Marr H H - OmicsDI

Show results for

Unknown (223)
Transcriptomics (12)
Proteomics (6)
Genomics (5)
Metabolomics (1)

Organisms

Streptococcus mutans (2)
Bacillus subtilis subsp. subtilis str. 168 (2)
Homo sapiens (2)
Salmonella enterica subsp. enterica serovar Typhimurium str. 14028S (1)
Staphylococcus aureus subsp. aureus USA300 (1)
Neisseria meningitidis (1)
Listeria monocytogenes (1)
Campylobacter jejuni (1)
Bacillus subtilis (1)
Streptococcus pneumoniae (1)
Ovis aries (1)
Drosophila melanogaster (1)
Brucella abortus 2308 (1)
Yersinia pestis biovar Microtus str. 91001 (1)
Mus musculus (1)

Organisms

Brucella abortus 2308 (1)
Streptococcus pneumoniae (1)
Homo sapiens (1)

Repository

biostudies-arrayexpress (12)
ENA (4)
pride (3)
iProX (2)
geo (1)
MetaboLights (1)
PAXDB (1)

Tissue

Skin (1)

Disease

Psoroptes ovis infestation (1)

Technology Type

Mass Spectrometry (3)
Shotgun proteomics (3)
Mass spectrometry (1)

Instrument Platform

ScanArray Express HT (1)
Illumina HiSeq 1500 (1)
Liquid Chromatography MS - positive (1)

Publication Date

2020 (3)
2012 (3)
2010 (3)
2023 (3)
2011 (2)
2015 (1)
2013 (1)
2008 (1)
2007 (1)
2026 (1)
2019 (1)

UNIPROT ID/AC

3MGA_BACSU (1)
3MGH_BACSU (1)
4OT_BACSU (1)
53DR_BACSU (1)
6PGDH_BACSU (1)
6PGD_BACSU (1)
6PGL_BACSU (1)
AADK_BACSU (1)
AAPA_BACSU (1)
AAT1_BACSU (1)
AAT3_BACSU (1)
ABH_BACSU (1)
ABRB_BACSU (1)
ACCA_BACSU (1)
ACCC1_BACSU (1)
ACCC2_BACSU (1)
ACCD_BACSU (1)
ACDA_BACSU (1)
ACDB_BACSU (1)
ACDC_BACSU (1)
ACKA_BACSU (1)
ACNA_BACSU (1)
ACOA_BACSU (1)
ACOB_BACSU (1)
ACOC_BACSU (1)
ACOR_BACSU (1)
ACPK_BACSU (1)
ACPS_BACSU (1)
ACP_BACSU (1)
ACSA_BACSU (1)

Metabolite Name

(+)-Bornyl diphosphate|(-)-Bornyl diphosphate (1)
(+)-Catechin|(-)-Epicatechin (1)
(+)-Epicubenol|alpha-Eudesmol|(+)-T-Muurolol (1)
(-)-Sedamine (1)
(1R,6R)-6-Hydroxy-2-succinylcyclohexa-2,4-diene-1-carboxylate (1)
(1R,6S)-1,6-Dihydroxycyclohexa-2,4-diene-1-carboxylate|(4R,5R)-4,5-Dihydroxycyclohexa-1(6),2-diene-1-carboxylate (1)
(1R,6S)-6-Amino-5-oxocyclohex-2-ene-1-carboxylate|(3S,5S)-Carbapem-3-carboxylic acid|(5S,6S)-6-Amino-5-hydroxycyclohexa-1,3-diene-1-carboxylate (1)
(2R)-O-Phospho-3-sulfolactate (1)
(2R,3S)-2,3-Dimethylmalate|(R)-2-Ethylmalate|(R)-3,3-Dimethylmalate (1)
(2R,3S)-2,3-Dimethylmalate|(R)-2-Ethylmalate|2-Dehydro-3-deoxy-L-rhamnote (1)
(2R,3S)-2,3-Dimethylmalate|3-Ethylmalate|2-Dehydro-3-deoxy-L-rhamnote (1)
(2R,3S)-2,3-Dimethylmalate|L-Rhamnote|D-Fucote (1)
(2S)-2-{[1-(R)-Carboxyethyl]amino}pentanoate (1)
(2S,3R)-3-Hydroxybutane-1,2,3-tricarboxylate|N-Succinyl-L-glutamate|2-(Acetamidomethylene)succite (1)
(2S,3R)-3-Hydroxybutane-1,2,3-tricarboxylate|N-Succinyl-L-glutamate|Homoisocitrate (1)
(2S,3S)-2-Hydroxytridecane-1,2,3-tricarboxylate (1)
(2S,3S)-2-Hydroxytridecane-1,2,3-tricarboxylate|(R)-Norreticuline (1)
(3E)-4-(2-Carboxyphenyl)-2-oxobut-3-enoate|(3Z)-4-(2-Carboxyphenyl)-2-oxobut-3-enoate (1)
(3S,4S)-3-Hydroxytetradecane-1,3,4-tricarboxylate (1)
(4S,5R)-4,5,6-Trihydroxy-2-iminohexanoate|(2Z,4S,5R)-2-Amino-4,5,6-trihydroxyhex-2-enoate (1)
(4S,5R)-4,5,6-Trihydroxy-2-iminohexanoate|(2Z,4S,5R)-2-Amino-4,5,6-trihydroxyhex-2-enoate|4-Hydroxy-4-methylglutamate (1)
(4S,5R)-4,5,6-Trihydroxy-2-iminohexanoate|2,3,4,5-Tetrahydrodipicolite|L-Dopachrome (1)
(4S,5R)-4,5,6-Trihydroxy-2-iminohexanoate|2-Hydroxyisophthalic acid|(2Z,4S,5R)-2-Amino-4,5,6-trihydroxyhex-2-enoate (1)
(4S,5R)-4,5,6-Trihydroxy-2-iminohexanoate|4-Hydroxy-4-methylglutamate|(2Z,4S,5R)-2-Amino-4,5,6-trihydroxyhex-2-enoate (1)
(5-L-Glutamyl)-L-amino acid|gamma-L-Glutamyl-D-alanine|L-Alanyl-D-glutamate (1)
(5-L-Glutamyl)-L-glutamate (1)
(6R)-10-Formyltetrahydropteroyldiglutamate (1)
(E)-2-Methylgeranyl diphosphate|2-Succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate (1)
(Indol-3-yl)acetamide|Indole-3-acetaldehyde oxime (1)
(R)-(Homo)2-citrate (1)

First Public Date

2024 (2)
2023 (1)
2014 (1)

Classification

bacteria (2)

Study type

Transcription profiling by array (10)
High-throughput sequencing (1)
RNA-seq of coding RNA (1)

Release Date

2025 (27)
2023 (27)
2022 (22)
2021 (19)
2020 (17)
2024 (15)
2018 (13)
2019 (12)
2012 (10)
2014 (10)
2011 (9)
2017 (9)
2016 (8)
2015 (8)
2010 (8)
2013 (7)
2007 (6)
2009 (4)
2008 (3)
2003 (1)

Lab affiliation

Freie Universität Berlin Institut für Biologie-Mikrobiologie (1)
Helmholtz Zentrum München, Institute of Lung Biology and Disease, Group Regenerative Biology and Medicine, Munich, Germany, Member of the German Centre for Lung Research (DZL) (1)
St. Giles Laboratory of Human Genetics of Infectious Diseases, The Rockefeller University, New York, New York, USA. (1)

Tags

pathogen (2)
pathogen:bacterium (2)
xref:PubMed:38422122 (1)
xref:PubMed:37847580 (1)
xref:PubMed:38614291 (1)
xref:PubMed:20804771 (1)

Previous page
1 / 25
You're on page 1
page 2
page 3
page 4
page 5
page ...
page 25
Next page

Sort by:

Relevance

Page size

The metalloregulatory site in Streptococcus pneumoniae AdcR, a zinc-activated MarR-family repressor

Streptococcus pneumoniae D39 AdcR (adhesion competence repressor) is the first metal-sensing member of the MarR (multiple antibiotic resistance repressor) family to be characterized. Expression profiling of a âˆ†adcR strain grown in liquid culture under microaerobic conditions revealed that transcr...

ORGANISM(S): Streptococcus pneumoniae

2010-10-01 | E-GEOD-21506 | biostudies-arrayexpress

Paralogous MarR/DUF24-family repressors YodB and CatR control expression of the catechol dioxygenase CatE in Bacillus subtilis

The redox-sensing MarR/DUF24-type repressor YodB controls expression of the azoreductase AzoR1 and the nitroreductase YodC that are involved in detoxification of quinones and diamide in Bacillus subtilis. In the present paper, we identified YodB and its paralog YvaP (CatR) as repressors of the yfiDE...

ORGANISM(S): Bacillus subtilis

2010-06-29 | E-GEOD-22603 | biostudies-arrayexpress

Brucella MucR acts as an H-NS-like protein to silence virulence genes and structure the nucleoid 

Histone-like nucleoid structuring (H-NS) and H-NS-like proteins serve as global gene silencers and work with antagonistic transcriptional activators (counter- silencers) to properly coordinate the expression of virulence genes in pathogenic bacteria. In Brucella, MucR has been proposed as a novel H-...

ORGANISM(S): Brucella abortus 2308

2023-09-16 | GSE234935 | GEO

MarR family proteins are important regulators of clinically relevant antibiotic resistance.

Not available

S-EPMC7020996 | biostudies-literature

Brucella MucR acts as an H-NS-like protein to silence virulence genes and structure the nucleoid 

PRJNA983775 | ENA

Oxidants induce Escherichia coli MarR glutathionylation in the presence of glutathione.

Not available

S-EPMC12017873 | biostudies-literature

Structural insights into the redox-switch mechanism of the MarR/DUF24-type regulator HypR.

Not available