ESD (gene): Difference between revisions
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'''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> | |||
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==References== | ==References== | ||
{{reflist | {{reflist}} | ||
==Further reading== | ==Further reading== | ||
{{refbegin | 2}} | {{refbegin | 2}} | ||
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*{{cite journal | | *{{cite journal | vauthors=Munier F, Balmer A, von Moos C |title=[Lausanne study of retinoblastoma, 1986-90: deletion of esterase D locus in a collective of 128 patients] |journal=Klinische Monatsblätter für Augenheilkunde |volume=198 |issue= 5 |pages= 419–24 |year= 1991 |pmid= 1886375 |doi=10.1055/s-2008-1045999 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Young LJ, Lee EY, To HA |title=Human esterase D gene: complete cDNA sequence, genomic structure, and application in the genetic diagnosis of human retinoblastoma. |journal=Hum. Genet. |volume=79 |issue= 2 |pages= 137–41 |year= 1988 |pmid= 3164702 |doi=10.1007/BF00280552 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Lee EY, Lee WH |title=Molecular cloning of the human esterase D gene, a genetic marker of retinoblastoma. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=83 |issue= 17 |pages= 6337–41 |year= 1986 |pmid= 3462698 |doi=10.1073/pnas.83.17.6337 | pmc=386498 }} | ||
*{{cite journal | | *{{cite journal | vauthors=Squire J, Dryja TP, Dunn J |title=Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=83 |issue= 17 |pages= 6573–7 |year= 1986 |pmid= 3462714 |doi=10.1073/pnas.83.17.6573 | pmc=386546 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Lee WH, Wheatley W, Benedict WF |title=Purification, biochemical characterization, and biological function of human esterase D. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=83 |issue= 18 |pages= 6790–4 |year= 1986 |pmid= 3462728 |doi=10.1073/pnas.83.18.6790 | pmc=386595 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Cortivo P, Caenazzo L, Crestani C |title=Genetic study of red cell esterase D polymorphism by ultrathin layer isoelectric focusing. Distribution in the Veneto population (Italy). |journal=Z. Rechtsmed. |volume=98 |issue= 1 |pages= 39–42 |year= 1987 |pmid= 3591015 |doi=10.1007/BF00200384 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Eiberg H, Mohr J |title=Identity of the polymorphisms for esterase D and S-formylglutathione hydrolase in red blood cells. |journal=Hum. Genet. |volume=74 |issue= 2 |pages= 174–5 |year= 1986 |pmid= 3770744 |doi=10.1007/BF00282085 }} | ||
*{{cite journal | | *{{cite journal | vauthors=Tsuchida S, Fukui E, Ikemoto S |title=Molecular analysis of esterase D polymorphism. |journal=Hum. Genet. |volume=93 |issue= 3 |pages= 255–8 |year= 1994 |pmid= 7907313 |doi=10.1007/BF00212018 }} | ||
*{{cite journal | | *{{cite journal | vauthors=Hu RM, Han ZG, Song HD |title=Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=97 |issue= 17 |pages= 9543–8 |year= 2000 |pmid= 10931946 |doi= 10.1073/pnas.160270997 | pmc=16901 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Strausberg RL, Feingold EA, Grouse LH |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Saito S, Iida A, Sekine A |title=Catalog of 680 variations among eight cytochrome p450 ( CYP) genes, nine esterase genes, and two other genes in the Japanese population. |journal=J. Hum. Genet. |volume=48 |issue= 5 |pages= 249–70 |year= 2003 |pmid= 12721789 |doi= 10.1007/s10038-003-0021-7 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Sergeev AS, Agapova RK, Bogadel'nikova IV, Perel'man MI |title=[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] |journal=Genetika |volume=39 |issue= 7 |pages= 996–1002 |year= 2003 |pmid= 12942785 |doi= }} | ||
*{{cite journal | | *{{cite journal | vauthors=Ota T, Suzuki Y, Nishikawa T |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Dunham A, Matthews LH, Burton J |title=The DNA sequence and analysis of human chromosome 13. |journal=Nature |volume=428 |issue= 6982 |pages= 522–8 |year= 2004 |pmid= 15057823 |doi= 10.1038/nature02379 | pmc=2665288 |display-authors=etal}} | ||
*{{cite journal | | *{{cite journal | vauthors=Gerhard DS, Wagner L, Feingold EA |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 |display-authors=etal}} | ||
}} | }} | ||
{{refend}} | {{refend}} | ||
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Revision as of 00:37, 31 August 2017
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External IDs | GeneCards: [1] | ||||||
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Species | Human | Mouse | |||||
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
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S-formylglutathione hydrolase is an enzyme that in humans is encoded by the ESD gene.[1]
References
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.
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