Ghent University Academic Bibliography

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Your filters: cql: author="Martin, Shaun" or (type any "bookEditor issueEditor" and editor="Martin, Shaun")

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ATP13A3 is a major component of the enigmatic mammalian polyamine transport system

Norin Nabil Hamouda, Chris Van den Haute, Roeland Vanhoutte, Ragna Sannerud, Mujahid Azfar, Rupert Mayer (UGent) , Alvaro Cortes Calabuig, Johannes V. Swinnen, Patrizia Agostinis, Veerle Baekelandt, et al.

(2021) JOURNAL OF BIOLOGICAL CHEMISTRY. 296.
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Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Daniel J. Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, Mahmoud Abdellatif, Asghar Abdoli, Steffen Abel, Hagai Abeliovich, Marie H. Abildgaard, Yakubu Princely Abudu, Abraham Acevedo-Arozena, et al.

(2021) AUTOPHAGY. 17(1). p.1-382
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Necroptosis in immuno-oncology and cancer immunotherapy

Jenny Sprooten, Pieter De Wijngaert, Isaure Vanmeerbeek, Shaun Martin, Peter Vangheluwe, Susan Schlenner, Dmitri Krysko (UGent) , Jan B. Parys, Geert Bultynck, Peter Vandenabeele (UGent) , et al.

(2020) CELLS. 9(8).
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Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export

Shaun Martin, Stefanie Smolders, Chris Van den Haute, Bavo Heeman, Sarah van Veen, David Crosiers, Igor Beletchi, Aline Verstraeten, Helena Gossye, Geraldine Gelders, et al.

(2020) ACTA NEUROPATHOLOGICA. 139(6). p.1001-1024
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A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics : the case of NPC1 deficiency

Arun Kumar Tharkeshwar Raghunath (UGent) , Jesse Trekker, Wendy Vermeire, Jarne Pauwels (UGent) , Ragna Sannerud, David A Priestman, Danielle te Vruchte, Katlijn Vints, Pieter Baatsen, Jean-Paul Decuypere, et al.

(2017) SCIENTIFIC REPORTS. 7.
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Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)

Alejandro Estrada-Cuzcano, Shaun Martin, Teodora Chamova, Matthis Synofzik, Dagmar Timmann, Tine Holemans, Albena Andreeva, Jennifer Reichbauer, Riet De Rycke (UGent) , Dae-In Chang, et al.

(2017) BRAIN. 140. p.287-305
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EV-TRACK : transparent reporting and centralizing knowledge in extracellular vesicle research

Jan Van Deun (UGent) , Pieter Mestdagh (UGent) , Patrizia Agostinis, Özden Akay, Sushma Anand, Jasper Anckaert, Zoraida Andreu Martinez, Tine Baetens, Els Beghein, Laurence Bertier (UGent) , et al.

(2017) NATURE METHODS. 14(3). p.228-232

Academic Bibliography

ATP13A3 is a major component of the enigmatic mammalian polyamine transport system

Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)

Necroptosis in immuno-oncology and cancer immunotherapy

Mutated ATP10B increases Parkinson's disease risk by compromising lysosomal glucosylceramide export

A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics : the case of NPC1 deficiency

Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)

EV-TRACK : transparent reporting and centralizing knowledge in extracellular vesicle research

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