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Matrix Biology : Journal of the International Society for Matrix Biology|December 2, 2017
Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategiesPeter D Yurchenco, Karen K McKee, Judith R Reinhard, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|February 4, 2026
Dual AAV gene therapy using laminin-linking proteins ameliorates muscle and nerve defects in LAMA2-related muscular dystrophyJudith R Reinhard, Shuo Lin, Eleonora Maino, et al.Skeletal Muscle|December 4, 2019
mTORC2 affects the maintenance of the muscle stem cell poolNathalie Rion, Perrine Castets, Shuo Lin, et al.PNAS Nexus|April 11, 2023
Nerve pathology is prevented by linker proteins in mouse models for LAMA2-related muscular dystrophyJudith R Reinhard, Emanuela Porrello, Shuo Lin, et al.Development (Cambridge, England)|March 16, 2019
mTOR controls embryonic and adult myogenesis via mTORC1Nathalie Rion, Perrine Castets, Shuo Lin, et al.Nature Communications|May 20, 2016
The calcium sensor Copine-6 regulates spine structural plasticity and learning and memoryJudith R Reinhard, Alexander Kriz, Milos Galic, et al.The Journal of Clinical Investigation|February 21, 2017
Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotypeKaren K McKee, Stephanie C Crosson, Sarina Meinen, et al.Nature Communications|November 27, 2025
Loss of cell-autonomously secreted laminin-α2 drives muscle stem cell dysfunction in LAMA2-related muscular dystrophyTimothy J McGowan, Judith R Reinhard, Nicolas Lewerenz, et al.Science Translational Medicine|June 30, 2017
Linker proteins restore basement membrane and correct LAMA2-related muscular dystrophy in miceJudith R Reinhard, Shuo Lin, Karen K McKee, et al.Nature Communications|September 10, 2020
The neuromuscular junction is a focal point of mTORC1 signaling in sarcopeniaDaniel J Ham, Anastasiya Börsch, Shuo Lin, et al.Pageof 1