Publications by authors named "Maya Barad"

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Skeletal diseases caused by mutations in show aberrant differentiation of skeletal progenitors due to dysregulation of DEPTOR.
Fabiana Csukasi, Michaela Bosakova, Tomas Barta, Jorge H Martin, Jesus Arcedo, Maya Barad

Front Cell Dev Biol· January 2023

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4-PBA Treatment Improves Bone Phenotypes in the Aga2 Mouse Model of Osteogenesis Imperfecta.
Ivan Duran, Jennifer Zieba, Fabiana Csukasi, Jorge H Martin, Davis Wachtell, Maya Barad

J Bone Miner Res· April 2022

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Biallelic mutations in LAMA5 disrupts a skeletal noncanonical focal adhesion pathway and produces a distinct bent bone dysplasia.
Maya Barad, Fabiana Csukasi, Michaela Bosakova, Jorge H Martin, Wenjuan Zhang

EBioMedicine· December 2020

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Dominant-negative SOX9 mutations in campomelic dysplasia.
Fabiana Csukasi, Ivan Duran, Wenjuan Zhang, Jorge H Martin, Maya Barad

Hum Mutat· December 2019

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The PTH/PTHrP-SIK3 pathway affects skeletogenesis through altered mTOR signaling.
Fabiana Csukasi, Ivan Duran, Maya Barad, Tomas Barta, Iva Gudernova

Sci Transl Med· September 2018

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