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Tag 22q13 [7 articles]

Articoli recentemente classificati sotto il tag 22q13.
  • Molecular and phenotypic characterization of ring chromosome 22
    American Journal of Medical Genetics Part A, Vol. 137A, No. 2. (2005), pp. 139-147.
    by Aaron R Jeffries, Sarah Curran, Frances Elmslie, Ajay Sharma, Sharon Wenger, Marybeth Hummel, John Powell
    posted to 22q13 by r03ert0 on 2006-08-25 08:02:56 as **
  • Expanded characterization of the social interaction abnormalities in mice lacking Dvl1.
    Genes Brain Behav, Vol. 3, No. 1. (February 2004), pp. 51-62.
    by JM Long, P LaPorte, R Paylor, A Wynshaw-Boris
    posted to 22q13 dvl by r03ert0 on 2006-07-28 10:30:08 as **
  • 22q13 deletion syndrome.
    Am J Med Genet, Vol. 101, No. 2. (15 June 2001), pp. 91-99.
    by MC Phelan, RC Rogers, RA Saul, GA Stapleton, K Sweet, H McDermid, SR Shaw, J Claytor, J Willis, DP Kelly
    posted to 22q13 by r03ert0 on 2006-07-20 10:54:46 as **
  • notes Direct interaction of post-synaptic density-95DlgZO-1 domain-containing synaptic molecule Shank3 with GluR1 -amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor
    Journal of Neurochemistry, Vol. 97, No. 4. (May 2006), pp. 1203-1214.
    by Shigeo Uchino, Hidenori Wada, Shizuyo Honda, Yasuko Nakamura, Yumiko Ondo, Takayoshi Uchiyama, Moe Tsutsumi, Eri Suzuki, Takae Hirasawa, Shinichi Kohsaka
    posted to 22q13 shank3 by r03ert0 on 2006-07-20 10:44:22 as **
  • Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons.
    J Neurosci, Vol. 25, No. 14. (6 April 2005), pp. 3560-3570.
    by G Roussignol, F Ango, S Romorini, JC Tu, C Sala, PF Worley, J Bockaert, L Fagni
    posted to 22q13 shank3 by r03ert0 on 2006-07-20 10:48:29 as **
  • Identification of a recurrent breakpoint within the SHANK3 gene in the 22q13.3 deletion syndrome.
    J Med Genet (11 November 2005)
    by Maria Clara C Bonaglia, Roberto Giorda, Elisa Mani, Giuseppe Aceti, Britt-Marie M Anderlid, Anna Baroncini, Tiziano Pramparo, Orsetta Zuffardi
    posted to 22q13 breakpoint by r03ert0 on 2006-07-20 10:53:48 as **
  • Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.
    Clin Genet, Vol. 57, No. 2. (February 2000), pp. 103-109.
    by C Prasad, AN Prasad, BN Chodirker, C Lee, AK Dawson, LJ Jocelyn, AE Chudley
    posted to pervasive disorders developmental deletion autism 22q13 by mgaldzic on 2007-02-02 06:02:49 as ** along with 1 group CHIP
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