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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Core clock regulators in dexamethasone-treated HEK 293T cells at 4 h intervals

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Συγγραφέας
Beta R.A.A., Arsenopoulou Z.V., Kanoura A., Dalkidis D., Avraamidou R., Balatsos N.A.A.
Ημερομηνία
2022
Γλώσσα
en
DOI
10.1186/s13104-021-05871-7
Λέξη-κλειδί
circadian rhythm signaling protein
dexamethasone
circadian rhythm
HEK293 cell line
human
metabolism
Circadian Clocks
Circadian Rhythm
Dexamethasone
HEK293 Cells
Humans
Period Circadian Proteins
BioMed Central Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Objective: The study of the circadian clock and its mechanisms is easily facilitated through clock resetting in cell culture. Among the various established synchronizers of the circadian clock in cell culture (temperature, serum shock, glucocorticoids), the artificial glucocorticoid Dexamethasone (DEX) is the most widely used. DEX treatment as a protocol to reset the circadian clock in culture gives simple readout with minimal laboratory requirements. Even though there are many studies regarding clock resetting in culture using DEX, reference points or expression patterns of core clock genes and their protein products are scarce and sometimes contradict other works with similar methodology. We synchronise a cell line of human origin with DEX to be used for studies on circadian rhythms. Results: We treat HEK 293T cells with DEX and describe the patterns of mRNA and proteins of core clock regulators, while making a clear point on how CLOCK is less than an ideal molecule to help monitor rhythms in this cell line. © 2022, The Author(s).
URI
http://hdl.handle.net/11615/71617
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19743]

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