نتایج جستجو برای: lrtomt
تعداد نتایج: 14 فیلتر نتایج به سال:
Cochlear implantation is currently the treatment of choice for children with severe to profound hearing impairment. However, the outcomes with cochlear implants (CIs) vary significantly among recipients. The purpose of the present study is to identify the genetic determinants of poor CI outcomes. Twelve children with poor CI outcomes (the "cases") and 30 "matched controls" with good CI outcomes...
We have identified a previously unannotated catechol-O-methyltranferase (COMT), here designated COMT2, through positional cloning of a chemically induced mutation responsible for a neurobehavioral phenotype. Mice homozygous for a missense mutation in Comt2 show vestibular impairment, profound sensorineuronal deafness, and progressive degeneration of the organ of Corti. Consistent with this phen...
v e l v l g e s n h e o p F l a t t i C d p P resynaptic neurexins and postsynaptic neuroligins are celladhesion proteins that interact across the synaptic cleft and influence synaptic function (1). These proteins have received recent attention in psychiatry because of genetic evidence linking them to schizophrenia, autism, and mental retardation (1). However, during the last 2 years, an additi...
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