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HSD17B4
An Error has occured retrieving Wikidata item for infobox HSD17B4 (Hydroxysteroid 17-beta dehydrogenase 4) هوَ بروتين يُشَفر بواسطة جين HSD17B4 في الإنسان.[1][1][2][3][4]
الوظيفة
![]() | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
![]() | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
- ^ أ ب Huyghe S، Mannaerts GP، Baes M، Van Veldhoven PP (2006). "Peroxisomal multifunctional protein-2: the enzyme, the patients and the knockout mouse model". Biochim. Biophys. Acta. ج. 1761 ع. 9: 973–94. DOI:10.1016/j.bbalip.2006.04.006. PMID:16766224.
- ^ Leenders F، Prescher G، Dolez V، Begue A، de Launoit Y، Adamski J (مارس 1997). "Assignment of human 17 beta-hydroxysteroid dehydrogenase IV to chromosome 5q2 by fluorescence in situ hybridization". Genomics. ج. 37 ع. 3: 403–4. DOI:10.1006/geno.1996.0578. PMID:8938456.
- ^ "Entrez Gene: HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4". مؤرشف من الأصل في 2010-12-05.
- ^ Persson B، Kallberg Y، Bray JE، Bruford E، Dellaporta SL، Favia AD، Duarte RG، Jornvall H، Kavanagh KL، Kedishvili N، Kisiela M، Maser E، Mindnich R، Orchard S، Penning TM، Thornton JM، Adamski J، Oppermann U (فبراير 2009). "The SDR (short-chain dehydrogenase/reductase and related enzymes) nomenclature initiative". Chem Biol Interact. ج. 178 ع. 1–3: 94–8. DOI:10.1016/j.cbi.2008.10.040. PMC:2896744. PMID:19027726.
قراءة متعمقة
- de Launoit Y، Adamski J (1999). "Unique multifunctional HSD17B4 gene product: 17beta-hydroxysteroid dehydrogenase 4 and D-3-hydroxyacyl-coenzyme A dehydrogenase/hydratase involved in Zellweger syndrome". J. Mol. Endocrinol. ج. 22 ع. 3: 227–40. DOI:10.1677/jme.0.0220227. PMID:10343282.
- Huyghe S، Mannaerts GP، Baes M، Van Veldhoven PP (2006). "Peroxisomal multifunctional protein-2: the enzyme, the patients and the knockout mouse model". Biochim. Biophys. Acta. ج. 1761 ع. 9: 973–94. DOI:10.1016/j.bbalip.2006.04.006. PMID:16766224.
- Palosaari PM، Hiltunen JK (1990). "Peroxisomal bifunctional protein from rat liver is a trifunctional enzyme possessing 2-enoyl-CoA hydratase, 3-hydroxyacyl-CoA dehydrogenase, and delta 3, delta 2-enoyl-CoA isomerase activities". J. Biol. Chem. ج. 265 ع. 5: 2446–9. PMID:2303409.
- Adamski J، Normand T، Leenders F، وآخرون (1995). "Molecular cloning of a novel widely expressed human 80 kDa 17 beta-hydroxysteroid dehydrogenase IV". Biochem. J. ج. 311 ع. 2: 437–43. PMC:1136019. PMID:7487879.
- Markus M، Husen B، Adamski J (1996). "The subcellular localization of 17 beta-hydroxysteroid dehydrogenase type 4 and its interaction with actin". J. Steroid Biochem. Mol. Biol. ج. 55 ع. 5–6: 617–21. DOI:10.1016/0960-0760(95)00213-8. PMID:8547189.
- Jiang LL، Kobayashi A، Matsuura H، وآخرون (1997). "Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase". J. Biochem. ج. 120 ع. 3: 624–32. DOI:10.1093/oxfordjournals.jbchem.a021458. PMID:8902629.
- Jiang LL، Miyazawa S، Souri M، Hashimoto T (1997). "Structure of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein". J. Biochem. ج. 121 ع. 2: 364–9. DOI:10.1093/oxfordjournals.jbchem.a021596. PMID:9089413.
- Jiang LL، Kurosawa T، Sato M، وآخرون (1997). "Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein". J. Biochem. ج. 121 ع. 3: 506–13. DOI:10.1093/oxfordjournals.jbchem.a021615. PMID:9133619.
- Novikov D، Dieuaide-Noubhani M، Vermeesch JR، وآخرون (1997). "The human peroxisomal multifunctional protein involved in bile acid synthesis: activity measurement, deficiency in Zellweger syndrome and chromosome mapping". Biochim. Biophys. Acta. ج. 1360 ع. 3: 229–40. DOI:10.1016/s0925-4439(97)00003-3. PMID:9197465.
- Suzuki Y، Jiang LL، Souri M، وآخرون (1997). "D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder". Am. J. Hum. Genet. ج. 61 ع. 5: 1153–62. DOI:10.1086/301599. PMC:1716023. PMID:9345094.
- van Grunsven EG، van Berkel E، IJlst L، وآخرون (1998). "Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency". Proc. Natl. Acad. Sci. U.S.A. ج. 95 ع. 5: 2128–33. DOI:10.1073/pnas.95.5.2128. PMC:19272. PMID:9482850.
- Dong Y، Qiu QQ، Debear J، وآخرون (1999). "17Beta-hydroxysteroid dehydrogenases in human bone cells". J. Bone Miner. Res. ج. 13 ع. 10: 1539–46. DOI:10.1359/jbmr.1998.13.10.1539. PMID:9783542.
- Leenders F، Dolez V، Begue A، وآخرون (1999). "Structure of the gene for the human 17beta-hydroxysteroid dehydrogenase type IV". Mamm. Genome. ج. 9 ع. 12: 1036–41. DOI:10.1007/s003359900921. PMID:9880674.
- Green VL، Speirs V، Landolt AM، وآخرون (1999). "17Beta-hydroxysteroid dehydrogenase type 1, 2, 3, and 4 expression and enzyme activity in human anterior pituitary adenomas". J. Clin. Endocrinol. Metab. ج. 84 ع. 4: 1340–5. DOI:10.1210/jc.84.4.1340. PMID:10199776.
- van Grunsven EG، Mooijer PA، Aubourg P، Wanders RJ (1999). "Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency". Hum. Mol. Genet. ج. 8 ع. 8: 1509–16. DOI:10.1093/hmg/8.8.1509. PMID:10400999.
- Itoh M، Suzuki Y، Takashima S (1999). "A novel peroxisomal enzyme, D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein: its expression in the developing human brain". Microsc. Res. Tech. ج. 45 ع. 6: 383–8. DOI:10.1002/(SICI)1097-0029(19990615)45:6<383::AID-JEMT5>3.0.CO;2-7. PMID:10402265.
- Möller G، Leenders F، van Grunsven EG، وآخرون (1999). "Characterization of the HSD17B4 gene: D-specific multifunctional protein 2/17beta-hydroxysteroid dehydrogenase IV". J. Steroid Biochem. Mol. Biol. ج. 69 ع. 1–6: 441–6. DOI:10.1016/S0960-0760(99)00066-7. PMID:10419023.
- Haapalainen AM، van Aalten DM، Meriläinen G، وآخرون (2001). "Crystal structure of the liganded SCP-2-like domain of human peroxisomal multifunctional enzyme type 2 at 1.75 A resolution". J. Mol. Biol. ج. 313 ع. 5: 1127–38. DOI:10.1006/jmbi.2001.5084. PMID:11700068.