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| 1 | Human apoE isoforms differentially regulate brain amyloid-显示文摘 | Castellano JM Kim J Stewart FR | 2011 | Sci Transl Med2011，3，： | 1 |
| 2 | Root replacement for all allografts in young recipients显示文摘 | O'Brien MF Stewart FR Stafford EC | 1993 | J Thorac Cardiovasc Surg1993，105，3： | 1 |
| 3 | Human apo E isoforms differentially regulate brainamyloid-beta peptide clearance显示文摘 | Castellano JM Kim J Stewart FR | 2011 | Sci Transl Med2011，3，： | 1 |
| 4 | In vivo microdialysis revea decrease of brain interstitia s age-dependent fluid tau levels in P301S human tau transgenic mice显示文摘 | Yamada K Cirrito JR Stewart FR | 2011 | J Neurosci2011，31，13： | 1 |
| 5 | Phenanthrene-4,5-quinones: a synthesis of morphenol 显示文摘 | Hewgill FR Stewart JM | 1988 | J Chem Soc Perkin Trans1988，46，6： | 1 |
| 6 | Ultrastructural studies in APP/PS1 mice expressing human ApoE isoforms: implications for Alzheimer's disease 显示文摘 | Dikranian K Kim J Stewart FR | 2012 | Int J Clin Exp Pathol2012，5，： | 1 |
| 7 | Human apo E isoforms differentially regulate brain amyloid-βpeptide clearance显示文摘 | Castellano JM Kim J Stewart FR | 2011 | Sci Transl Med2011，3，89： | 1 |
| 8 | Human apoE isoforms differentially regulate brain amyloid-β peptide clearance显示文摘 | Castellano JM Kim J Stewart FR | 2011 | Sci Transl Med2011，3，89： | 1 |
| 9 | Human apoE isoforms differentially regulate brain amyloid-13 peptide clearance 显示文摘 | Castellano JM Kim J Stewart FR | 2011 | Sci Transl Med2011，3，89： | 1 |
| 10 | In vivo mierodialysis reveals age-dependent decrease of brain interstitial fluid tau levels in P301S human tan transgenic mice 显示文摘 | Yamada K Cirrito JR Stewart FR | 2011 | Neurosci2011，31，13： | 1 |
| 11 | Human apoE isoforms differentially regulate brain amyloid-beta peptide clearance 显示文摘 | Castellano JM Kim J Stewart FR | 2011 | Sci Transl Med2011，3，89： | 1 |
| 12 | Global Transcriptional Profile of Tranosema rostrale Ichnovirus Genes in Infected Lepidopteran Hosts and Wasp Ovaries显示文摘The ichnovirus TrIV, transmitted by the endoparasitic wasp Tranosema rostrale to its lepidopteran host during oviposition, replicates asymptomatically in wasp ovaries and causes physiological dysfunctions in parasitized caterpillars. The need to identify ichnoviral genes responsible for disturbances induced in lepidopteran hosts has provided the impetus for the sequencing and annotation of ichnovirus genomes, including that of TrIV. In the latter, 86 putative genes were identified, including 35 that could be assigned to recognized ichnoviral gene families. With the aim of assessing the relative importance of each TrIV gene, as inferred from its level of expression, and evaluating the accuracy of the gene predictions made during genome annotation, the present study builds on an earlier qPCR quantification of transcript abundance of TrIV rep ORFs, in both lepidopteran and wasp hosts, extending it to other gene families as well as to a sample of unassigned ORFs. We show that the majority (91%) of putative ORFs assigned to known gene families are expressed in infected larvae, while this proportion is lower (67%) for a sample taken among the remaining ORFs. Selected members of the TrV and rep gene families are shown to be transcribed in infected larvae at much higher levels than genes from any other TrIV gene family, pointing to their likely involvement in host subjugation. In wasp ovaries, the transcriptional profile is dominated by a rep gene and a member of a newly described gene family encoding secreted proteins displaying a novel cysteine motif, which we identified among previously unassigned ORFs. | Asieh Rasoolizadeh Frédéric Dallaire Don Stewart Catherine Béliveau Renée Lapointe Michel Cusson | 2009 | Virologica Sinica2009，24，5： | 0 |
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