[cite web | title = Entrez Gene: GJA3 gap junction protein, alpha 3, 46kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2700| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Hsieh CL, Kumar NM, Gilula NB, Francke U |title=Distribution of genes for gap junction membrane channel proteins on human and mouse chromosomes. |journal=Somat. Cell Mol. Genet. |volume=17 |issue= 2 |pages= 191–200 |year= 1991 |pmid= 1849321 |doi=
*cite journal | author=Willecke K, Jungbluth S, Dahl E, "et al." |title=Six genes of the human connexin gene family coding for gap junctional proteins are assigned to four different human chromosomes. |journal=Eur. J. Cell Biol. |volume=53 |issue= 2 |pages= 275–80 |year= 1991 |pmid= 1964417 |doi=
*cite journal | author=Rosenberg AM, Gole GA |title=Morning Glory Syndrome: a report of two cases. |journal=Australian journal of ophthalmology |volume=9 |issue= 4 |pages= 263–5 |year= 1982 |pmid= 7342922 |doi=
*cite journal | author=Mackay D, Ionides A, Berry V, "et al." |title=A new locus for dominant "zonular pulverulent" cataract, on chromosome 13. |journal=Am. J. Hum. Genet. |volume=60 |issue= 6 |pages= 1474–8 |year= 1997 |pmid= 9199569 |doi=
*cite journal | author=Gong X, Li E, Klier G, "et al." |title=Disruption of alpha3 connexin gene leads to proteolysis and cataractogenesis in mice. |journal=Cell |volume=91 |issue= 6 |pages= 833–43 |year= 1998 |pmid= 9413992 |doi=
*cite journal | author=Dunia I, Recouvreur M, Nicolas P, "et al." |title=Assembly of connexins and MP26 in lens fiber plasma membranes studied by SDS-fracture immunolabeling. |journal=J. Cell. Sci. |volume=111 ( Pt 15) |issue= |pages= 2109–20 |year= 1998 |pmid= 9664032 |doi=
*cite journal | author=Mackay D, Ionides A, Kibar Z, "et al." |title=Connexin46 mutations in autosomal dominant congenital cataract. |journal=Am. J. Hum. Genet. |volume=64 |issue= 5 |pages= 1357–64 |year= 1999 |pmid= 10205266 |doi=
*cite journal | author=Rees MI, Watts P, Fenton I, "et al." |title=Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA3). |journal=Hum. Genet. |volume=106 |issue= 2 |pages= 206–9 |year= 2000 |pmid= 10746562 |doi=
*cite journal | author=Das Sarma J, Meyer RA, Wang F, "et al." |title=Multimeric connexin interactions prior to the trans-Golgi network. |journal=J. Cell. Sci. |volume=114 |issue= Pt 22 |pages= 4013–24 |year= 2002 |pmid= 11739633 |doi=
*cite journal | author=Schubert AL, Schubert W, Spray DC, Lisanti MP |title=Connexin family members target to lipid raft domains and interact with caveolin-1. |journal=Biochemistry |volume=41 |issue= 18 |pages= 5754–64 |year= 2002 |pmid= 11980479 |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=Nielsen PA, Baruch A, Shestopalov VI, "et al." |title=Lens connexins alpha3Cx46 and alpha8Cx50 interact with zonula occludens protein-1 (ZO-1). |journal=Mol. Biol. Cell |volume=14 |issue= 6 |pages= 2470–81 |year= 2004 |pmid= 12808044 |doi= 10.1091/mbc.E02-10-0637
*cite journal | author=Jiang H, Jin Y, Bu L, "et al." |title=A novel mutation in GJA3 (connexin46) for autosomal dominant congenital nuclear pulverulent cataract. |journal=Mol. Vis. |volume=9 |issue= |pages= 579–83 |year= 2003 |pmid= 14627959 |doi=
*cite journal | author=Dunham A, Matthews LH, Burton J, "et al." |title=The DNA sequence and analysis of human chromosome 13. |journal=Nature |volume=428 |issue= 6982 |pages= 522–8 |year= 2004 |pmid= 15057823 |doi= 10.1038/nature02379
*cite journal | author=Bennett TM, Mackay DS, Knopf HL, Shiels A |title=A novel missense mutation in the gene for gap-junction protein alpha3 (GJA3) associated with autosomal dominant "nuclear punctate" cataracts linked to chromosome 13q. |journal=Mol. Vis. |volume=10 |issue= |pages= 376–82 |year= 2004 |pmid= 15208569 |doi=
*cite journal | author=Burdon KP, Wirth MG, Mackey DA, "et al." |title=A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance. |journal=J. Med. Genet. |volume=41 |issue= 8 |pages= e106 |year= 2004 |pmid= 15286166 |doi= 10.1136/jmg.2004.018333
*cite journal | author=Lin D, Lobell S, Jewell A, Takemoto DJ |title=Differential phosphorylation of connexin46 and connexin50 by H2O2 activation of protein kinase Cgamma. |journal=Mol. Vis. |volume=10 |issue= |pages= 688–95 |year= 2004 |pmid= 15467523 |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=Devi RR, Reena C, Vijayalakshmi P |title=Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population. |journal=Mol. Vis. |volume=11 |issue= |pages= 846–52 |year= 2006 |pmid= 16254549 |doi=
*cite journal | author=Addison PK, Berry V, Holden KR, "et al." |title=A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family. |journal=Mol. Vis. |volume=12 |issue= |pages= 791–5 |year= 2006 |pmid= 16885921 |doi=
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