References: Parvoviridae

 

Adeyemi, R. O. & Pintel, D. J. (2014). The ATR signaling pathway is disabled during infection with the parvovirus minute virus of mice. J Virol 88, 10189-10199. [PubMed]

Agbandje-McKenna, M. & Kleinschmidt, J. (2011). AAV capsid structure and cell interactions. Methods in Molecular Biology 807, 47-92. [PubMed]

Agbandje-McKenna, M., Llamas-Saiz, A. L., Wang, F., Tattersall, P. & Rossmann, M. G. (1998). Functional implications of the structure of the murine parvovirus, minute virus of mice. Structure 6, 1369-1381. [PubMed]

Allander, T., Tammi, M. T., Eriksson, M., Bjerkner, A., Tiveljung-Lindell, A. & Andersson, B. (2005). Cloning of a human parvovirus by molecular screening of respiratory tract samples. Proc Natl Acad Sci USA 102, 12891-12896. [PubMed]

Allison, A. B., Kohler, D. J., Ortega, A., Hoover, E. A., Grove, D. M., Holmes, E. C. & Parrish, C. R. (2014). Host-specific parvovirus evolution in nature is recapitulated by in vitro adaptation to different carnivore species. PLoS Pathog 10, e1004475. [PubMed]

Anderson, S., Momoeda, M., Kawase, M., Kajigaya, S. & Young, N. S. (1995). Peptides derived from the unique region of B19 parvovirus minor capsid protein elicit neutralizing antibodies in rabbits. Virology 206, 626-632. [PubMed]

Angelova, A. L., Barf, M., Geletneky, K., Unterberg, A. & Rommelaere, J. (2017). Immunotherapeutic potential of pncolytic H-1 parvovirus: hints of glioblastoma microenvironment conversion towards immunogenicity. Viruses 9. [PubMed

Arthur, J. L., Higgins, G. D., Davidson, G. P., Givney, R. C. & Ratcliff, R. M. (2009). A novel bocavirus associated with acute gastroenteritis in Australian children. PLoS Pathog 5, e1000391. [PubMed]

Atchison, R. W., Casto, B. C. & Hammon, W. M. (1965). Adenovirus-associated defective virus particles. Science 149, 754-756. [PubMed]

Aydemir, F., Salganik, M., Resztak, J., Singh, J., Bennett, A., Agbandje-McKenna, M. & Muzyczka, N. (2016). Mutants at the 2-fold interface of adeno-associated virus type 2 (AAV2) structural proteins suggest a role in viral transcription for AAV capsids. J Virol 90, 7196-7204. [PubMed

Bär, S., Daeffler, L., Rommelaere, J. & Nüesch, J. P. (2008). Vesicular egress of non-enveloped lytic parvoviruses depends on gelsolin functioning. PLoS Pathog 4, e1000126. [PubMed]

Bär, S., Rommelaere, J. & Nüesch, J. P. (2013). Vesicular transport of progeny parvovirus particles through ER and Golgi regulates maturation and cytolysis. PLoS Pathog 9, e1003605. [PubMed]

Beierwaltes, W. H. (1991). Endocrine imaging in the management of goiter and thyroid nodules: Part I. J Nucl Med 32, 1455-1461. [PubMed]

Bennett, A. D., Wong, K., Lewis, J., Tseng, Y. S., Smith, J. K., Chipman, P., McKenna, R., Samulski, R. J., Kleinschmidt, J. & Agbandje-McKenna, M. (2018). AAV6 K531 serves a dual function in selective receptor and antibody ADK6 recognition. Virology 518, 369-376. [PubMed]

Berns, K. I. & Parrish, C. R. (2013). Parvoviridae. In Fields Virology, 6th Edition, pp. 1768-1791. Edited by D. M. Knipe & P. Howley. Philadelphia: Lippincott Williams &Wilkins. 

Best, S. M., Shelton, J. F., Pompey, J. M., Wolfinbarger, J. B. & Bloom, M. E. (2003). Caspase cleavage of the nonstructural protein NS1 mediates replication of Aleutian mink disease parvovirus. J Virol 77, 5305-5312. [PubMed]

Binn, L. N., Lazar, E. C., Eddy, G. A. & Kajima, M. (1970). Recovery and characterization of a minute virus of canines. Infect Immun 1, 503-508. [PubMed]

Bloom, M. E., Best, S. M., Hayes, S. F., Wells, R. D., Wolfinbarger, J. B., McKenna, R. & Agbandje-McKenna, M. (2001). Identification of aleutian mink disease parvovirus capsid sequences mediating antibody-dependent enhancement of infection, virus neutralization, and immune complex formation. J Virol 75, 11116-11127. [PubMed]

Blümel, J., Eis-Hübinger, A. M., Stühler, A., Bönsch, C., Gessner, M. & Löwer, J. (2005). Characterization of Parvovirus B19 genotype 2 in KU812Ep6 cells. J Virol 79, 14197-14206. [PubMed]

Bodendorf, U., Cziepluch, C., Jauniaux, J. C., Rommelaere, J. & Salomé, N. (1999). Nuclear export factor CRM1 interacts with nonstructural proteins NS2 from parvovirus minute virus of mice. J Virol 73, 7769-7779. [PubMed]

Bönsch, C., Zuercher, C., Lieby, P., Kempf, C. & Ros, C. (2010). The globoside receptor triggers structural changes in the B19 virus capsid that facilitate virus internalization. J Virol 84, 11737-11746. [PubMed

Boublik, Y., Jousset, F. X. & Bergoin, M. (1994). Complete nucleotide sequence and genomic organization of the Aedes albopictus parvovirus (AaPV) pathogenic for Aedes aegypti larvae. Virology 200, 752-763. [PubMed]

Brockhaus, K., Plaza, S., Pintel, D. J., Rommelaere, J. & Salomé, N. (1996). Nonstructural proteins NS2 of minute virus of mice associate in vivo with 14-3-3 protein family members. J Virol 70, 7527-7534. [PubMed]

Brown & Young (1997). The simian parvoviruses. Rev Med Virol 7, 211-218. [PubMed]

Canaan, S., Zádori, Z., Ghomashchi, F., Bollinger, J., Sadilek, M., Moreau, M. E., Tijssen, P. & Gelb, M. H. (2004). Interfacial enzymology of parvovirus phospholipases A2. J Biol Chem 279, 14502-14508. [PubMed]

Canuti, M., Doyle, H. E., A, P. B. & Lang, A. S. (2017). Full genetic characterization and epidemiology of a novel amdoparvovirus in striped skunk (Mephitis mephitis). Emerg Microbes Infect 6, e30. [PubMed]

Canuti, M., Eis-Huebinger, A. M., Deijs, M., de Vries, M., Drexler, J. F., Oppong, S. K., Müller, M. A., Klose, S. M., Wellinghausen, N., Cottontail, V. M., Kalko, E. K., Drosten, C. & van der Hoek, L. (2011). Two novel parvoviruses in frugivorous New and Old World bats. PLoS One 6, e29140. [PubMed]

Canuti, M., O'Leary, K. E., Hunter, B. D., Spearman, G., Ojkic, D., Whitney, H. G. & Lang, A. S. (2016). Driving forces behind the evolution of the Aleutian mink disease parvovirus in the context of intensive farming. Virus Evol 2, vew004. [PubMed

Canuti, M., Whitney, H. G. & Lang, A. S. (2015). Amdoparvoviruses in small mammals: expanding our understanding of parvovirus diversity, distribution, and pathology. Front Microbiol 6, 1119. [PubMed]

Carrasco, C., Carreira, A., Schaap, I. A., Serena, P. A., Gómez-Herrero, J., Mateu, M. G. & de Pablo, P. J. (2006). DNA-mediated anisotropic mechanical reinforcement of a virus. Proc Natl Acad Sci USA 103, 13706-13711. [PubMed]

Carrasco, C., Castellanos, M., de Pablo, P. J. & Mateu, M. G. (2008). Manipulation of the mechanical properties of a virus by protein engineering. Proc Natl Acad Sci USA 105, 4150-4155. [PubMed]

Chang, S. F., Sgro, J. Y. & Parrish, C. R. (1992). Multiple amino acids in the capsid structure of canine parvovirus coordinately determine the canine host range and specific antigenic and hemagglutination properties. J Virol 66, 6858-6867. [PubMed]

Chapman, M. S. & Rossmann, M. G. (1995). Single-stranded DNA-protein interactions in canine parvovirus. Structure 3, 151-162. [PubMed]

Chen, A. Y., Cheng, F., Lou, S., Luo, Y., Liu, Z., Delwart, E., Pintel, D. & Qiu, J. (2010a). Characterization of the gene expression profile of human bocavirus. Virology 403, 145-154. [PubMed]

Chen, A. Y., Zhang, E. Y., Guan, W., Cheng, F., Kleiboeker, S., Yankee, T. M. & Qiu, J. (2010b). The small 11 kDa nonstructural protein of human parvovirus B19 plays a key role in inducing apoptosis during B19 virus infection of primary erythroid progenitor cells. Blood 115, 1070-1080. [PubMed]

Chen, K. C., Shull, B. C., Moses, E. A., Lederman, M., Stout, E. R. & Bates, R. C. (1986). Complete nucleotide sequence and genome organization of bovine parvovirus. J Virol 60, 1085-1097. [PubMed]

Chen, Z., Guan, W., Cheng, F., Chen, A. Y. & Qiu, J. (2009). Molecular characterization of human parvovirus B19 genotypes 2 and 3. Virology 394, 276-285. [PubMed]

Cheng, F., Chen, A. Y., Best, S. M., Bloom, M. E., Pintel, D. & Qiu, J. (2010). The capsid proteins of Aleutian mink disease virus activate caspases and are specifically cleaved during infection. J Virol 84, 2687-2696. [PubMed]

Chiorini, J. A. (2016). And one to bind them all. Oral diseases 22, 716-718. [PubMed]

Choi, E. Y., Newman, A. E., Burger, L. & Pintel, D. (2005). Replication of minute virus of mice DNA is critically dependent on accumulated levels of NS2. J Virol 79, 12375-12381. [PubMed]

Christensen, J., Cotmore, S. F. & Tattersall, P. (1995). Minute virus of mice transcriptional activator protein NS1 binds directly to the transactivation region of the viral P38 promoter in a strictly ATP-dependent manner. J Virol 69, 5422-5430. [PubMed]

Christensen, J., Cotmore, S. F. & Tattersall, P. (2001). Minute virus of mice initiator protein NS1 and a host KDWK family transcription factor must form a precise ternary complex with origin DNA for nicking to occur. J Virol 75, 7009-7017. [PubMed]

Cotmore, S. F., Christensen, J., Nüesch, J. P. & Tattersall, P. (1995). The NS1 polypeptide of the murine parvovirus minute virus of mice binds to DNA sequences containing the motif [ACCA" target="ictvref">PubMed]2-3. J Virol 69, 1652-1660. [PubMed]

Cotmore, S. F., Christensen, J. & Tattersall, P. (2000). Two widely spaced initiator binding sites create an HMG1-dependent parvovirus rolling-hairpin replication origin. J Virol 74, 1332-1341. [PubMed]

Cotmore, S. F., D'Abramo, A. M., Jr., Carbonell, L. F., Bratton, J. & Tattersall, P. (1997). The NS2 polypeptide of parvovirus MVM is required for capsid assembly in murine cells. Virology 231, 267-280. [PubMed]

Cotmore, S. F., Hafenstein, S. & Tattersall, P. (2010). Depletion of virion-associated divalent cations induces parvovirus minute virus of mice to eject its genome in a 3'-to-5' direction from an otherwise intact viral particle. J Virol 84, 1945-1956. [PubMed]

Cotmore, S. F. & Tattersall, P. (1984). Characterization and molecular cloning of a human parvovirus genome. Science 226, 1161-1165. [PubMed]

Cotmore, S. F. & Tattersall, P. (1989). A genome-linked copy of the NS-1 polypeptide is located on the outside of infectious parvovirus particles. J Virol 63, 3902-3911. [PubMed]

Cotmore, S. F. & Tattersall, P. (2003). Resolution of parvovirus dimer junctions proceeds through a novel heterocruciform intermediate. J Virol 77, 6245-6254. [PubMed]

Cotmore, S. F. & Tattersall, P. (2005a). Encapsidation of minute virus of mice DNA: aspects of the translocation mechanism revealed by the structure of partially packaged genomes. Virology 336, 100-112. [PubMed

Cotmore, S. F. & Tattersall, P. (2005b). Genome packaging sense is controlled by the efficiency of the nick site in the right-end replication origin of parvoviruses minute virus of mice and LuIII. J Virol 79, 2287-2300. [PubMed]

Cotmore, S. F. & Tattersall, P. (2012). 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. J Virol 86, 69-80. [PubMed]

Cotmore, S. F. & Tattersall, P. (2014). Parvoviruses: small does not mean simple. Annu Rev Virol 1, 517-537. [PubMed]

Crispino, G., Galindo Ramirez, F., Campioni, M., Zorzi, V., Praetorius, M., Di Pasquale, G., Chiorini, J. A. & Mammano, F. (2017). In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors. Sci Rep 7, 6567. [PubMed]

Deng, X., Yan, Z., Cheng, F., Engelhardt, J. F. & Qiu, J. (2016). Replication of an autonomous human parvovirus in non-dividing human airway epithelium is facilitated through the DNA damage and repair pathways. PLoS Pathog 12, e1005399. [PubMed

Dhar, A. K., Robles-Sikisaka, R., Saksmerprome, V. & Lakshman, D. K. (2014). Biology, genome organization, and evolution of parvoviruses in marine shrimp. Adv Virus Res 89, 85-139. [PubMed]

Dijkman, R., Koekkoek, S. M., Molenkamp, R., Schildgen, O. & van der Hoek, L. (2009). Human bocavirus can be cultured in differentiated human airway epithelial cells. J Virol 83, 7739-7748. [PubMed]

Earley, L. F., Powers, J. M., Adachi, K., Baumgart, J. T., Meyer, N. L., Xie, Q., Chapman, M. S. & Nakai, H. (2017). Adeno-associated virus (AAV) assembly-activating protein is not an essential requirement for capsid assembly of AAV serotypes 4, 5, and 11. J Virol 91. [PubMed]

Eichwald, V., Daeffler, L., Klein, M., Rommelaere, J. & Salomé, N. (2002). The NS2 proteins of parvovirus minute virus of mice are required for efficient nuclear egress of progeny virions in mouse cells. J Virol 76, 10307-10319. [PubMed]

Ekman, A., Hokynar, K., Kakkola, L., Kantola, K., Hedman, L., Bondén, H., Gessner, M., Aberham, C., Norja, P., Miettinen, S., Hedman, K. & Söderlund-Venermo, M. (2007). Biological and immunological relations among human parvovirus B19 genotypes 1 to 3. J Virol 81, 6927-6935. [PubMed]

Engelsma, D., Valle, N., Fish, A., Salomé, N., Almendral, J. M. & Fornerod, M. (2008). A supraphysiological nuclear export signal is required for parvovirus nuclear export. Molecular biology of the cell 19, 2544-2552. [PubMed]

Farkas, S. L., Zádori, Z., Benko, M., Essbauer, S., Harrach, B. & Tijssen, P. (2004). A parvovirus isolated from royal python (Python regius) is a member of the genus DependovirusJ Gen Virol 85, 555-561. [PubMed]

Farr, G. A., Zhang, L. G. & Tattersall, P. (2005). Parvoviral virions deploy a capsid-tethered lipolytic enzyme to breach the endosomal membrane during cell entry. Proc Natl Acad Sci USA 102, 17148-17153. [PubMed

Fasina, O. O., Dong, Y. & Pintel, D. J. (2016). NP1 protein of the bocaparvovirus minute virus of canines controls access to the viral capsid genes via its role in RNA processing. J Virol 90, 1718-1728. [PubMed]

Fasina, O. O., Stupps, S., Figueroa-Cuilan, W. & Pintel, D. J. (2017). Minute virus of canines NP1 protein governs the expression of a subset of essential nonstructural proteins via its role in RNA processing. J Virol 91. [PubMed]

Filippone, C., Zhi, N., Wong, S., Lu, J., Kajigaya, S., Gallinella, G., Kakkola, L., Söderlund-Venermo, M., Young, N. S. & Brown, K. E. (2008). VP1u phospholipase activity is critical for infectivity of full-length parvovirus B19 genomic clones. Virology 374, 444-452. [PubMed]

Fuller, M. S., Majumder, K. & Pintel, D. J. (2017). Minute virus of mice inhibits transcription of the cyclin B1 gene during infection. J Virol 91. [PubMed]

Ganaie, S. S., Chen, A. Y., Huang, C., Xu, P., Kleiboeker, S., Du, A. & Qiu, J. (2018). RNA binding protein RBM38 regulates expression of the 11-kilodalton protein of parvovirus B19, which cacilitates viral DNA replication. J Virol 92. [PubMed]

Ganaie, S. S., Zou, W., Xu, P., Deng, X., Kleiboeker, S. & Qiu, J. (2017). Phosphorylated STAT5 directly facilitates parvovirus B19 DNA replication in human erythroid progenitors through interaction with the MCM complex. PLoS Pathog 13, e1006370. [PubMed]

Geletneky, K., Hajda, J., Angelova, A. L., Leuchs, B., Capper, D., Bartsch, A. J., Neumann, J. O., Schöning, T., Hüsing, J., Beelte, B., Kiprianova, I., Roscher, M., Bhat, R., von Deimling, A., Brück, W., Just, A., Frehtman, V., Löbhard, S., Terletskaia-Ladwig, E., Fry, J., Jochims, K., Daniel, V., Krebs, O., Dahm, M., Huber, B., Unterberg, A. & Rommelaere, J. (2017). Oncolytic H-1 parvovirus shows safety and signs of immunogenic activity in a first phase I/IIa glioblastoma trial. Mol Ther 25, 2620-2634. [PubMed]

Geletneky, K., Nüesch, J. P., Angelova, A., Kiprianova, I. & Rommelaere, J. (2015). Double-faceted mechanism of parvoviral oncosuppression. Curr Opin Virol 13, 17-24. [PubMed

Gil-Ranedo, J., Hernando, E., Riolobos, L., Domínguez, C., Kann, M. & Almendral, J. M. (2015). The mammalian cell cycle regulates parvovirus nuclear capsid assembly. PLoS Pathog 11, e1004920. [PubMed]

Girod, A., Wobus, C. E., Zádori, Z., Ried, M., Leike, K., Tijssen, P., Kleinschmidt, J. A. & Hallek, M. (2002). The VP1 capsid protein of adeno-associated virus type 2 is carrying a phospholipase A2 domain required for virus infectivity. J Gen Virol 83, 973-978. [PubMed]

Green, S. W., Malkovska, I., O'Sullivan, M. G. & Brown, K. E. (2000). Rhesus and pig-tailed macaque parvoviruses: identification of two new members of the Erythrovirus genus in monkeys. Virology 269, 105-112. [PubMed

Grekova, S., Zawatzky, R., Hörlein, R., Cziepluch, C., Mincberg, M., Davis, C., Rommelaere, J. & Daeffler, L. (2010). Activation of an antiviral response in normal but not transformed mouse cells: a new determinant of minute virus of mice oncotropism. J Virol 84, 516-531. [PubMed

Gu, Z., Plaza, S., Perros, M., Cziepluch, C., Rommelaere, J. & Cornelis, J. J. (1995). NF-Y controls transcription of the minute virus of mice P4 promoter through interaction with an unusual binding site. J Virol 69, 239-246. [PubMed]

Guan, W., Cheng, F., Yoto, Y., Kleiboeker, S., Wong, S., Zhi, N., Pintel, D. J. & Qiu, J. (2008). Block to the production of full-length B19 virus transcripts by internal polyadenylation is overcome by replication of the viral genome. J Virol 82, 9951-9963. [PubMed

Hafenstein, S., Bowman, V. D., Sun, T., Nelson, C. D., Palermo, L. M., Chipman, P. R., Battisti, A. J., Parrish, C. R. & Rossmann, M. G. (2009). Structural comparison of different antibodies interacting with parvovirus capsids. J Virol 83, 5556-5566. [PubMed]

Halder, S., Nam, H. J., Govindasamy, L., Vogel, M., Dinsart, C., Salomé, N., McKenna, R. & Agbandje-McKenna, M. (2013). Structural characterization of H-1 parvovirus: comparison of infectious virions to empty capsids. J Virol 87, 5128-5140. [PubMed]

Haut, D. D. & Pintel, D. J. (1999). Inclusion of the NS2-specific exon in minute virus of mice mRNA is facilitated by an intronic splicing enhancer that affects definition of the downstream small intron. Virology 258, 84-94. [PubMed

Hickman, A. B., Ronning, D. R., Perez, Z. N., Kotin, R. M. & Dyda, F. (2004). The nuclease domain of adeno-associated virus rep coordinates replication initiation using two distinct DNA recognition interfaces. Mol Cell 13, 403-414. [PubMed]

Hokynar, K., Norja, P., Hedman, K. & Söderlund-Venermo, M. (2007). Tissue persistence and prevalence of B19 virus types 1–3. Future Medicine 2, 377-388. [

Hokynar, K., Söderlund-Venermo, M., Pesonen, M., Ranki, A., Kiviluoto, O., Partio, E. K. & Hedman, K. (2002). A new parvovirus genotype persistent in human skin. Virology 302, 224-228. [PubMed

Huang, L. Y., Halder, S. & Agbandje-McKenna, M. (2014a). Parvovirus glycan interactions. Curr Opin Virol 7, 108-118. [PubMed]

Huang, L. Y., Patel, A., Ng, R., Miller, E. B., Halder, S., McKenna, R., Asokan, A. & Agbandje-McKenna, M. (2016). Characterization of the adeno-associated virus 1 and 6 sialic acid binding site. J Virol 90, 5219-5230. [PubMed]

Huang, Q., Deng, X., Yan, Z., Cheng, F., Luo, Y., Shen, W., Lei-Butters, D. C., Chen, A. Y., Li, Y., Tang, L., Söderlund-Venermo, M., Engelhardt, J. F. & Qiu, J. (2012). Establishment of a reverse genetics system for studying human bocavirus in human airway epithelia. PLoS Pathog 8, e1002899. [PubMed]

Huang, Q., Luo, Y., Cheng, F., Best, S. M., Bloom, M. E. & Qiu, J. (2014b). Molecular characterization of the small nonstructural proteins of parvovirus Aleutian mink disease virus (AMDV) during infection. Virology 452-453, 23-31. [PubMed]

Hulks, G., Cowan, M. D. & Kerr, J. W. (1990). Asymptomatic renal thoracic ectopia, pulmonary hypoplasia, and Bochdalek hernia. Thorax 45, 635-636. [PubMed]

Ilyas, M., Mietzsch, M., Kailasan, S., Väisänen, E., Luo, M., Chipman, P., Smith, J. K., Kurian, J., Sousa, D., McKenna, R., Söderlund-Venermo, M. & Agbandje-McKenna, M. (2018). Atomic resolution structures of human bufaviruses determined by cryo-electron microscopy. Viruses 10. [PubMed]

Im, D. S. & Muzyczka, N. (1990). The AAV origin binding protein Rep68 is an ATP-dependent site-specific endonuclease with DNA helicase activity. Cell 61, 447-457. [PubMed]

James, J. A., Escalante, C. R., Yoon-Robarts, M., Edwards, T. A., Linden, R. M. & Aggarwal, A. K. (2003). Crystal structure of the SF3 helicase from adeno-associated virus type 2. Structure 11, 1025-1035. [PubMed

Jartti, T., Hedman, K., Jartti, L., Ruuskanen, O., Allander, T. & Söderlund-Venermo, M. (2012). Human bocavirus-the first 5 years. Rev Med Virol 22, 46-64. [PubMed]

Jones, M. S., Kapoor, A., Lukashov, V. V., Simmonds, P., Hecht, F. & Delwart, E. (2005). New DNA viruses identified in patients with acute viral infection syndrome. J Virol 79, 8230-8236. [PubMed]

Kailasan, S., Agbandje-McKenna, M. & Parrish, C. R. (2015a). Parvovirus family conundrum: what makes a killer? Annu Rev Virol 2, 425-450. [PubMed]

Kailasan, S., Garrison, J., Ilyas, M., Chipman, P., McKenna, R., Kantola, K., Söderlund-Venermo, M., Kučinskaitė-Kodzė, I., Žvirblienė, A. & Agbandje-McKenna, M. (2016). Mapping antigenic epitopes on the human bocavirus capsid. J Virol 90, 4670-4680. [PubMed]

Kailasan, S., Halder, S., Gurda, B., Bladek, H., Chipman, P. R., McKenna, R., Brown, K. & Agbandje-McKenna, M. (2015b). Structure of an enteric pathogen, bovine parvovirus. J Virol 89, 2603-2614. [PubMed]

Kaján, G. L., Davison, A. J., Palya, V., Harrach, B. & Benko, M. (2012). Genome sequence of a waterfowl aviadenovirus, goose adenovirus 4. J Gen Virol 93, 2457-2465. [PubMed]

Kanaan, N. M., Sellnow, R. C., Boye, S. L., Coberly, B., Bennett, A., Agbandje-McKenna, M., Sortwell, C. E., Hauswirth, W. W., Boye, S. E. & Manfredsson, F. P. (2017). Rationally engineered AAV capsids improve transduction and volumetric spread in the CNS. Molecular therapy Nucleic acids 8, 184-197. [PubMed

Kantola, K., Hedman, L., Tanner, L., Simell, V., Mäkinen, M., Partanen, J., Sadeghi, M., Veijola, R., Knip, M., Ilonen, J., Hyöty, H., Toppari, J., Simell, O., Hedman, K. & Söderlund-Venermo, M. (2015). B-cell responses to human bocaviruses 1-4: new insights from a childhood follow-up study. PLoS One 10, e0139096. [PubMed]

Kapoor, A., Simmonds, P., Slikas, E., Li, L., Bodhidatta, L., Sethabutr, O., Triki, H., Bahri, O., Oderinde, B. S., Baba, M. M., Bukbuk, D. N., Besser, J., Bartkus, J. & Delwart, E. (2010). Human bocaviruses are highly diverse, dispersed, recombination prone, and prevalent in enteric infections. J Infect Dis 201, 1633-1643. [PubMed

Kapoor, A., Slikas, E., Simmonds, P., Chieochansin, T., Naeem, A., Shaukat, S., Alam, M. M., Sharif, S., Angez, M., Zaidi, S. & Delwart, E. (2009). A newly identified bocavirus species in human stool. J Infect Dis 199, 196-200. [PubMed]

Kaufmann, B., Bowman, V. D., Li, Y., Szelei, J., Waddell, P. J., Tijssen, P. & Rossmann, M. G. (2010). Structure of Penaeus stylirostris densovirus, a shrimp pathogen. J Virol 84, 11289-11296. [PubMed]

Kaufmann, B., Chipman, P. R., Kostyuchenko, V. A., Modrow, S. & Rossmann, M. G. (2008). Visualization of the externalized VP2 N termini of infectious human parvovirus B19. J Virol 82, 7306-7312. [PubMed

Kaufmann, B., El-Far, M., Plevka, P., Bowman, V. D., Li, Y., Tijssen, P. & Rossmann, M. G. (2011). Structure of Bombyx mori densovirus 1, a silkworm pathogen. J Virol 85, 4691-4697. [PubMed]

Kaufmann, B., Simpson, A. A. & Rossmann, M. G. (2004). The structure of human parvovirus B19. Proc Natl Acad Sci USA 101, 11628-11633. [PubMed]

Kerr, J. R. (2016). The role of parvovirus B19 in the pathogenesis of autoimmunity and autoimmune disease. J Clin Pathol 69, 279-291. [PubMed

Kerr, J. R. & Linden, R. M. (2006). Human dependovirus infection. In Parvoviruses, pp. 381-384. Edited by J. Kerr, S. Cotmore, M. E. Bloom, R. M. Linden & C. R. Parrish. London: Hodder Arnold.  

Kilham, L. & Olivier, L. J. (1959). A latent virus of rats isolated in tissue culture. Virology 7, 428-437. [PubMed]

King, J. A., Dubielzig, R., Grimm, D. & Kleinschmidt, J. A. (2001). DNA helicase-mediated packaging of adeno-associated virus type 2 genomes into preformed capsids. EMBO J 20, 3282-3291. [PubMed]

Kontou, M., Govindasamy, L., Nam, H. J., Bryant, N., Llamas-Saiz, A. L., Foces-Foces, C., Hernando, E., Rubio, M. P., McKenna, R., Almendral, J. M. & Agbandje-McKenna, M. (2005). Structural determinants of tissue tropism and in vivo pathogenicity for the parvovirus minute virus of mice. J Virol 79, 10931-10943. [PubMed]

Koonin, E. V. & Ilyina, T. V. (1993). Computer-assisted dissection of rolling circle DNA replication. BioSyst 30, 241-268. [PubMed]

Krupovic, M. & Koonin, E. V. (2014). Evolution of eukaryotic single-stranded DNA viruses of the Bidnaviridae family from genes of four other groups of widely different viruses. Sci Rep 4, 5347. [PubMed]

Lahtinen, A., Kivelä, P., Hedman, L., Kumar, A., Kantele, A., Lappalainen, M., Liitsola, K., Ristola, M., Delwart, E., Sharp, C., Simmonds, P., Söderlund-Venermo, M. & Hedman, K. (2011). Serodiagnosis of primary infections with human parvovirus 4, Finland. Emerg Infect Dis 17, 79-82. [PubMed]

Lau, S. K., Woo, P. C., Tse, H., Fu, C. T., Au, W. K., Chen, X. C., Tsoi, H. W., Tsang, T. H., Chan, J. S., Tsang, D. N., Li, K. S., Tse, C. W., Ng, T. K., Tsang, O. T., Zheng, B. J., Tam, S., Chan, K. H., Zhou, B. & Yuen, K. Y. (2008). Identification of novel porcine and bovine parvoviruses closely related to human parvovirus 4. J Gen Virol 89, 1840-1848. [PubMed]

Leisi, R., Ruprecht, N., Kempf, C. & Ros, C. (2013). Parvovirus B19 uptake is a highly selective process controlled by VP1u, a novel determinant of viral tropism. J Virol 87, 13161-13167. [PubMed]

Leisi, R., Von Nordheim, M., Ros, C. & Kempf, C. (2016). The VP1u receptor restricts parvovirus B19 uptake to permissive erythroid cells. Viruses 8. [PubMed]

Li, L., Pesavento, P. A., Woods, L., Clifford, D. L., Luff, J., Wang, C. & Delwart, E. (2011). Novel amdovirus in gray foxes. Emerg Infect Dis 17, 1876-1878. [PubMed]

Li, L. & Pintel, D. J. (2012). Splicing of goose parvovirus pre-mRNA influences cytoplasmic translation of the processed mRNA. Virology 426, 60-65. [PubMed

Li, L., Qiu, J. & Pintel, D. J. (2009). The choice of translation initiation site of the rep proteins from goose parvovirus P9-generated mRNA is governed by splicing and the nature of the excised intron. J Virol 83, 10264-10268. [PubMed]

Li, P., Li, J., Zhang, R., Chen, J., Wang, W., Lan, J., Xie, Z. & Jiang, S. (2018). Duck "beak atrophy and dwarfism syndrome" disease complex: Interplay of novel goose parvovirus-related virus and duck circovirus? Transbound Emerg Dis 65, 345-351. [PubMed]

Liu, K., Li, Y., Jousset, F. X., Zadori, Z., Szelei, J., Yu, Q., Pham, H. T., Lépine, F., Bergoin, M. & Tijssen, P. (2011). The Acheta domesticus densovirus, isolated from the European house cricket, has evolved an expression strategy unique among parvoviruses. J Virol 85, 10069-10078. [PubMed]

Liu, Z., Qiu, J., Cheng, F., Chu, Y., Yoto, Y., O'Sullivan, M. G., Brown, K. E. & Pintel, D. J. (2004). Comparison of the transcription profile of simian parvovirus with that of the human erythrovirus B19 reveals a number of unique features. J Virol 78, 12929-12939. [PubMed]

Lombardo, E., Ramírez, J. C., Agbandje-McKenna, M. & Almendral, J. M. (2000). A beta-stranded motif drives capsid protein oligomers of the parvovirus minute virus of mice into the nucleus for viral assembly. J Virol 74, 3804-3814. [PubMed]

López-Bueno, A., Mateu, M. G. & Almendral, J. M. (2003). High mutant frequency in populations of a DNA virus allows evasion from antibody therapy in an immunodeficient host. J Virol 77, 2701-2708. [PubMed]

López-Bueno, A., Segovia, J. C., Bueren, J. A., O'Sullivan, M. G., Wang, F., Tattersall, P. & Almendral, J. M. (2008). Evolution to pathogenicity of the parvovirus minute virus of mice in immunodeficient mice involves genetic heterogeneity at the capsid domain that determines tropism. J Virol 82, 1195-1203. [PubMed]

López-Bueno, A., Valle, N., Gallego, J. M., Pérez, J. & Almendral, J. M. (2004). Enhanced cytoplasmic sequestration of the nuclear export receptor CRM1 by NS2 mutations developed in the host regulates parvovirus fitness. J Virol 78, 10674-10684. [PubMed]

Lorson, C., Burger, L. R., Mouw, M. & Pintel, D. J. (1996). Efficient transactivation of the minute virus of mice P38 promoter requires upstream binding of NS1. J Virol 70, 834-842. [PubMed]

Lou, S., Xu, B., Huang, Q., Zhi, N., Cheng, F., Wong, S., Brown, K., Delwart, E., Liu, Z. & Qiu, J. (2012). Molecular characterization of the newly identified human parvovirus 4 in the family ParvoviridaeVirology 422, 59-69. [PubMed]

Luo, Y. & Qiu, J. (2013). Parvovirus infection-induced DNA damage response. Future virology 8, 245-257. [PubMed]

Luo, Y. & Qiu, J. (2015). Human parvovirus B19: a mechanistic overview of infection and DNA replication. Future virology 10, 155-167. [PubMed]

Majumder, K., Etingov, I. & Pintel, D. J. (2017). Protoparvovirus interactions with the cellular DNA damage response. Viruses 9. [PubMed]

Mäntylä, E., Kann, M. & Vihinen-Ranta, M. (2017). Protoparvovirus knocking at the nuclear door. Viruses 9. [PubMed]

Maroto, B., Valle, N., Saffrich, R. & Almendral, J. M. (2004). Nuclear export of the nonenveloped parvovirus virion is directed by an unordered protein signal exposed on the capsid surface. J Virol 78, 10685-10694. [PubMed

Mattei, L. M., Cotmore, S. F., Tattersall, P. & Iwasaki, A. (2013). Parvovirus evades interferon-dependent viral control in primary mouse embryonic fibroblasts. Virology 442, 20-27. [PubMed]

Matthews, P. C., Sharp, C., Simmonds, P. & Klenerman, P. (2017). Human parvovirus 4 'PARV4' remains elusive despite a decade of study. F1000Research 6, 82. [PubMed]

McKenna, R., Olson, N. H., Chipman, P. R., Baker, T. S., Booth, T. F., Christensen, J., Aasted, B., Fox, J. M., Bloom, M. E., Wolfinbarger, J. B. & Agbandje-McKenna, M. (1999). Three-dimensional structure of Aleutian mink disease parvovirus: implications for disease pathogenicity. J Virol 73, 6882-6891. [PubMed]

Meng, G., Zhang, X., Plevka, P., Yu, Q., Tijssen, P. & Rossmann, M. G. (2013). The structure and host entry of an invertebrate parvovirus. J Virol 87, 12523-12530. [PubMed]

Mészáros, I., Olasz, F., Cságola, A., Tijssen, P. & Zádori, Z. (2017a). Biology of porcine parvovirus (Ungulate parvovirus 1). Viruses 9. [PubMed]

Mészáros, I., Tóth, R., Olasz, F., Tijssen, P. & Zádori, Z. (2017b). The SAT protein of porcine parvovirus accelerates viral spreading through induction of irreversible endoplasmic reticulum stress. J Virol 91. [PubMed]

Mietzsch, M., Kailasan, S., Garrison, J., Ilyas, M., Chipman, P., Kantola, K., Janssen, M. E., Spear, J., Sousa, D., McKenna, R., Brown, K., Söderlund-Venermo, M., Baker, T. & Agbandje-McKenna, M. (2017). Structural insights into human bocaparvoviruses. J Virol 91. [PubMed]

Mihaylov, I. S., Cotmore, S. F. & Tattersall, P. (2014). Complementation for an essential ancillary non-structural protein function across parvovirus genera. Virology 468-470, 226-237. [PubMed]

Miller, C. L. & Pintel, D. J. (2002). Interaction between parvovirus NS2 protein and nuclear export factor Crm1 is important for viral egress from the nucleus of murine cells. J Virol 76, 3257-3266. [PubMed]

Modha, S., Thanki, A. S., Cotmore, S. F., Davison, A. J. & Hughes, J. (2018). ViCTree: an automated framework for taxonomic classification from protein sequences. Bioinformatics 34, 2195-2200. [PubMed]

Moesker, F. M., van Kampen, J. J., van der Eijk, A. A., van Rossum, A. M., de Hoog, M., Schutten, M., Smits, S. L., Bodewes, R., Osterhaus, A. D. & Fraaij, P. L. (2015). Human bocavirus infection as a cause of severe acute respiratory tract infection in children. Clin Microbiol Infect 21, 964.e961-968. [PubMed

Mollerup, S., Fridholm, H., Vinner, L., Kjartansdóttir, K. R., Friis-Nielsen, J., Asplund, M., Herrera, J. A., Steiniche, T., Mourier, T., Brunak, S., Willerslev, E., Izarzugaza, J. M., Hansen, A. J. & Nielsen, L. P. (2017). Cutavirus in cutaneous malignant melanoma. Emerg Infect Dis 23, 363-365. [PubMed]

Mori, D., Ranawaka, U., Yamada, K., Rajindrajith, S., Miya, K., Perera, H. K., Matsumoto, T., Dassanayake, M., Mitui, M. T., Mori, H., Nishizono, A., Söderlund-Venermo, M. & Ahmed, K. (2013). Human bocavirus in patients with encephalitis, Sri Lanka, 2009-2010. Emerg Infect Dis 19, 1859-1862. [PubMed]

Mouw, M. B. & Pintel, D. J. (2000). Adeno-associated virus RNAs appear in a temporal order and their splicing is stimulated during coinfection with adenovirus. J Virol 74, 9878-9888. [PubMed]

Naeger, L. K., Cater, J. & Pintel, D. J. (1990). The small nonstructural protein (NS2) of the parvovirus minute virus of mice is required for efficient DNA replication and infectious virus production in a cell-type-specific manner. J Virol 64, 6166-6175. [PubMed]

Nguyen, Q. T., Sifer, C., Schneider, V., Allaume, X., Servant, A., Bernaudin, F., Auguste, V. & Garbarg-Chenon, A. (1999). Novel human erythrovirus associated with transient aplastic anemia. J Clin Microbiol 37, 2483-2487. [PubMed]

Nguyen, Q. T., Wong, S., Heegaard, E. D. & Brown, K. E. (2002). Identification and characterization of a second novel human erythrovirus variant, A6. Virology 301, 374-380. [PubMed]

Ning, K., Wang, M., Qu, S., Lv, J., Yang, L. & Zhang, D. (2017). Pathogenicity of Pekin duck- and goose-origin parvoviruses in Pekin ducklings. Vet Microbiol 210, 17-23. [PubMed]

Norja, P., Hokynar, K., Aaltonen, L. M., Chen, R., Ranki, A., Partio, E. K., Kiviluoto, O., Davidkin, I., Leivo, T., Eis-Hübinger, A. M., Schneider, B., Fischer, H. P., Tolba, R., Vapalahti, O., Vaheri, A., Söderlund-Venermo, M. & Hedman, K. (2006). Bioportfolio: lifelong persistence of variant and prototypic erythrovirus DNA genomes in human tissue. Proc Natl Acad Sci USA 103, 7450-7453. [PubMed]

Paloniemi, M., Lappalainen, S., Salminen, M., Kätkä, M., Kantola, K., Hedman, L., Hedman, K., Söderlund-Venermo, M. & Vesikari, T. (2014). Human bocaviruses are commonly found in stools of hospitalized children without causal association to acute gastroenteritis. Eur J Pediatr 173, 1051-1057. [PubMed]

Panning, M., Kobbe, R., Vollbach, S., Drexler, J. F., Adjei, S., Adjei, O., Drosten, C., May, J. & Eis-Hubinger, A. M. (2010). Novel human parvovirus 4 genotype 3 in infants, Ghana. Emerg Infect Dis 16, 1143-1146. [PubMed

Parker, J. S., Murphy, W. J., Wang, D., O'Brien, S. J. & Parrish, C. R. (2001). Canine and feline parvoviruses can use human or feline transferrin receptors to bind, enter, and infect cells. J Virol 75, 3896-3902. [PubMed]

Pearson, J. L. & Pintel, D. J. (2000). Recombination within the nonstructural genes of the parvovirus minute virus of mice (MVM) generates functional levels of wild-type NS1, which can be detected in the absence of selective pressure following transfection of nonreplicating plasmids. Virology 269, 128-136. [PubMed]

Pénzes, J. J., Pham, H. T., Benkö, M. & Tijssen, P. (2015). Novel parvoviruses in reptiles and genome sequence of a lizard parvovirus shed light on Dependoparvovirus genus evolution. J Gen Virol 96, 2769-2779. [PubMed

Pereira, D. J., McCarty, D. M. & Muzyczka, N. (1997). The adeno-associated virus (AAV) Rep protein acts as both a repressor and an activator to regulate AAV transcription during a productive infection. J Virol 71, 1079-1088. [PubMed]

Pettersen, E. F., Goddard, T. D., Huang, C. C., Couch, G. S., Greenblatt, D. M., Meng, E. C. & Ferrin, T. E. (2004). UCSF Chimera--a visualization system for exploratory research and analysis. J Comp Chem 25, 1605-1612. [PubMed]

Pham, H. T., Jousset, F. X., Perreault, J., Shike, H., Szelei, J., Bergoin, M. & Tijssen, P. (2013a). Expression strategy of Aedes albopictus densovirus. J Virol 87, 9928-9932. [PubMed

Pham, H. T., Yu, Q., Bergoin, M. & Tijssen, P. (2013b). A novel ambisense densovirus, Acheta domesticus mini ambidensovirus, from Crickets. Genome Announc 1. [PubMed]

Phan, T. G., Dreno, B., da Costa, A. C., Li, L., Orlandi, P., Deng, X., Kapusinszky, B., Siqueira, J., Knol, A. C., Halary, F., Dantal, J., Alexander, K. A., Pesavento, P. A. & Delwart, E. (2016). A new protoparvovirus in human fecal samples and cutaneous T cell lymphomas (mycosis fungoides). Virology 496, 299-305. [PubMed]

Phan, T. G., Sdiri-Loulizi, K., Aouni, M., Ambert-Balay, K., Pothier, P., Deng, X. & Delwart, E. (2014). New parvovirus in child with unexplained diarrhea, Tunisia. Emerg Infect Dis 20, 1911-1913. [PubMed]

Phan, T. G., Vo, N. P., Bonkoungou, I. J., Kapoor, A., Barro, N., O'Ryan, M., Kapusinszky, B., Wang, C. & Delwart, E. (2012). Acute diarrhea in West African children: diverse enteric viruses and a novel parvovirus genus. J Virol 86, 11024-11030. [PubMed]

Pillay, S., Zou, W., Cheng, F., Puschnik, A. S., Meyer, N. L., Ganaie, S. S., Deng, X., Wosen, J. E., Davulcu, O., Yan, Z., Engelhardt, J. F., Brown, K. E., Chapman, M. S., Qiu, J. & Carette, J. E. (2017). AAV serotypes have distinctive interactions with domains of the cellular receptor AAVR. J Virol. [PubMed]

Pillet, S., Le Guyader, N., Hofer, T., NguyenKhac, F., Koken, M., Aubin, J. T., Fichelson, S., Gassmann, M. & Morinet, F. (2004). Hypoxia enhances human B19 erythrovirus gene expression in primary erythroid cells. Virology 327, 1-7. [PubMed]

Pintel, D., Dadachanji, D., Astell, C. R. & Ward, D. C. (1983). The genome of minute virus of mice, an autonomous parvovirus, encodes two overlapping transcription units. Nucleic Acids Res 11, 1019-1038. [PubMed]

Plevka, P., Hafenstein, S., Li, L., D'Abrgamo, A., Jr., Cotmore, S. F., Rossmann, M. G. & Tattersall, P. (2011). Structure of a packaging-defective mutant of minute virus of mice indicates that the genome is packaged via a pore at a 5-fold axis. J Virol 85, 4822-4827. [PubMed]

Prasad, K. M. & Trempe, J. P. (1995). The adeno-associated virus Rep78 protein is covalently linked to viral DNA in a preformed virion. Virology 214, 360-370. [PubMed]

Pyöriä, L., Toppinen, M., Mäntylä, E., Hedman, L., Aaltonen, L. M., Vihinen-Ranta, M., Ilmarinen, T., Söderlund-Venermo, M., Hedman, K. & Perdomo, M. F. (2017). Extinct type of human parvovirus B19 persists in tonsillar B cells. Nat Commun 8, 14930. [PubMed]

Qiu, J., Cheng, F., Burger, L. R. & Pintel, D. (2006a). The transcription profile of Aleutian mink disease virus in CRFK cells is generated by alternative processing of pre-mRNAs produced from a single promoter. J Virol 80, 654-662. [PubMed]

Qiu, J., Cheng, F., Johnson, F. B. & Pintel, D. (2007). The transcription profile of the bocavirus bovine parvovirus is unlike those of previously characterized parvoviruses. J Virol 81, 12080-12085. [PubMed]

Qiu, J., Cheng, F. & Pintel, D. (2006b). Molecular characterization of caprine adeno-associated virus (AAV-Go.1) reveals striking similarity to human AAV5. Virology 356, 208-216. [PubMed]

Qiu, J., Cheng, F. & Pintel, D. J. (2006c). Expression profiles of bovine adeno-associated virus and avian adeno-associated virus display significant similarity to that of adeno-associated virus type 5. J Virol 80, 5482-5493. [PubMed]

Qiu, J., Cheng, F., Yoto, Y., Zádori, Z. & Pintel, D. (2005). The expression strategy of goose parvovirus exhibits features of both the Dependovirus and Parvovirus genera. J Virol 79, 11035-11044. [PubMed]

Qiu, J. & Pintel, D. J. (2002). The adeno-associated virus type 2 Rep protein regulates RNA processing via interaction with the transcription template. Mol Cell Biol 22, 3639-3652. [PubMed]

Qiu, J., Söderlund-Venermo, M. & Young, N. S. (2017). Human parvoviruses. Clin Microbiol Rev 30, 43-113. [PubMed]

Riolobos, L., Valle, N., Hernando, E., Maroto, B., Kann, M. & Almendral, J. M. (2010). Viral oncolysis that targets Raf-1 signaling control of nuclear transport. J Virol 84, 2090-2099. [PubMed

Ros, C., Bayat, N., Wolfisberg, R. & Almendral, J. M. (2017). Protoparvovirus cell entry. Viruses 9. [PubMed]

Ruiz, Z., D'Abramo, A., Jr. & Tattersall, P. (2006). Differential roles for the C-terminal hexapeptide domains of NS2 splice variants during MVM infection of murine cells. Virology 349, 382-395. [PubMed

Saksmerprome, V., Jitrakorn, S., Chayaburakul, K., Laiphrom, S., Boonsua, K. & Flegel, T. W. (2011). Additional random, single to multiple genome fragments of Penaeus stylirostris densovirus in the giant tiger shrimp genome have implications for viral disease diagnosis. Virus Res 160, 180-190. [PubMed]

Samulski, R. J. & Muzyczka, N. (2014). AAV-mediated gene therapy for research and therapeutic purposes. Annu Rev Virol 1, 427-451. [PubMed]

Schlehofer, J. R., Ehrbar, M. & zur Hausen, H. (1986). Vaccinia virus, herpes simplex virus, and carcinogens induce DNA amplification in a human cell line and support replication of a helpervirus dependent parvovirus. Virology 152, 110-117. [PubMed]

Schrodinger, LLC (2015). The PyMOL Molecular Graphics System, Version 1.8. 

Servant, A., Laperche, S., Lallemand, F., Marinho, V., De Saint Maur, G., Meritet, J. F. & Garbarg-Chenon, A. (2002). Genetic diversity within human erythroviruses: identification of three genotypes. J Virol 76, 9124-9134. [PubMed]

Shackelton, L. A. & Holmes, E. C. (2006). Phylogenetic evidence for the rapid evolution of human B19 erythrovirus. J Virol 80, 3666-3669. [PubMed

Shackelton, L. A., Parrish, C. R., Truyen, U. & Holmes, E. C. (2005). High rate of viral evolution associated with the emergence of carnivore parvovirus. Proc Natl Acad Sci USA 102, 379-384. [PubMed]

Shade, R. O., Blundell, M. C., Cotmore, S. F., Tattersall, P. & Astell, C. R. (1986). Nucleotide sequence and genome organization of human parvovirus B19 isolated from the serum of a child during aplastic crisis. J Virol 58, 921-936. [PubMed]

Shao, X. Q., Wen, Y. J., Ba, H. X., Zhang, X. T., Yue, Z. G., Wang, K. J., Li, C. Y., Qiu, J. & Yang, F. H. (2014). Novel amdoparvovirus infecting farmed raccoon dogs and arctic foxes. Emerg Infect Dis 20, 2085-2088. [PubMed]

Sharp, C. P., Lail, A., Donfield, S., Simmons, R., Leen, C., Klenerman, P., Delwart, E., Gomperts, E. D. & Simmonds, P. (2009). High frequencies of exposure to the novel human parvovirus PARV4 in hemophiliacs and injection drug users, as detected by a serological assay for PARV4 antibodies. J Infect Dis 200, 1119-1125. [PubMed

Shen, W., Deng, X., Zou, W., Cheng, F., Engelhardt, J. F., Yan, Z. & Qiu, J. (2015). Identification and functional analysis of novel nonstructural proteins of human bocavirus 1. J Virol 89, 10097-10109. [PubMed]

Simpson, A. A., Chipman, P. R., Baker, T. S., Tijssen, P. & Rossmann, M. G. (1998). The structure of an insect parvovirus (Galleria mellonella densovirus) at 3.7  Å resolution. Structure 6, 1355-1367. [PubMed]

Simpson, A. A., Hébert, B., Sullivan, G. M., Parrish, C. R., Zádori, Z., Tijssen, P. & Rossmann, M. G. (2002). The structure of porcine parvovirus: comparison with related viruses. J Mol Biol 315, 1189-1198. [PubMed]

Slavov, S. N., Otaguiri, K. K., Smid, J., de Oliveira, A. C., Casseb, J., Martinez, E. Z., Covas, D. T., Eis-Hübinger, A. M. & Kashima, S. (2017). Human parvovirus 4 prevalence among HTLV-1/2 infected individuals in Brazil. J Med Virol 89, 748-752. [PubMed]

Snyder, R. O., Samulski, R. J. & Muzyczka, N. (1990). In vitro resolution of covalently joined AAV chromosome ends. Cell 60, 105-113. [PubMed]

Söderlund-Venermo, M., Hokynar, K., Nieminen, J., Rautakorpi, H. & Hedman, K. (2002). Persistence of human parvovirus B19 in human tissues. Pathologie-biologie 50, 307-316. [PubMed]

Söderlund, M., von Essen, R., Haapasaari, J., Kiistala, U., Kiviluoto, O. & Hedman, K. (1997). Persistence of parvovirus B19 DNA in synovial membranes of young patients with and without chronic arthropathy. Lancet 349, 1063-1065. [PubMed]

Sonntag, F., Bleker, S., Leuchs, B., Fischer, R. & Kleinschmidt, J. A. (2006). 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. J Virol 80, 11040-11054. [PubMed]

Sonntag, F., Schmidt, K. & Kleinschmidt, J. A. (2010). A viral assembly factor promotes AAV2 capsid formation in the nucleolus. Proc Natl Acad Sci USA 107, 10220-10225. [PubMed

Subramanian, S., Organtini, L. J., Grossman, A., Domeier, P. P., Cifuente, J. O., Makhov, A. M., Conway, J. F., D'Abramo, A., Jr., Cotmore, S. F., Tattersall, P. & Hafenstein, S. (2017). Cryo-EM maps reveal five-fold channel structures and their modification by gatekeeper mutations in the parvovirus minute virus of mice (MVM) capsid. Virology 510, 216-223. [PubMed]

Sukhu, L., Fasina, O., Burger, L., Rai, A., Qiu, J. & Pintel, D. J. (2013). Characterization of the nonstructural proteins of the bocavirus minute virus of canines. J Virol 87, 1098-1104. [PubMed]

Sukhumsirichart, W., Attasart, P., Boonsaeng, V. & Panyim, S. (2006). Complete nucleotide sequence and genomic organization of hepatopancreatic parvovirus (HPV) of Penaeus monodonVirology 346, 266-277. [PubMed]

Sun, Y., Chen, A. Y., Cheng, F., Guan, W., Johnson, F. B. & Qiu, J. (2009). Molecular characterization of infectious clones of the minute virus of canines reveals unique features of bocaviruses. J Virol 83, 3956-3967. [PubMed]

Tattersall, P. & Ward, D. C. (1976). Rolling hairpin model for replication of parvovirus and linear chromosomal DNA. Nature 263, 106-109. [PubMed]

Tewary, S. K., Liang, L., Lin, Z., Lynn, A., Cotmore, S. F., Tattersall, P., Zhao, H. & Tang, L. (2015). Structures of minute virus of mice replication initiator protein N-terminal domain: Insights into DNA nicking and origin binding. Virology 476, 61-71. [PubMed]

Tewary, S. K., Zhao, H., Shen, W., Qiu, J. & Tang, L. (2013). Structure of the NS1 protein N-terminal origin recognition/nickase domain from the emerging human bocavirus. J Virol 87, 11487-11493. [PubMed

Tijssen, P., Li, Y., El-Far, M., Szelei, J., Letarte, M. & Zádori, Z. (2003). Organization and expression strategy of the ambisense genome of densonucleosis virus of Galleria mellonellaJ Virol 77, 10357-10365. [PubMed]

Tijssen, P., Pénzes, J. J., Yu, Q., Pham, H. T. & Bergoin, M. (2016). Diversity of small, single-stranded DNA viruses of invertebrates and their chaotic evolutionary past. J Invertebr Pathol 140, 83-96. [PubMed

Toppinen, M., Perdomo, M. F., Palo, J. U., Simmonds, P., Lycett, S. J., Söderlund-Venermo, M., Sajantila, A. & Hedman, K. (2015). Bones hold the key to DNA virus history and epidemiology. Sci Rep 5, 17226. [PubMed]

Tse, H., Tsoi, H. W., Teng, J. L., Chen, X. C., Liu, H., Zhou, B., Zheng, B. J., Woo, P. C., Lau, S. K. & Yuen, K. Y. (2011). Discovery and genomic characterization of a novel ovine partetravirus and a new genotype of bovine partetravirus. PLoS One 6, e25619. [PubMed]

Tse, L. V., Klinc, K. A., Madigan, V. J., Castellanos Rivera, R. M., Wells, L. F., Havlik, L. P., Smith, J. K., Agbandje-McKenna, M. & Asokan, A. (2017). Structure-guided evolution of antigenically distinct adeno-associated virus variants for immune evasion. Proc Natl Acad Sci USA 114, E4812-e4821. [PubMed]

Tse, L. V., Moller-Tank, S., Meganck, R. M. & Asokan, A. (2018). Mapping and engineering functional domains of the assembly-activating protein of adeno-associated viruses. J Virol 92. [PubMed]

Tseng, Y. S., Gurda, B. L., Chipman, P., McKenna, R., Afione, S., Chiorini, J. A., Muzyczka, N., Olson, N. H., Baker, T. S., Kleinschmidt, J. & Agbandje-McKenna, M. (2015). Adeno-associated virus serotype 1 (AAV1)- and AAV5-antibody complex structures reveal evolutionary commonalities in parvovirus antigenic reactivity. J Virol 89, 1794-1808. [PubMed]

Väisänen, E., Fu, Y., Hedman, K. & Söderlund-Venermo, M. (2017). Human protoparvoviruses. Viruses 9. [PubMed]

Väisänen, E., Mohanraj, U., Kinnunen, P. M., Jokelainen, P., Al-Hello, H., Barakat, A. M., Sadeghi, M., Jalilian, F. A., Majlesi, A., Masika, M., Mwaengo, D., Anzala, O., Delwart, E., Vapalahti, O., Hedman, K. & Söderlund-Venermo, M. (2018). Global distribution of human protoparvoviruses. Emerg Infect Dis 24, 1292-1299. [PubMed]

Vendeville, A., Ravallec, M., Jousset, F. X., Devise, M., Mutuel, D., López-Ferber, M., Fournier, P., Dupressoir, T. & Ogliastro, M. (2009). Densovirus infectious pathway requires clathrin-mediated endocytosis followed by trafficking to the nucleus. J Virol 83, 4678-4689. [PubMed]

Venkatakrishnan, B., Yarbrough, J., Domsic, J., Bennett, A., Bothner, B., Kozyreva, O. G., Samulski, R. J., Muzyczka, N., McKenna, R. & Agbandje-McKenna, M. (2013). Structure and dynamics of adeno-associated virus serotype 1 VP1-unique N-terminal domain and its role in capsid trafficking. J Virol 87, 4974-4984. [PubMed]

Wang, Z., Deng, X., Zou, W., Engelhardt, J. F., Yan, Z. & Qiu, J. (2017a). Human bocavirus 1 is a novel helper for adeno-associated virus replication. J Virol. [PubMed

Wang, Z., Shen, W., Cheng, F., Deng, X., Engelhardt, J. F., Yan, Z. & Qiu, J. (2017b). Parvovirus expresses a small noncoding RNA that plays an essential role in virus replication. J Virol 91. [PubMed]

Wigfield, D. C. & Eatock, S. A. (1990). The effect of metals on the activity of L-phenylalanine hydroxylase. J Trace Elem Elect Health Dis 4, 143-146. [PubMed]

Wu, H., Keller, W. & Rossmann, M. G. (1993). Determination and refinement of the canine parvovirus empty-capsid structure. Acta Crystallogr D Biol Crystallogr 49, 572-579. [PubMed

Xie, Q. & Chapman, M. S. (1996). Canine parvovirus capsid structure, analyzed at 2.9 Å resolution. J Mol Biol 264, 497-520. [PubMed]

Xie, Q., Spear, J. M., Noble, A. J., Sousa, D. R., Meyer, N. L., Davulcu, O., Zhang, F., Linhardt, R. J., Stagg, S. M. & Chapman, M. S. (2017). The 2.8 Å electron microscopy structure of adeno-associated virus-DJ bound by a heparinoid pentasaccharide. Mol Ther Met Clin Dev 5, 1-12. [PubMed]

Yahiro, T., Wangchuk, S., Tshering, K., Bandhari, P., Zangmo, S., Dorji, T., Tshering, K., Matsumoto, T., Nishizono, A., Söderlund-Venermo, M. & Ahmed, K. (2014). Novel human bufavirus genotype 3 in children with severe diarrhea, Bhutan. Emerg Infect Dis 20, 1037-1039. [PubMed

Ye, C. & Pintel, D. J. (2008). The transcription strategy of bovine adeno-associated virus (B-AAV) combines features of both adeno-associated virus type 2 (AAV2) and type 5 (AAV5). Virology 370, 392-402. [PubMed]

Yoon-Robarts, M., Blouin, A. G., Bleker, S., Kleinschmidt, J. A., Aggarwal, A. K., Escalante, C. R. & Linden, R. M. (2004). Residues within the B' motif are critical for DNA binding by the superfamily 3 helicase Rep40 of adeno-associated virus type 2. J Biol Chem 279, 50472-50481. [PubMed

Yu, Q. & Tijssen, P. (2014). Gene expression of five different iteradensoviruses: Bombyx mori densovirus, Casphalia extranea densovirus, Papilio polyxenes densovirus, Sibine fusca densovirus, and Danaus plexippus densovirus. J Virol 88, 12152-12157. [PubMed

Zádori, Z., Stefancsik, R., Rauch, T. & Kisary, J. (1995). Analysis of the complete nucleotide sequences of goose and muscovy duck parvoviruses indicates common ancestral origin with adeno-associated virus 2. Virology 212, 562-573. [PubMed]

Zádori, Z., Szelei, J., Kiss, I. & Tijssen, P. (2006). Waterfowl parvoviruses. In Parvoviruses. Edited by J. Kerr, S. Cotmore, M. E. Bloom, R. M. Linden & C. R. Parrish. London: Hodder Arnold. 

Zádori, Z., Szelei, J., Lacoste, M. C., Li, Y., Gariépy, S., Raymond, P., Allaire, M., Nabi, I. R. & Tijssen, P. (2001). A viral phospholipase A2 is required for parvovirus infectivity. Dev Cell 1, 291-302. [PubMed]

Zádori, Z., Szelei, J. & Tijssen, P. (2005). SAT: a late NS protein of porcine parvovirus. J Virol 79, 13129-13138. [PubMed]

Zhi, N., Zádori, Z., Brown, K. E. & Tijssen, P. (2004). Construction and sequencing of an infectious clone of the human parvovirus B19. Virology 318, 142-152. [PubMed]

Zinn, E. & Vandenberghe, L. H. (2014). Adeno-associated virus: fit to serve. Curr Opin Virol 8, 90-97. [PubMed]

Zolotukhin, S., Byrne, B. J., Mason, E., Zolotukhin, I., Potter, M., Chesnut, K., Summerford, C., Samulski, R. J. & Muzyczka, N. (1999). Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Ther 6, 973-985. [PubMed

Zou, W., Cheng, F., Shen, W., Engelhardt, J. F., Yan, Z. & Qiu, J. (2016). Nonstructural protein NP1 of human bocavirus 1 plays a critical role in the expression of viral capsid proteins. J Virol 90, 4658-4669. [PubMed]

Zou, W., Wang, Z., Xiong, M., Chen, A. Y., Xu, P., Ganaie, S. S., Badawi, Y., Kleiboeker, S., Nishimune, H., Ye, S. Q. & Qiu, J. (2018). Human parvovirus B19 utilizes cellular DNA replication machinery for viral DNA replication. J Virol 92. [PubMed

Zsak, L., Cha, R. M. & Day, J. M. (2013). Chicken parvovirus-induced runting-stunting syndrome in young broilers. Avian Dis 57, 123-127. [PubMed]

Zsak, L., Cha, R. M., Li, F. & Day, J. M. (2015). Host specificity and phylogenetic relationships of chicken and turkey parvoviruses. Avian Dis 59, 157-161. [PubMed