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Journal of Inherited Metabolic Disease|September 10, 2020
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 mitochondriaMiroslav P Milev, Djenann Saint-Dic, Khashayar Zardoui, et al.
Nucleic Acids Research|December 22, 2011
Differential effects of hnRNP D/AUF1 isoforms on HIV-1 gene expressionNicole Lund, Miroslav P Milev, Raymond Wong, et al.
Scientific Reports|July 16, 2017
HIV-1 enhances mTORC1 activity and repositions lysosomes to the periphery by co-opting Rag GTPasesAlessandro Cinti, Valerie Le Sage, Miroslav P Milev, et al.
Journal of Medical Genetics|October 7, 2016
A novel <i>TRAPPC11</i> mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrimaKatrin Koehler, Miroslav P Milev, Keshika Prematilake, et al.
Journal of Cell Science|January 8, 2010
Novel Staufen1 ribonucleoproteins prevent formation of stress granules but favour encapsidation of HIV-1 genomic RNALevon G Abrahamyan, Laurent Chatel-Chaix, Lara Ajamian, et al.
Plos One|July 19, 2012
Naturally-occurring genetic variants in human DC-SIGN increase HIV-1 capture, cell-transfer and risk of mother-to-child transmissionGeneviève Boily-Larouche, Miroslav P Milev, Lynn S Zijenah, et al.
Molecular Biology of the Cell|February 26, 2016
trappc11 is required for protein glycosylation in zebrafish and humansCharles DeRossi, Ana Vacaru, Ruhina Rafiq, et al.
American Journal of Human Genetics|August 5, 2017
Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi DysfunctionMiroslav P Milev, Megan E Grout, Djenann Saint-Dic, et al.
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