About: Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease

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scientific journal article

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rdf:type	Item
description	artículu científicu espublizáu en 1994 (ast) vědecký článek publikovaný v roce 1994 (cs) 1994 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в березні 1994 (uk) 1994 թվականի մարտին հրատարակված գիտական հոդված (hy) vedecký článok (publikovaný 1994/03/01) (sk) مقالة علمية (نشرت في مارس 1994) (ar) wetenschappelijk artikel (gepubliceerd op 1994/03/01) (nl) article scientifique publié en 1994 (fr) scientific journal article (en) im März 1994 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28510609-BCFF7BF3-1FC2-487D-B7ED-19F3DBCFF306
publication date	1994-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q28510609-169AFFB3-1917-4890-9104-C965089A31FD
language of work or name	English
author name string	wds:Q28510609-2620D555-59EF-4DD7-A9DC-A4B033A44C2C wds:Q28510609-3025A7D3-CC46-46C9-82D4-D673AFAA0FB4 wds:Q28510609-5BE13F6C-E8C4-4221-A188-0C33AC46C8A9 wds:Q28510609-5F20BBF0-08CA-4C41-8CC7-9FC3C74C5E12 wds:Q28510609-6F2EEC6F-5473-44D5-B0F1-EBE631C5AE0C wds:Q28510609-86626CC7-897D-4855-B971-8C4A2D649519 wds:Q28510609-AA968987-D927-4220-A8AF-A39FC60324AB wds:Q28510609-EDA5753C-A80D-4F3E-B313-1A309A1A20CD wds:Q28510609-EE26F6E6-5C5F-42CF-B5FE-5997E5EC77C6
OpenCitations bibliographic resource ID	wds:Q28510609-9247054F-C0BA-4BC7-A04C-7C9440C532C5
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1600906
author name string	K Y Lee M Goldstein H A Jinnah M Hunt T Friedmann J K Wamsley P J Langlais N Narang B E Wojcik
OpenCitations bibliographic resource ID	1600906
rdfs:label	Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (en) Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (nl) Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (ast)
skos:prefLabel	Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (en) Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (nl) Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (ast)
name	Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (en) Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (nl) Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (ast)
title	wds:Q28510609-398AC9B3-6F70-4AA3-965F-DFB29E2B9CED
title	Dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease (en)
page(s)	wds:Q28510609-2F521138-C67E-4DC2-831A-76D95AB57845
page(s)	1164-1175
instance of	wds:Q28510609-EFEA1FEA-3EF0-46B2-A270-A5FBB3C0D8FA
instance of	scholarly article
main subject	wds:Q28510609-36D4FAC3-24AF-47F2-951A-AC47BE669E1C wds:Q28510609-634482e5-d889-4d00-809a-130de1406192 wds:Q28510609-B4597B28-973F-4855-8D50-D917599934D8
main subject	Lesch-Nyhan syndrome wd:Q170304 Hypoxanthine guanine phosphoribosyl transferase
PubMed ID	wds:Q28510609-5DD179A8-5FC6-4962-BE65-4B1171D39841
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7509865
PubMed ID	7509865
published in	wds:Q28510609-D23243F5-9879-4DFF-A54A-0687CFEAE9C5
published in	Journal of Neuroscience
issue	wds:Q28510609-1988C051-7169-416A-9A0B-06AFB756E9F7
volume	wds:Q28510609-6AE892ED-7121-4E6F-827D-F89FD5F28158
issue	3 Pt 1
volume	14
DOI	wds:Q28510609-AC78AB6B-C3D6-473D-880F-060C6A01E30F
DOI	http://dx.doi.org/10.1523/JNEUROSCI.14-03-01164.1994
DOI	10.1523/JNEUROSCI.14-03-01164.1994
PMCID	wds:Q28510609-98DD4A6A-A167-4A08-8B21-5DF90B5390FC
PMCID	6577527
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28510609
is cites work of	Convergent mechanisms in etiologically-diverse dystonias Dystonia as a network disorder: what is the role of the cerebellum? Functional analysis of dopaminergic systems in a DYT1 knock-in mouse model of dystonia The housekeeping gene hypoxanthine guanine phosphoribosyltransferase (HPRT) regulates multiple developmental and metabolic pathways of murine embryonic stem cell neuronal differentiation Neurotransmitter changes in the pathophysiology of Lesch-Nyhan syndrome MicroRNA-mediated dysregulation of neural developmental genes in HPRT deficiency: clues for Lesch-Nyhan disease? Basal ganglia dopamine loss due to defect in purine recycling Hypoxanthine-guanine phosphoribosyl transferase regulates early developmental programming of dopamine neurons: implications for Lesch-Nyhan disease pathogenesis Adenosine, dopamine and serotonin receptors imbalance in lymphocytes of Lesch-Nyhan patients Lesch-Nyhan disease and the basal ganglia Lesch-Nyhan disease: from mechanism to model and back again Tissue-specific aberrations of gene expression in HPRT-deficient mice: functional complexity in a monogenic disease? PRTFDC1 is a genetic modifier of HPRT-deficiency in the mouse Induction of basal cell carcinoma features in transgenic human skin expressing Sonic Hedgehog Dopamine transporters are markedly reduced in Lesch-Nyhan disease in vivo Cutaneous gene therapy Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse. Levodopa is not a useful treatment for Lesch-Nyhan disease Loss of dopamine phenotype among midbrain neurons in Lesch-Nyhan disease Genotype-phenotype correlations in neurogenetics: Lesch-Nyhan disease as a model disorder Oxidative stress and dopamine deficiency in a genetic mouse model of Lesch-Nyhan disease Mutational and biochemical analysis of dopamine in dystonia: evidence for decreased dopamine D2 receptor inhibition Attenuated variants of Lesch-Nyhan disease Adenoviruses encoding HPRT correct biochemical abnormalities of HPRT-deficient cells and allow their survival in negative selection medium Hypoxanthine-guanine phosophoribosyltransferase (HPRT) deficiency: Lesch-Nyhan syndrome Elevated UTP and CTP content in cultured neurons from HPRT-deficient transgenic mice The effects of sapropterin on urinary monoamine metabolites in phenylketonuria.

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