntington's disease.Pedigree parables.Review and hypotheses: somatic mosaicism: observations related to clinical genetics.The selective vulnerability of nerve cells in Huntington's disease.The Huntington disease locus is most likely within 325 kilobases of the chromosome 4p telomereTrinucleotide repeat length instability and age of onset in Huntington's disease.Comparison of modules of wild type and mutant Huntingtin and TP53 protein interaction networks: implications in biological processes and functions.HD CAG-correlated gene expression changes support a simple dominant gain of function.Clinical and research advances in Huntington's disease.Homozygotes for the autosomal dominant neoplasia syndrome (MEN1).Epigene conversion: a proposal with implications for gene mapping in humans.The paradigm of Huntington disease
P2860
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P2860
description
1987 nî lūn-bûn
@nan
1987 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի մարտին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Homozygotes for Huntington's disease.
@ast
Homozygotes for Huntington's disease.
@en
Homozygotes for Huntington's disease.
@nl
type
label
Homozygotes for Huntington's disease.
@ast
Homozygotes for Huntington's disease.
@en
Homozygotes for Huntington's disease.
@nl
prefLabel
Homozygotes for Huntington's disease.
@ast
Homozygotes for Huntington's disease.
@en
Homozygotes for Huntington's disease.
@nl
P2093
P356
P1433
P1476
Homozygotes for Huntington's disease.
@en
P2093
Ramos Arroyo MA
Shoulson I
Snodgrass SR
Starosta-Rubinstein S
P2888
P304
P356
10.1038/326194A0
P407
P577
1987-03-01T00:00:00Z
P5875
P6179
1012101430