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{{Underlinked|date=March 2014}}
{{Infobox_gene}}
{{Infobox_gene}}
'''S-formylglutathione hydrolase''' is an [[enzyme]] that in humans is encoded by the ''ESD'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: ESD esterase D/formylglutathione hydrolase| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2098| accessdate = }}</ref>
'''S-formylglutathione hydrolase''' is an [[enzyme]] that in humans is encoded by the ''ESD'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: ESD esterase D/formylglutathione hydrolase| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2098| accessdate = }}</ref>
Munier F, Balmer A, von Moos C, et al. (1991). "[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients]". Klinische Monatsblätter für Augenheilkunde. 198 (5): 419–24. doi:10.1055/s-2008-1045999. PMID1886375.
Young LJ, Lee EY, To HA, et al. (1988). "Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma". Hum. Genet. 79 (2): 137–41. doi:10.1007/BF00280552. PMID3164702.
Cortivo P, Caenazzo L, Crestani C, et al. (1987). "Genetic study of red cell esterase D polymorphism by ultrathin layer isoelectric focusing. Distribution in the Veneto population (Italy)". Z. Rechtsmed. 98 (1): 39–42. doi:10.1007/BF00200384. PMID3591015.
Eiberg H, Mohr J (1986). "Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cells". Hum. Genet. 74 (2): 174–5. doi:10.1007/BF00282085. PMID3770744.
Tsuchida S, Fukui E, Ikemoto S (1994). "Molecular analysis of esterase D polymorphism". Hum. Genet. 93 (3): 255–8. doi:10.1007/BF00212018. PMID7907313.
Saito S, Iida A, Sekine A, et al. (2003). "Catalog of 680 variations among eight cytochrome p450 ( CYP) genes, nine esterase genes, and two other genes in the Japanese population". J. Hum. Genet. 48 (5): 249–70. doi:10.1007/s10038-003-0021-7. PMID12721789.
Sergeev AS, Agapova RK, Bogadel'nikova IV, Perel'man MI (2003). "[The use of discrete characters in discriminant analysis for diagnosis of pulmonary tuberculosis and for classification of patients differing in treatment efficiency based on polymorphisms at nine codominant loci-HP, GC, TF, PI, PGM1, GLO1, C3, ACP1 and ESD]". Genetika. 39 (7): 996–1002. PMID12942785.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID14702039.