ACAD8: Difference between revisions
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==References== | ==References== | ||
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==Further reading== | ==Further reading== | ||
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Revision as of 13:51, 4 September 2012
WikiDoc Resources for ACAD8 |
Articles |
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Media |
Evidence Based Medicine |
Clinical Trials |
Ongoing Trials on ACAD8 at Clinical Trials.gov Clinical Trials on ACAD8 at Google
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Guidelines / Policies / Govt |
US National Guidelines Clearinghouse on ACAD8
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Books |
News |
Commentary |
Definitions |
Patient Resources / Community |
Directions to Hospitals Treating ACAD8 Risk calculators and risk factors for ACAD8
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Healthcare Provider Resources |
Continuing Medical Education (CME) |
International |
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Business |
Experimental / Informatics |
Acyl-Coenzyme A dehydrogenase family, member 8, also known as ACAD8, is a human gene.[1]
References
Further reading
- Näär AM, Beaurang PA, Zhou S; et al. (1999). "Composite co-activator ARC mediates chromatin-directed transcriptional activation". Nature. 398 (6730): 828–32. doi:10.1038/19789. PMID 10235267.
- Telford EA, Moynihan LM, Markham AF, Lench NJ (1999). "Isolation and characterisation of a cDNA encoding the precursor for a novel member of the acyl-CoA dehydrogenase gene family". Biochim. Biophys. Acta. 1446 (3): 371–6. PMID 10524212.
- Andresen BS, Christensen E, Corydon TJ; et al. (2000). "Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism". Am. J. Hum. Genet. 67 (5): 1095–103. PMID 11013134.
- Nguyen TV, Andresen BS, Corydon TJ; et al. (2003). "Identification of isobutyryl-CoA dehydrogenase and its deficiency in humans". Mol. Genet. Metab. 77 (1–2): 68–79. PMID 12359132.
- 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. PMID 12477932.
- 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.
- Battaile KP, Nguyen TV, Vockley J, Kim JJ (2004). "Structures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenases". J. Biol. Chem. 279 (16): 16526–34. doi:10.1074/jbc.M400034200. PMID 14752098.
- 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. PMID 15489334.
- Ma J, Dempsey AA, Stamatiou D; et al. (2007). "Identifying leukocyte gene expression patterns associated with plasma lipid levels in human subjects". Atherosclerosis. 191 (1): 63–72. doi:10.1016/j.atherosclerosis.2006.05.032. PMID 16806233.