A monoclonal antibody reactive with a 15-kDa cytoplasmic granule-associated protein defines a subpopulation of CD8+ T lymphocytes.
about
Fas-activated serine/threonine kinase (FAST) phosphorylates TIA-1 during Fas-mediated apoptosisThe splicing regulator TIA-1 interacts with U1-C to promote U1 snRNP recruitment to 5' splice sites.Identification and functional characterization of a TIA-1-related nucleolysinThe RNA-binding protein TIAR is translocated from the nucleus to the cytoplasm during Fas-mediated apoptotic cell deathMutation of Mapped TIA-1/TIAR Binding Sites in the 3' Terminal Stem-Loop of West Nile Virus Minus-Strand RNA in an Infectious Clone Negatively Affects Genomic RNA AmplificationCharacterization of GMP-17, a granule membrane protein that moves to the plasma membrane of natural killer cells following target cell recognition.Analysis of the human thymic perivascular space during agingCharacterization of the host immune response in human Ganglia after herpes zoster.Stepwise maturation of lytic granules during differentiation and activation of human CD8+ T lymphocytes.B7-H1 and B7-H3 are independent predictors of poor prognosis in patients with non-small cell lung cancerMycobacterium tuberculosis growth at the cavity surface: a microenvironment with failed immunityEvidence that intestinal intraepithelial lymphocytes are activated cytotoxic T cells in celiac disease but not in giardiasis.Granzyme B expression in Reed-Sternberg cells of Hodgkin's disease.T-cell-rich large-B-cell lymphomas contain non-activated CD8+ cytolytic T cells, show increased tumor cell apoptosis, and have lower Bcl-2 expression than diffuse large-B-cell lymphomasExpression of cytotoxic proteins by neoplastic T cells in mycosis fungoides increases with progression from plaque stage to tumor stage diseaseHigh prevalence of activated intraepithelial cytotoxic T lymphocytes and increased neoplastic cell apoptosis in colorectal carcinomas with microsatellite instability.Primary cutaneous CD8-positive epidermotropic cytotoxic T cell lymphomas. A distinct clinicopathological entity with an aggressive clinical behavior.Identification of tissue-infiltrating lymphocytes expressing PEN5, a mucin-like glycoprotein selectively expressed on natural killer cellsImmunohistochemical localization of granzyme B antigen in cytotoxic cells in human tissues.Immunohistochemical identification of cytotoxic lymphocytes using human perforin monoclonal antibodyCytotoxic effector cell granules recognized by the monoclonal antibody TIA-1 are present in CD8+ lymphocytes in lymph nodes of human immunodeficiency virus-1-infected patientsIn situ detection of activated cytotoxic cells in follicular lymphomas.Tumor-infiltrating lymphocytes predict response to anthracycline-based chemotherapy in estrogen receptor-negative breast cancer.Definition of a natural killer NKR-P1A+/CD56-/CD16- functionally immature human NK cell subset that differentiates in vitro in the presence of interleukin 12.The unenlarged lymph nodes of HIV-1-infected, asymptomatic patients with high CD4 T cell counts are sites for virus replication and CD4 T cell proliferation. The impact of highly active antiretroviral therapyAntiviral cytotoxic T lymphocytes in vaginal mucosa of simian immunodeficiency virus-infected rhesus macaquesControl of alternative splicing in immune responses: many regulators, many predictions, much still to learnA cytotoxic phenotype does not predict clinical outcome in anaplastic large cell lymphomas.Cytotoxic T cell response against the chimeric ETV6-AML1 protein in childhood acute lymphoblastic leukemia.Cytotoxic CD4 T Cells-Friend or Foe during Viral Infection?Neuroimmunity of HTLV-I Infection.Predicting treatment outcome in classical Hodgkin lymphoma: genomic advancesDysregulated expression of lipid storage and membrane dynamics factors in Tia1 knockout mouse nervous tissue.Expression of TIA-1 and TIA-2 in T cell malignancies and T cell lymphocytosis.Decreased in situ expression of interleukin-10 receptor is correlated with the exacerbated inflammatory and cytotoxic responses observed in mucosal leishmaniasis.NK cells, displaying early activation, cytotoxicity and adhesion molecules, are associated with mild dengue disease.Most CD8+ cells in skin lesions of CD3+ CD4+ mycosis fungoides are CD3+ T cells that lack CD11b, CD16, CD56, CD57, and human Hanukah factor mRNA.Recruitment of CD8(+) T cells expressing granzyme A is associated with lesion progression in human cutaneous leishmaniasis.Expression of killer cell inhibitory receptors is restricted to true NK cell lymphomas and a subset of intestinal enteropathy-type T cell lymphomas with a cytotoxic phenotype.Activation of infiltrating cytotoxic T lymphocytes and lymphoma cell apoptotic rates in gastric MALT lymphomas. Differences between high-grade and low-grade cases
P2860
Q24307757-D8D76C45-2688-407B-B91B-F746792E2C23Q24337164-EAF6CF4A-A52D-4664-B502-B8973583C336Q24337248-A1F12BA0-CB37-4F24-9348-09D2E03A3574Q24563323-3F4D3430-5C70-44A1-B03A-5AF1F6D7EBDFQ27487114-2F6A2A8B-E220-410A-BA6F-6F81B01BE9EBQ33571226-689E0F91-13BD-46EA-9762-2F828D85850CQ33859403-AF5B3030-AD1F-45A6-BEB6-B683EA157AE2Q34055440-F5D8EA03-05BF-42FE-A4CA-A237331ABEFCQ34071769-DB1AD4EE-BBE6-461C-B723-8B844D18A4CFQ34459048-0769B895-890C-4C1E-92AA-D6CFCF15DA90Q34945420-B02FB7A6-11E1-44B1-9850-95FDEC6A0FCEQ35773749-2DE7922E-7330-4257-8280-F4C355EFE2A0Q35773794-C3B0CACE-F693-486E-951C-F0E99BBC81C0Q35786017-AF37A3D3-03A6-4F8C-8EBE-9424BEC6DE44Q35786883-60CA15A8-5C82-4FB5-BD92-8467C65C0EECQ35787046-D1496BBF-72F3-4C48-A172-8A63F9AF1690Q35787772-C0095383-79EB-4660-992A-B018B6752FEBQ35796248-5E3C5D3A-A046-4691-AB77-E40A1F9B6CA7Q35830318-B86877A3-A688-43EB-B450-D60F19895F7AQ35831708-DB5DEDC7-0A73-40A1-B32D-1EC38B766847Q35833022-0089747D-5E62-4D5F-9186-A5948C1E6F6BQ35833276-2A5E0257-26E4-49C3-B97A-E3F42DA60229Q35889643-17D9279A-398B-4B83-BF50-D622CDC024A1Q36367558-5F009A3E-1C28-4CEE-82D4-CC985FA39513Q36400457-19AA6206-3314-49B4-BA12-53B8830B449EQ36546178-23F5D993-97A9-48F3-9403-9F25933C6ACEQ36751866-90C938A8-ECDE-4069-880D-91738528CE54Q37230518-09BED711-DBE5-4907-9AC4-FD1FC1DC7630Q37384003-81311DCF-4F28-49AD-8976-28DFAAD95EBEQ37597931-C45C459B-6FB0-4C36-97B8-EC55A7BE0E6CQ37741036-ABC628F6-6EA5-44C1-8222-1DF913CBEF6FQ37872044-FE6DC1F4-8596-4F49-8CED-25F9AFC21204Q38308258-17EAE7EB-0C1A-41A2-83BC-E8EFF64AF547Q39582507-AC77447C-66EB-45E7-B017-1BFB52B6F9B0Q40380946-0D8AB33E-CB45-4E22-A385-D4F92EF6D901Q40488687-3802973E-E3A6-4E76-BB90-31EE840B6081Q41971887-2EA98C25-BFA5-4AE9-A7AB-0085E2FC2DCFQ41983589-2862F824-AC4B-4B1E-998B-1127D935A161Q42041467-43D5E1AD-C6A2-4BFB-B62B-F80AE190D49BQ42048881-C1ED1624-DA66-46A8-9275-F7ED86CC0A57
P2860
A monoclonal antibody reactive with a 15-kDa cytoplasmic granule-associated protein defines a subpopulation of CD8+ T lymphocytes.
description
1990 nî lūn-bûn
@nan
1990 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1990 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
name
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@ast
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@en
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@nl
type
label
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@ast
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@en
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@nl
prefLabel
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@ast
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@en
A monoclonal antibody reactive ...... ulation of CD8+ T lymphocytes.
@nl
P2093
P1476
A monoclonal antibody reactive ...... pulation of CD8+ T lymphocytes
@en
P2093
Anderson P
Nagler-Anderson C
Schlossman SF
Slayter HS
P304
P407
P577
1990-01-01T00:00:00Z