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Items: 4

1.

Selective Translation Complex Profiling in yeast and human Reveals Staged Initiation and Co-translational Assembly of Initiation Factor Complexes [Human]

(Submitter supplied) Translational control targeting mainly the initiation phase is central to the regulation of gene expression. Understanding all of its aspects requires substantial technological advancements. Here we modified yeast Translational Complex Profile sequencing (TCP-seq), related to ribosome profiling, and adopted it for mammalian cells. Human TCP-seq, capable of capturing footprints of 40S subunits (40Ses) in addition to 80S ribosomes (80Ses), revealed that mammalian and yeast 40Ses distribute similarly across 5’UTRs indicating considerable evolutionary conservation. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL20795 GPL16791
6 Samples
Download data: CSV, XLS
Series
Accession:
GSE139131
ID:
200139131

PubMed Full text in PMC Similar studies SRA Run Selector

2.

Selective Translation Complex Profiling in yeast and human Reveals Staged Initiation and Co-translational Assembly of Initiation Factor Complexes

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens; Saccharomyces cerevisiae
Type:
Expression profiling by high throughput sequencing; Other
Platforms:
GPL20795 GPL16791 GPL17342
22 Samples
Download data
Series
Accession:
GSE139132
ID:
200139132

PubMed Full text in PMC Similar studies

3.

HiSeq X Ten (Homo sapiens)

Organism:
Homo sapiens
2127 Series
36413 Samples
Download data
Platform
Accession:
GPL20795
ID:
100020795

4.

human eIF3b bound 40S 1

Organism:
Homo sapiens
Source name:
HEK293T cells
Platform:
GPL20795
Series:
GSE139131 GSE139132
Download data
Sample
Accession:
GSM4131412
ID:
304131412

SRA Run Selector

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db=gds|term=GSM4131412[Accession]|query=1|qty=3|blobid=MCID_677b2f6a0bdf8a6e73ed4292|ismultiple=true|min_list=5|max_list=20|def_tree=20|def_list=|def_view=|url=/Taxonomy/backend/subset.cgi?|trace_url=/stat?
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