(Glyco)sphingolipids Are Sorted in Sub-Apical Compartments in HepG2 Cells: A Role for Non-Golgi–Related Intracellular Sites in the Polarized Distribution of (Glyco)sphingolipids

por van IJzendoorn, Sven C.D., Hoekstra, Dick
Publicado 1998

Letter to the Editor: Liver Cell Models for Premature Termination Codon Readthrough Analyses

por Matakovic, Lavinija, Li, Qinghong, van Ijzendoorn, Sven C.D.
Publicado 2021

Segregation of Glucosylceramide and Sphingomyelin Occurs in the Apical to Basolateral Transcytotic Route in HepG2 Cells

por van IJzendoorn, Sven C.D., Zegers, Mirjam M.P., Kok, Jan Willem, Hoekstra, Dick
Publicado 1997

The Na(+)/H(+) Exchanger NHE6 in the Endosomal Recycling System Is Involved in the Development of Apical Bile Canalicular Surface Domains in HepG2 Cells

por Ohgaki, Ryuichi, Matsushita, Masafumi, Kanazawa, Hiroshi, Ogihara, Satoshi, Hoekstra, Dick, van IJzendoorn, Sven C.D.
Publicado 2010

A Functional Relationship Between UNC45A and MYO5B Connects Two Rare Diseases With Shared Enteropathy

por Li, Qinghong, Zhou, Zhe, Sun, Yue, Sun, Chang, Klappe, Karin, van IJzendoorn, Sven C.D.
Publicado 2022

Par1b links lumen polarity with LGN–NuMA positioning for distinct epithelial cell division phenotypes

por Lázaro-Diéguez, Francisco, Cohen, David, Fernandez, Dawn, Hodgson, Louis, van IJzendoorn, Sven C.D., Müsch, Anne
Publicado 2013

Unequal Effects of Myosin 5B Mutations in Liver and Intestine Determine the Clinical Presentation of Low‐Gamma‐Glutamyltransferase Cholestasis

por van IJzendoorn, Sven C.D., Li, Qinghong, Qiu, Yi‐ling, Wang, Jian‐She, Overeem, Arend W.
Publicado 2020

Adenosine A(2B) receptor-mediated leukemia inhibitory factor release from astrocytes protects cortical neurons against excitotoxicity

por Moidunny, Shamsudheen, Vinet, Jonathan, Wesseling, Evelyn, Bijzet, Johan, Shieh, Chu-Hsin, van Ijzendoorn, Sven CD, Bezzi, Paola, Boddeke, Hendrikus WGM, Biber, Knut
Publicado 2012

A Molecular Mechanism Underlying Genotype‐Specific Intrahepatic Cholestasis Resulting From MYO5B Mutations

por Overeem, Arend W., Li, Qinghong, Qiu, Yi‐Ling, Cartón‐García, Fernando, Leng, Changsen, Klappe, Karin, Dronkers, Just, Hsiao, Nai‐Hua, Wang, Jian‐She, Arango, Diego, van Ijzendoorn, Sven C.D.
Publicado 2020

MYO5B, STX3, and STXBP2 mutations reveal a common disease mechanism that unifies a subset of congenital diarrheal disorders: A mutation update

por Dhekne, Herschel S., Pylypenko, Olena, Overeem, Arend W., Ferreira, Rosaria J., van der Velde, K. Joeri, Rings, Edmond H.H.M., Posovszky, Carsten, Swertz, Morris A., Houdusse, Anne, van IJzendoorn, Sven C.D.
Publicado 2018

Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility

por Yeshaw, Wondwossen M, van der Zwaag, Marianne, Pinto, Francesco, Lahaye, Liza L, Faber, Anita IE, Gómez-Sánchez, Rubén, Dolga, Amalia M, Poland, Conor, Monaco, Anthony P, van IJzendoorn, Sven CD, Grzeschik, Nicola A, Velayos-Baeza, Antonio, Sibon, Ody CM
Publicado 2019

Wilson Disease Protein ATP7B Utilizes Lysosomal Exocytosis to Maintain Copper Homeostasis

por Polishchuk, Elena V., Concilli, Mafalda, Iacobacci, Simona, Chesi, Giancarlo, Pastore, Nunzia, Piccolo, Pasquale, Paladino, Simona, Baldantoni, Daniela, van IJzendoorn, Sven C.D., Chan, Jefferson, Chang, Christopher J., Amoresano, Angela, Pane, Francesca, Pucci, Piero, Tarallo, Antonietta, Parenti, Giancarlo, Brunetti-Pierri, Nicola, Settembre, Carmine, Ballabio, Andrea, Polishchuk, Roman S.
Publicado 2014