PDSS2

An Error has occured retrieving Wikidata item for infobox PDSS2‏ (Decaprenyl diphosphate synthase subunit 2) هوَ بروتين يُشَفر بواسطة جين PDSS2 في الإنسان.

قراءة متعمقة

• Talmud PJ، Drenos F، Shah S، وآخرون (2009). "Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip". Am. J. Hum. Genet. ج. 85 ع. 5: 628–42. DOI:10.1016/j.ajhg.2009.10.014. PMC:2775832. PMID:19913121.
• Mungall AJ، Palmer SA، Sims SK، وآخرون (2003). "The DNA sequence and analysis of human chromosome 6". Nature. ج. 425 ع. 6960: 805–11. DOI:10.1038/nature02055. PMID:14574404.
• Diomedi-Camassei F، Di Giandomenico S، Santorelli FM، وآخرون (2007). "COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement". J. Am. Soc. Nephrol. ج. 18 ع. 10: 2773–80. DOI:10.1681/ASN.2006080833. PMID:17855635.
• 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.
• Maruyama K، Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
• Cui TZ، Kaino T، Kawamukai M (2010). "A subunit of decaprenyl diphosphate synthase stabilizes octaprenyl diphosphate synthase in Escherichia coli by forming a high-molecular weight complex". FEBS Lett. ج. 584 ع. 4: 652–6. DOI:10.1016/j.febslet.2009.12.029. PMID:20051244.
• Strausberg RL، Feingold EA، Grouse LH، وآخرون (2002). "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.
• Saiki R، Nagata A، Kainou T، وآخرون (2005). "Characterization of solanesyl and decaprenyl diphosphate synthases in mice and humans". FEBS J. ج. 272 ع. 21: 5606–22. DOI:10.1111/j.1742-4658.2005.04956.x. PMID:16262699.
• Machuca E، Benoit G، Nevo F، وآخرون (2010). "Genotype-phenotype correlations in non-Finnish congenital nephrotic syndrome". J. Am. Soc. Nephrol. ج. 21 ع. 7: 1209–17. DOI:10.1681/ASN.2009121309. PMC:3152225. PMID:20507940.
• Chen P، Zhao SH، Chu YL، وآخرون (2009). "Anticancer activity of PDSS2, prenyl diphosphate synthase, subunit 2, in gastric cancer tissue and the SGC7901 cell line". Anticancer Drugs. ج. 20 ع. 2: 141–8. DOI:10.1097/CAD.0b013e32832016a9. PMID:19209031.
• Hendrickson SL، Lautenberger JA، Chinn LW، وآخرون (2010). "Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression". PLoS ONE. ج. 5 ع. 9: e12862. DOI:10.1371/journal.pone.0012862. PMC:2943476. PMID:20877624.
• Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، وآخرون (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
• Vieira AR، McHenry TG، Daack-Hirsch S، وآخرون (2008). "Candidate gene/loci studies in cleft lip/palate and dental anomalies finds novel susceptibility genes for clefts". Genet. Med. ج. 10 ع. 9: 668–74. DOI:10.1097/GIM.0b013e3181833793. PMC:2734954. PMID:18978678.
• Bailey SD، Xie C، Do R، وآخرون (2010). "Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study". Diabetes Care. ج. 33 ع. 10: 2250–3. DOI:10.2337/dc10-0452. PMC:2945168. PMID:20628086.