[cite web | title = Entrez Gene: RASSF8 Ras association (RalGDS/AF-6) domain family 8| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=11228| accessdate = ] ] PBB_Summary
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References
Further reading
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citations =
*cite journal | author=Falvella FS, Spinola M, Manenti G, "et al." |title=Common polymorphisms in D12S1034 flanking genes RASSF8 and BHLHB3 are not associated with lung adenocarcinoma risk. |journal=Lung Cancer |volume=56 |issue= 1 |pages= 1-7 |year= 2007 |pmid= 17194498 |doi= 10.1016/j.lungcan.2006.11.008
*cite journal | author=Falvella FS, Manenti G, Spinola M, "et al." |title=Identification of RASSF8 as a candidate lung tumor suppressor gene. |journal=Oncogene |volume=25 |issue= 28 |pages= 3934-8 |year= 2006 |pmid= 16462760 |doi= 10.1038/sj.onc.1209422
*cite journal | author=Rual JF, Venkatesan K, Hao T, "et al." |title=Towards a proteome-scale map of the human protein-protein interaction network. |journal=Nature |volume=437 |issue= 7062 |pages= 1173-8 |year= 2005 |pmid= 16189514 |doi= 10.1038/nature04209
*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=Jin J, Smith FD, Stark C, "et al." |title=Proteomic, functional, and domain-based analysis of in vivo 14-3-3 binding proteins involved in cytoskeletal regulation and cellular organization. |journal=Curr. Biol. |volume=14 |issue= 16 |pages= 1436-50 |year= 2004 |pmid= 15324660 |doi= 10.1016/j.cub.2004.07.051
*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=Debeer P, Schoenmakers EF, Twal WO, "et al." |title=The fibulin-1 gene (FBLN1) is disrupted in a t(12;22) associated with a complex type of synpolydactyly. |journal=J. Med. Genet. |volume=39 |issue= 2 |pages= 98-104 |year= 2002 |pmid= 11836357 |doi=
*cite journal | author=Debeer P, Schoenmakers EF, Thoelen R, "et al." |title=Physical map of a 1.5 mb region on 12p11.2 harbouring a synpolydactyly associated chromosomal breakpoint. |journal=Eur. J. Hum. Genet. |volume=8 |issue= 8 |pages= 561-70 |year= 2000 |pmid= 10951517 |doi= 10.1038/sj.ejhg.5200497
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