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November 2017
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Cover Image
Cover Image
An epifluorescence image of HEK293 cells expressing mKate2–GPER (red) and loaded with the Ca2+ indicator fura-2/AM (blue). The approach allows for direct comparison of Ca2+ signals in cells transfected with or without mKate2–GPER in the same microscopic field. In this issue of the Biochemical Journal, Terry et al. report on how activation of GPER (G protein-coupled estrogen receptor 1) “clamps” cytoplasmic Ca2+ signals via suppression of store-operated Ca2+ entry and Ca2+ efflux; see pages 3627–3642 for details.
ISSN 0264-6021
EISSN 1470-8728
In this Issue
Review Articles
Kinetochore–microtubule interactions in chromosome segregation: lessons from yeast and mammalian cells
Biochem J (2017) 474 (21): 3559–3577.
Research Articles
Escherichia coli and Neisseria gonorrhoeae UvrD helicase unwinds G4 DNA structures
Biochem J (2017) 474 (21): 3579–3597.
VPS18 recruits VPS41 to the human HOPS complex via a RING–RING interaction
Biochem J (2017) 474 (21): 3615–3626.
Suppression of store-operated Ca2+ entry by activation of GPER: contribution to a clamping effect on endothelial Ca2+ signaling
Biochem J (2017) 474 (21): 3627–3642.
AtSPX1 affects the AtPHR1–DNA-binding equilibrium by binding monomeric AtPHR1 in solution
Biochem J (2017) 474 (21): 3675–3687.
The spliceosomal proteins PPIH and PRPF4 exhibit bi-partite binding
Biochem J (2017) 474 (21): 3689–3704.