DRUG TARGETING TO LYSOSOMES

被引：10

作者：

DUNCAN, R ^{[1
]}

KOPECEK, J ^{[1
]}

LLOYD, JB ^{[1
]}

机构：

[1] CZECHOSLOVAK ACAD SCI, INST MACROMOLEC SCI, CS-16206 PRAGUE 6, CZECHOSLOVAKIA

来源：

BIOCHEMICAL SOCIETY TRANSACTIONS | 1984年 / 12卷 / 06期

关键词：

D O I：

10.1042/bst0120913

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：913 / 915

页数：3

共 34 条

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[3]

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[4]

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[6]

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[7]

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[8] EFFECT OF MOLECULAR-SIZE OF I-125-LABELED POLY(VINYLPYRROLIDONE) ON ITS PINOCYTOSIS BY RAT VISCERAL YOLK SACS AND RAT PERITONEAL-MACROPHAGES [J].

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[9] PINOCYTOSIS OF POLY(ALPHA,BETA-(N-2-HYDROXYETHYL))-DL-ASPARTAMIDE AND A TYRAMINE DERIVATIVE BY RAT VISCERAL YOLK SACS CULTURED INVITRO - ABILITY OF PHENOLIC RESIDUES TO ENHANCE THE RATE OF PINOCYTIC CAPTURE OF A MACROMOLECULE [J].

DUNCAN, R ;

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[10] DEGRADATION OF SIDE-CHAINS OF N-(2-HYDROXYPROPYL) METHACRYLAMIDE CO-POLYMERS BY LYSOSOMAL-ENZYMES [J].

DUNCAN, R ;

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KOPECEK, J .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1980, 94 (01) :284-290

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