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Home › Dataset Library › Expression data from E18.5 Igf1 -/- (homozygous mutant) and Igf1+/+ (normal wild type control) mouse lungs

Dataset: Expression data from E18.5 Igf1 -/- (homozygous mutant) and Igf1+/+ (normal wild type control) mouse lungs

Insight into the role of Insulin-like Growth Factor (IGF) in development of lungs has come from the study of genetically modified mice....

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Insight into the role of Insulin-like Growth Factor (IGF) in development of lungs has come from the study of genetically modified mice. IGF1 is a key factor during lung development. IGF1 deficiency in the neonatal mouse causes respiratory failure collapsed alveoli and altered alveolar septa. To further characterize IGF1 function during lung development we analyzed Igf1-/- mouse prenatal lungs in a C57Bl/6 genetic background. Mutant lungs showed disproportional hypoplasia, disorganized extracellular matrix and dilated alveolar capillaries. IGF1 target genes during lung maturation were identified by analyzing RNA differential expression in Igf1-/- lungs using microarrays. Lungs from E18.5 were isolated from both Igf1+/+ wild type and Igf1-/- null mice and pooled to obtain RNA. Heterozygous male and female with a genetic background C57BL/6J were mated to obtain embryos at embrionic (E) stage 18.5 days post coitum (E18.5). 3 biological replicates per genotype.

Species:
mouse

Samples:
6

Source:
E-GEOD-17157

PubMed:
24391734

Updated:
Dec.12, 2014

Registered:
Nov.24, 2014


Factors: (via ArrayExpress)
Sample GENOTYPE
GSM429107 Igf1-/- (homozygous mutant)
GSM429107 Igf1-/- (homozygous mutant)
GSM429107 Igf1-/- (homozygous mutant)
GSM429110 Igf1+/+ (normal wild type control)
GSM429110 Igf1+/+ (normal wild type control)
GSM429110 Igf1+/+ (normal wild type control)

Tags

  • insulin
  • lung
  • respiratory failure

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