The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.
about
Machado-Joseph Disease: from first descriptions to new perspectives.Caspase cleavage of gene products associated with triplet expansion disorders generates truncated fragments containing the polyglutamine tractAmyloid-like fibril formation by polyQ proteins: a critical balance between the polyQ length and the constraints imposed by the host proteinMultiple system atrophy: a sporadic synucleinopathy.Huntington disease models and human neuropathology: similarities and differencesThe selective vulnerability of nerve cells in Huntington's disease.Brain pathology of spinocerebellar ataxias.Broad distribution of ataxin 1 silencing in rhesus cerebella for spinocerebellar ataxia type 1 therapy.Gene suppression strategies for dominantly inherited neurodegenerative diseases: lessons from Huntington's disease and spinocerebellar ataxia.Distinct neurochemical profiles of spinocerebellar ataxias 1, 2, 6, and cerebellar multiple system atrophy.The androgen receptor: structure, mutations, and antiandrogens.Psychotic-affective symptoms and multiple system atrophy expand phenotypes of spinocerebellar ataxia type 2.TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions.Emerging chemotherapeutic strategies for Huntington's disease.Transglutaminase aggregates huntingtin into nonamyloidogenic polymers, and its enzymatic activity increases in Huntington's disease brain nuclei.The cerebellar component of Friedreich's ataxiaA Tale of Two Maladies? Pathogenesis of Depression with and without the Huntington's Disease Gene Mutation.RNAi prevents and reverses phenotypes induced by mutant human ataxin-1.Movement disorders in spinocerebellar ataxias.Mahogunin Ring Finger-1 (MGRN1), a Multifaceted Ubiquitin Ligase: Recent Unraveling of Neurobiological Mechanisms.Spinal Cord Damage in Spinocerebellar Ataxia Type 1.An isoform of ataxin-3 accumulates in the nucleus of neuronal cells in affected brain regions of SCA3 patients.Pattern of peripheral nerve involvement in Machado-Joseph disease: neuronopathy or distal axonopathy? A clinical and neurophysiological evaluation.Pattern of Peripheral Nerve Involvement in Spinocerebellar Ataxia Type 2: a Neurophysiological Assessment.Spinocerebellar ataxia type 1 (SCA1): new pathoanatomical and clinico-pathological insights.Prospective study of peripheral neuropathy in Machado-Joseph disease
P2860
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P2860
The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.
description
1997 nî lūn-bûn
@nan
1997年の論文
@ja
1997年論文
@yue
1997年論文
@zh-hant
1997年論文
@zh-hk
1997年論文
@zh-mo
1997年論文
@zh-tw
1997年论文
@wuu
1997年论文
@zh
1997年论文
@zh-cn
name
The neuropathology of CAG repe ...... enetic and molecular features.
@en
type
label
The neuropathology of CAG repe ...... enetic and molecular features.
@en
prefLabel
The neuropathology of CAG repe ...... enetic and molecular features.
@en
P2093
P2860
P1433
P1476
The neuropathology of CAG repe ...... enetic and molecular features.
@en
P2093
Lopes-Cendes I
Robitaille Y
P2860
P304
P356
10.1111/J.1750-3639.1997.TB00893.X
P577
1997-07-01T00:00:00Z