Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Masoud M. Toloue"'
Autor:
Hanane Ennajdaoui, Jonathan M. Howard, Timothy Sterne-Weiler, Fereshteh Jahanbani, Doyle J. Coyne, Philip J. Uren, Marija Dargyte, Sol Katzman, Jolene M. Draper, Andrew Wallace, Oscar Cazarez, Suzanne C. Burns, Mei Qiao, Lindsay Hinck, Andrew D. Smith, Masoud M. Toloue, Benjamin J. Blencowe, Luiz O.F. Penalva, Jeremy R. Sanford
Publikováno v:
Cell Reports, Vol 15, Iss 9, Pp 1876-1883 (2016)
Insulin-like growth factor 2 mRNA binding protein 3 (IGF2BP3) expression correlates with malignancy, but its role(s) in pathogenesis remains enigmatic. We interrogated the IGF2BP3-RNA interaction network in pancreatic ductal adenocarcinoma (PDAC) cel
Externí odkaz:
https://doaj.org/article/4c64e93800e542b284ebe625acd620b5
Autor:
Garam Kim, Jonathan M. Howard, Andrew J. Wallace, Jolene M. Draper, Maximilian Haeussler, Sol Katzman, Hai Lin, Masoud M. Toloue, Yunlong Liu, Jeremy R. Sanford
Publikováno v:
Genome research, vol 28, iss 5
Alternative pre-mRNA splicing plays a major role in expanding the transcript output of human genes. This process is regulated, in part, by the interplay of trans-acting RNA binding proteins (RBPs) with myriad cis-regulatory elements scattered through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5307f29995f0a524431f26a37e6589
https://europepmc.org/articles/PMC5932609/
https://europepmc.org/articles/PMC5932609/
Autor:
Maximilian Haeussler, Jeremy R. Sanford, Sol Katzman, Hai Lin, Garam Kim, Jolene M. Draper, Masoud M. Toloue, Jonathan M. Howard, Yunlong Liu
Alternative pre-mRNA splicing plays a major role in expanding the transcript output of human genes. This process is regulated, in part, by the interplay of trans-acting RNA binding proteins (RBPs) with myriad cis-regulatory elements scattered through
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e5b00a4c527c6a01559c1f9ecb73135
Autor:
Fereshteh Jahanbani, Masoud M. Toloue, Andrew J. Wallace, Oscar Cazarez, Mei Qiao, Sol Katzman, Luiz O. F. Penalva, Suzanne C. Burns, Timothy Sterne-Weiler, Marija Dargyte, Philip J. Uren, Jonathan M. Howard, Doyle Coyne, Andrew D. Smith, Lindsay Hinck, Benjamin J. Blencowe, Jolene M. Draper, Jeremy R. Sanford, Hanane Ennajdaoui
Publikováno v:
Ennajdaoui, H; Howard, JM; Sterne-Weiler, T; Jahanbani, F; Coyne, DJ; Uren, PJ; et al.(2016). IGF2BP3 Modulates the Interaction of Invasion-Associated Transcripts with RISC. Cell Reports, 15(9), 1876-1883. doi: 10.1016/j.celrep.2016.04.083. UC Santa Cruz: Retrieved from: http://www.escholarship.org/uc/item/784385x0
Cell Reports, Vol 15, Iss 9, Pp 1876-1883 (2016)
Cell reports, vol 15, iss 9
Cell Reports, Vol 15, Iss 9, Pp 1876-1883 (2016)
Cell reports, vol 15, iss 9
© 2016 The Author(s). Insulin-like growth factor 2 mRNA binding protein 3 (IGF2BP3) expression correlates with malignancy, but its role(s) in pathogenesis remains enigmatic. We interrogated the IGF2BP3-RNA interaction network in pancreatic ductal ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7111c59b318b39b4370a6656fc2c2af7
http://www.escholarship.org/uc/item/784385x0
http://www.escholarship.org/uc/item/784385x0
Autor:
Giuseppe Basso, Thilini Fernando, Jonathan M. Howard, Tiffany M. Tran, Jayanth Kumar Palanichamy, Martina Pigazzi, Masoud M. Toloue, Dinesh S. Rao, Weihong Yan, Timothy Sterne-Weiler, Jeremy R. Sanford, Jorge R. Contreras, Sol Katzman
Publikováno v:
The Journal of clinical investigation, vol 126, iss 4
Posttranscriptional control of gene expression is important for defining both normal and pathological cellular phenotypes. In vitro, RNA-binding proteins (RBPs) have recently been shown to play important roles in posttranscriptional regulation; howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f565623b395fd94091ae03e3c1f80e3
http://hdl.handle.net/11577/3186845
http://hdl.handle.net/11577/3186845
Autor:
Sayaka Inukai, Gina E. Sosinsky, Amy Smock, Yoko Hiroaki, Angela C. Cone, Bruce J. Nicholson, Atsunori Oshima, Masoud M. Toloue, Kazutoshi Tani, Yoshinori Fujiyoshi
Publikováno v:
Journal of Molecular Biology. 405:724-735
Gap junction channels are unique in that they possess multiple mechanisms for channel closure, several of which involve the N terminus as a key component in gating, and possibly assembly. Here, we present electron crystallographic structures of a mut
Autor:
Lance P. Ford, Masoud M. Toloue
Publikováno v:
Wiley Interdisciplinary Reviews. RNA
Delivering polynucleotides into animals has been a major challenge facing their success as therapeutic agents. Given the matured understanding of antibody‐mediated delivery techniques, it is possible to rationally design delivery vehicles that circ
Autor:
Bruce J. Nicholson, Zifei Jade Zhou, Eric A. Banks, Jean X. Jiang, Qian Shi, Jialu Liu, Masoud M. Toloue
Publikováno v:
Journal of Cell Science. 122:378-388
The connexin (Cx) 50, E48K, mutation is associated with a human dominant congenital cataract; however, the underlying molecular mechanism has not been characterized. The glutamate (E) residue at position 48 is highly conserved across animal species a
Autor:
Anitha D. Jayaprakash, Luca Lambertini, Masoud M. Toloue, Ravi Sachidanandam, Raymond Liang, Jaehee V. Shim, Michael Wigler, Stuart A. Aaronson, Swapna Gone, Erica K. Benson
Publikováno v:
Nucleic Acids Research
Eukaryotic cells carry two genomes, nuclear (nDNA) and mitochondrial (mtDNA), which are ostensibly decoupled in their replication, segregation and inheritance. It is increasingly appreciated that heteroplasmy, the occurrence of multiple mtDNA haploty
Autor:
Shoshanna N. Zucker, Galen M. Hand, Anjana Chandrasekhar, Guido M. Gaietta, Gina E. Sosinsky, Masoud M. Toloue, Bruce J. Nicholson, A. Oshima, Amy Smock, Derek L. Beahm
Publikováno v:
Journal of Biological Chemistry. 281:7994-8009
Single site mutations in connexins have provided insights about the influence specific amino acids have on gap junction synthesis, assembly, trafficking, and functionality. We have discovered a single point mutation that eliminates functionality with