5 of 38 articles - Show All
  1. Signature combinatorial splicing profiles of rat cardiac- and smooth-muscle Cav1.2 channels with distinct biophysical properties

    Cell calcium , Volume 41 , Issue 5 (2007)
    Tang Z , Hong X , Wang J , Soong T
  2. Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism.

    Cell , Volume 119 , Issue 1 (2004)
    Splawski I , Timothy K W , Sharpe L M , Decher N , Kumar P , Bloise R , Napolitano C , Schwartz P J , Joseph R M , Condouris K , Tager-Flusberg H , Priori S G , Sanguinetti M C , Keating M T
  3. The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene

    JOURNAL OF HUMAN GENETICS , Volume 49 , Issue 6 (2004)
    K B , HA P , J C , OLD M , JC M , H E , AE G , G K , DF C
  4. Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.

    American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics , Volume 144B , Issue 7 (2007)
    Martin C L , Duvall J A , Ilkin Y , Simon J S , Arreaza M G , Wilkes K , Alvarez-Retuerto A , Whichello A , Powell C M , Rao K , Cook E , Geschwind D H
  5. Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

    Cell , Volume 102 , Issue 1 (2000)
    Platzer J , Engel J , Schrott-Fischer A , Stephan K , Bova S , Chen H , Zheng H , Striessnig J
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