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资源简介：
A shared gene expression signature in human blastocyst embryos affected by a mitochondrial defect.
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创建时间：
2025-07-08
相关数据集
Expression data from mouse muscle
The knock-out of calpain 3 (C3KO) is a murine model for calpainopathies wich shows a mild dystrophic phenotype with signs of muscle degeneration. Adult (A) mice show a more severe phenotype than young
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Agilent microarray analysis between a Dullard-heterozygous and a Dullard-homozygous E7.5 embryo. Mus musculus
To explore the loss of Dullurd function in mouse embryo development, we have performed the Agilent microarray analysis between a Dullard-heterozygous and a Dullard-homozygous E7.5 embryo. Our findings
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Mitochondrial disorders
Extremely variable clinic and genetic features characterize Mitochondrial Encephalomyopathy Disorders (MED). Pathogenic mitochondrial DNA (mtDNA) defects can be divided into large-scale rearrangements
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Comparison of gene expression between Ftx KO eyes and wild type eyes
Gene expression of embryonic eye (e13.5) in Ftx KO females, Ftx KO males, WT females and WT males. Ftx KO females, Ftx KO males, WT females and WT males.
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Differential Gene Expression in Uterine Endometrium during Implantation in Pigs. Sus scrofa
This study provide an opportunity to elucidate the genetic control of fetal implantation and improve our understanding of fetal implantation and gestation maintenance, thus make further improvement fo
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