Consequences of impaired purine recycling in dopaminergic neurons.
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Transiently transfected purine biosynthetic enzymes form stress bodiesHPRT-deficiency dysregulates cAMP-PKA signaling and phosphodiesterase 10A expression: mechanistic insight and potential target for Lesch-Nyhan Disease?Striatal neurodevelopment is dysregulated in purine metabolism deficiency and impacts DARPP-32, BDNF/TrkB expression and signaling: new insights on the molecular and cellular basis of Lesch-Nyhan Syndrome.Attenuated variants of Lesch-Nyhan diseaseHPRT deficiency coordinately dysregulates canonical Wnt and presenilin-1 signaling: a neuro-developmental regulatory role for a housekeeping gene?Severe gouty arthritis and mild neurologic symptoms due to F199C, a newly identified variant of the hypoxanthine guanine phosphoribosyltransferase.Clinical severity in Lesch-Nyhan disease: the role of residual enzyme and compensatory pathwaysConsequences of impaired purine recycling on the proteome in a cellular model of Lesch-Nyhan disease.Ageing as a primary risk factor for Parkinson's disease: evidence from studies of non-human primates.Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease.Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesisPurine metabolism during neuronal differentiation: the relevance of purine synthesis and recycling.Deficiency of the purine metabolic gene HPRT dysregulates microRNA-17 family cluster and guanine-based cellular functions: a role for EPAC in Lesch-Nyhan syndrome.Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder.Xanthine oxido-reductase, free radicals and cardiovascular disease. A critical review.Transcriptomic approach to Lesch-Nyhan disease.The Use of Perinatal 6-Hydroxydopamine to Produce a Rodent Model of Lesch-Nyhan Disease.Effects of methylmercury on dopamine release in MN9D neuronal cells.Lesch-Nyhan Syndrome: Models, Theories, and Therapies.Deficiency of the housekeeping gene hypoxanthine-guanine phosphoribosyltransferase (HPRT) dysregulates neurogenesis.Lesch-Nyhan disease: from mechanism to model and back again.
P2860
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P2860
Consequences of impaired purine recycling in dopaminergic neurons.
description
2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
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2008年学术文章
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name
Consequences of impaired purine recycling in dopaminergic neurons.
@ast
Consequences of impaired purine recycling in dopaminergic neurons.
@en
type
label
Consequences of impaired purine recycling in dopaminergic neurons.
@ast
Consequences of impaired purine recycling in dopaminergic neurons.
@en
prefLabel
Consequences of impaired purine recycling in dopaminergic neurons.
@ast
Consequences of impaired purine recycling in dopaminergic neurons.
@en
P2093
P2860
P1433
P1476
Consequences of impaired purine recycling in dopaminergic neurons.
@en
P2093
H A Jinnah
I Ceballos-Picot
J C Lewers
T L Shirley
P2860
P304
P356
10.1016/J.NEUROSCIENCE.2007.10.065
P407
P577
2008-01-17T00:00:00Z