
Publications
Scientific articles and outputs from PGNM teams and collaborators.
About
PGNM publications reflect the scientific output of the laboratory’s teams and collaborators, spanning fundamental mechanisms, disease models, technologies and translational research.
2011
Junctophilin 1 and 2 proteins interact with the L-type Ca2+ channel dihydropyridine receptors (DHPRs) in skeletal muscle.,
J Biol Chem 2011 Dec; 286(51): 43717-43725.
2011
Myopathy caused by mammalian target of rapamycin complex 1 (mTORC1) inactivation is not reversed by restoring mitochondrial function.,
Proc Natl Acad Sci U S A 2011 Dec; 108(51): 20808-13.
2011
Defects in Ca2+ release associated with local expression of pathological ryanodine receptors in mouse muscle fibres.,
J Physiol 2011 Nov; 589(Pt 22): 5361-82.
2011
DNA Damage Response,
Cold Spring Harbor Perspectives in Biology.
2010
Replication factor C recruits DNA polymerase delta to sites of nucleotide excision repair but is not required for PCNA recruitment.,
Mol Cell Biol 2010 Oct; 30(20): 4828-39.
2010
In vivo expression of G-protein beta1gamma2 dimer in adult mouse skeletal muscle alters L-type calcium current and excitation-contraction coupling.,
J Physiol 2010 Aug; 588(Pt 15): 2945-60.
2010
Interactome mapping of the phosphatidylinositol 3-kinase-mammalian target of rapamycin pathway identifies deformed epidermal autoregulatory factor-1 as a new glycogen synthase kinase-3 interactor.,
Mol Cell Proteomics 2010 Jul; 9(7): 1578-93.
2010
Compressed Sensing with off-axis frequency-shifting holography,
Optics Letters.
2010
Altered myoplasmic Ca(2+) handling in rat fast-twitch skeletal muscle fibres during disuse atrophy.,
Pflugers Arch 2010 Mar; 459(4): 631-44.
2010
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis.,
EMBO J 2010 Feb; 29(3): 643-54.
2009
Muscle inactivation of mTOR causes metabolic and dystrophin defects leading to severe myopathy.,
J Cell Biol 2009 Dec; 187(6): 859-74.
2009
T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase.,
Proc Natl Acad Sci U S A 2009 Nov; 106(44): 18763-8.
2009
Differentiation Driven Changes in the Dynamic Organization of Basal Transcription Initiation,
PLoS Biology.
2009
Probing PML body function in ALT cells reveals spatiotemporal requirements for telomere recombination,
Proc Natl Acad Sci U S A 2009 Sep; 106(37): 15726-31.
2009
Identification of an agrin mutation that causes congenital myasthenia and affects synapse function.,
Am J Hum Genet 2009 Aug; 85(2): 155-67.
2009
Silencing rapsyn in vivo decreases acetylcholine receptors and augments sodium channels and secondary postsynaptic membrane folding.,
Neurobiol Dis 2009 Jul; 35(1): 14-23.
2009
Hemoglobin and hematocrit are not such good candidates to detect autologous blood doping,
International Journal of Hematology.
2009
Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons.,
PLoS One 2009 ; 4(4): e5390.
2008
Effect of Proliferating Cell Nuclear Antigen Ubiquitination and Chromatin Structure on the Dynamic Properties of the Y-family DNA Polymerases,
Molecular Biology of the Cell.
2008
Expression of the muscular dystrophy-associated caveolin-3(P104L) mutant in adult mouse skeletal muscle specifically alters the Ca(2+) channel function of the dihydropyridine receptor.,
Pflugers Arch 2008 Nov; 457(2): 361-75.