A New Molybdophosphate Constructed From Mo 2V O4(H2O)62+ and 1-Hydroxyethylidenediphosphonate -
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A New Molybdophosphate Constructed F ...
A new molybdophosphate (NH4)8{Mo2VO4[(Mo2VIO6)CH3C(O)(PO3)2]2}?14H2O (1), has been synthesized by the reaction of {Mo2VO4(H2O)6}2+ fragments with 1-hydroxyethylidenediphosphonate (hedp HOC(CH3)(PO3H2)2), and it is characterized by 31P NMR, IR, UV, element analysis, TG and single-crystal X-ray analysis. The structure analysis reveals that the polyoxoanion can be described as two {(Mo2VIO6)(CH3C(O)(PO3)2} units connected by a {Mo2VO4}2+ moiety. In the structure, the six Mo atoms are arranged into a new “W-shaped” structure, which represents a new kind of molybdophosphate.
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Transcriptome-wide mega-analyses reveal joint dysregulation of immunologic genes and transcription regulators in brain and blood in schizophrenia
Hess, Jonathan L.,
Tylee, Daniel S.,
Scott, Rodney J.,
Yasawardene, Surangi,
Perera, Antionette,
Mendis, Jayan,
Carr, Vaughan,
Kelly, Brian,
Cairns, Murray,
Tsuang, Ming T.,
Glatt, Stephen J.,
Barve, Rahul,
de Jong, Simone,
Ophoff, Roel A.,
Kumarasinghe, Nishantha,
Tooney, Paul,
Schall, Ulrich,
Gardiner, Erin,
Beveridge, Natalie Jane
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AMA - American Medical Association, 9th Edition
JAMA - Journal of the American Medical Association
New England Journal of Medicine
Chicago 15th Edition (Author-Date System)
Council of Biology Editors - CBE 6th, Citation-Sequence
MLA 6th Edition
NLM - National Library of Medicine
Turabian (Reference List) 6th Edition
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http://hdl.handle.net/8053
Transcriptome-wide mega-analyses reveal joint dysregulation of immunologic genes and transcription regulators in brain and blood in schizophrenia
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journal article
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The application of microarray technology in schizophrenia research was heralded as paradigm-shifting, as it allowed for high-throughput assessment of cell and tissue function. This technology was widely adopted, initially in studies of postmortem brain tissue, and later in studies of peripheral blood. The collective body of schizophrenia microarray literature contains apparent inconsistencies between studies, with failures to replicate top hits, in part due to small sample sizes, cohort-specific effects, differences in array types, and other confounders. In an attempt to summarize existing studies of schizophrenia cases and non-related comparison subjects, we performed two mega-analyses of a combined set of microarray data from postmortem prefrontal cortices (n = 315) and from ex-vivo blood tissues (n = 578). We adjusted regression models per gene to remove non-significant covariates, providing best-estimates of transcripts dysregulated in schizophrenia. We also examined dysregulation of functionally related gene sets and gene co-expression modules, and assessed enrichment of cell types and genetic risk factors. The identities of the most significantly dysregulated genes were largely distinct for each tissue, but the findings indicated common emergent biological functions (e.g. immunity) and regulatory factors (e.g., predicted targets of transcription factors and miRNA species across tissues). Our network-based analyses converged upon similar patterns of heightened innate immune gene expression in both brain and blood in schizophrenia. We also constructed generalizable machine-learning classifiers using the blood-based microarray data. Our study provides an informative atlas for future pathophysiologic and biomarker studies of schizophrenia.
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