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Human Molecular Genetics|September 30, 2010
Correction of CNS defects in the MPSII mouse model via systemic enzyme replacement therapyVinicia Assunta Polito, Serena Abbondante, Roman S Polishchuk, et al.
Cell|June 17, 2008
Transport through the Golgi apparatus by rapid partitioning within a two-phase membrane systemGeorge H Patterson, Koret Hirschberg, Roman S Polishchuk, et al.
The EMBO Journal|August 23, 2012
A new class of carriers that transport selective cargo from the trans Golgi network to the cell surfaceYuichi Wakana, Josse van Galen, Felix Meissner, et al.
Cells|January 21, 2022
TFEB Regulates ATP7B Expression to Promote Platinum Chemoresistance in Human Ovarian Cancer CellsRaffaella Petruzzelli, Marta Mariniello, Rossella De Cegli, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 25, 2010
Golgi-modifying properties of macfarlandin E and the synthesis and evaluation of its 2,7-dioxabicyclo[3.2.1]octan-3-one coreMartin J Schnermann, Christopher M Beaudry, Anastasia V Egorova, et al.
Molecular Biology of the Cell|November 28, 2008
Mitochondria are linked to calcium stores in striated muscle by developmentally regulated tethering structuresSimona Boncompagni, Ann E Rossi, Massimo Micaroni, et al.
The EMBO Journal|May 29, 2002
A tubular EHD1-containing compartment involved in the recycling of major histocompatibility complex class I molecules to the plasma membraneSteve Caplan, Naava Naslavsky, Lisa M Hartnell, et al.
Scientific Reports|June 24, 2020
Author Correction: Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cellsSilvia Parisi, Elena V Polishchuk, Simona Allocca, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 8, 2020
Pharmacoproteomics pinpoints HSP70 interaction for correction of the most frequent Wilson disease-causing mutant of ATP7BMafalda Concilli, Raffaella Petruzzelli, Silvia Parisi, et al.
Scientific Reports|April 21, 2018
Characterization of the most frequent ATP7B mutation causing Wilson disease in hepatocytes from patient induced pluripotent stem cellsSilvia Parisi, Elena V Polishchuk, Simona Allocca, et al.
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