Argyle, D

Cannon, C

Dunsford, T

Flynn, J N

Hosie, M J

Jarrett, O

Mackay, N A

Miyazawa, T

Neil, J C

Onions, D E

Rigby, M A

Willett, B J

English

Edinburgh Research Explorer

     Edinburgh Research Explorer                                      DNA vaccination affords significant protection against felineimmunodeficiency virus infection without inducing detectableantiviral antibodies (vol 72, pg 7310, 1998)Citation for published version:Hosie, MJ, Flynn, JN, Rigby, MA, Cannon, C, Dunsford, T, Mackay, NA, Argyle, D, Willett, BJ, Miyazawa, T,Onions, DE, Jarrett, O & Neil, JC 1998, 'DNA vaccination affords significant protection against felineimmunodeficiency virus infection without inducing detectable antiviral antibodies (vol 72, pg 7310, 1998)'Journal of Virology, vol 72, no. 10, pp. 8460-8460.Link:Link to publication record in Edinburgh Research ExplorerDocument Version:Author final version (often known as postprint)Published In:Journal of VirologyGeneral rightsCopyright for the publications made accessible via the Edinburgh Research Explorer is retained by the author(s)and / or other copyright owners and it is a condition of accessing these publications that users recognise andabide by the legal requirements associated with these rights.Take down policyThe University of Edinburgh has made every reasonable effort to ensure that Edinburgh Research Explorercontent complies with UK legislation. If you believe that the public display of this file breaches copyright pleasecontact openaccess@ed.ac.uk providing details, and we will remove access to the work immediately andinvestigate your claim.Download date: 20. Feb. 2015ERRATAMoloney Murine Leukemia Virus Envelope Protein Subunits,gp70 and Pr15E, Form a Stable Disulfide-Linked ComplexDIRK-JAN E. OPSTELTEN, MICHAEL WALLIN, AND HENRIK GAROFFDepartment for Biosciences at Novum, Karolinska Institute, S-141 57 Huddinge, SwedenVolume 72, no. 8, p. 6537–6545, 1998. Page 6540, Fig. 3C should appear as shown below.The Second Extracellular Loop of CXCR4 Determines Its Functionas a Receptor for Feline Immunodeficiency VirusBRIAN J. WILLETT, KAREN ADEMA, NIKOLAUS HEVEKER, ANNE BRELOT, LAURENT PICARD,MARC ALIZON, JULIE D. TURNER, JAMES A. HOXIE, STEPHEN PEIPER,JAMES C. NEIL, AND MARGARET J. HOSIEDepartment of Veterinary Pathology, University of Glasgow Veterinary School, Glasgow G61 1QH, United Kingdom;INSERM U.332, Institute Cochin de Ge´ne´tique Mole´culaire, 75014 Paris, France; University of Pennsylvania,Philadelphia, Pennsylvania 19104; and Department of Pathology, James Graham BrownCancer Center, University of Louisville, Louisville, Kentucky 40202Volume 72, no. 8, p. 6475–6481, 1998. Page 6475, column 2, line 16: “C” should read “R;” line 17, “C5” should read “R5.”DNA Vaccination Affords Significant Protection against FelineImmunodeficiency Virus Infection without InducingDetectable Antiviral AntibodiesMARGARET J. HOSIE, J. NORMAN FLYNN, MARK A. RIGBY, CELIA CANNON, THOMAS DUNSFORD, NANCY A. MACKAY,DAVID ARGYLE, BRIAN J. WILLETT, TAKAYUKI MIYAZAWA, DAVID E. ONIONS,OSWALD JARRETT, AND JAMES C. NEILRetrovirus Research Laboratory, Department of Veterinary Pathology, University of Glasgow, Bearsden, Glasgow G61 1QH, United KingdomVolume 72, no. 9, p. 7310–7319, 1998. Page 7316, Table 1, line 1 of data: Trial 1, FIVDRT, 12-week postchallenge response,“2, 0, blank” should read “1, 2, 0.”FIG. 3C.8460Functional Interaction of Human Immunodeficiency VirusType 1 Vpu and Gag with a Novel Member of theTetratricopeptide Repeat Protein FamilyMICHAEL A. CALLAHAN, MARK A. HANDLEY, YUNG-HUI LEE, KATRIN J. TALBOT,J. WADE HARPER, AND ANTONITO T. PANGANIBANMcArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison, Wisconsin 53706, andVerna and Marrs McLean Department of Biochemistry, Baylor College of Medicine, Houston, Texas 77030Volume 72, no. 6, p. 5189–5197, 1998. Page 5192: We found that nucleotide 932 (G) was omitted from the originally publishedubp sequence. This resulted in changes in all the encoded amino acids following this position. The ubp cDNA is 2,222 bp long, witha 942-bp open reading frame and a 1,242-bp 39 untranslated region. The ubp open reading frame is predicted to encode a 313-residue protein with a molecular mass of 34.1 kDa, which is consistent with the mobility of UBP on polyacrylamide gels. Thesechanges do not alter the conclusions made in the original publication. Figure 1 should appear as shown below.FIG. 1.VOL. 72, 1998 ERRATA 8461

DNA vaccination affords significant protection against feline immunodeficiency virus infection without inducing detectable antiviral antibodies (vol 72, pg 7310, 1998)

DNA vaccination affords significant protection against feline immunodeficiency virus infection without inducing detectable antiviral antibodies (vol 72, pg 7310, 1998)

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