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dbpedia-es:Tirosin_hidroxilasa
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dbpedia-es:Tirosina_hidroxilasa
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dbpedia-es:Tirosín_hidroxilasa
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dbpedia-es:Tirosina_hidroxilasa
Subject Item
dbr:Tyrosine_hydroxylase
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dbpedia-es:Tirosina_hidroxilasa
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dbpedia-es:Tirosina_hidroxilasa
rdf:type
dbo:Biomolecule wikidata:Q8054 wikidata:Q206229 owl:Thing dbo:Protein
rdfs:label
Tirosina hidroxilasa
rdfs:comment
La tirosina hidroxilasa o tirosina 3-monooxigenasa (EC 1.14.16.2) es la enzima responsable de catalizar la conversión del aminoácido L-tirosina a dihidroxifenilalanina (DOPA). La DOPA es el precursor de la dopamina, que a su vez es también el precursor de la noradrenalina y la adrenalina. En humanos, la tirosina hidroxilasa es codificada por el gen TH.​
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category-es:Hidroxilasas category-es:Neurotransmisores category-es:Oxigenasas
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wikipedia-es:Tirosina_hidroxilasa
prop-es:altsymbols
DYT14; DYT5b; TYH
prop-es:autor
Zhou QY, Quaife CJ, Palmiter RD Kobayashi K, Kaneda N, Ichinose H, et al. Knappskog PM, Flatmark T, Mallet J, et al. Le Bourdellès B, Boularand S, Boni C, et al. Meloni R, Biguet NF, Mallet J Lüdecke B, Bartholomé K Haycock JW, Ahn NG, Cobb MH, Krebs EG Craig SP, Buckle VJ, Lamouroux A, et al. Lüdecke B, Dworniczak B, Bartholomé K Kaneda N, Kobayashi K, Ichinose H, et al. Ginns EI, Rehavi M, Martin BM, et al. Grima B, Lamouroux A, Boni C, et al. Haycock JW O'Malley KL, Anhalt MJ, Martin BM, et al. Joh TH, Park DH, Reis DJ Masserano JM, Weiner N Vulliet PR, Woodgett JR, Cohen P Coker GT, Vinnedge L, O'Malley KL
prop-es:año
1979 1983 2002 1986 1987 1984 1990 1988 1989 1995 1992 1996
prop-es:banda
155
prop-es:brazo
p
prop-es:chembl
1969
prop-es:cromosoma
11
prop-es:doi
101111 101093 101016 101021 101007 101038 101385 101159 101073
prop-es:ecnumber
114162
prop-es:geneatlasImage
PBB_GE_TH_208291_s_at_tn.png
prop-es:hgncid
11782
prop-es:homologene
307
prop-es:hsEnsembl
ENSG00000180176
prop-es:hsEntrezgene
7054
prop-es:hsGenlocChr
11
prop-es:hsGenlocDb
hg19
prop-es:hsGenlocEnd
2193107
prop-es:hsGenlocStart
2185159
prop-es:hsRefseqmrna
NM_000360
prop-es:hsRefseqprotein
NP_000351
prop-es:hsUniprot
P07101
prop-es:mmEnsembl
ENSMUSG00000000214
prop-es:mmEntrezgene
21823
prop-es:mmGenlocChr
7
prop-es:mmGenlocEnd
142931128
prop-es:mmGenlocStart
142892752
prop-es:mmRefseqmrna
NM_009377
prop-es:mmRefseqprotein
NP_033403
prop-es:mmUniprot
P24529
prop-es:name
Tirosina hidroxilasa
prop-es:número
6523 6114 6 7 1 2 3 15 10 20 22 16
prop-es:omim
191290
prop-es:pmc
336196 306135 48658
prop-es:pmid
2892893 2896667 8528210 6137760 2902075 7715703 2882428 7814018 2888085 1347949 6150037 2905129 2887169 2892528 2872999 12428766 7789962 1973163 33381
prop-es:publicación
Hum. Mol. Genet. J. Biochem. Nucleic Acids Res. Nature J. Neurochem. Biochem. Biophys. Res. Commun. Cytogenet. Cell Genet. Hum. Genet. Mol. Cell. Biochem. Mol. Neurobiol. J. Biol. Chem. Biochemistry Proc. Natl. Acad. Sci. U.S.A.
prop-es:páginas
11682 907 123 640 6910 1341 389 988 971 129 707 716 6733 4744 29 7406 1209 13680 2365
prop-es:símbolo
TH
prop-es:título
Isolation of a full-length cDNA clone encoding human tyrosine hydroxylase type 3. A single human gene encoding multiple tyrosine hydroxylases with different predicted functional characteristics. A point mutation in the tyrosine hydroxylase gene associated with Segawa's syndrome. Tyrosine hydroxylase regulation in the central nervous system. ERK1 and ERK2, two microtubule-associated protein 2 kinases, mediate the phosphorylation of tyrosine hydroxylase at serine-31 in situ. Characterization of rat and human tyrosine hydroxylase genes: functional expression of both promoters in neuronal and non-neuronal cell types. Post-genomic era and gene discovery for psychiatric diseases: there is a new art of the trade? The example of the HUMTH01 microsatellite in the Tyrosine Hydroxylase gene. Isolation and characterization of the human tyrosine hydroxylase gene: identification of 5' alternative splice sites responsible for multiple mRNAs. Isolation of a novel cDNA clone for human tyrosine hydroxylase: alternative RNA splicing produces four kinds of mRNA from a single gene. Recessively inherited L-DOPA-responsive dystonia caused by a point mutation in the tyrosine hydroxylase gene. Phosphorylation of tyrosine hydroxylase by calmodulin-dependent multiprotein kinase. Structure of the human tyrosine hydroxylase gene: alternative splicing from a single gene accounts for generation of four mRNA types. Analysis of the 5' region of the human tyrosine hydroxylase gene: combinatorial patterns of exon splicing generate multiple regulated tyrosine hydroxylase isoforms. Phosphorylation of tyrosine hydroxylase in situ at serine 8, 19, 31, and 40. Targeted disruption of the tyrosine hydroxylase gene reveals that catecholamines are required for mouse fetal development. Direct phosphorylation of brain tyrosine hydroxylase by cyclic AMP-dependent protein kinase: mechanism of enzyme activation. Expression of human tyrosine hydroxylase cDNA in invertebrate cells using a baculovirus vector. Localization of the human tyrosine hydroxylase gene to 11p15: gene duplication and evolution of metabolic pathways. Frequent sequence variant in the human tyrosine hydroxylase gene.
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,
prop-es:volumen
146 157 42 50 53 4 15 26 259 263 103 265 75 374 89 95 326
prop-es:width
230
prop-es:ecNumber
114162
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1240859
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130159170
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11966
dbo:arm
p
dbo:band
15.5
dbo:chromosome
11
dbo:ecNumber
1.14.16.2
dbo:hgncid
11782
dbo:omim
191290
dbo:symbol
TH DYT14; DYT5b; TYH
prov:wasDerivedFrom
n15:0
dbo:abstract
La tirosina hidroxilasa o tirosina 3-monooxigenasa (EC 1.14.16.2) es la enzima responsable de catalizar la conversión del aminoácido L-tirosina a dihidroxifenilalanina (DOPA). La DOPA es el precursor de la dopamina, que a su vez es también el precursor de la noradrenalina y la adrenalina. En humanos, la tirosina hidroxilasa es codificada por el gen TH.​
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