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International Clinical Psychopharmacology|January 1, 1993
Seizures induced by combined levomepromazine-fluvoxamine treatmentA Grinshpoon, Y Berg, T Mozes, et al.Worm|October 4, 2016
Probing and rearranging the transcription factor network controlling the C. elegans endodermTobias Wiesenfahrt, Erin Osborne Nishimura, Janette Y Berg, et al.Journal of Psychiatry & Neuroscience : JPN|November 1, 1992
Delayed amnesia and disorientation after electroconvulsive treatmentA Grinshpoon, R Mester, B Spivak, et al.Accident; Analysis and Prevention|November 27, 1999
Sixteen years age limit for learner drivers in Sweden--an evaluation of safety effectsN P Gregersen, H Y Berg, I Engström, et al.Biochemical and Biophysical Research Communications|December 23, 2021
The effects of the tropomyosin cardiomyopathy mutations on the calcium regulation of actin-myosin interaction in the atrium and ventricle differGalina V Kopylova, Valentina Y Berg, Anastasia M Kochurova, et al.Journal of Muscle Research and Cell Motility|January 3, 2021
Acidosis modifies effects of phosphorylated tropomyosin on the actin-myosin interaction in the myocardiumGalina V Kopylova, Alexander M Matyushenko, Valentina Y Berg, et al.Development (Cambridge, England)|December 25, 2015
The function and regulation of the GATA factor ELT-2 in the C. elegans endodermTobias Wiesenfahrt, Janette Y Berg, Erin Osborne Nishimura, et al.Biochemical and Biophysical Research Communications|June 10, 2020
Myosin from the ventricle is more sensitive to omecamtiv mecarbil than myosin from the atriumDaniil V Shchepkin, Salavat R Nabiev, Larisa V Nikitina, et al.Biochemical and Biophysical Research Communications|December 15, 2018
Structural and functional properties of αβ-heterodimers of tropomyosin with myopathic mutations Q147P and K49del in the β-chainAlexander M Matyushenko, Daniil V Shchepkin, Denis S Susorov, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|August 16, 2020
Mechanisms of disturbance of the contractile function of slow skeletal muscles induced by myopathic mutations in the tropomyosin TPM3 geneAlexander M Matyushenko, Victoria V Nefedova, Daniil V Shchepkin, et al.Pageof 3