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TranscriptomicsTranscription profiling of mouse skin, dermis, and epidermis of epithelial activated beta-catenin mutant embryo
This SuperSeries is composed of the following subset Series:; GSE10726: Expression data from skin of epithelial activated beta-catenin mutant mouse embryo; GSE10727: Expression data from dermis of epithelial activated beta-catenin mutant mouse embryo; GSE10728: Expression data from epidermis of epit...
ORGANISM(S): Mus musculus 
2008-06-20 | E-GEOD-10733 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse skin from epithelial activated beta-catenin mutant embryo
β-catenin signaling is required for hair follicle development, but it is unknown whether it is sufficient to activate expression of hair follicle genes in embryonic skin. To address this we profiled gene expression in skin dissected from E14.5 KRT14-Cre Ctnnb1(Ex3)fl/+ embryos carrying an activatin...
ORGANISM(S): Mus musculus 
2008-06-20 | E-GEOD-10726 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse dermis from epithelial activated beta-catenin mutant embryo
β-catenin signaling is required for hair follicle development, but it is unknown whether it is sufficient to activate expression of hair follicle genes in embryonic skin. To address this we profiled gene expression in dermis from E15.5 KRT14-Cre Ctnnb1(Ex3)fl/+ embryos carrying an activating mutati...
ORGANISM(S): Mus musculus 
2008-06-20 | E-GEOD-10727 | biostudies-arrayexpress
TranscriptomicsTranscription profiling of mouse epidermis from epithelial activated beta-catenin mutant embryo
β-catenin signaling is required for hair follicle development, but it is unknown whether it is sufficient to activate expression of hair follicle genes in embryonic skin. To address this we profiled gene expression in epidermis from E15.5 KRT14-Cre Ctnnb1(Ex3)fl/+ embryos carrying an activating mut...
ORGANISM(S): Mus musculus 
2008-06-20 | E-GEOD-10728 | biostudies-arrayexpress
TranscriptomicsA Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders
Human peroxisome biogenesis disorders are lethal genetic disease in which abnormal peroxisome assembly compromises overall peroxisome and cellular function. Peroxisomes are ubiquitous membrane-bound organelles involved in several important biochemical processes, notably lipid metabolism and the use ...
ORGANISM(S): Drosophila melanogaster 
2011-07-02 | E-GEOD-30362 | biostudies-arrayexpress
UnknownPhase 2 study of the focal adhesion kinase inhibitor defactinib (VS-6063) in previously treated advanced KRAS mutant non-small cell lung cancer.
Not available
S-EPMC6942685 | biostudies-literature
TranscriptomicsSpecific functions for ERK/MAPK signaling during PNS development
We have established functions of the stimulus dependent MAPKs, ERK1/2 and ERK5 in DRG, motor neuron, and Schwann cell development. Surprisingly, many aspects of early DRG and motor neuron development were found to be ERK1/2 independent and Erk5 deletion had no obvious effect on embryonic PNS. In con...
ORGANISM(S): Mus musculus 
2010-10-16 | E-GEOD-24730 | biostudies-arrayexpress
GenomicsPCGP Ph-likeALL RNASeq - samples
DATA FILES FOR SJPhLike-RNASeq
EGAD00001001016 | EGA
GenomicsPCGP Ph-likeALL SNP6 - samples
PCGP Ph-likeALL SNP6
EGAD00010000598 | EGA
GenomicsPCGP Ph-likeALL WES - samples
DATA FILES FOR Ph-likeALL WES
EGAD00001001054 | EGA
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