Registrera dig | Logga in | FAQ      [?] 

Taggat som: 22q13 [7 articles]

Senaste hänvisningarna som insorterats under taggen 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
    • Du kan hänvisa till den här sidan som: http://www.citeulike.org/tag/22q13

    RIS BibTeX
    CiteULike organises scholarly (or academic) papers or literature and provides bibliographic (which means it makes bibliographies) for universities and higher education establishments. It helps undergraduates and postgraduates. People studying for PhDs or in postdoctoral (postdoc) positions. The service is similar in scope to EndNote or RefWorks or any other reference manager like BibTeX, but it is a social bookmarking service for scientists and humanities researchers.