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Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation O'Connell, Amy E.; Gerashchenko, Maxim V.; O'Donohue, Marie-Francoise; Rosen, Samantha M.; Huntzinger, Eric; Gleeson, Diane; Galli, Antonella; Ryder, Edward; Cao, Siqi; Murphy, Quinn; Kazerounian, Shideh; Morton, Sarah U.; Schmitz-Abe, Klaus; Gladyshev, Vadim N.; Gleizes, Pierre-Emmanuel; Seraphin, Bertrand; Agrawal, Pankaj B. Share Save
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Architecture of the yeast Elongator complex Dauden, Maria I.; Kosinski, Jan; Kolaj-Robin, Olga; Desfosses, Ambroise; Ori, Alessandro; Faux, Celine; Hoffmann, Niklas A.; Onuma, Osita F.; Breunig, Karin D.; Beck, Martin; Sachse, Carsten; Seraphin, Bertrand; Glatt, Sebastian; Mueller, Christoph W. Share Save
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Structural basis for tRNA modification by Elp3 from Dehalococcoides mccartyi Glatt, Sebastian; Zabel, Rene; Kolaj-Robin, Olga; Onuma, Osita F.; Baudin, Florence; Graziadei, Andrea; Taverniti, Valerio; Lin, Ting-Yu; Baymann, Frauke; Seraphin, Bertrand; Breunig, Karin D.; Mueller, Christoph W. Share Save
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Loss of the scavenger mRNA decapping enzyme DCPS causes syndromic intellectual disability with neuromuscular defects Ng, Calista K. L.; Shboul, Mohammad; Taverniti, Valerio; Bonnard, Carine; Lee, Hane; Eskin, Ascia; Nelson, Stanley F.; Al-Raqad, Mohammed; Altawalbeh, Samah; Seraphin, Bertrand; Reversade, Bruno Share Save
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