5 edition of Characterization of the human RB1 promoter and of elements involved in transcriptional autoregulation found in the catalog.
Published 1993 by Administrator in National Library of Canada = Bibliothèque nationale du Canada
University Microfilms order no. UMI00431289.Thesis (M.Sc.)--University of Toronto, 1993.Includes bibliographical references.
|Statement||National Library of Canada = Bibliothèque nationale du Canada|
|Publishers||National Library of Canada = Bibliothèque nationale du Canada|
|The Physical Object|
|Pagination||xvi, 57 p. :|
|Number of Pages||51|
|2||Canadian theses = Thèses canadiennes|
nodata File Size: 3MB.
Global review of challenges and good practices in support of displaced women in conflict and post-conflict situations
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TDP-43 is deposited in the Guam parkinsonism-dementia complex brains. Cshowing that MIZF binds to its cognate site in the Rb promoter in vivo. B Illustration of DREAM and PRC1. In order to investigate the regulation of RB expression by RB family members in vivo, we sought to develop a tool that would allow us to track changes in the transcription of the mouse Rb mRNA in cells, including cells with genetic inactivation of the Rb gene itself. a Knockdown of ncRNA-RB1 in A549 cells using two different siRNAs against ncRNA-RB1.
46 Hamel PA, Gill RM, Phillips RA, Gallie BL., Research has mostly been focused on the functional characterization of long ncRNAs originating from genomic regions that do not overlap with protein-coding genes PCGs and hence those transcripts that are expressed from independent promoters.
In osteosarcoma, although frequently affected by RB1 allelic losses , complete absence of gene expression is rarely seen, indicating that a residual function of the wt RB1 protein is compatible with or maybe even accelerates OS growth Additional file.
For instance, the HPV E7 and PyV TAg oncoproteins may trigger A3B upregulation directly by dissociating repressive E2F complexes. The RB pathway regulates RB expression. 55 Trapnell C, Pachter L, Salzberg SL.To further study the regulation of CALR by ncRNA-RB1, we monitored CALR protein levels following knockdown of ncRNA-RB1.
Sorting was performed at the Stanford Shared FACS Facility on a Vantage machine. The secondary rabbit anti-mouse IgG was purchased from MP Biomedicals 55436. The eGFP cassette contains two polyadenylation polyA sequences.
Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: A functional link with disease penetrance. Expression of eGFP largely parallels that of Rb in transgenic embryos and adult mice. mRNA expression for each gene was calculated relative to that for the liver. We next investigated the potentially dynamic binding of E2F and RB family members to the RB promoter as a function of the cell cycle through ChIP analysis of synchronized T98G cells.
A recent multi-center GWAS study on osteosacoma identified 2 novel candidate loci for OS susceptibility with odds-ratios of 1.
Clones were PCR-screened for alleles mimicking the natural A3B deletion.
Together, these observations suggest a complex model of Rb transcriptional regulation in which a combination of tissue-specific and general transcription factors, including E2F, ATF, and Sp1, together control Rb transcription.
The y axis represents ncRNA expression level and the x-axis represents mRNA expression level for nine cell lines A549, HEK293, HeLa, HepG2, IMR90, K562, MCF7, Thp1 and U2OS.