[cite web | title = Entrez Gene: AHI1 Abelson helper integration site 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=54806| accessdate = ] ] PBB_Summary
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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=Hartley JL, Temple GF, Brasch MA |title=DNA cloning using in vitro site-specific recombination. |journal=Genome Res. |volume=10 |issue= 11 |pages= 1788–95 |year= 2001 |pmid= 11076863 |doi=
*cite journal | author=Wiemann S, Weil B, Wellenreuther R, "et al." |title=Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. |journal=Genome Res. |volume=11 |issue= 3 |pages= 422–35 |year= 2001 |pmid= 11230166 |doi= 10.1101/gr.154701
*cite journal | author=Jiang X, Hanna Z, Kaouass M, "et al." |title=Ahi-1, a novel gene encoding a modular protein with WD40-repeat and SH3 domains, is targeted by the Ahi-1 and Mis-2 provirus integrations. |journal=J. Virol. |volume=76 |issue= 18 |pages= 9046–59 |year= 2002 |pmid= 12186888 |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=Mungall AJ, Palmer SA, Sims SK, "et al." |title=The DNA sequence and analysis of human chromosome 6. |journal=Nature |volume=425 |issue= 6960 |pages= 805–11 |year= 2003 |pmid= 14574404 |doi= 10.1038/nature02055
*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=Jiang X, Zhao Y, Chan WY, "et al." |title=Deregulated expression in Ph+ human leukemias of AHI-1, a gene activated by insertional mutagenesis in mouse models of leukemia. |journal=Blood |volume=103 |issue= 10 |pages= 3897–904 |year= 2004 |pmid= 14751929 |doi= 10.1182/blood-2003-11-4026
*cite journal | author=Lagier-Tourenne C, Boltshauser E, Breivik N, "et al." |title=Homozygosity mapping of a third Joubert syndrome locus to 6q23. |journal=J. Med. Genet. |volume=41 |issue= 4 |pages= 273–7 |year= 2004 |pmid= 15060101 |doi=
*cite journal | author=Close J, Game L, Clark B, "et al." |title=Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adults. |journal=BMC Genomics |volume=5 |issue= 1 |pages= 33 |year= 2004 |pmid= 15169551 |doi= 10.1186/1471-2164-5-33
*cite journal | author=Ferland RJ, Eyaid W, Collura RV, "et al." |title=Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. |journal=Nat. Genet. |volume=36 |issue= 9 |pages= 1008–13 |year= 2004 |pmid= 15322546 |doi= 10.1038/ng1419
*cite journal | author=Dixon-Salazar T, Silhavy JL, Marsh SE, "et al." |title=Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria. |journal=Am. J. Hum. Genet. |volume=75 |issue= 6 |pages= 979–87 |year= 2005 |pmid= 15467982 |doi= 10.1086/425985
*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=Wiemann S, Arlt D, Huber W, "et al." |title=From ORFeome to biology: a functional genomics pipeline. |journal=Genome Res. |volume=14 |issue= 10B |pages= 2136–44 |year= 2004 |pmid= 15489336 |doi= 10.1101/gr.2576704
*cite journal | author=Parisi MA, Doherty D, Eckert ML, "et al." |title=AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndrome. |journal=J. Med. Genet. |volume=43 |issue= 4 |pages= 334–9 |year= 2006 |pmid= 16155189 |doi= 10.1136/jmg.2005.036608
*cite journal | author=Utsch B, Sayer JA, Attanasio M, "et al." |title=Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome. |journal=Pediatr. Nephrol. |volume=21 |issue= 1 |pages= 32–5 |year= 2006 |pmid= 16240161 |doi= 10.1007/s00467-005-2054-y
*cite journal | author=Mehrle A, Rosenfelder H, Schupp I, "et al." |title=The LIFEdb database in 2006. |journal=Nucleic Acids Res. |volume=34 |issue= Database issue |pages= D415–8 |year= 2006 |pmid= 16381901 |doi= 10.1093/nar/gkj139
*cite journal | author=Valente EM, Brancati F, Silhavy JL, "et al." |title=AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. |journal=Ann. Neurol. |volume=59 |issue= 3 |pages= 527–34 |year= 2006 |pmid= 16453322 |doi= 10.1002/ana.20749
*cite journal | author=Amann-Zalcenstein D, Avidan N, Kanyas K, "et al." |title=AHI1, a pivotal neurodevelopmental gene, and C6orf217 are associated with susceptibility to schizophrenia. |journal=Eur. J. Hum. Genet. |volume=14 |issue= 10 |pages= 1111–9 |year= 2006 |pmid= 16773125 |doi= 10.1038/sj.ejhg.5201675
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