OmicsDI
Toggle navigation
Browse
Submit Data
Databases
API
Help
Advanced
Search
205
Results
Show all
Save search
Copy query
Show results for
Unknown
(99)
Genomics
(46)
Proteomics
(38)
Transcriptomics
(18)
Other
(4)
Organisms
Homo sapiens
(26)
Aerococcus urinae NBRC 15544 = CCUG 36881
(19)
Andropogon gerardi
(19)
Bacteria
(19)
Bartonella quintana JK 31
(19)
Canis lupus familiaris
(19)
Cnidaria
(19)
Ectopseudomonas oleovorans CECT 5344
(19)
Ensifer adhaerens
(19)
Halictus scabiosae
(19)
Human immunodeficiency virus 1
(19)
Mesocricetus auratus
(19)
Miscanthus x giganteus
(19)
Morchella importuna
(19)
Mus musculus
(19)
Panicum virgatum
(19)
Pseudomonas aeruginosa PA103
(19)
Pseudomonas aeruginosa SJTD-1
(19)
Mus musculus
(13)
Escherichia coli
(2)
Saccharomyces cerevisiae
(1)
Escherichia coli str. K-12 substr. MG1655
(1)
Oryza sativa Japonica Group
(1)
Bacillus subtilis subsp. subtilis str. 168
(1)
Bacillus thuringiensis HD-771
(1)
Clostridium butyricum DORA_1
(1)
Edwardsiella piscicida EIB202
(1)
Mycolicibacterium smegmatis MC2 51
(1)
Staphylococcus aureus
(1)
Priestia megaterium NBRC 15308 = ATCC 14581
(1)
Organisms
Homo sapiens
(18)
Mus musculus
(9)
Oryza sativa Japonica Group
(1)
Repository
ENA
(32)
geo
(29)
pride
(19)
iProX
(11)
biostudies-arrayexpress
(7)
MassIVE
(5)
jPOST
(3)
Tissue
Cell culture
(4)
Early embryonic cell
(4)
Brain
(3)
Liver
(2)
Testis
(2)
Breast
(1)
Cecum
(1)
Cell suspension culture
(1)
Colon
(1)
Epithelial cell
(1)
Heart
(1)
Kidney
(1)
Leaf
(1)
Permanent cell line cell
(1)
Seed
(1)
Spleen
(1)
Whole body
(1)
Disease
Disease free
(2)
Cervix carcinoma
(1)
Technology Type
Mass Spectrometry
(19)
Shotgun proteomics
(7)
Affinity purification coupled with mass spectrometry proteomics
(5)
Bottom-up proteomics
(5)
Gel-based experiment
(5)
Data-dependent acquisition
(3)
Affinity proteomics
(1)
Chemical cross-linking coupled with mass spectrometry proteomics
(1)
Top-down proteomics
(1)
Instrument Platform
Q Exactive
(2)
Illumina MiSeq
(1)
Illumina HiSeq 3000
(1)
NextSeq 500
(1)
Orbitrap Exploris 480
(1)
Q Exactive HF
(1)
TimsTOF fleX
(1)
TripleTOF 6600
(1)
Publication Date
2026
(12)
2025
(12)
2021
(11)
2022
(10)
2023
(9)
2016
(5)
2024
(5)
2020
(2)
2018
(2)
2017
(2)
2010
(1)
2008
(1)
2019
(1)
2015
(1)
First Public Date
2026
(8)
2021
(8)
2023
(5)
2025
(4)
2020
(2)
2017
(2)
2024
(1)
2018
(1)
2016
(1)
Modification
N6
(2)
N6-dimethyl-L-lysine
(2)
Study type
Transcription profiling by array
(2)
Animal - High-throughput sequencing
(1)
Ribo-seq
(1)
Other
(1)
DNA-seq
(1)
Methylation profiling by high throughput sequencing
(1)
Release Date
2022
(14)
2024
(13)
2021
(12)
2018
(11)
2023
(10)
2017
(9)
2016
(6)
2020
(5)
2019
(5)
2025
(4)
2010
(3)
2008
(2)
2015
(2)
2014
(2)
2011
(2)
2013
(1)
2012
(1)
2009
(1)
2007
(1)
2006
(1)
2001
(1)
Lab affiliation
1 Department of Hepatobiliary Surgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, 230001, China. 2 Anhui Province Key Laboratory of Hepatopancreatobiliary Surgery, Hefei, Anhui, 230001, China. 3 Anhui Provincial Clinical Research Center for Hepatobiliary Diseases, Hefei, Anhui, 230001, China.
(1)
1Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China 2Academy of Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China 3Synthetic and Functional Biomolecules Center, Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China
(1)
Department of Chemistry and Biochemistry, University of California, Los Angeles, CA,USA David Geffen School of Medicine, Department of Biological Chemistry, University of California, Los Angeles, CA, USA UCLA-DOE Institute, University of California, Los Angeles, CA, USA UCLA Molecular Biology Institute, University of California, Los Angeles, CA, USA
(1)
Department of Chemistry and Chemical Biology
(1)
Div. Biol. Geosci., Grad. Sch. Sci., Osaka City Univ., Japan
(1)
EDyP/BGE/IRIG/CEA Grenoble
(1)
European Instutute of Oncology, Milan
(1)
Inserm UMRS 1256 N-GERE (Nutrition-Genetics-Environmental Risks)
(1)
Institute of Paulownia, Henan Agricultural University, Zhengzhou, Henan, 450002, P. R. China
(1)
Institute of Plant Science of Paris-Saclay (IPS2), CNRS, INRA, Université Paris-sud 11, Université Paris-Saclay, 91405 Orsay, France
(1)
PhD candidate, Faculty of Medicine, University of Oslo, Norway
(1)
Professor and Chair of Chemical Biology, Peking-Tsinghua Center for Life Sciences Peking University, Beijing, China. Associate Editor, ACS Chemical Biology
(1)
Professor and Chair of Chemical Biology, Peking-Tsinghua Center for Life Sciences Peking University, Beijing, China. Exceutive Editor, ACS Chemical Biology (lab head)
(1)
Professor and Chair of Chemical Biology, Peking-Tsinghua Center for Life Sciences Peking University, Beijing, China. Executive Editor, ACS Chemical Biology
(1)
The NNF Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, 2200 Copenhagen, Denmark
(1)
University Grenoble Alpes, CEA, INSERM, UA13 BGE, CNRS, CEA, Grenoble, France
(1)
University of Ottawa
(1)
University of Pennsylvania
(1)
Wuhan Botanical Garden, CAS
(1)
Tags
xref:PubMed:34320364
(7)
xref:PubMed:41421336
(5)
xref:PubMed:36868209
(5)
xref:PubMed:29058708
(2)
xref:PubMed:33512761
(1)
xref:PubMed:30253806
(1)
xref:PubMed:27105113
(1)
Previous
page
1 / 21
You're on page
1
page
2
page
3
page
4
page
5
page
...
page
21
Next
page
Sort
by:
Relevance
Page size
10
H4K16 acylations fine-tune transcriptional response during metabolic perturbations (ChIP-seq)
H4K16 acylations fine-tune transcriptional response during metabolic perturbations (ChIP-seq)
PRJNA1153613
|
ENA
Cite
H4K16 acylations fine-tune transcriptional response during metabolic perturbations (ATAC-seq)
H4K16 acylations fine-tune transcriptional response during metabolic perturbations (ATAC-seq)
PRJNA1153609
|
ENA
Cite
H4K16 acylations fine-tune transcriptional response during metabolic perturbations (RNA-seq)
H4K16 acylations fine-tune transcriptional response during metabolic perturbations (RNA-seq)
PRJNA1153614
|
ENA
Cite
Evolved, Selective Erasers of Distinct Lysine Acylations.
Not available
S-EPMC7317389
|
biostudies-literature
Cite
Characterization of acidic lysine acylations in mycobacteria.
Not available
S-EPMC11667787
|
biostudies-literature
Cite
HBO1 is a versatile histone acyltransferase critical for promoter histone acylations.
Not available
S-EPMC8661427
|
biostudies-literature
Cite
Mapping histone acylations in mouse liver
Comparison of histone acylations in liver from fed and fasted mice. We have mapped H3K9ac, H3K14pr and H3K14bu by ChIP-seq in livers of either re-fed or 48h fasted mice.
ORGANISM(S):
Mus musculus
2017-10-01
|
GSE101597
|
GEO
Cite
H4K16 acylations fine-tune transcriptional response to short-chain acyl-CoA dehydrogenase deficiency (ATAC-seq)
H4K16 acylations fine-tune transcriptional response to short-chain acyl-CoA dehydrogenase deficiency (ATAC-seq)
PRJNA1262310
|
ENA
Cite
H4K16 acylations fine-tune transcriptional response to short-chain acyl-CoA dehydrogenase deficiency (RNA-seq)
H4K16 acylations fine-tune transcriptional response to short-chain acyl-CoA dehydrogenase deficiency (RNA-seq)
PRJNA1262312
|
ENA
Cite
Mechanochemical Friedel-Crafts acylations.
Not available
S-EPMC6604704
|
biostudies-literature
Cite
Previous
page
1 / 21
You're on page
1
page
2
page
3
page
4
page
5
page
...
page
21
Next
page
Sort
by:
Relevance
Page size
10
OmicsDI
is part of the ELIXIR infrastructure
OmicsDI is an Elixir interoperability service.
Learn more ›
Tweets