TRAPPopathies: An emerging set of disorders linked to variations in the genes encoding transport protein particle (TRAPP)‐associated proteins von Sacher, Michael, Shahrzad, Nassim, Kamel, Hiba, Milev, Miroslav P.

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Lipidomic analysis of human TANGO2-deficient cells suggests a lipid imbalance as a cause of TANGO2 deficiency disease von Mehranfar, Mahsa, Asadi, Paria, Shokohi, Rozmehr, Milev, Miroslav P., Gamberi, Chiara, Sacher, Michael

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TRAPPC11 functions in autophagy by recruiting ATG2B‐WIPI4/WDR45 to preautophagosomal membranes von Stanga, Daniela, Zhao, Qingchuan, Milev, Miroslav P., Saint‐Dic, Djenann, Jimenez‐Mallebrera, Cecilia, Sacher, Michael

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Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice von Rawlins, Lettie E, Almousa, Hashem, Khan, Shazia, Collins, Stephan C, Milev, Miroslav P, Leslie, Joseph, Saint-Dic, Djenann, Khan, Valeed, Hincapie, Ana Maria, Day, Jacob O, McGavin, Lucy, Rowley, Christine, Harlalka, Gaurav V, Vancollie, Valerie E, Ahmad, Wasim, Lelliott, Christopher J, Gul, Asma, Yalcin, Binnaz, Crosby, Andrew H, Sacher, Michael, Baple, Emma L

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Vitamin B5, a coenzyme A precursor, rescues TANGO2 deficiency disease‐associated defects in Drosophila and human cells von Asadi, Paria, Milev, Miroslav P., Saint‐Dic, Djenann, Gamberi, Chiara, Sacher, Michael

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The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER‐to‐Golgi transport and at the mitochondria von Milev, Miroslav P., Saint‐Dic, Djenann, Zardoui, Khashayar, Klopstock, Thomas, Law, Christopher, Distelmaier, Felix, Sacher, Michael

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HIV-1 enhances mTORC1 activity and repositions lysosomes to the periphery by co-opting Rag GTPases von Cinti, Alessandro, Le Sage, Valerie, Milev, Miroslav P., Valiente-Echeverría, Fernando, Crossie, Christina, Miron, Marie-Joelle, Panté, Nelly, Olivier, Martin, Mouland, Andrew J.

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TRAMM/TrappC12 plays a role in chromosome congression, kinetochore stability, and CENP-E recruitment von Milev, Miroslav P, Hasaj, Benedeta, Saint-Dic, Djenann, Snounou, Sary, Zhao, Qingchuan, Sacher, Michael

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Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction von Milev, Miroslav P., Grout, Megan E., Saint-Dic, Djenann, Cheng, Yong-Han Hank, Glass, Ian A., Hale, Christopher J., Hanna, David S., Dorschner, Michael O., Prematilake, Keshika, Shaag, Avraham, Elpeleg, Orly, Sacher, Michael, Doherty, Dan, Edvardson, Simon

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Dynamic regulation of inter-organelle communication by ubiquitylation controls skeletal muscle development and disease onset von Mansur, Arian, Joseph, Remi, Kim, Euri S, Jean-Beltran, Pierre M, Udeshi, Namrata D, Pearce, Cadence, Jiang, Hanjie, Iwase, Reina, Milev, Miroslav P, Almousa, Hashem A, McNamara, Elyshia, Widrick, Jeffrey, Perez, Claudio, Ravenscroft, Gianina, Sacher, Michael, Cole, Philip A, Carr, Steven A, Gupta, Vandana A

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TRAPPC11‐related muscular dystrophy with hypoglycosylation of alpha‐dystroglycan in skeletal muscle and brain von Munot, Pinki, McCrea, Nadine, Torelli, Silvia, Manzur, Adnan, Sewry, Caroline, Chambers, Darren, Feng, Lucy, Ala, Pierpaolo, Zaharieva, Irina, Ragge, Nicola, Roper, Helen, Marton, Tamas, Cox, Phil, Milev, Miroslav P., Liang, Wen‐Chen, Maruyama, Shinsuke, Nishino, Ichizo, Sacher, Michael, Phadke, Rahul, Muntoni, Francesco

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Characterization of three TRAPPC11 variants suggests a critical role for the extreme carboxy terminus of the protein von Milev, Miroslav P., Stanga, Daniela, Schänzer, Anne, Nascimento, Andrés, Saint-Dic, Djenann, Ortez, Carlos, Natera-de Benito, Daniel, Barrios, Desiré González, Colomer, Jaume, Badosa, Carmen, Jou, Cristina, Gallano, Pia, Gonzalez-Quereda, Lidia, Töpf, Ana, Johnson, Katherine, Straub, Volker, Hahn, Andreas, Sacher, Michael, Jimenez-Mallebrera, Cecilia

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Differential effects of hnRNP D/AUF1 isoforms on HIV-1 gene expression von Lund, Nicole, Milev, Miroslav P, Wong, Raymond, Sanmuganantham, Tharmila, Woolaway, Kathryn, Chabot, Benoit, Abou Elela, Sherif, Mouland, Andrew J, Cochrane, Alan

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TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy von Larson, Austin A, Baker, 2nd, Peter R, Milev, Miroslav P, Press, Craig A, Sokol, Ronald J, Cox, Mary O, Lekostaj, Jacqueline K, Stence, Aaron A, Bossler, Aaron D, Mueller, Jennifer M, Prematilake, Keshika, Tadjo, Thierry Fotsing, Williams, Charles A, Sacher, Michael, Moore, Steven A

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A Humanized Yeast Model for Studying TRAPP Complex Mutations; Proof-of-Concept Using Variants from an Individual with a TRAPPC1 -Associated Neurodevelopmental Syndrome von Zykaj, Erta, Abboud, Chelsea, Asadi, Paria, Warsame, Simane, Almousa, Hashem, Milev, Miroslav P, Greco, Brittany M, López-Sánchez, Marcos, Bratkovic, Drago, Kachroo, Aashiq H, Pérez-Jurado, Luis Alberto, Sacher, Michael

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Intracellular Transport of Human Immunodeficiency Virus Type 1 Genomic RNA and Viral Production Are Dependent on Dynein Motor Function and Late Endosome Positioning von Lehmann, Martin, Milev, Miroslav P., Abrahamyan, Levon, Yao, Xiao-Jian, Pante, Nelly, Mouland, Andrew J.

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Live cell visualization of the interactions between HIV-1 Gag and the cellular RNA-binding protein Staufen1 von Milev, Miroslav P, Brown, Chris M, Mouland, Andrew J

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trappc11 is required for protein glycosylation in zebrafish and humans von DeRossi, Charles, Vacaru, Ana, Rafiq, Ruhina, Cinaroglu, Ayca, Imrie, Dru, Nayar, Shikha, Baryshnikova, Anastasia, Milev, Miroslav P, Stanga, Daniela, Kadakia, Dhara, Gao, Ningguo, Chu, Jaime, Freeze, Hudson H, Lehrman, Mark A, Sacher, Michael, Sadler, Kirsten C

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Novel Staufen1 ribonucleoproteins prevent formation of stress granules but favour encapsidation of HIV-1 genomic RNA von Abrahamyan, Levon G, Chatel-Chaix, Laurent, Ajamian, Lara, Milev, Miroslav P, Monette, Anne, Clément, Jean-François, Song, Rujun, Lehmann, Martin, DesGroseillers, Luc, Laughrea, Michael, Boccaccio, Graciela, Mouland, Andrew J

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Mitotic transformation of TRAMM/TrappC12 von Milev, Miroslav P, Sacher, Michael

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