ETFA
ETFA (Electron transfer flavoprotein subunit alpha) هوَ بروتين يُشَفر بواسطة جين ETFA في الإنسان.[1]
المراجع
- "Entrez Gene: ETFA electron-transfer-flavoprotein, alpha polypeptide (glutaric aciduria II)"، مؤرشف من الأصل في 7 مارس 2010.
قراءة متعمقة
- Frerman FE (1988)، "Acyl-CoA dehydrogenases, electron transfer flavoprotein and electron transfer flavoprotein dehydrogenase."، Biochem. Soc. Trans.، 16 (3): 416–8، PMID 3053288.
- "Glutaric acidemia type II. Heterogeneity in beta-oxidation flux, polypeptide synthesis, and complementary DNA mutations in the alpha subunit of electron transfer flavoprotein in eight patients."، J. Clin. Invest.، 90 (5): 1679–86، 1992، doi:10.1172/JCI116040، PMC 443224، PMID 1430199.
- "Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstable mature protein in a patient."، Am. J. Hum. Genet.، 49 (3): 575–80، 1991، PMC 1683153، PMID 1882842.
- "Molecular cloning and nucleotide sequence of cDNAs encoding the alpha-subunit of human electron transfer flavoprotein."، J. Biol. Chem.، 263 (30): 15773–80، 1988، PMID 3170610.
- "Assignment of Etfdh, Etfb, and Etfa to chromosomes 3, 7, and 13: the mouse homologs of genes responsible for glutaric acidemia type II in human."، Genomics، 33 (1): 131–4، 1996، doi:10.1006/geno.1996.0170، PMID 8617498.
- "Three-dimensional structure of human electron transfer flavoprotein to 2.1-A resolution."، Proc. Natl. Acad. Sci. U.S.A.، 93 (25): 14355–60، 1997، doi:10.1073/pnas.93.25.14355، PMC 26136، PMID 8962055.
- "A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation."، Mol. Genet. Metab.، 67 (2): 138–47، 1999، doi:10.1006/mgme.1999.2856، PMID 10356313.
- "Electron transfer and conformational change in complexes of trimethylamine dehydrogenase and electron transferring flavoprotein."، J. Biol. Chem.، 277 (10): 8457–65، 2002، doi:10.1074/jbc.M111105200، PMID 11756429.
- "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، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency."، Hum. Mutat.، 22 (1): 12–23، 2003، doi:10.1002/humu.10226، PMID 12815589.
- "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes."، Genome Res.، 16 (1): 55–65، 2006، doi:10.1101/gr.4039406، PMC 1356129، PMID 16344560.
- "Electron transfer flavoprotein deficiency: functional and molecular aspects."، Mol. Genet. Metab.، 88 (2): 153–8، 2006، doi:10.1016/j.ymgme.2006.01.009، PMID 16510302.
- "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks."، Cell، 127 (3): 635–48، 2006، doi:10.1016/j.cell.2006.09.026، PMID 17081983.
- "Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency."، Mol. Genet. Metab.، 92 (1–2): 109–14، 2007، doi:10.1016/j.ymgme.2007.06.017، PMID 17689999.
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