There was no effect of season on the proportion of oocytes developing to the blastocyst stage from small follicles. In this study we were interested in exploring which known or newly discovered PGRMC1 functions are related to these phosphorylation events.
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GO pathways enrichment results. Pharmacol Ther. Please note that Subject Outlines and assessment tasks are updated each session. Mol BioSyst. Peter Thomson is acknowledged for his statistical assistance. Pathways enrichment suggests altered cell cycle control proteins.
Lf intervention increased the level of polySia-NCAM expression in the hippocampus and prefrontal cortex of postnatal piglets as confirmed by Western blot analyses. Reichardt LF. These changes were mediated, at least in part, by the Lf-induced upregulation of the BDNF signaling pathway.
Expert Opin Ther Targets. Meiosis- Cell division involving sex cells. No outliers were identified using the principal component analysis method with Partek software. Electronic supplementary material Below is the link to the electronic supplementary material.
PGRMC1 phosphorylation site mutations cause pronounced metabolic changes, genomic mutation rates, and altered genomic CpG methylation, without affecting progesterone-dependent doxycycline resistance. NpFR1 reveals differences in cytoplasmic redox status.
Conclusion Our work was inspired by the discovery that PGRMC1 phosphorylation differs between breast cancer subtypes differing in estrogen receptor expression, that also exhibit starkly contrasting levels of patient survival [ 9 ].
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