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20 July 1998
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Contrasting sites for expression of MIP-3α and MIP-3β in human tonsils. In vivo MIP-3α (top) and MIP-3β (bottom) expression by in situ hybridization of tonsils. The two darkfield illuminations represent the same area (serial cryostat sections; original magnification: ×40). mRNA for MIP-3α (top) is detected at high levels in epithelial crypts only, whereas MIP-3β expression (bottom) is restricted to T cell–rich areas. MIP-3α and MIP-3β attract immature and mature dendritic cells, respectively. See related article in this issue by Dieu et al., pp. 373–386.
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ISSN 0022-1007
EISSN 1540-9538
In this Issue
Article
gp100/pmel 17 Is a Murine Tumor Rejection Antigen: Induction of “Self”-reactive, Tumoricidal T Cells Using High-affinity, Altered Peptide Ligand
Willem W. Overwijk,Allan Tsung,Kari R. Irvine,Maria R. Parkhurst,Theresa J. Goletz,Kangla Tsung,Miles W. Carroll,Chunlei Liu,Bernard Moss,Steven A. Rosenberg,Nicholas P. Restifo
Cerebral Ischemia Enhances Polyamine Oxidation: Identification of Enzymatically Formed 3-Aminopropanal as an Endogenous Mediator of Neuronal and Glial Cell Death
Svetlana Ivanova,Galina I. Botchkina,Yousef Al-Abed,Malcolm Meistrell, III,Franak Batliwalla,Janet M. Dubinsky,Constantino Iadecola,Haichao Wang,Peter K. Gregersen,John W. Eaton,Kevin J. Tracey
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