Tunicamycin treatment of CHO cells abrogates multiple blocks to retrovirus infection, one of which is due to a secreted inhibitor.
about
A human cell-surface receptor for xenotropic and polytropic murine leukemia viruses: possible role in G protein-coupled signal transductionSodium-dependent neutral amino acid transporter type 1 is an auxiliary receptor for baboon endogenous retrovirus.The mouse "xenotropic" gammaretroviruses and their XPR1 receptorA family of retroviruses that utilize related phosphate transporters for cell entryPit2 assemblies at the cell surface are modulated by extracellular inorganic phosphate concentrationThe envelope glycoprotein of an amphotropic murine retrovirus binds specifically to the cellular receptor/phosphate transporter of susceptible speciesDifferential coupling of the human P2Y(11) receptor to phospholipase C and adenylyl cyclaseCloning of the cellular receptor for amphotropic murine retroviruses reveals homology to that for gibbon ape leukemia virusMurine endogenous retrovirusesThe avian XPR1 gammaretrovirus receptor is under positive selection and is disabled in bird species in contact with virus-infected wild miceEfficient transduction by an amphotropic retrovirus vector is dependent on high-level expression of the cell surface virus receptorGibbon ape leukemia virus receptor functions of type III phosphate transporters from CHOK1 cells are disrupted by two distinct mechanisms.Host range and interference studies of three classes of pig endogenous retrovirus.Retrovirus packaging cells expressing the Mus dunni endogenous virus envelope facilitate transduction of CHO and primary hematopoietic cells.Cellular and species resistance to murine amphotropic, gibbon ape, and feline subgroup C leukemia viruses is strongly influenced by receptor expression levels and by receptor masking mechanisms.Retroviral vectors pseudotyped with lymphocytic choriomeningitis virus.Transmembrane topology of PiT-2, a phosphate transporter-retrovirus receptor.Receptors and entry cofactors for retroviruses include single and multiple transmembrane-spanning proteins as well as newly described glycophosphatidylinositol-anchored and secreted proteins.Membrane fusion and cell entry of XMRV are pH-independent and modulated by the envelope glycoprotein's cytoplasmic tailEvolution of functional and sequence variants of the mammalian XPR1 receptor for mouse xenotropic gammaretroviruses and the human-derived retrovirus XMRV.Resistance to infection by subgroups B, D, and E avian sarcoma and leukosis viruses is explained by a premature stop codon within a resistance allele of the tvb receptor gene.Similar regulation of cell surface human T-cell leukemia virus type 1 (HTLV-1) surface binding proteins in cells highly and poorly transduced by HTLV-1-pseudotyped virionsFeline leukemia virus infection requires a post-receptor binding envelope-dependent cellular component.Naturally Occurring Polymorphisms of the Mouse Gammaretrovirus Receptors CAT-1 and XPR1 Alter Virus Tropism and Pathogenicity.A novel murine retrovirus identified during testing for helper virus in human gene transfer trials.Analysis of the unique hamster cell tropism of ecotropic murine leukemia virus PVC-211.Murine retroviruses use at least six different receptors for entry into Mus dunni cellsGene transfer to human cells using retrovirus vectors produced by a new polytropic packaging cell lineCapillary endothelial cell tropism of PVC-211 murine leukemia virus and its application for gene transductionIdentification of envelope protein residues required for the expanded host range of 10A1 murine leukemia virus.Second site mutation in the virus envelope expands the host range of a cytopathic variant of Moloney murine leukemia virus.Role of receptor polymorphism and glycosylation in syncytium induction and host range variation of ecotropic mouse gammaretroviruses.Properties of a unique form of the murine amphotropic leukemia virus receptor expressed on hamster cells.Introduction of human genomic sequences renders CHO-K1 cells susceptible to infection by amphotropic retroviruses.A phenotypic host range alteration determines RD114 virus restriction in feline embryonic cellsInhibitors of retrovirus infection are secreted by several hamster cell lines and are also present in hamster seraGibbon ape leukemia virus and the amphotropic murine leukemia virus 4070A exhibit an unusual interference pattern on E36 Chinese hamster cells.The requirements for viral entry differ from those for virally induced syncytium formation in NIH 3T3/DTras cells exposed to Moloney murine leukemia virus.Identification of an extracellular domain within the human PiT2 receptor that is required for amphotropic murine leukemia virus bindingInhibition of MHC class I-restricted antigen presentation by gamma 2-herpesviruses
P2860
Q22001445-59C69131-84B2-4174-AA4C-5FE812207432Q24527201-685E0898-026F-4A9F-A3C7-18414F72223FQ24622259-13A5F026-C1FD-4F50-9109-18429C451318Q24645533-A5DDDFF2-817D-4C9D-AB54-1C7D3F0D38B5Q24673772-7C132B83-6619-412A-8B13-EF3F328E55D6Q24675131-34B55E20-5D4E-49E5-8EF7-3CF7BAC66745Q28345903-7512238B-9FF0-4A7C-B552-4558F7593E84Q28576023-AEF39BA3-4F9D-409D-B0ED-B656CD7B229DQ28602246-591ECC9E-7B01-4591-94F9-6C90A02C63C1Q28681423-C8746C08-0D96-45EB-B8BA-A0BA6851AD74Q33639579-09D88E11-FF2A-4503-9E1E-E930F42B9112Q33643741-6DDEE476-EA88-439A-AA60-EBD54E6A2C43Q33786110-87145F7E-8AA6-44E6-8191-79A7810262C3Q33786362-57567E15-32B5-4214-ADFA-08099B0FB86AQ33812075-ACFB7363-25EC-483F-8C5F-6A796E47BE72Q33816040-2BAD4472-60A0-46DE-8348-4D250CC271D6Q33841953-6DD3FA8A-28FF-4461-BE56-B4BFB7964819Q34010373-7CF5D4B9-A8A5-41A2-8914-B7E4F42188FDQ34221609-422567F1-0466-485F-8E04-5076CF6EBB47Q34296049-A37458BF-CD5D-4443-AE7F-9C92BA06BBBAQ34343436-198FC41D-6C9C-497E-82A5-CC2A858C496AQ34354324-5034FB90-4AFB-4D73-AAC9-2A0B557D3774Q35531590-58B21D8E-581D-4730-97A3-BE13973C328FQ35692374-A23ECDD7-4BDC-47AD-8BDE-43767220021EQ35857136-BE0960EC-6DA7-43D4-B393-FD5BCF9FAA52Q35873475-EB32651F-5941-4589-B6A8-B4B26EED6AD2Q35886705-11663A5A-A9E3-40B1-8B71-1DFD47B2C4DCQ35887352-127C56AC-9723-45BF-B742-2DC78377749BQ35890403-2C661DA0-53BA-47E4-B977-8B958AB4634FQ35897703-4E1CCACB-2E8D-4FD8-BA51-F3C86A3BB0AFQ36240769-09E3E571-B526-48AE-A35C-2456D77B6514Q36471170-3EF48275-4A3D-4279-8460-6F353290B44DQ36637612-FA86DFFC-5229-4FA9-83A9-0CF1835B016EQ36642298-4D4490A8-6AE6-462A-BA4C-6F49F24F472CQ36651072-6B1E99E4-DA6B-4EAD-BBB6-758F7020F4FAQ36651916-CFC249E8-D017-444E-96A6-9DFE79CF3B17Q36652085-44F7D791-E8E7-49D1-8E29-366DFF2623EAQ36687255-AD1ABC60-C4BF-4833-9E17-D125C3929641Q36943559-1BD77FE3-85A1-424B-8855-8922E3A55D56Q37228775-CA12458A-E223-49C2-BA92-0017A8754DF2
P2860
Tunicamycin treatment of CHO cells abrogates multiple blocks to retrovirus infection, one of which is due to a secreted inhibitor.
description
1992 nî lūn-bûn
@nan
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
1992年论文
@zh
1992年论文
@zh-cn
name
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@ast
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@en
type
label
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@ast
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@en
prefLabel
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@ast
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@en
P2860
P1433
P1476
Tunicamycin treatment of CHO c ...... s due to a secreted inhibitor.
@en
P2093
P2860
P407
P577
1992-01-01T00:00:00Z