Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Ina Hollerer"'
Autor:
Ina Hollerer, Juliet C. Barker, Victoria Jorgensen, Amy Tresenrider, Claire Dugast-Darzacq, Leon Y. Chan, Xavier Darzacq, Robert Tjian, Elçin Ünal, Gloria A. Brar
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 9, Iss 4, Pp 1045-1053 (2019)
We recently described an unconventional mode of gene regulation in budding yeast by which transcriptional and translational interference collaborate to down-regulate protein expression. Developmentally timed transcriptional interference inhibited pro
Externí odkaz:
https://doaj.org/article/fbddfaee35014676a9c0c782a5c6f2d3
Publikováno v:
STAR Protocols, Vol 2, Iss 1, Pp 100250- (2021)
Summary: Translation initiation site (TIS) profiling allows for the genome-wide identification of TISs in vivo by exclusively capturing mRNA fragments within ribosomes that have just completed translation initiation. It leverages translation inhibito
Externí odkaz:
https://doaj.org/article/daf0bd892ae543528367b78ea4871ad3
Autor:
Christian Hauer, Jana Sieber, Thomas Schwarzl, Ina Hollerer, Tomaz Curk, Anne-Marie Alleaume, Matthias W. Hentze, Andreas E. Kulozik
Publikováno v:
Cell Reports, Vol 16, Iss 6, Pp 1588-1603 (2016)
The exon junction complex (EJC) connects spliced mRNAs to posttranscriptional processes including RNA localization, transport, and regulated degradation. Here, we provide a comprehensive analysis of bona fide EJC binding sites across the transcriptom
Externí odkaz:
https://doaj.org/article/55c4f6dafa4a4fb68e162596c8e9bec5
Publikováno v:
Haematologica, Vol 102, Iss 5 (2017)
Mutations in the HFE (hemochromatosis) gene cause hereditary hemochromatosis, an iron overload disorder that is hallmarked by excessive accumulation of iron in parenchymal organs. The HFE mutation p.Cys282Tyr is pathologically most relevant and occur
Externí odkaz:
https://doaj.org/article/be581c59fcff4a4286dc048f868fd69b
Publikováno v:
EMBO Molecular Medicine, Vol 6, Iss 1, Pp 16-26 (2013)
Abstract Recent advances reveal mRNA 3′end processing as a highly regulated process that fine‐tunes posttranscriptional gene expression. This process can affect the site and/or the efficiency of 3′end processing, controlling the quality and the
Externí odkaz:
https://doaj.org/article/cc8ecc3b40a3408a8e04b0d4945df54d
Autor:
Tina L Sing, Katie Conlon, Stephanie H Lu, Nicole Madrazo, Kaitlin Morse, Juliet C Barker, Ina Hollerer, Gloria A Brar, Peter H Sudmant, Elçin Ünal
Publikováno v:
Genetics
Gametogenesis is an evolutionarily conserved developmental program whereby a diploid progenitor cell undergoes meiosis and cellular remodeling to differentiate into haploid gametes, the precursors for sexual reproduction. Even in the simple eukaryoti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::375481396d59e374f07b680a52e97b2a
https://europepmc.org/articles/PMC9157139/
https://europepmc.org/articles/PMC9157139/
Autor:
Sing Tl, Elçin Ünal, Lu Sh, Madrazo N, Ina Hollerer, Conlon K, Gloria A. Brar, Peter H. Sudmant, Juliet C Barker
Gametogenesis is a highly regulated and dynamic developmental program where a diploid progenitor cell differentiates into haploid gametes, the precursors for sexual reproduction. During meiosis, several pathways converge to initiate ploidy reduction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::621a76c7ed29c29942f05ae867cdcd48
https://doi.org/10.1101/2021.05.10.443361
https://doi.org/10.1101/2021.05.10.443361
Autor:
Irwin Jungreis, Ina Hollerer, Paige D. Diamond, Amy Rose Eisenberg, Andrea Higdon, Gloria A. Brar, Marko Jovanovic, Manolis Kellis, Alexander P. Fields
Publikováno v:
Cell systems, vol 11, iss 2
Elsevier
Cell Syst
Elsevier
Cell Syst
Genomic analyses in budding yeast have helped define the foundational principles of eukaryotic gene expression. However, in the absence of empirical methods for defining coding regions, these analyses have historically excluded specific classes of po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8641beb4caca6de2d67b2cc16fd22bf6
https://escholarship.org/uc/item/14n8b37q
https://escholarship.org/uc/item/14n8b37q
Publikováno v:
Haematologica
Mutations in the HFE (hemochromatosis) gene cause hereditary hemochromatosis, an iron overload disorder that is hallmarked by excessive accumulation of iron in parenchymal organs. The HFE mutation p.Cys282Tyr is pathologically most relevant and occur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a668b58da1fb6f24ad9670ac2a818710
http://europepmc.org/articles/PMC5477599
http://europepmc.org/articles/PMC5477599
Publikováno v:
STAR Protocols, Vol 2, Iss 1, Pp 100250-(2021)
STAR Protocols
STAR protocols, vol 2, iss 1
STAR Protocols
STAR protocols, vol 2, iss 1
Summary Translation initiation site (TIS) profiling allows for the genome-wide identification of TISs in vivo by exclusively capturing mRNA fragments within ribosomes that have just completed translation initiation. It leverages translation inhibitor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9847cd7c20a29e31c307df6ba8a750a2
https://doi.org/10.1016/j.xpro.2020.100250
https://doi.org/10.1016/j.xpro.2020.100250