gp120s derived from four syncytiuminducing HIV-1 strains induce different patterns of CD4 association with lymphocyte surface molecules
スポンサーリンク
概要
著者
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DIANZANI Umberto
Laboratory of Immunology, Department of Medical Science, A. Avogadro University of Eastern Piedmont
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Dianzani Umberto
Interdisciplinary Research Center Of Autoimmune Disease Department Of Medical Sciences A. Avogadro U
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Dianzani Umberto
Dipartimento Di Scienze Mediche University 'a. Avogadro' Of Eastern Piedmont
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Feito Maria
Dipartimento Di Scienze Mediche University 'a. Avogadro' Of Eastern Piedmont
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Malavasi Fabio
Istituto Di Biologia E Genetica University Of Ancona
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Bonissoni Sara
Dipartimento Di Scienze Mediche University 'a. Avogadro' Of Eastern Piedmont
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Buonfiglio Donatella
Laboratorio Di Immunologia Dipartimento Di Scienza Mediche University Of Turin At Novara
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Flafia Bottarel
Dipartimento Di Scienze Mediche University 'a. Avogadro' Of Eastern Piedmont
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Dianzani U
Interdisciplinary Research Center Of Autoimmune Disease Department Of Medical Sciences A. Avogadro U
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Bragardo Manuela
Dipartimento Di Scienze Mediche University 'a. Avogadro' Of Eastern Piedmont
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FEITO Maria
Laboratorio di Immunologia, Dipartimento di Scienza Mediche, University of Turin at Novara
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BRAGARDO Manuela
Laboratorio di Immunologia, Dipartimento di Scienza Mediche, University of Turin at Novara
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BONISSONI Sara
Laboratorio di Immunologia, Dipartimento di Scienza Mediche, University of Turin at Novara
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FLAFIA Bottarel
Laboratorio di Immunologia, Dipartimento di Scienza Mediche, University of Turin at Novara
関連論文
- CD44 signaling through p56^ involves lateral association with CD4 in human CD4^+ T cells
- Possible involvement of T cell co-stimulation in pustulosis palmaris et plantaris via the induction of inducible co-stimulator in chronic focal infections
- A co-stimulatory molecule on activated T cells, H4/ICOS, delivers specific signals in T_h cells and regulates their responses
- gp120s derived from four syncytiuminducing HIV-1 strains induce different patterns of CD4 association with lymphocyte surface molecules