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Links from GEO DataSets

Items: 20

1.

Global gene expression in Moraxella catarrhalis ATCC 43617 grown under iron-replete and iron-limiting conditions

(Submitter supplied) Total RNA samples were isolated from M. catarrhalis grown in BHI (iron-replete condition, designated DF0) and in BHI containing 30 mM Desferal (iron-limiting condition, designated DF30). Total RNA and M. catarrhalis genome-directed primers (GDPs) were used for synthesis of Cy3- or Cy5-labeled cDNA samples. Three independent M. catarrhalis growth experiments and total RNA isolations were used for synthesis of cDNA samples, and a total of six DNA microarray hybridizations were performed in this study. more...
Organism:
Moraxella catarrhalis
Type:
Expression profiling by array
Platforms:
GPL3478 GPL3479
6 Samples
Download data: GPR
Series
Accession:
GSE4346
ID:
200004346
2.

Global gene expression in Moraxella catarrhalis ATCC43617 cells grown in the planktonic and in biofilm states

(Submitter supplied) Total RNA samples were isolated from M. catarrhalis grown in the planktonic state (i.e., in broth) and in a biofilm. Biofilms were generated by growing this strain in the continuous-flow Sorbarod filter system for three days. Total RNA samples and M. catarrhalis genome-directed primers (GDPs) were used for synthesis of Cy3- or Cy5-labeled cDNA samples. Five independent M. catarrhalis growth experiments and total RNA isolations were used for the synthesis of cDNA samples, and a total of six DNA microarray hybridizations were performed in this study. more...
Organism:
Moraxella catarrhalis
Type:
Expression profiling by array
Platforms:
GPL3478 GPL3479
6 Samples
Download data: GPR
Series
Accession:
GSE4348
ID:
200004348
3.

EJH Mcat Oligo-DNA Microarray 3

(Submitter supplied) The oligonucleotides were synthesized by Qiagen and spotted in triplicate on Corning UltraGapII slides
Organism:
Moraxella catarrhalis
8 Series
40 Samples
Download data
Platform
Accession:
GPL7398
ID:
100007398
4.

Identification of genes essential for Moraxella catarrhalis growth under iron-limiting conditions

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Moraxella catarrhalis BBH18
Type:
Expression profiling by array; Other; Genome variation profiling by genome tiling array
Platforms:
GPL16171 GPL16172
100 Samples
Download data: PAIR
Series
Accession:
GSE41548
ID:
200041548
5.

Identification of genes essential for Moraxella catarrhalis growth under iron-limiting conditions using Genomic Array Footprinting (GAF): Expression analysis of directed gene deletion mutants.

(Submitter supplied) Iron-sequestration by the human host is a first line defense against respiratory pathogens like Moraxella catarrhalis, which consequently experiences a period of iron-starvation during colonization and infection. We determined the genetic requirements for M. catarrhalis growth during iron-starvation using the high-throughput genome-wide screening technology genomic array footprinting (GAF). To further characterize the functional consequences of the gene deletions (GAF identified genes), we determined transcriptome profiles of the wild-type and directed mutant strains during exponential growth in BHI medium. more...
Organism:
Moraxella catarrhalis BBH18
Type:
Expression profiling by array
Platform:
GPL16172
76 Samples
Download data: PAIR
Series
Accession:
GSE41547
ID:
200041547
6.

Identification of genes essential for Moraxella catarrhalis growth under iron-limiting conditions using Genomic Array Footprinting (GAF)

(Submitter supplied) Iron-sequestration by the human host is a first line defense against respiratory pathogens like Moraxella catarrhalis, which consequently experiences a period of iron-starvation during colonization and infection. We determined the genetic requirements for M. catarrhalis growth during iron-starvation using the high-throughput genome-wide screening technology genomic array footprinting (GAF). To this end, a large marinerT7 transposon mutant library (~28,000 independent transposon mutants) was grown under iron-limiting conditions, achieved by sequestration of iron by 30 µM Desferal (DF30), and under control growth conditions (brain heart infusion broth, DF0). more...
Organism:
Moraxella catarrhalis BBH18
Type:
Genome variation profiling by genome tiling array; Other
Platform:
GPL16171
24 Samples
Download data: PAIR
Series
Accession:
GSE41546
ID:
200041546
7.

Expression profiling of Moraxella catarrhalis RH4 during in vitro growth in brain heart infusion (BHI) medium

(Submitter supplied) Transcriptome analysis of M. catarrhalis RH4 predicted coding sequences and clustered regularly interspaced short palindromic repeats (CRISPRs) regions. The results described in this study are further discussed in De Vries, S.P.W., van Hijum, S.A.F.T., Schueler, W., Riesbeck, K., Hays, J.P., Hermans, P.W.M., Bootsma, H.J.; Genome analysis of Moraxella catarrhalis strain RH4: a human respiratory tract pathogen; Journal of Bacteriology
Organism:
Moraxella catarrhalis RH4; Moraxella catarrhalis BBH18
Type:
Expression profiling by genome tiling array
Platform:
GPL10378
18 Samples
Download data: PAIR
Series
Accession:
GSE21632
ID:
200021632
8.

Transcriptional Profile of Lactobacillus helveticus grown in milk vs. MRS medium

(Submitter supplied) L. helveticus is used to modulate cheese flavor and as a starter organism in certain cheese varieties. Our group has compiled a draft (4x) sequence for the 2.4 Mb genome of an industrial strain L. helveticus CNRZ32. The primary aim was to investigate expression of 168 completely sequenced genes during growth in milk and MRS medium using microarrays. Oligonucleotide probes against each of the completely sequenced genes were compiled on maskless photolithography-based DNA microarrays. more...
Organism:
Lactobacillus helveticus; Lactobacillus helveticus CNRZ32
Type:
Expression profiling by array
Platform:
GPL4817
12 Samples
Download data: DATA, PAIR
Series
Accession:
GSE7005
ID:
200007005
9.

NimbleGen Lactobacillus helveticus CNRZ32 169/tiling

(Submitter supplied) High-density microarrays based on Maskless Array Synthesizer technology.
Organism:
Lactobacillus helveticus CNRZ32
1 Series
12 Samples
Download data: TXT
Platform
Accession:
GPL4817
ID:
100004817
10.

RNA-seq-based analysis of the physiologic cold shock-induced changes in Moraxella catarrhalis gene expression

(Submitter supplied) Background: Moraxella catarrhalis, a major nasopharyngeal pathogen of the human respiratory tract, is exposed to rapid downshifts of environmental temperature when humans breathe cold air. The prevalence of pharyngeal colonization and respiratory tract infections caused by M. catarrhalis is greatest in winter. We investigated how M. catarrhalis uses the physiologic exposure to cold air to regulate pivotal survival systems that may contribute to M. more...
Organism:
Moraxella catarrhalis O35E
Type:
Expression profiling by high throughput sequencing
Platform:
GPL17097
6 Samples
Download data: BED, TSV
Series
Accession:
GSE46256
ID:
200046256
11.

Differential gene expression profile of Streptococcus pneumoniae early biofilm cells and planktonic cells

(Submitter supplied) Otitis media, pneumonia, sinusitis and as well as severe diseases such as meningitis and bacteraemia are related to biofilm-like diseases, in which Streptococcus pneumoniae demonstrated differential and tissue specific gene expressions. In this study, we reported the differential gene expression profile of early in vitro biofilm and planktonic cell in c-DNA microarray analysis. The microarray analysis was performed on total RNA extracted from biofilms grown in 24-well microtiter plate and mid-log grown planktonic cells. more...
Organism:
Streptococcus pneumoniae R6
Type:
Expression profiling by array
Platform:
GPL15071
3 Samples
Download data: GPR
Series
Accession:
GSE34751
ID:
200034751
12.

M. catarrhalis Gene Expression in the Chinchilla Nasopharynx

(Submitter supplied) M. catarrhalis strain O35E.rpsl was inoculated into the nasopharynx of healthy, male adult chinchillas. 24 hours later the nasopharyngeal tissues were extracted and homogenized. Total RNA was extracted from these tissue samples. Subsequently, M. catarrhalis genome directed primers were utilized to synthesize cDNA from the total RNA sample. As a control, M.catarrhalis strain O35E.rpsl was grown in BHI broth to a Klett density of 200 units and underwent RNA extraction per standard protocols. more...
Organism:
Moraxella catarrhalis
Type:
Expression profiling by array
Platform:
GPL7398
5 Samples
Download data: GPR
Series
Accession:
GSE13559
ID:
200013559
13.

Identification of Gene Products Involved in the Oxidative Stress Response of Moraxella catarrhalis: Evaluation of OxyR dependent Genes

(Submitter supplied) Series of DNA microarrays (4) comparing the M. catarrhalis strain 035E and M. catarrhalis oxyR mutant response to 50 mM hydrogen peroxide.
Organism:
Moraxella catarrhalis
Type:
Expression profiling by array
Platform:
GPL7398
4 Samples
Download data: GPR
Series
Accession:
GSE24351
ID:
200024351
14.

Identification of Gene Products Involved in the Oxidative Stress Response of Moraxella catarrhalis

(Submitter supplied) Series of DNA microarrays (4) comparing the M. catarrhalis strain 035E response to 50 mM hydrogen peroxide relative to a water-only control.
Organism:
Moraxella catarrhalis
Type:
Expression profiling by array
Platform:
GPL7398
4 Samples
Download data: GPR
Series
Accession:
GSE24331
ID:
200024331
15.

Gene expression in E.coli K-12 MC4100 at 37˚C and 23˚C in M9 glycerol exponential phase growth

(Submitter supplied) Because many virulence genes in E. coli and other pathogens are regulated by temperature, we wanted to determine on a genome-wide scale which genes are modulated in adapting to both human host temperature (37˚C) and ambient room temperature (23˚C). Overall, 126 genes were found to be more highly expressed at 37˚C (1) whereas 297 genes were more highly expressed at 23˚C (2). Genes involved in the uptake and utilization of amino acids, carbohydrates, and iron dominated the 37˚C list, supporting a model in which temperature serves as a host cue to increase expression of bacterial genes needed for growth. more...
Organism:
Escherichia coli
Type:
Expression profiling by array
Platform:
GPL5942
5 Samples
Download data: GPR, TXT
Series
Accession:
GSE9197
ID:
200009197
16.

Univerisity of Wisconsin Gene Expression Center_Escherichia coli_4.2K_Eco15

(Submitter supplied) Microarray consists of full-length PCR products from all 4,290 annotated open reading frames (ORFs) in E. coli mg1655 (1). PCR products are printed in replicate on standard, 1” X 3”, poly-l-lysine coated glass microscope slides. Greater than 95% have been shown to migrate as a single band, of the predicted molecular weight, as determined by gel electrophoresis and ethidium bromide staining. Also printed on each microarray are >200 control spots consisting of: fragmented E. more...
Organism:
Escherichia coli
1 Series
5 Samples
Download data: TXT
Platform
Accession:
GPL5942
ID:
100005942
17.

Expression data from planktonic and biofilm cultures of Mycobacterium smegmatis

(Submitter supplied) Transition of microbial growth from planktonic to biofilm is associated with programmed changes in the global patterns of gene expression. These changes are likely to faciliate the appropriate physiological and metabolic adjustments that bacteria need to make during the development of biofilms. Using microarrays we have examined the changes in pattern of gene expression associated with growth of Mycobacterium smegmatis in various stages of planktonic and biofilm cultures. more...
Organism:
Mycolicibacterium smegmatis
Type:
Expression profiling by array
Platform:
GPL4686
12 Samples
Download data: GPR
Series
Accession:
GSE6935
ID:
200006935
18.

HatfullPitt Mycobacterium smegmatis 30K v2

(Submitter supplied) Slide Information Array Name : Mycobacterium smegmatis microarray version 2 Elements on Array : 29184 Elements on Array (minus empties): 28904 Grids: 48 Array Type : ss_oligo (70-mer) Surface Coating: Epoxy Printing Buffer(s): Nexterion with .01 CTAB, Schott buffer LEB E2 Arraying Machine(s): Genetix Oligo Replicates : 4x Oligos Designed : 6746 ORFs w/o oligo*: 1 Controls: 480 A. thaliana (70-mers) Strain Information Design Strain : ORFs in Design: Oligos Designed **: MC2 155 6898 6746 TIGR Spotfinder Printing Pattern MetaRow 12 MetaColumn 4 Pix X (pix) 450 Pin Y (pix) 450 Row Number 25 Column Number 25 X Spacing (pix) 17 Y Spacing (pix) 17 The user should remove slides from their packaging as soon as possible and store them at room temperature in a desiccator or a Rubbermaid® or Tupperware® container containing a bottom layer of anhydrous calcium sulfate such as Drierite®. more...
Organism:
Mycolicibacterium smegmatis
1 Series
12 Samples
Download data
Platform
Accession:
GPL4686
ID:
100004686
19.

Analysis of the mesSR regulon in M. catarrhalis

(Submitter supplied) Transcription profile analysis of a wild type ETSU9 strain and its isogenic non-polar in frame mesR mutant.
Organism:
Moraxella catarrhalis
Type:
Expression profiling by array
Platform:
GPL7398
6 Samples
Download data: GPR
Series
Accession:
GSE50229
ID:
200050229
20.

RNA-seq of Moraxella catarrhalis CCRI-195ME ModM3 ON and ModM3 OFF phase variants

(Submitter supplied) Moraxella catarrhalis contains an N6-adenine DNA-methyltransferase (ModM3), that is subject to phase variable expression (random ON/OFF switching). Phase-variable switching of DNA methyltransferase activity results in the presence or absence of methylation at a specific target sequence, leading to co-ordinated, epigenetically-regulated switching of expression of multiple genes across the genome. The suite of genes thus regulated are known as a phasevarion (phase-variable regulon). more...
Organism:
Moraxella catarrhalis
Type:
Expression profiling by high throughput sequencing
Platform:
GPL27756
6 Samples
Download data: TXT
Series
Accession:
GSE140417
ID:
200140417
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