Infection of Glial Cells by the Human Polyomavirus JC Is Mediated by an N-Linked Glycoprotein Containing Terminal α(2-6)-Linked Sialic Acids
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[1] W. Atwood,et al. The human polyomavirus, JCV, does not share receptor specificity with SV40 on human glial cells. , 1998, Journal of neurovirology.
[2] S. Harrison,et al. High‐resolution structure of a polyomavirus VP1‐oligosaccharide complex: implications for assembly and receptor binding , 1997, The EMBO journal.
[3] M. Pawlita,et al. Consequences of a subtle sialic acid modification on the murine polyomavirus receptor , 1997, Journal of virology.
[4] T. Benjamin,et al. Roles ofN-Glycans with α2,6 as well as α2,3 Linked Sialic Acid in Infection by Polyoma Virus , 1997 .
[5] L. Mitnaul,et al. Receptor specificity of influenza A viruses correlates with the agglutination of erythrocytes from different animal species. , 1997, Virology.
[6] T. Benjamin,et al. Roles of N-glycans with alpha2,6 as well as alpha2,3 linked sialic acid in infection by polyoma virus. , 1997, Virology.
[7] J. Kartenbeck,et al. Major histocompatibility complex class I molecules mediate association of SV40 with caveolae. , 1997, Molecular biology of the cell.
[8] R. Chammas,et al. Sialic Acid 9-O-Acetylation on Murine Erythroleukemia Cells Affects Complement Activation, Binding to I-type Lectins, and Tissue Homing* , 1996, The Journal of Biological Chemistry.
[9] L. Norkin,et al. Bound simian virus 40 translocates to caveolin-enriched membrane domains, and its entry is inhibited by drugs that selectively disrupt caveolae. , 1996, Molecular biology of the cell.
[10] E. Major,et al. JC virus infection of hematopoietic progenitor cells, primary B lymphocytes, and tonsillar stromal cells: implications for viral latency , 1996, Journal of virology.
[11] P. Cinque,et al. JCV-DNA and BKV-DNA in the CNS tissue and CSF of AIDS patients and normal subjects. Study of 41 cases and review of the literature. , 1996, Journal of acquired immune deficiency syndromes and human retrovirology : official publication of the International Retrovirology Association.
[12] E. Jones,et al. Characterization of the Sialic Acid-binding Site in Sialoadhesin by Site-directed Mutagenesis (*) , 1996, The Journal of Biological Chemistry.
[13] J. Ragnaud,et al. Detection of JC virus DNA in the peripheral blood leukocytes of HIV‐infected patients , 1996, AIDS.
[14] H. Klenk,et al. Transfer of an esterase-resistant receptor analog to the surface of influenza C virions results in reduced infectivity due to aggregate formation. , 1996, Virology.
[15] A. Varki,et al. I-type Lectins (*) , 1995, The Journal of Biological Chemistry.
[16] A. Varki,et al. CD22-mediated Cell Adhesion to Cytokine-activated Human Endothelial Cells , 1995, The Journal of Biological Chemistry.
[17] M. Pawlita,et al. Biosynthetic Modulation of Sialic Acid-dependent Virus-Receptor Interactions of Two Primate Polyoma Viruses (*) , 1995, The Journal of Biological Chemistry.
[18] E. Major,et al. Evaluation of the role of cytokine activation in the multiplication of JC virus (JCV) in human fetal glial cells. , 1995, Journal of neurovirology.
[19] M. Concha,et al. Progressive multifocal leukoencephalopathy: the evolution of a disease once considered rare. , 1995, Journal of neurovirology.
[20] G. Wadell,et al. Molecular determinants of adenovirus tropism. , 1995, Current topics in microbiology and immunology.
[21] R. Weiss,et al. Retrovirus receptors , 1995, Cell.
[22] M. Pawlita,et al. Regulation of susceptibility and cell surface receptor for the B-lymphotropic papovavirus by N glycosylation , 1994, Journal of virology.
[23] M G Rossmann,et al. Viral cell recognition and entry. , 1994, Protein science : a publication of the Protein Society.
[24] E. Major,et al. JC virus: Current concepts and controversies in the molecular virology and pathogenesis of progressive multifocal leucoencephalopathy , 1994 .
[25] Thilo Stehle,et al. Structure of murine polyomavirus complexed with an oligosaccharide receptor fragment , 1994, Nature.
[26] I. Stamenkovic,et al. Cytokine-induced beta-galactoside alpha-2,6-sialyltransferase in human endothelial cells mediates alpha 2,6-sialylation of adhesion molecules and CD22 ligands. , 1994, The Journal of biological chemistry.
[27] A M Haywood,et al. Virus receptors: binding, adhesion strengthening, and changes in viral structure , 1994, Journal of virology.
[28] S. Günther,et al. Infection of human polyomaviruses JC and BK in peripheral blood leukocytes from immunocompetent individuals. , 1994, Virology.
[29] H. Zentgraf,et al. The cell surface receptor is a major determinant restricting the host range of the B-lymphotropic papovavirus , 1993, Journal of virology.
[30] B. Harfe,et al. Mutations that alter an Arg-Gly-Asp (RGD) sequence in the adenovirus type 2 penton base protein abolish its cell-rounding activity and delay virus reproduction in flat cells , 1993, Journal of virology.
[31] G. Nemerow,et al. Integrins α v β 3 and α v β 5 promote adenovirus internalization but not virus attachment , 1993, Cell.
[32] K. Dörries,et al. High frequency of polyomavirus infection in lymphoid cell preparations after allogeneic bone marrow transplantation. , 1993, Transplantation proceedings.
[33] R. Weiss. Cellular Receptors and Viral Glycoproteins Involved in Retrovirus Entry , 1993 .
[34] K. Dörries,et al. Evidence of human polyomavirus BK and JC infection in normal brain tissue. , 1992, Virology.
[35] E. Major,et al. Interaction of the human polyomavirus, JCV, with human B-lymphocytes. , 1992, Virology.
[36] V. Pietropaolo,et al. Role of phospholipids in BK virus infection and haemagglutination. , 1992, Microbiologica.
[37] R. Frisque,et al. JC virus DNA is present in many human brain samples from patients without progressive multifocal leukoencephalopathy , 1992, Journal of virology.
[38] S. Kenney,et al. Subclinical central nervous system infection with JC virus in patients with AIDS. , 1992, The Journal of infectious diseases.
[39] R. Jaenisch,et al. Infection by polyomavirus of murine cells deficient in class I major histocompatibility complex expression , 1992, Journal of virology.
[40] W. Atwood,et al. Class I major histocompatibility proteins are an essential component of the simian virus 40 receptor , 1992, Journal of virology.
[41] E. Major,et al. Pathogenesis and molecular biology of progressive multifocal leukoencephalopathy, the JC virus-induced demyelinating disease of the human brain , 1992, Clinical Microbiology Reviews.
[42] H. Greenberg,et al. Strategies for the identification of icosahedral virus receptors. , 1992, The Journal of clinical investigation.
[43] R. Liddington,et al. Structure of simian virus 40 at 3.8-Å resolution , 1991, Nature.
[44] H. Greenberg,et al. Identification and partial characterization of a rhesus rotavirus binding glycoprotein on murine enterocytes. , 1991, Virology.
[45] M. Hsu,et al. Inhibition of DNA replication of adenovirus type 5 and simian virus 40 by tunicamycin. , 1991, Virology.
[46] H. Lipton. Is JC Virus latent in brain? , 1991, Annals of neurology.
[47] M. Tajima,et al. JC virus detection by in situ hybridization in brain tissue from elderly patients , 1991, Annals of neurology.
[48] J. Assouline,et al. Human fetal Schwann cells support JC virus multiplication , 1991, Journal of virology.
[49] R. Garcea,et al. A single-amino-acid substitution in polyomavirus VP1 correlates with plaque size and hemagglutination behavior , 1991, Journal of virology.
[50] T. Benjamin,et al. Polyomavirus tumor induction in mice: effects of polymorphisms of VP1 and large T antigen , 1991, Journal of virology.
[51] E. Major,et al. Glial cells of the human developing brain and B cells of the immune system share a common DNA binding factor for recognition of the regulatory sequences of the human polyomavirus, JCV , 1990, Journal of neuroscience research.
[52] R. Yolken,et al. Rotaviruses specifically bind to the neutral glycosphingolipid asialo-GM1 , 1990, Journal of virology.
[53] V. Racaniello. Cell receptors for picornaviruses. , 1990, Current topics in microbiology and immunology.
[54] A. Helenius,et al. Virus Entry into Animal Cells , 1989, Advances in Virus Research.
[55] W. Atwood,et al. Class I major histocompatibility proteins as cell surface receptors for simian virus 40 , 1989, Journal of virology.
[56] E. Major,et al. Human Fetal Astrocytes in Culture Support the Growth of the Neurotropic Human Polyomavirus, JCV , 1989, Journal of neuropathology and experimental neurology.
[57] J. Tomassini,et al. cDNA cloning reveals that the major group rhinovirus receptor on HeLa cells is intercellular adhesion molecule 1. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[58] K. Shah,et al. Detection of BK virus and JC virus in urine and brain tissue by the polymerase chain reaction , 1989, Journal of clinical microbiology.
[59] E. Major,et al. Extension of JC virus host range to monkey cells by insertion of a simian virus 40 enhancer into the JC virus regulatory region. , 1989, Virology.
[60] E. Wimmer,et al. Cellular receptor for poliovirus: Molecular cloning, nucleotide sequence, and expression of a new member of the immunoglobulin superfamily , 1989, Cell.
[61] R. Compans,et al. Characterization of simian virus 40 receptor moieties on the surfaces of Vero C1008 cells , 1989, Journal of virology.
[62] C. Kufta,et al. Involvement of JC virus-infected mononuclear cells from the bone marrow and spleen in the pathogenesis of progressive multifocal leukoencephalopathy. , 1988, The New England journal of medicine.
[63] E. Harlow,et al. Antibodies: A Laboratory Manual , 1988 .
[64] D. Walker,et al. The Biology and Molecular Biology of JC Virus , 1986 .
[65] E. Major,et al. Establishment of a line of human fetal glial cells that supports JC virus multiplication. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[66] L. Norkin,et al. Human glioblastoma cells persistently infected with simian virus 40 carry nondefective episomal viral DNA and acquire the transformed phenotype and numerous chromosomal abnormalities , 1985, Journal of virology.
[67] Luc Montagnier,et al. T-lymphocyte T4 molecule behaves as the receptor for human retrovirus LAV , 1984, Nature.
[68] M. Greaves,et al. The CD4 (T4) antigen is an essential component of the receptor for the AIDS retrovirus , 1984, Nature.
[69] J. Paulson,et al. Sialyloligosaccharide receptors of binding variants of polyoma virus. , 1983, Virology.
[70] Padgett Bl,et al. Virologic and serologic studies of progressive multifocal leukoencephalopathy. , 1983 .
[71] B. Padgett,et al. Virologic and serologic studies of progressive multifocal leukoencephalopathy. , 1983, Progress in clinical and biological research.
[72] L. Norkin. Papovaviral persistent infections. , 1982, Microbiological reviews.
[73] F. Superti,et al. Receptors for BK virus on human erythrocytes. , 1981, Acta virologica.
[74] J. Paulson,et al. Polyoma virus recognizes specific sialyligosaccharide receptors on host cells. , 1981, Virology.
[75] J. Paulson,et al. Polyoma virus adsorbs to specific sialyloligosaccharide receptors on erythrocytes. , 1980, Virology.
[76] B. Padgett,et al. JC virus, a human polyomavirus associated with progressive multifocal leukoencephalopathy: additional biological characteristics and antigenic relationships , 1977, Infection and immunity.
[77] R. Mäntyjärvi,et al. Hemagglutination by BK Virus, a Tentative New Member of the Papovavirus Group , 1972, Infection and immunity.
[78] U. Pettersson,et al. Virus-Receptor Interaction in an Adenovirus System , 1968, Journal of virology.