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Items: 5

1.

Analgesia of naloxone and morphine in wild-type and NY1DD sickle cell mice using BMAP cDNA microarrays

(Submitter supplied) Sickle cell disease is the most common genetic disorder in African-Americans. The opioid analgesic, morphine, has long been the treatment for the severe pain associated with this disease. Here we reveal that the opioid antagonist, naloxone, possesses potent analgesic activity in two strains of sickle cell mice (NY1DD and hBERK1) and not in their respective controls (ICR-CD1 and C57BL/6J) when administered by three parenteral routes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Platform:
GPL4464
12 Samples
Download data: GPS
Series
Accession:
GSE6479
ID:
200006479
2.

Analgesia of naloxone in wild-type and NY1DD transgenic mouse model of sickle cell anemia using BMAP cDNA microarrays

(Submitter supplied) Sickle cell disease is the most common genetic disorder in African-Americans. The opioid analgesic, morphine, has long been the treatment for the severe pain associated with this disease. Here we reveal that the opioid antagonist, naloxone, possesses potent analgesic activity in two strains of sickle cell mice (NY1DD and hBERK1) and not in their respective controls (ICR-CD1 and C57BL/6J) when administered by three parenteral routes. more...
Organism:
Mus musculus
Type:
Expression profiling by array
Dataset:
GDS2826
Platform:
GPL4464
6 Samples
Download data: GPS
Series
Accession:
GSE6578
ID:
200006578
3.
Full record GDS2826

Sickle cell anemia model: brain response to naloxone

Analysis of brains of NY1DD transgenic animals treated with naloxone. The NY1DD strain is a model for sickle cell anemia. Naloxone is an opioid antagonist that possesses potent analgesic activity in NY1DD animals. Results provide insight into the mechanism of action of naloxone in this model.
Organism:
Mus musculus
Type:
Expression profiling by array, log ratio, 2 strain sets
Platform:
GPL4464
Series:
GSE6578
6 Samples
Download data: GPS
4.

UMN Mouse 11K V 11_22_04 BMAP

(Submitter supplied) Basic protocol for generation of mouse microarrays i) Obtain cDNA library (1) thousands of bacterial stocks in 96-well plates (2) each bacterial stock contains a standard eukaryotic expression plasmid that contains a unique stretch of mouse cDNA inserted in the multiple cloning site ii) Replicate the library iii) PCR amplify each cDNA clone in 96 well reactions iv) Check PCR reactions on an agarose gel v) Purify PCR reactions with a Millipore filter vi) Elute purified DNA with 3XSSC (spotting buffer) vii) Spot DNA onto glass slides using a DNA spotting robot
Organism:
Mus musculus
1 DataSet
2 Series
12 Samples
Download data
Platform
Accession:
GPL4464
ID:
100004464
5.

NY1DD Sickle Cell Mouse brains, NLX treated, 10mins. SCNLX-I 817

Organism:
Mus musculus
Source name:
NY1DD Sickle Cell Mouse brains, NLX treated, 10mins. (channel 1) NY1DD Sickle Cell Mouse brains, Saline treated, 10 mins. (channel 2)
Platform:
GPL4464
Series:
GSE6479 GSE6578
Dataset:
GDS2826
Download data: GPS
Sample
Accession:
GSM141569
ID:
300141569
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