| Q30445618 | A common mechanism for cytoplasmic dynein-dependent microtubule binding shared among adeno-associated virus and adenovirus serotypes |
| Q39306165 | Adeno-associated virus type 2 capsids with externalized VP1/VP2 trafficking domains are generated prior to passage through the cytoplasm and are maintained until uncoating occurs in the nucleus |
| Q37945241 | Adenovirus recruits dynein by an evolutionary novel mechanism involving direct binding to pH-primed hexon |
| Q30492884 | Adenovirus transport via direct interaction of cytoplasmic dynein with the viral capsid hexon subunit |
| Q38860287 | Autonomous parvoviruses neither stimulate nor are inhibited by the type I interferon response in human normal or cancer cells |
| Q28473771 | Chloroquine and its derivatives exacerbate B19V-associated anemia by promoting viral replication |
| Q28534023 | Comparative molecular docking analysis of cytoplasmic dynein light chain DYNLL1 with pilin to explore the molecular mechanism of pathogenesis caused by Pseudomonas aeruginosa PAO |
| Q40537831 | Comparative protein profiling of B16 mouse melanoma cells susceptible and non-susceptible to alphavirus infection: Effect of the tumor microenvironment. |
| Q30501771 | Coxsackievirus B3-induced cellular protrusions: structural characteristics and functional competence |
| Q34116174 | Cyclic stretch-induced reorganization of the cytoskeleton and its role in enhanced gene transfer |
| Q40054442 | Cyclophilin A is required for CXCR4-mediated nuclear export of heterogeneous nuclear ribonucleoprotein A2, activation and nuclear translocation of ERK1/2, and chemotactic cell migration |
| Q30448880 | Cytoplasmic dynein mediates adenovirus binding to microtubules |
| Q30525258 | Cytoplasmic trafficking, endosomal escape, and perinuclear accumulation of adeno-associated virus type 2 particles are facilitated by microtubule network |
| Q39605035 | Deletion of a Predicted β-Sheet Domain within the Amino Terminus of Herpes Simplex Virus Glycoprotein K Conserved among Alphaherpesviruses Prevents Virus Entry into Neuronal Axons |
| Q39882481 | Densovirus infectious pathway requires clathrin-mediated endocytosis followed by trafficking to the nucleus |
| Q40446928 | Dynein light chain DYNLL1 subunit facilitates porcine circovirus type 2 intracellular transports along microtubules. |
| Q30445612 | Eclipse phase of herpes simplex virus type 1 infection: Efficient dynein-mediated capsid transport without the small capsid protein VP26. |
| Q40814763 | Effect of inhibition of dynein function and microtubule-altering drugs on AAV2 transduction. |
| Q24541472 | Effect of protein kinase A on accumulation of brefeldin A-inhibited guanine nucleotide-exchange protein 1 (BIG1) in HepG2 cell nuclei |
| Q39807196 | Equine herpesvirus type 1 (EHV-1) utilizes microtubules, dynein, and ROCK1 to productively infect cells |
| Q40473158 | Expression and subcellular targeting of canine parvovirus capsid proteins in baculovirus-transduced NLFK cells. |
| Q48291591 | Expression of transferrin receptor 1, proliferating cell nuclear antigen, p27(Kip1) and calbindin in the fetal and neonatal feline cerebellar cortex |
| Q34387725 | Highly dynamic microtubules improve the effectiveness of early stages of human influenza A/NWS/33 virus infection in LLC-MK2 cells |
| Q92789289 | How non-enveloped viruses hijack host machineries to cause infection |
| Q33834978 | Improvement in nuclear entry and transgene expression of baculoviruses by disintegration of microtubules in human hepatocytes |
| Q36218205 | Intracellular trafficking of nonviral vectors |
| Q36316640 | Intracellular trafficking of nucleic acids |
| Q36700696 | Intracellular transport of hepatitis B virus |
| Q39948612 | Late steps of parvoviral infection induce changes in cell morphology |
| Q40280143 | Lipid-mediated introduction of hepatitis B virus capsids into nonsusceptible cells allows highly efficient replication and facilitates the study of early infection events |
| Q39642528 | Mechanisms of cell death in canine parvovirus-infected cells provide intuitive insights to developing nanotools for medicine |
| Q40399389 | Microtubule-dependent and microtubule-independent steps in Crimean-Congo hemorrhagic fever virus replication cycle |
| Q41962853 | Multiple pathways involved in porcine parvovirus cellular entry and trafficking toward the nucleus |
| Q35665949 | Mutations at the base of the icosahedral five-fold cylinders of minute virus of mice induce 3'-to-5' genome uncoating and critically impair entry functions |
| Q35076773 | Nuclear envelope disruption involving host caspases plays a role in the parvovirus replication cycle |
| Q30476771 | Nuclear localization signal peptides induce molecular delivery along microtubules |
| Q33841475 | Nuclear targeting of adenovirus type 2 requires CRM1-mediated nuclear export |
| Q36926777 | Parvoviral host range and cell entry mechanisms |
| Q64889980 | Parvovirus B19 Uncoating Occurs in the Cytoplasm without Capsid Disassembly and It Is Facilitated by Depletion of Capsid-Associated Divalent Cations. |
| Q34150166 | Parvovirus infection of cells by using variants of the feline transferrin receptor altering clathrin-mediated endocytosis, membrane domain localization, and capsid-binding domains |
| Q34512255 | Parvovirus particles and movement in the cellular cytoplasm and effects of the cytoskeleton |
| Q56115905 | Parvoviruses: structure and infection |
| Q35803571 | Pathways of cell infection by parvoviruses and adeno-associated viruses |
| Q38838492 | Porcine circovirus type 2 ORF4 protein binds heavy chain ferritin |
| Q46274294 | Protoparvovirus Cell Entry. |
| Q41925259 | Protoparvovirus Knocking at the Nuclear Door. |
| Q61800857 | Real-time analysis of quantum dot labeled single porcine epidemic diarrhea virus moving along the microtubules using single particle tracking |
| Q27313339 | Rotavirus viroplasm fusion and perinuclear localization are dynamic processes requiring stabilized microtubules |
| Q40484000 | Selective alterations of the host cell architecture upon infection with parvovirus minute virus of mice |
| Q24308845 | Testis-specific human small heat shock protein HSPB9 is a cancer/testis antigen, and potentially interacts with the dynein subunit TCTEL1 |
| Q38003158 | The HIV-1 passage from cytoplasm to nucleus: the process involving a complex exchange between the components of HIV-1 and cellular machinery to access nucleus and successful integration. |
| Q33967271 | The association of viral proteins with host cell dynein components during virus infection. |
| Q52718934 | The cytoplasmic dynein transport machinery and its many cargoes. |
| Q28116141 | The herpesvirus VP1/2 protein is an effector of dynein-mediated capsid transport and neuroinvasion |
| Q39128466 | The intermediate filament network protein, vimentin, is required for parvoviral infection |
| Q48134366 | The precise subcellular localization of Dlg in the Drosophila larva body wall using improved pre-embedding immuno-EM. |
| Q27325499 | Trafficking of Sendai virus nucleocapsids is mediated by intracellular vesicles |
| Q39895207 | Translocation of incoming pseudorabies virus capsids to the cell nucleus is delayed in the absence of tegument protein pUL37. |
| Q40529887 | Transport of African swine fever virus from assembly sites to the plasma membrane is dependent on microtubules and conventional kinesin |
| Q41952996 | Truncated forms of viral VP2 proteins fused to EGFP assemble into fluorescent parvovirus-like particles |
| Q38754437 | Tubulins interact with porcine and human S proteins of the genus Alphacoronavirus and support successful assembly and release of infectious viral particles |
| Q47551667 | Viral highway to nucleus exposed by image correlation analyses |
| Q36392210 | Viral interactions with the cytoskeleton: a hitchhiker's guide to the cell |