Deafness mutation in the MYO3A motor domain impairs actin protrusion elongation mechanism

por Gunther, Laura K., Cirilo, Joseph A., Desetty, Rohini, Yengo, Christopher M.
Publicado 2022

Mutations of the SLX4 gene in Fanconi anemia

por Kim, Yonghwan, Lach, Francis P., Desetty, Rohini, Hanenberg, Helmut, Auerbach, Arleen D., Smogorzewska, Agata
Publicado 2011

Long noncoding RNA PANDA and scaffold-attachment-factor SAFA control senescence entry and exit

por Puvvula, Pavan Kumar, Desetty, Rohini Devi, Pineau, Pascal, Marchio, Agnés, Moon, Anne, Dejean, Anne, Bischof, Oliver
Publicado 2014

Dilated cardiomyopathy mutation E525K in human beta-cardiac myosin stabilizes the interacting-heads motif and super-relaxed state of myosin

por Rasicci, David V, Tiwari, Prince, Bodt, Skylar ML, Desetty, Rohini, Sadler, Fredrik R, Sivaramakrishnan, Sivaraj, Craig, Roger, Yengo, Christopher M
Publicado 2022