Neurodegeneration in hereditary nucleotide repair disorders.
about
Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiencyOxidative stress and disturbed glutamate transport in hereditary nucleotide repair disorders.Cockayne syndrome in adults: review with clinical and pathologic study of a new case.Brainstem and basal ganglia lesions in xeroderma pigmentosum group A.Impaired genome maintenance suppresses the growth hormone--insulin-like growth factor 1 axis in mice with Cockayne syndrome.Cockayne syndrome group B cellular and biochemical functions.DNA repair on the brain.Premature aging and cancer in nucleotide excision repair-disorders.Age-related neuronal degeneration: complementary roles of nucleotide excision repair and transcription-coupled repair in preventing neuropathologyOn the traces of XPD: cell cycle matters - untangling the genotype-phenotype relationship of XPD mutationsNeuroimaging features of xeroderma pigmentosum group A.Endogenous formation and repair of oxidatively induced G[8-5 m]T intrastrand cross-link lesion.Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic diseaseCockayne syndrome B protects against methamphetamine-enhanced oxidative DNA damage in murine fetal brain and postnatal neurodevelopmental deficitsXeroderma Pigmentosum Group A Suppresses Mutagenesis Caused by Clustered Oxidative DNA Adducts in the Human GenomeThe case for 8,5'-cyclopurine-2'-deoxynucleosides as endogenous DNA lesions that cause neurodegeneration in xeroderma pigmentosum.Do all of the neurologic diseases in patients with DNA repair gene mutations result from the accumulation of DNA damage?The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging.The influence of DNA repair on neurological degeneration, cachexia, skin cancer and internal neoplasms: autopsy report of four xeroderma pigmentosum patients (XP-A, XP-C and XP-D).DNA repair deficiency and neurological disease.Genetic disorders associated with postnatal microcephaly.Quantitative and in situ detection of oxidatively generated DNA damage 8,5'-cyclo-2'-deoxyadenosine using an immunoassay with a novel monoclonal antibody.Sources and consequences of oxidative damage from mitochondria and neurotransmitter signaling.Cockayne syndrome: Clinical features, model systems and pathways.Brain vascular changes in Cockayne syndrome.Cockayne syndrome: a diffusion tensor imaging and volumetric study.Neuroimaging in Cockayne syndrome.
P2860
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P2860
Neurodegeneration in hereditary nucleotide repair disorders.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Neurodegeneration in hereditary nucleotide repair disorders.
@ast
Neurodegeneration in hereditary nucleotide repair disorders.
@en
type
label
Neurodegeneration in hereditary nucleotide repair disorders.
@ast
Neurodegeneration in hereditary nucleotide repair disorders.
@en
prefLabel
Neurodegeneration in hereditary nucleotide repair disorders.
@ast
Neurodegeneration in hereditary nucleotide repair disorders.
@en
P2093
P1476
Neurodegeneration in hereditary nucleotide repair disorders.
@en
P2093
Minagawa M
Morimatsu Y
Tamagawa K
P304
P356
10.1016/S0387-7604(99)00033-9
P577
1999-07-01T00:00:00Z