36 research outputs found

    Clinical descriptors for the TRD and healthy control groups in the structural MRI analysis.

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    <p>*chi-square test with other tests being t-tests.</p><p>Variables are shown as mean (standard deviation).</p

    Treatment Resistance, State Illness Severity and Current Medication.

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    <p>No patients had psychotic symptoms and quetiapine was prescribed as an augmentation agent for antidepressants [<a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0132958#pone.0132958.ref071" target="_blank">71</a>], similar to the long established use of lithium, L-tryptophan and tri-iodothyronine in treatment resistant depression. No obvious relationships between current medication and treatment resistance/state illness severity were present. ‘mg’ indicates total dose per day, ‘mcg’ total micrograms per day.</p

    Overlapping grey matter regions between features selected during classification (purple/blue) and regions selected in the VBM analysis (red/purple).

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    <p>Overlapping grey matter regions between features selected during classification (purple/blue) and regions selected in the VBM analysis (red/purple).</p

    The TriTryp Phosphatome: analysis of the protein phosphatase catalytic domains-2

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    <p><b>Copyright information:</b></p><p>Taken from "The TriTryp Phosphatome: analysis of the protein phosphatase catalytic domains"</p><p>http://www.biomedcentral.com/1471-2164/8/434</p><p>BMC Genomics 2007;8():434-434.</p><p>Published online 26 Nov 2007</p><p>PMCID:PMC2175518.</p><p></p>d as markers. Phosphatase domains are indicated by systematic gene IDs. Sequences are colour-coded by organism: blue for (), () and (F); red for human (); brown for () and green for (). Protein names replace Swiss-Prot IDs for some human, yeast and plant sequences. Results of the four phylogenetic methods are shown: bootstrap values > 70 are black for Neighbour-Joining, brown for Bayesian and purple for Maximum Parsimony. Asterisks (*) show Maximum Likelihood support

    The TriTryp Phosphatome: analysis of the protein phosphatase catalytic domains-9

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    <p><b>Copyright information:</b></p><p>Taken from "The TriTryp Phosphatome: analysis of the protein phosphatase catalytic domains"</p><p>http://www.biomedcentral.com/1471-2164/8/434</p><p>BMC Genomics 2007;8():434-434.</p><p>Published online 26 Nov 2007</p><p>PMCID:PMC2175518.</p><p></p>ifferent families: S/T Phosphatases, Protein tyrosine phosphatases, Dual-specificity phosphatases and PTEN/MTM lipid phosphatases. Phosphatase complements are shown for , , , in comparison with those for the Human [24, 26, 29, 128], [129, 130] and [76, 131] genomes. ACR2/cdc25-like are included in the DSP group

    The TriTryp Phosphatome: analysis of the protein phosphatase catalytic domains-5

    No full text
    <p><b>Copyright information:</b></p><p>Taken from "The TriTryp Phosphatome: analysis of the protein phosphatase catalytic domains"</p><p>http://www.biomedcentral.com/1471-2164/8/434</p><p>BMC Genomics 2007;8():434-434.</p><p>Published online 26 Nov 2007</p><p>PMCID:PMC2175518.</p><p></p>man, and as markers. Phosphatase domains are indicated by systematic gene IDs. Sequences are colour-coded by organism: blue for (), () and (F); red for human (); brown for () and green for (). Protein names replace Swiss-Prot IDs for some human, yeast and plant sequences. The results of the four phylogenetic methods are shown: bootstrap values > 70 are black for Neighbour-Joining, brown for Bayesian and purple for Maximum Parsimony. Asterisks (*) show Maximum Likelihood support
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