MURAMYL DIPEPTIDE BOUND TO POLY-L-LYSINE SUBSTITUTED WITH MANNOSE AND GLUCONOYL RESIDUES AS MACROPHAGE ACTIVATORS

被引：70

作者：

DERRIEN, D

MIDOUX, P

PETIT, C

NEGRE, E

MAYER, R

MONSIGNY, M

ROCHE, AC

机构：

[1] INSERM, CNRS,CTR BIOPHYS MOLEC, DEPT BIOCHIM GLYCOCONJUGUES & LECTINES ENDOGENES, 1 RUE HAUTE, F-45071 ORLEANS 02, FRANCE

[2] UNIV ORLEANS, F-45071 ORLEANS, FRANCE

来源：

GLYCOCONJUGATE JOURNAL | 1989年 / 6卷 / 02期

关键词：

D O I：

10.1007/BF01050652

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：241 / 255

页数：15

共 46 条

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[7] DUNCAN R, 1985, Critical Reviews in Therapeutic Drug Carrier Systems, V1, P281
[8] ERADICATION OF SPONTANEOUS METASTASES AND ACTIVATION OF ALVEOLAR MACROPHAGES BY INTRAVENOUS-INJECTION OF LIPOSOMES CONTAINING MURAMYL DIPEPTIDE
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[10] Fields R, 1972, Methods Enzymol, V25, P464, DOI 10.1016/S0076-6879(72)25042-X

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