[cite web | title = Entrez Gene: CC2D1A coiled-coil and C2 domain containing 1A| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54862| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Albert PR, Lemonde S |title=5-HT1A receptors, gene repression, and depression: guilt by association. |journal=The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry |volume=10 |issue= 6 |pages= 575–93 |year= 2005 |pmid= 15534042 |doi= 10.1177/1073858404267382
*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=Matsuda A, Suzuki Y, Honda G, "et al." |title=Large-scale identification and characterization of human genes that activate NF-kappaB and MAPK signaling pathways. |journal=Oncogene |volume=22 |issue= 21 |pages= 3307–18 |year= 2003 |pmid= 12761501 |doi= 10.1038/sj.onc.1206406
*cite journal | author=Basel-Vanagaite L, Alkelai A, Straussberg R, "et al." |title=Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity. |journal=J. Med. Genet. |volume=40 |issue= 10 |pages= 729–32 |year= 2003 |pmid= 14569116 |doi=
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*cite journal | author=Lemonde S, Rogaeva A, Albert PR |title=Cell type-dependent recruitment of trichostatin A-sensitive repression of the human 5-HT1A receptor gene. |journal=J. Neurochem. |volume=88 |issue= 4 |pages= 857–68 |year= 2004 |pmid= 14756806 |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=Rush J, Moritz A, Lee KA, "et al." |title=Immunoaffinity profiling of tyrosine phosphorylation in cancer cells. |journal=Nat. Biotechnol. |volume=23 |issue= 1 |pages= 94–101 |year= 2005 |pmid= 15592455 |doi= 10.1038/nbt1046
*cite journal | author=Basel-Vanagaite L, Attia R, Yahav M, "et al." |title=The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation. |journal=J. Med. Genet. |volume=43 |issue= 3 |pages= 203–10 |year= 2006 |pmid= 16033914 |doi= 10.1136/jmg.2005.035709
*cite journal | author=Beausoleil SA, Villén J, Gerber SA, "et al." |title=A probability-based approach for high-throughput protein phosphorylation analysis and site localization. |journal=Nat. Biotechnol. |volume=24 |issue= 10 |pages= 1285–92 |year= 2006 |pmid= 16964243 |doi= 10.1038/nbt1240
*cite journal | author=Rogaeva A, Ou XM, Jafar-Nejad H, "et al." |title=Differential repression by freud-1/CC2D1A at a polymorphic site in the dopamine-D2 receptor gene. |journal=J. Biol. Chem. |volume=282 |issue= 29 |pages= 20897–905 |year= 2007 |pmid= 17535813 |doi= 10.1074/jbc.M610038200
*cite journal | author=Rogaeva A, Albert PR |title=The mental retardation gene CC2D1A/Freud-1 encodes a long isoform that binds conserved DNA elements to repress gene transcription. |journal=Eur. J. Neurosci. |volume=26 |issue= 4 |pages= 965–74 |year= 2007 |pmid= 17714190 |doi= 10.1111/j.1460-9568.2007.05727.x
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