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pro vyhledávání: '"Brian J Reon"'
Autor:
Brian J Reon, Jordan Anaya, Ying Zhang, James Mandell, Benjamin Purow, Roger Abounader, Anindya Dutta
Publikováno v:
PLoS Medicine, Vol 13, Iss 12, p e1002192 (2016)
BackgroundEach year, over 16,000 patients die from malignant brain cancer in the US. Long noncoding RNAs (lncRNAs) have recently been shown to play critical roles in regulating neurogenesis and brain tumor progression. To better understand the role o
Externí odkaz:
https://doaj.org/article/a1e3e0b04b7f4bf8968e275245fa1185
Autor:
Masamitsu Negishi, Somsakul P Wongpalee, Sukumar Sarkar, Jonghoon Park, Kyung Yong Lee, Yoshiyuki Shibata, Brian J Reon, Roger Abounader, Yutaka Suzuki, Sumio Sugano, Anindya Dutta
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e95216 (2014)
Long noncoding RNAs (lncRNAs) have emerged as a major regulator of cell physiology, but many of which have no known function. CDKN1A/p21 is an important inhibitor of the cell-cycle, regulator of the DNA damage response and effector of the tumor suppr
Externí odkaz:
https://doaj.org/article/dbe43e105b9249f599e1f75789e33cc3
Supplementary Information. Supplementary material and method, figure legend and references
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72837da662ee99fa2ddf6bb6cc15a102
https://doi.org/10.1158/1541-7786.22514520
https://doi.org/10.1158/1541-7786.22514520
Supplementary Figures 1-3, Table 1. Supplementary Figure 1: Cellular localization of DRAIC and 3'RACE of DRAIC gene Supplementary Figure 2: Transcriptional variants of DRAIC gene Supplementary Figure 3: AR, FOXA1 and NKX3-1 binding sequences at DRAIC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::508422e6c6a8b75119bf8dad53b22561
https://doi.org/10.1158/1541-7786.22514523.v1
https://doi.org/10.1158/1541-7786.22514523.v1
Fold changes of indicated genes (log 2) after knockdown or overexpression of LINC00152 or M8.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab5b33d37e7b68666a613d687a761208
https://doi.org/10.1158/1541-7786.22512958.v1
https://doi.org/10.1158/1541-7786.22512958.v1
LINC00152 full length and deletion mutants. A) Predicted secondary structures of LINC00152 deletion mutants. M2 and M3 lack the protein bound stem-loop. M8 is highlighted by the boxed area (nucleotides 280-401). On the other hand, M4 through M8 conta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a52028eb97dd56d94c20d44151c5be9
https://doi.org/10.1158/1541-7786.22512964.v1
https://doi.org/10.1158/1541-7786.22512964.v1
LINC00152 does not affect U87 cell proliferation rate. A) qRT-PCR showing knockdown of LINC00152 after treatment with two different siRNAs. B) Cell proliferation rate measured by MTT assay of U87 cells treated with two different siRNA against LINC001
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::097e5a556b163da00a5b8723201e8c56
https://doi.org/10.1158/1541-7786.22512973.v1
https://doi.org/10.1158/1541-7786.22512973.v1
Expression of genes involved in EMT are decreased by si LINC00152 rescued by LINC00152 m8 overexpression. A-G) qRT-PCR showing (A) LINC00152, (B) TPM2, (C) PTX3, (D) IGFBP4, (E) TGM2, (F) SPP1, (G) LUM expression after siGL2 and pcDNA3, or siLINC0015
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39da164c71dc5e2b09bf67536ec9427a
https://doi.org/10.1158/1541-7786.22512970.v1
https://doi.org/10.1158/1541-7786.22512970.v1
A protein-bound stem loop in LINC00152. A and B) The two lowest free-energy structures of LINC00152, predicted by mfold. Boxed areas show overlapping stem-loop regions between the structures which also overlaps with the PARIS reads and Ribo-seq reads
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56365bcab34f5232cc14f62f032ad6e0
https://doi.org/10.1158/1541-7786.22512967.v1
https://doi.org/10.1158/1541-7786.22512967.v1
LINC00152 knockdown leads to changes in gene expression. A) Heatmap showing clustering of replicates from the same condition (with or without LINC00152 knockdown) based on differentially regulated genes in U87 cells. Three biological replicates for e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fa894a4f8136a60169816723dfc173f
https://doi.org/10.1158/1541-7786.22512961
https://doi.org/10.1158/1541-7786.22512961