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Nature Communications|February 25, 2022
A fast Myosin super enhancer dictates muscle fiber phenotype through competitive interactions with Myosin genesMatthieu Dos Santos, Stéphanie Backer, Frédéric Auradé, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 22, 2014
AMPK controls exercise endurance, mitochondrial oxidative capacity, and skeletal muscle integrityLouise Lantier, Joachim Fentz, Rémi Mounier, et al.
Ebiomedicine|December 12, 2018
Installation of a cancer promoting WNT/SIX1 signaling axis by the oncofusion protein MLL-AF9Li-Shu Zhang, Xunlei Kang, Jianming Lu, et al.
EMBO Molecular Medicine|July 15, 2024
DiPRO1 distinctly reprograms muscle and mesenchymal cancer cellsJeremy Rich, Melanie Bennaroch, Laura Notel, et al.
Journal of Medical Genetics|January 13, 2021
Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disordersEduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
JCI Insight|April 14, 2022
Sine oculis homeobox homolog 1 plays a critical role in pulmonary fibrosisCory Wilson, Tinne Cj Mertens, Pooja Shivshankar, et al.
Cell Reports|January 23, 2026
Retinal determination network reactivation drives chemoresistance and blocks myeloid differentiation in acute myeloid leukemiaLiam Clayfield, Divya Malik, Jessica Whittle, et al.
Elife|June 14, 2018
Signals from the brain and olfactory epithelium control shaping of the mammalian nasal capsule cartilageMarketa Kaucka, Julian Petersen, Marketa Tesarova, et al.
Molecular Metabolism|April 2, 2021
Compound- and fiber type-selective requirement of AMPKγ3 for insulin-independent glucose uptake in skeletal musclePhilipp Rhein, Eric M Desjardins, Ping Rong, et al.
Nature Genetics|June 15, 2007
The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndromeMarion Delous, Lekbir Baala, Rémi Salomon, et al.
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