ESD (gene)
S-formylglutathione hydrolase is an enzyme that in humans is encoded by the ESD gene.[1]
Further reading
Further reading
- 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. PMID 1886375.
- 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. PMID 3164702.
- Lee EY, Lee WH (1986). “Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma”. Proc. Natl. Acad. Sci. U.S.A. 83 (17): 6337–41. doi:10.1073/pnas.83.17.6337. PMC 386498. PMID 3462698.
- Squire J, Dryja TP, Dunn J, et al. (1986). “Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13”. Proc. Natl. Acad. Sci. U.S.A. 83 (17): 6573–7. doi:10.1073/pnas.83.17.6573. PMC 386546. PMID 3462714.
- Lee WH, Wheatley W, Benedict WF, et al. (1986). “Purification, biochemical characterization, and biological function of human esterase D.” Proc. Natl. Acad. Sci. U.S.A. 83 (18): 6790–4. doi:10.1073/pnas.83.18.6790. PMC 386595. PMID 3462728.
- 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. PMID 3591015.
- 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. PMID 3770744.
- Tsuchida S, Fukui E, Ikemoto S (1994). “Molecular analysis of esterase D polymorphism”. Hum. Genet. 93 (3): 255–8. doi:10.1007/BF00212018. PMID 7907313.
- Hu RM, Han ZG, Song HD, et al. (2000). “Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning”. Proc. Natl. Acad. Sci. U.S.A. 97 (17): 9543–8. doi:10.1073/pnas.160270997. PMC 16901. PMID 10931946.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). “Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences”. Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- 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. PMID 12721789.
- 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. PMID 12942785.
- 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. PMID 14702039.
- Dunham A, Matthews LH, Burton J, et al. (2004). “The DNA sequence and analysis of human chromosome 13”. Nature. 428 (6982): 522–8. doi:10.1038/nature02379. PMC 2665288. PMID 15057823.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)”. Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Looking for the patient version?
© 2026 MyEClinic – IFTM Institut für Telematik in der Medizin GmbH