ETFA
من أرابيكا، الموسوعة العربية الحرة
المزيد من اللغات
المزيد من الإجراءات
An Error has occured retrieving Wikidata item for infobox ETFA (Electron transfer flavoprotein subunit alpha) هوَ بروتين يُشَفر بواسطة جين ETFA في الإنسان.[1]
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
- ^ "Entrez Gene: ETFA electron-transfer-flavoprotein, alpha polypeptide (glutaric aciduria II)". مؤرشف من الأصل في 2010-03-07.
قراءة متعمقة
- Frerman FE (1988). "Acyl-CoA dehydrogenases, electron transfer flavoprotein and electron transfer flavoprotein dehydrogenase". Biochem. Soc. Trans. ج. 16 ع. 3: 416–8. PMID:3053288.
- Freneaux E، Sheffield VC، Molin L، وآخرون (1992). "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. ج. 90 ع. 5: 1679–86. DOI:10.1172/JCI116040. PMC:443224. PMID:1430199.
- Indo Y، Glassberg R، Yokota I، Tanaka K (1991). "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. ج. 49 ع. 3: 575–80. PMC:1683153. PMID:1882842.
- Finocchiaro G، Ito M، Ikeda Y، Tanaka K (1988). "Molecular cloning and nucleotide sequence of cDNAs encoding the alpha-subunit of human electron transfer flavoprotein". J. Biol. Chem. ج. 263 ع. 30: 15773–80. PMID:3170610.
- White RA، Dowler LL، Angeloni SV، Koeller DM (1996). "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. ج. 33 ع. 1: 131–4. DOI:10.1006/geno.1996.0170. PMID:8617498.
- Roberts DL، Frerman FE، Kim JJ (1997). "Three-dimensional structure of human electron transfer flavoprotein to 2.1-A resolution". Proc. Natl. Acad. Sci. U.S.A. ج. 93 ع. 25: 14355–60. DOI:10.1073/pnas.93.25.14355. PMC:26136. PMID:8962055.
- Bross P، Pedersen P، Winter V، وآخرون (1999). "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. ج. 67 ع. 2: 138–47. DOI:10.1006/mgme.1999.2856. PMID:10356313.
- Jones M، Talfournier F، Bobrov A، وآخرون (2002). "Electron transfer and conformational change in complexes of trimethylamine dehydrogenase and electron transferring flavoprotein". J. Biol. Chem. ج. 277 ع. 10: 8457–65. DOI:10.1074/jbc.M111105200. PMID:11756429.
- Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Olsen RK، Andresen BS، Christensen E، وآخرون (2003). "Clear relationship between ETF/ETFDH genotype and phenotype in patients with multiple acyl-CoA dehydrogenation deficiency". Hum. Mutat. ج. 22 ع. 1: 12–23. DOI:10.1002/humu.10226. PMID:12815589.
- Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
- Kimura K، Wakamatsu A، Suzuki Y، وآخرون (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. ج. 16 ع. 1: 55–65. DOI:10.1101/gr.4039406. PMC:1356129. PMID:16344560.
- Schiff M، Froissart R، Olsen RK، وآخرون (2006). "Electron transfer flavoprotein deficiency: functional and molecular aspects". Mol. Genet. Metab. ج. 88 ع. 2: 153–8. DOI:10.1016/j.ymgme.2006.01.009. PMID:16510302.
- Olsen JV، Blagoev B، Gnad F، وآخرون (2006). "Global, in vivo, and site-specific phosphorylation dynamics in signaling networks". Cell. ج. 127 ع. 3: 635–48. DOI:10.1016/j.cell.2006.09.026. PMID:17081983.
- Chiong MA، Sim KG، Carpenter K، وآخرون (2007). "Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiency". Mol. Genet. Metab. ج. 92 ع. 1–2: 109–14. DOI:10.1016/j.ymgme.2007.06.017. PMID:17689999.