Citations for
1CTNNA1, CTNNA2, LRRTM1, LRRTM2
Bidirectional transcription from human LRRTM2/CTNNA1 and LRRTM1/CTNNA2 gene loci leads to expression of N-terminally truncated CTNNA1 and CTNNA2 isoforms.
Kask M, Pruunsild P, Timmusk T.
Biochem Biophys Res Commun 411(1):56-61. Epub 2011 Jun 17. 2011
2CTNNA2
Regulation of a novel alphaN-catenin splice variant in schizophrenic smokers.
Mexal S, Berger R, Pearce L, Barton A, Logel J, Adams CE, Ross RG, Freedman R, Leonard S.
Am J Med Genet B Neuropsychiatr Genet 147B(6):759-68. 2008
3CTNNA2
Alpha N-catenin deficiency causes defects in axon migration and nuclear organization in restricted regions of the mouse brain.
Uemura M, Takeichi M.
Dev Dyn 235(9):2559-66. 2006
4ACTR1B, B3GALT1, C2orf19, C2orf27A, C2orf29, C2orf39, C4orf23, C4orf28, CCDC104, CCDC74A, CCDC75, CSRNP3, CTNNA2, ELOVL6, EMX1, FASTKD2, INMT, INPP4A, KIF1A, MMADHC, OTX1, RFTN2, RNF103, TBC1D14, TSSC1, ZNF514
Generation and annotation of the DNA sequences of human chromosomes 2 and 4.
Hillier LW, Graves TA, Fulton RS, Fulton LA, Pepin KH, Minx P, Wagner-McPherson C, Layman D, Wylie K, Sekhon M, Becker MC, Fewell GA, Delehaunty KD, Miner TL, Nash WE, Kremitzki C, Oddy L, Du H, Sun H, Bradshaw-Cordum H, Ali J, Carter J, Cordes M, Harris A, Isak A, van Brunt A, Nguyen C, Du F, Courtney L, Kalicki J, Ozersky P, Abbott S, Armstrong J, Belter EA, Caruso L, Cedroni M, Cotton M, Davidson T, Desai A, Elliott G, Erb T, Fronick C, Gaige T, Haakenson W, Haglund K, Holmes A, Harkins R, Kim K, Kruchowski SS, Strong CM, Grewal N, Goyea E, Hou S, Levy A, Martinka S, Mead K, McLellan MD, Meyer R, Randall-Maher J, Tomlinson C, Dauphin-Kohlberg S, Kozlowicz-Reilly A, Shah N, Swearengen-Shahid S, Snider J, Strong JT, Thompson J, Yoakum M, Leonard S, Pearman C, Trani L, Radionenko M, Waligorski JE, Wang C, Rock SM, Tin-Wollam AM, Maupin R, Latreille P, Wendl MC, Yang SP, Pohl C, Wallis JW, Spieth J, Bieri TA, Berkowicz N, Nelson JO, Osborne J, Ding L, Meyer R, Sabo A, Shotland Y, Sinha P, Wohldmann PE, Cook LL, Hickenbotham MT, Eldred J, Williams D, Jones TA, She X, Ciccarelli FD, Izaurralde E, Taylor J, Schmutz J, Myers RM, Cox DR, Huang X, McPherson JD, Mardis ER, Clifton SW, Warren WC, Chinwalla AT, Eddy SR, Marra MA, Ovcharenko I, Furey TS, Miller W, Eichler EE, Bork P, Suyama M, Torrents D, Waterston RH, Wilson RK.
Nature 434(7034):724-31. 2005
5CTNNA1, CTNNA2, CTNNB1, JUP
Expression of Catenin family members CTNNA1, CTNNA2, CTNNB1 and JUP in the primate prefrontal cortex and hippocampus.
Smith A, Bourdeau I, Wang J, Bondy CA.
Brain Res Mol Brain Res 135(1-2):225-31. 2005
6CTNNA2
Expression of N-cadherin and alphaN-catenin in the degeneration/regeneration process of rat skeletal muscle after nerve injury.
Hatoko M, Niitsuma K, Tanaka A, Kuwahara M, Iioka H.
J Reconstr Microsurg 20(3):267-73. 2004
7CTNNA2
Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulation.
Park C, Falls W, Finger JH, Longo-Guess CM, Ackerman SL.
Nat Genet 31(3):279-84. 2002
8CTNNA2
Characterization and chromosomal assignment of a human cDNA encoding a protein related to the murine 102-kDa cadherin-associated protein (alpha-catenin).
Claverie JM, et al.
Genomics 15 : 13-20. 1993