Golgi organization is regulated by proteasomal degradation by Eisenberg-Lerner, Avital, Benyair, Ron, Hizkiahou, Noa, Nudel, Neta, Maor, Roey, Kramer, Matthias P., Shmueli, Merav D., Zigdon, Inbal, Cherniavsky Lev, Marina, Ulman, Adi, Sagiv, Jitka Yehudith, Dayan, Molly, Dassa, Bareket, Rosenwald, Mercedes, Shachar, Idit, Li, Jie, Wang, Yanzhuang, Dezorella, Nili, Khan, Suman, Porat, Ziv, Shimoni, Eyal, Avinoam, Ori, Merbl, Yifat

Glycan regulation of ER-associated degradation through compartmentalization by Benyair, Ron, Ogen-Shtern, Navit, Lederkremer, Gerardo Z.

Maintaining Golgi Homeostasis: A Balancing Act of Two Proteolytic Pathways by Benyair, Ron, Eisenberg-Lerner, Avital, Merbl, Yifat

ER Stress-Induced eIF2-alpha Phosphorylation Underlies Sensitivity of Striatal Neurons to Pathogenic Huntingtin by Leitman, Julia, Barak, Boaz, Benyair, Ron, Shenkman, Marina, Ashery, Uri, Hartl, F. Ulrich, Lederkremer, Gerardo Z.

Mannosidase activity of EDEM1 and EDEM2 depends on an unfolded state of their glycoprotein substrates by Shenkman, Marina, Ron, Efrat, Yehuda, Rivka, Benyair, Ron, Khalaila, Isam, Lederkremer, Gerardo Z.

Common fixation–permeabilization methods cause artifactual localization of a type II transmembrane protein by Benyair, Ron, Lederkremer, Gerardo Z.

Upregulation of the ESCRT pathway and multivesicular bodies accelerates degradation of proteins associated with neurodegeneration by Benyair, Ron, Panapakkam Giridharan, Sai Srinivas, Rivero-Ríos, Pilar, Hasegawa, Junya, Bristow, Emily, Eskelinen, Eeva-Liisa, Shmueli, Merav D, Fishbain-Yoskovitz, Vered, Merbl, Yifat, Sharkey, Lisa M, Paulson, Henry L., Hanson, Phyllis I, Patnaik, Samarjit, Al-Ramahi, Ismael, Botas, Juan, Marugan, Juan, Weisman, Lois S.

Constant serum levels of secreted asialoglycoprotein receptor sH2a and decrease with cirrhosis by Benyair, Ron

Bur1 functions with TORC1 for vacuole‐mediated cell cycle progression by Jin, Yui, Jin, Natsuko, Oikawa, Yu, Benyair, Ron, Koizumi, Michiko, Wilson, Thomas E, Ohsumi, Yoshinori, Weisman, Lois S

Mammalian ER mannosidase I resides in quality control vesicles, where it encounters its glycoprotein substrates by Benyair, Ron, Ogen-Shtern, Navit, Mazkereth, Niv, Shai, Ben, Ehrlich, Marcelo, Lederkremer, Gerardo Z.

Mannosidase IA is in Quality Control Vesicles and Participates in Glycoprotein Targeting to ERAD by Ogen-Shtern, Navit, Avezov, Edward, Shenkman, Marina, Benyair, Ron, Lederkremer, Gerardo Z.

Helical charge distribution at the transmembrane-luminal interface determines subcellular localization by Saad, Haddas, Benyair, Ron, Mazor, Tal, Lederkremer, Gerardo Z.