The tripartite leader sequence is required for ectopic expression of HAdV-B and HAdV-E E3 CR1 genes.

[1]  H. Clark,et al.  Corrigendum: The extracellular interactome of the human adenovirus family reveals diverse strategies for immunomodulation , 2017, Nature Communications.

[2]  H. Clark,et al.  The extracellular interactome of the human adenovirus family reveals diverse strategies for immunomodulation , 2016, Nature Communications.

[3]  E. Hage,et al.  Human mastadenovirus type 70: a novel, multiple recombinant species D mastadenovirus isolated from diarrhoeal faeces of a haematopoietic stem cell transplantation recipient. , 2015, The Journal of general virology.

[4]  P. Lu,et al.  Molecular Epidemiology and Phylogenetic Analysis of Human Adenovirus Caused an Outbreak in Taiwan during 2011 , 2015, PloS one.

[5]  Wenbo Xu,et al.  Adenoviruses Associated with Acute Respiratory Diseases Reported in Beijing from 2011 to 2013 , 2015, PloS one.

[6]  K. Excoffon,et al.  Adenovirus Entry From the Apical Surface of Polarized Epithelia Is Facilitated by the Host Innate Immune Response , 2015, PLoS pathogens.

[7]  E. Kremmer,et al.  A unique secreted adenovirus E3 protein binds to the leukocyte common antigen CD45 and modulates leukocyte functions , 2013, Proceedings of the National Academy of Sciences.

[8]  D. Seto,et al.  Molecular evolution of human adenoviruses , 2013, Scientific Reports.

[9]  Jian-hua Zhou,et al.  Hepatitis B virus X protein up-regulates tumor necrosis factor-α expression in cultured mesangial cells via ERKs and NF-κB pathways. , 2013, Asian Pacific journal of tropical biomedicine.

[10]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[11]  Xiaohong Zhou,et al.  The E3 CR1-gamma gene in human adenoviruses associated with epidemic keratoconjunctivitis. , 2011, Virus research.

[12]  M. J. Mahon,et al.  Vectors bicistronically linking a gene of interest to the SV40 large T antigen in combination with the SV40 origin of replication enhance transient protein expression and luciferase reporter activity. , 2011, BioTechniques.

[13]  P. Murtagh,et al.  Acute Lower Respiratory Tract Infections by Adenovirus in Children: Histopathologic Findings in 18 Fatal Cases , 2011, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

[14]  S. K. Campos,et al.  Open Reading Frame E3-10.9K of Subspecies B1 Human Adenoviruses Encodes a Family of Late Orthologous Proteins That Vary in Their Predicted Structural Features and Subcellular Localization , 2010, Journal of Virology.

[15]  O. W. Lindwasser,et al.  A Diacidic Motif in Human Immunodeficiency Virus Type 1 Nef Is a Novel Determinant of Binding to AP-2 , 2007, Journal of Virology.

[16]  W. Schaffner,et al.  The nucleotide sequence and a first generation gene transfer vector of species B human adenovirus serotype 3 , 2005, Virology.

[17]  R. Cuesta,et al.  Regulation of Translation by Ribosome Shunting through Phosphotyrosine-Dependent Coupling of Adenovirus Protein 100k to Viral mRNAs , 2005, Journal of Virology.

[18]  R. Cuesta,et al.  Tethering of eIF4G to adenoviral mRNAs by viral 100k protein drives ribosome shunting. , 2004, Genes & development.

[19]  W. Wold,et al.  FUNCTIONS AND MECHANISMS OF ACTION OF THE ADENOVIRUS E3 PROTEINS , 2004, International reviews of immunology.

[20]  A. Hilgendorf,et al.  Immune evasion by adenovirus E3 proteins: exploitation of intracellular trafficking pathways. , 2004, Current topics in microbiology and immunology.

[21]  Andreas Elsing,et al.  Two Distinct Transport Motifs in the Adenovirus E3/10.4-14.5 Proteins Act in Concert to Down-modulate Apoptosis Receptors and the Epidermal Growth Factor Receptor* , 2003, Journal of Biological Chemistry.

[22]  A. Davison,et al.  Genetic content and evolution of adenoviruses. , 2003, The Journal of general virology.

[23]  W. Wold,et al.  Adenovirus ADP protein (E3-11.6K), which is required for efficient cell lysis and virus release, interacts with human MAD2B. , 2003, Virology.

[24]  P. Griffiths,et al.  Homology between the human cytomegalovirus RL11 gene family and human adenovirus E3 genes. , 2003, The Journal of general virology.

[25]  F. Deryckère,et al.  The novel early region 3 protein E3/49K is specifically expressed by adenoviruses of subgenus D: implications for epidemic keratoconjunctivitis and adenovirus evolution. , 2002, Virology.

[26]  H. Burgert,et al.  Characterization of E3/49K, a Novel, Highly Glycosylated E3 Protein of the Epidemic Keratoconjunctivitis-Causing Adenovirus Type 19a , 2002, Journal of Virology.

[27]  P. Sharp,et al.  Spliced segments at the 5' terminus of adenovirus 2 late mRNA. 1977. , 2000, Reviews in Medical Virology.

[28]  W. Wold,et al.  Identification and characterization of a 30K protein (Ad4E3-30K) encoded by the E3 region of human adenovirus type 4. , 2000, Virology.

[29]  A. Yueh,et al.  Translation by ribosome shunting on adenovirus and hsp70 mRNAs facilitated by complementarity to 18S rRNA. , 2000, Genes & development.

[30]  H. Burgert,et al.  Immunomodulatory functions encoded by the E3 transcription unit of adenoviruses. , 2000 .

[31]  J. Gaydos,et al.  Reemergence of adenovirus type 4 acute respiratory disease in military trainees: report of an outbreak during a lapse in vaccination. , 1999, The Journal of infectious diseases.

[32]  S. J. Flint,et al.  The Tripartite Leader Sequence of Subgroup C Adenovirus Major Late mRNAs Can Increase the Efficiency of mRNA Export , 1998, Journal of Virology.

[33]  M. Mathews,et al.  Structure, function, and evolution of adenovirus-associated RNA: a phylogenetic approach , 1996, Journal of virology.

[34]  F. Deryckère,et al.  Early region 3 of adenovirus type 19 (subgroup D) encodes an HLA-binding protein distinct from that of subgroups B and C , 1996, Journal of virology.

[35]  J. Ryerse,et al.  The adenovirus death protein (E3-11.6K) is required at very late stages of infection for efficient cell lysis and release of adenovirus from infected cells , 1996, Journal of virology.

[36]  W. Wold,et al.  The E3-20.5K membrane protein of subgroup B human adenoviruses contains O-linked and complex N-linked oligosaccharides. , 1995, Virology.

[37]  W. Wold,et al.  A 20,500-Dalton protein is coded by region E3 of subgroup B but not subgroup C human adenoviruses. , 1995, Virology.

[38]  W. Wold,et al.  E3 transcription unit of adenovirus. , 1995, Current topics in microbiology and immunology.

[39]  R. Dornburg,et al.  Downstream insertion of the adenovirus tripartite leader sequence enhances expression in universal eukaryotic vectors. , 1993, BioTechniques.

[40]  S. K. Saha,et al.  The 11,600-MW protein encoded by region E3 of adenovirus is expressed early but is greatly amplified at late stages of infection , 1992, Journal of virology.

[41]  T. Linné.  Differences in the E3 regions of the canine adenovirus type 1 and type 2. , 1992, Virus research.

[42]  R. Kaufman,et al.  Improved vectors for stable expression of foreign genes in mammalian cells by use of the untranslated leader sequence from EMC virus. , 1991, Nucleic acids research.

[43]  R. Schneider,et al.  Translation by the Adenovirus Tripartite Leader: Elements Which Determine Independence from Cap-Binding Protein Complex , 1990, Journal of virology.

[44]  龍喜 荒尾,et al.  メラノサイト系腫瘍におけるGrowth factor receptorの局在 , 1990 .

[45]  R. Schneider,et al.  Secondary structure analysis of adenovirus tripartite leader. , 1989, Journal of Biological Chemistry.

[46]  V. Pathak,et al.  The phosphorylation state of eucaryotic initiation factor 2 alters translational efficiency of specific mRNAs , 1989, Molecular and cellular biology.

[47]  R. Schneider,et al.  The adenovirus tripartite leader may eliminate the requirement for cap-binding protein complex during translation initiation , 1988, Journal of virology.

[48]  M. Katze,et al.  Efficient transcription, not translation, is dependent on adenovirus tripartite leader sequences at late times of infection , 1988, Journal of virology.

[49]  U. Pettersson,et al.  Subtypes of bovine adenovirus type 2 exhibit major differences in region E3. , 1986, Virology.

[50]  A. Davis,et al.  Expression of hepatitis B surface antigen with a recombinant adenovirus. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[51]  G. Akusjärvi,et al.  Adenovirus VA RNAI mediates a translational stimulation which is not restricted to the viral mRNAs. , 1985, The EMBO journal.

[52]  P. Sharp,et al.  Effect of the tripartite leader on synthesis of a non-viral protein in an adenovirus 5 recombinant. , 1985, Nucleic acids research.

[53]  R. Kaufman.  Identification of the components necessary for adenovirus translational control and their utilization in cDNA expression vectors. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[54]  T. Shenk,et al.  Adenovirus VAI RNA facilitates the initiation of translation in virus-infected cells , 1984, Cell.

[55]  C. V. van Beveren,et al.  The nucleotide sequence of the gene for protein IVa2 and of the 5' leader segment of the major late mRNAs of adenovirus type 5. , 1981, Gene.

[56]  P. Higgins,et al.  An outbreak of adenovirus type 4 conjunctivitis. , 1980, The British journal of ophthalmology.

[57]  L. Chow,et al.  Complex splicing patterns of RNAs from the early regions of adenovirus-2. , 1979, Journal of molecular biology.

[58]  Richard J. Roberts,et al.  Nucleotide sequence analysis of the leader segments in a cloned copy of adenovirus 2 fiber mRNA , 1979, Cell.

[59]  T. R. Broker,et al.  The spliced structures of adenovirus 2 fiber message and the other late mRNAs , 1978, Cell.

[60]  P. Sharp,et al.  Spliced segments at the 5′ terminus of adenovirus 2 late mRNA* , 1977, Proceedings of the National Academy of Sciences.

[61]  T. Kelly,et al.  Use of Nondefective Adenovirus-Simian Virus 40 Hybrids for Mapping the Simian Virus 40 Genome , 1973, Journal of virology.