<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets"</p><p>http://www.biomedcentral.com/1471-2350/8/36</p><p>BMC Medical Genetics 2007;8():36-36.</p><p>Published online 20 Jun 2007</p><p>PMCID:PMC1931432.</p><p></p> Cerebellum microarray expression data (M) are compared with qRT-PCR data from cerebellum (RC), forebrain (RF) and hippocampus (RH). For RC of and , the 8 wk samples from the microarray analysis were used. RC2 data are derived from an independent set of litters at 7.5 to 8 wk. Error bars represent SEM. One asterisk indicates < 0.05, two asterisks indicate < 0.001. expression was markedly increased in the cerebellum of 8 wk B-allele mic...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p>F test was calculated for pairwise comparison of RT-PCR results for MECP2e1 or e2 versus eGFP inf...
Abstract Background MeCP2, methyl-CpG-binding protein 2, binds to methylated cytosines at CpG dinucl...
<p>Hippocampus mRNA was extracted and level of mRNA detected using microarrays or qRT-PCR. <i>A</i>,...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p><b>Copyright information:</b></p><p>Taken from "Cerebellar gene expression profiles of mouse mode...
<p>F test was calculated for pairwise comparison of RT-PCR results for MECP2e1 or e2 versus eGFP inf...
Abstract Background MeCP2, methyl-CpG-binding protein 2, binds to methylated cytosines at CpG dinucl...
<p>Hippocampus mRNA was extracted and level of mRNA detected using microarrays or qRT-PCR. <i>A</i>,...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...
Rett syndrome is a rare neuropsychiatric disorder with a wide symptomatology including impaired comm...
Mutations in MECP2 are responsible for Rett syndrome (RTT), a severe X-linked neurological disorder ...