TYPE-VII COLLAGEN AND 19-DEJ-1 ANTIGEN - COMPARISON OF EXPRESSION IN INVERSA AND GENERALIZED VARIANTS OF RECESSIVE DYSTROPHIC EPIDERMOLYSIS-BULLOSA

被引：15

作者：

FINE, JD

JOHNSON, LB

WRIGHT, T

机构：

[1] UNIV N CAROLINA,SCH MED,DEPT DERMATOL,CHAPEL HILL,NC 27514

[2] UNIV ALABAMA,SCH DENT,DEPT PEDIAT DENT,BIRMINGHAM,AL 35294

[3] NATL EPIDERMOLYSIS BULLOSA REGISTRY,SO CLIN CTR,CHAPEL HILL,NC

来源：

ARCHIVES OF DERMATOLOGY | 1990年 / 126卷 / 12期

关键词：

D O I：

10.1001/archderm.126.12.1587

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

引用

页码：1587 / 1593

页数：7

共 26 条

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[2] TYPE-VII COLLAGEN IS EXPRESSED BUT ANCHORING FIBRILS ARE DEFECTIVE IN DYSTROPHIC EPIDERMOLYSIS-BULLOSA INVERSA
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[5] KF-1 MONOCLONAL-ANTIBODY DEFINES A SPECIFIC BASEMENT-MEMBRANE ANTIGEN DEFECT IN DYSTROPHIC FORMS OF EPIDERMOLYSIS BULLOSA
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[7] CHONDROITIN 6-SULFATE PROTEOGLYCAN BUT NOT HEPARAN-SULFATE PROTEOGLYCAN IS ABNORMALLY EXPRESSED IN SKIN BASEMENT-MEMBRANE FROM PATIENTS WITH DOMINANT AND RECESSIVE DYSTROPHIC EPIDERMOLYSIS BULLOSA
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[9] 19-DEJ-1, A HEMIDESMOSOME-ANCHORING FILAMENT COMPLEX-ASSOCIATED MONOCLONAL-ANTIBODY - DEFINITION OF A NEW SKIN BASEMENT-MEMBRANE ANTIGENIC DEFECT IN JUNCTIONAL AND DYSTROPHIC EPIDERMOLYSIS BULLOSA
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[10] 19-DEJ-1, A MONOCLONAL-ANTIBODY TO THE HEMIDESMOSOME-ANCHORING FILAMENT COMPLEX, IS THE ONLY RELIABLE IMMUNOHISTOCHEMICAL PROBE FOR ALL MAJOR FORMS OF JUNCTIONAL EPIDERMOLYSIS-BULLOSA
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