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Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden
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discovery, everything about DHT, 3β-Adiol, CYP7β1, and ERβ fell into place and a new endocrine pathway was unveiled ( Fig. 1 ) ( Weihua et al. 2002 ). Figure 1 A novel role for dihydrotestosterone (DHT) in estrogen signaling. How does
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evidence described in the literature have shown that the phosphoinositide 3-kinase (PI3K)/PTEN/Akt and TSC/mTOR signaling pathways are critical regulators of ovarian function including dormancy and activation of PFs, oocyte maintenance and activation, and
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embryonic development by melatonin via the nuclear factor erythroid 2-related factor 2/antioxidant-responsive element (Nrf2/ARE) signaling pathway. Nuclear factor erythroid 2-related factor 2, also known as NFE2L2 or Nrf2, is a potential transcription
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chain of proteins that transduces a signal from a membrane receptor to the nucleus. In many cancers, including BRAFV600E-driven tumors, the sustained activation of this pathway causes uncontrolled growth and cell survival, promoting carcinogenesis
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et al . 2007 ). Unfortunately, resistance to all endocrine therapies has been documented in both laboratory and clinical experiments, thereby necessitating novel strategies for targeting ER signaling to combat ER-positive breast cancer drug resistance
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provide another level of regulation to T3 distribution. All these observations suggest that T3 signaling in the developing brain can be modulated at several levels by both intracellular and extracellular events and does not directly reflect T3
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Department of Internal Medicine, Fujian Provincial Hospital South Branch, Fuzhou, Fujian, China
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Department of Endocrinology, Fujian Provincial Hospital, Fuzhou, Fujian, China
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). However, there have been no studies on the effects of LF in senile osteoporosis to date. The insulin/IGF1 signaling pathway was the first cell signaling mechanism that has been clearly shown to influence aging ( Kenyon et al. 2010 ). IGF1 is a critical
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Institut für Experimentelle Pädiatrische Endokrinologie, Department of Cell and Molecular Biology, Institut für Biochemie, Institut für Experimentelle Endokrinologie, Charité‐Universitätsmedizin Berlin, Augustenburger Platz 1, 13353 Berlin, Germany
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3-T1AM also binds to the α-2A-adrenergic receptor (ADRA2A), a receptor that influences glucose homeostasis ( Regard et al . 2007 ), but the underlying mechanism is still unclear. We consequently hypothesized that signaling of ADRA2A is induced or
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latter studies suggest the possibility of interactivity between NPs and VEGF variants ( Bijsmans et al . 2017 , Kamai et al . 2018 , Spes et al . 2019 ). This study’s over-riding objective was to extend the current knowledge of NP signalling in the
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to support fetal growth, responds to maternal nutrient availability and fetal demand to orchestrate the allocation of nutrients to meet energy and nutritional needs. Placental signaling pathways regulate fetal growth by sensing and integrating