Organization and nucleotide sequences of the human tyrosinase gene and a truncated tyrosinase-related segment.Giebel L.B., Strunk K.M., Spritz R.A.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenomics 9:435-445 (1991)Cited in11
Isolation and sequence of a cDNA clone for human tyrosinase that maps at the mouse c-albino locus.Kwon B.S., Haq A.K., Pomerantz S.H., Halaban R.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 84:7473-7477 (1987)Cited in1Mapped to7
No title available.Kwon B.S., Haq A.K., Pomerantz S.H., Halaban R.Cited forERRATUM OF PUBMED:2823263, SEQUENCE REVISION TO 384-398CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Proc. Natl. Acad. Sci. U.S.A. 85:6352-6352 (1988)Cited in1
Induction of pigmentation in mouse fibroblasts by expression of human tyrosinase cDNA.Bouchard B., Fuller B.B., Vijayasaradhi S., Houghton A.N.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)TissueMelanomaCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Exp. Med. 169:2029-2042 (1989)Cited in1
A single base insertion in the putative transmembrane domain of the tyrosinase gene as a cause for tyrosinase-negative oculocutaneous albinism.Chintamaneni C.D., Halaban R., Kobayashi Y., Witkop C.J., Kwon B.S.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 88:5272-5276 (1991)Cited in1
The tyrosinase gene codes for an antigen recognized by autologous cytolytic T lymphocytes on HLA-A2 melanomas.Brichard V., van Pel A., Woelfel T., Woelfel C., de Plaen E., Lethe B.G., Coulie P., Boon T.View abstractCited forNUCLEOTIDE SEQUENCE (ISOFORM 1)TissueMelanoma, T-cellCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Exp. Med. 178:489-495 (1993)Cited in1
The tyrosinase gene in gorillas and the albinism of 'Snowflake'.Martinez-Arias R., Comas D., Andres A., Abello M.-T., Domingo-Roura X., Bertranpetit J.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA] (ISOFORM 1), VARIANT TYR-192CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCPigment Cell Res. 13:467-470 (2000)Cited in2
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2)TissueSkinCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
Characteristic sequences in the upstream region of the human tyrosinase gene.Kikuchi H., Miura H., Yamamoto H., Takeuchi T., Dei T., Watanabe M.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 1-272TissueLiverCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochim. Biophys. Acta 1009:283-286 (1989)Cited in1
Functional analysis of the cDNA encoding human tyrosinase precursor.Takeda A., Tomita Y., Okinaga S., Tagami H., Shibahara S.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] OF 1-32CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochem. Biophys. Res. Commun. 162:984-990 (1989)Cited in1
Molecular phylogenetics and the origins of placental mammals.Murphy W.J., Eizirik E., Johnson W.E., Zhang Y.-P., Ryder O.A., O'Brien S.J.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 54-195, VARIANT TYR-192CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 409:614-618 (2001)Cited in599+Mapped to78
Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase gene.Oetting W.S., King R.A.View abstractCited forREVIEW ON OCA VARIANTSCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mutat. 2:1-6 (1993)Cited in1
Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism.Oetting W.S., King R.A.View abstractCited forREVIEW ON OCA1 VARIANTSCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCHum. Mutat. 13:99-115 (1999)Cited in4
Proteomic analysis of early melanosomes: identification of novel melanosomal proteins.Basrur V., Yang F., Kushimoto T., Higashimoto Y., Yasumoto K., Valencia J., Muller J., Vieira W.D., Watabe H.[...], Appella E.View abstractCited forSUBCELLULAR LOCATION [LARGE SCALE ANALYSIS]TissueMelanomaCategoriesSubcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Proteome Res. 2:69-79 (2003)Cited in29
Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes.Chi A., Valencia J.C., Hu Z.-Z., Watabe H., Yamaguchi H., Mangini N.J., Huang H., Canfield V.A., Cheng K.C.[...], Hunt D.F.View abstractCited forSUBCELLULAR LOCATION [LARGE SCALE ANALYSIS]TissueMelanomaCategoriesSubcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Proteome Res. 5:3135-3144 (2006)Cited in80
Structure of Human Tyrosinase Related Protein1 Reveals a Binuclear Zinc Active Site Important for Melanogenesis.Lai X., Wichers H.J., Soler-Lopez M., Dijkstra B.W.View abstractCited forFUNCTION, CATALYTIC ACTIVITYCategoriesFunctionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCAngew. Chem. Int. Ed. Engl. 56:9812-9815 (2017)Cited in2
Melanocytes Sense Blue Light and Regulate Pigmentation through Opsin-3.Regazzetti C., Sormani L., Debayle D., Bernerd F., Tulic M.K., De Donatis G.M., Chignon-Sicard B., Rocchi S., Passeron T.View abstractCited forINTERACTION WITH DCTCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Invest. Dermatol. 138:171-178 (2018)Cited in4
Detection of mutations in the tyrosinase gene in a patient with type IA oculocutaneous albinism.Spritz R.A., Strunk K.M., Giebel L.B., King R.A.Cited forVARIANTS OCA1A LYS-373 AND ASN-383, VARIANTS TYR-192 AND GLN-402CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCN. Engl. J. Med. 322:1724-1728 (1990)Cited in1
A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinism.Giebel L.B., Strunk K.M., King R.A., Hanifin J.M., Spritz R.A.View abstractCited forVARIANT OCA1A LEU-81CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 87:3255-3258 (1990)Cited in1
Tyrosinase gene mutations associated with type IB ('yellow') oculocutaneous albinism.Giebel L.B., Tripathi R.K., Strunk K.M., Hanifin J.M., Jackson C.E., King R.A., Spritz R.A.View abstractCited forVARIANTS OCA1B PHE-275 AND LEU-406CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCAm. J. Hum. Genet. 48:1159-1167 (1991)Cited in1Mapped to6
No title available.Giebel L.B., Tripathi R.K., Strunk K.M., Hanifin J.M., Jackson C.E., King R.A., Spritz R.A.Cited forERRATUM OF PUBMED:1903591SourceUniProtKB reviewed (Swiss-Prot)Am. J. Hum. Genet. 49:696-696 (1991)Cited in1
Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutions.Tripathi R.K., Strunk K.M., Giebel L.B., Weleber R.G., Spritz R.A.View abstractCited forVARIANTS OCA1A SER-21; TRP-217; HIS-299; SER-403; SER-446 AND ASN-448CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCAm. J. Med. Genet. 43:865-871 (1992)Cited in1
Homozygous tyrosinase gene mutation in an American black with tyrosinase- negative (type IA) oculocutaneous albinism.Spritz R.A., Strunk K.M., Hsieh C.-L., Sekhon G.S., Francke U.View abstractCited forVARIANT OCA1A ARG-89CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCAm. J. Hum. Genet. 48:318-324 (1991)Cited in1
A tyrosinase gene missense mutation in temperature-sensitive type I oculocutaneous albinism. A human homologue to the Siamese cat and the Himalayan mouse.Giebel L.B., Tripathi R.K., King R.A., Spritz R.A.View abstractCited forVARIANT OCA1B GLN-422CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Clin. Invest. 87:1119-1122 (1991)Cited in1
Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinism.King R.A., Mentink M.M., Oetting W.S.View abstractCited forVARIANTS OCA1A GLY-42; TYR-55; THR-206 AND ARG-419CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Biol. Med. 8:19-29 (1991)Cited in1