[cite web | title = Entrez Gene: CENTA2 centaurin, alpha 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55803| accessdate = ] ] PBB_Summary
section_title =
summary_text =
References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Jenne DE, Tinschert S, Stegmann E, "et al." |title=A common set of at least 11 functional genes is lost in the majority of NF1 patients with gross deletions. |journal=Genomics |volume=66 |issue= 1 |pages= 93–7 |year= 2000 |pmid= 10843809 |doi= 10.1006/geno.2000.6179
*cite journal | author=Whitley P, Gibbard AM, Koumanov F, "et al." |title=Identification of centaurin-alpha2: a phosphatidylinositide-binding protein present in fat, heart and skeletal muscle. |journal=Eur. J. Cell Biol. |volume=81 |issue= 4 |pages= 222–30 |year= 2003 |pmid= 12018390 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Hanck T, Stricker R, Sedehizade F, Reiser G |title=Identification of gene structure and subcellular localization of human centaurin alpha 2, and p42IP4, a family of two highly homologous, Ins 1,3,4,5-P4-/PtdIns 3,4,5-P3-binding, adapter proteins. |journal=J. Neurochem. |volume=88 |issue= 2 |pages= 326–36 |year= 2004 |pmid= 14690521 |doi=
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Venturin M, Bentivegna A, Moroni R, "et al." |title=Evidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion interval. |journal=Ann. Hum. Genet. |volume=69 |issue= Pt 5 |pages= 508–16 |year= 2005 |pmid= 16138909 |doi= 10.1111/j.1529-8817.2005.00203.x
*cite journal | author=Douglas J, Cilliers D, Coleman K, "et al." |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083
PBB_Controls
update_page = yes
require_manual_inspection = no
update_protein_box = yes
update_summary = yes
update_citations = yes
