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Hepatology (Baltimore, Md.)|May 26, 2007
Activation of endoplasmic reticulum stress response by hepatitis viruses up-regulates protein phosphatase 2AVerena Christen, Susan Treves, Francois H T Duong, et al.The Journal of Biological Chemistry|October 18, 2008
Ryanodine receptor activation by Ca v 1.2 is involved in dendritic cell major histocompatibility complex class II surface expressionMirko Vukcevic, Giulio C Spagnoli, Giandomenica Iezzi, et al.Peerj|January 30, 2016
The metabolomic profile of gamma-irradiated human hepatoma and muscle cells reveals metabolic changes consistent with the Warburg effectMin Wang, Adrian Keogh, Susan Treves, et al.Annals of the New York Academy of Sciences|March 8, 2007
Multiple levels of control of the expression of the human A beta H-J-J locus encoding aspartyl-beta-hydroxylase, junctin, and junctateGiordana Feriotto, Alessia Finotti, Giulia Breveglieri, et al.The FEBS Journal|August 8, 2007
Transcriptional activity and Sp 1/3 transcription factor binding to the P1 promoter sequences of the human AbetaH-J-J locusGiordana Feriotto, Alessia Finotti, Giulia Breveglieri, et al.Human Molecular Genetics|February 13, 2025
5-aza-2-deoxycytidine improves skeletal muscle function in a mouse model for recessive RYR1-related congenital myopathyAlexis Ruiz, Faiza Noreen, Hervé Meier, et al.Journal of Cell Science|June 15, 2007
Ca2+ signaling through ryanodine receptor 1 enhances maturation and activation of human dendritic cellsLaura Bracci, Mirko Vukcevic, Giulio Spagnoli, et al.The Journal of Physiology|May 1, 2009
Minor sarcoplasmic reticulum membrane components that modulate excitation-contraction coupling in striated musclesSusan Treves, Mirko Vukcevic, Marcin Maj, et al.Immunobiology|July 4, 2012
Ectosomes of polymorphonuclear neutrophils activate multiple signaling pathways in macrophagesCeylan Eken, Salima Sadallah, Perrine J Martin, et al.Human Molecular Genetics|December 24, 2016
Cellular, biochemical and molecular changes in muscles from patients with X-linked myotubular myopathy due to MTM1 mutationsChristoph Bachmann, Heinz Jungbluth, Francesco Muntoni, et al.Pageof 10