Publications
Download CSV
Download XLSX
Download TXT
Tables
2024 (574)
2023 (878)
2022 (829)
2021 (892)
2020 (640)
2019 (727)
2018 (651)
2017 (681)
2016 (664)
2015 (429)
2014 (376)
2013 (319)
2012 (245)
2011 (163)
2010 (139)
All (8207)
Infrastructure Units
Infrastructure Units list
Infrastructure Units table
Researchers
Subset
Documentation
About
Contact
Software
Login
BMC Res Notes
JSON
ISSN
1756-0500
ISSN-L
1756-0500
IUID
3b1d83ccfdd94244b9c0c8fd6ff47170
Modified
2020-11-27T13:14:06.898Z
Created
2017-05-09T09:12:50.377Z
Year 2023
PubMed
DOI
Crossref
Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH.
Lysenkova Wiklander M, Övernäs E, Lagensjö J, ..., Liljedahl U, Nordlund J
BMC Res Notes
16
(1) 265 [2023-10-10; online 2023-10-10]
Bioinformatics Support for Computational Resources [Service]
NGI Short read [Collaborative]
NGI Uppsala (SNP&SEQ Technology Platform) [Collaborative]
NGI Uppsala (Uppsala Genome Center) [Collaborative]
National Genomics Infrastructure [Collaborative]
Year 2019
PubMed
DOI
Crossref
Mebendazole-induced M1 polarisation of THP-1 macrophages may involve DYRK1B inhibition.
Blom K, Rubin J, Berglund M, ..., Nygren P, Larsson R
BMC Res Notes
12
(1) 234 [2019-04-22; online 2019-04-22]
Drug Discovery and Development (DDD) [Service]
Year 2018
PubMed
DOI
Crossref
EMBLmyGFF3: a converter facilitating genome annotation submission to European Nucleotide Archive
Norling M, Jareborg N, Dainat J
BMC Res Notes
11
(1) - [2018-12-00; online 2018-08-13]
Bioinformatics Support and Infrastructure [Technology development]
Bioinformatics Support, Infrastructure and Training [Technology development]
Year 2012
PubMed
DOI
Crossref
Sequence based analysis of U-2973, a cell line established from a double-hit B-cell lymphoma with concurrent MYC and BCL2 rearrangements.
Hooper SD, Jiao X, Sundström E, ..., Sjöblom T,
Cavelier L
BMC Res Notes
5
(-) 648 [2012-11-22; online 2012-11-22]
NGI Uppsala (Uppsala Genome Center)
National Genomics Infrastructure
Year 2011
PubMed
DOI
Crossref
FATP4 missense and nonsense mutations cause similar features in Ichthyosis Prematurity Syndrome.
Sobol M, Dahl N, Klar J
BMC Res Notes
4
(-) 90 [2011-03-30; online 2011-03-30]
NGI Uppsala (Uppsala Genome Center)
National Genomics Infrastructure
SciLifeLab Data Centre
Publications
9.5.1