在营养不良性大疱性表皮松解症中，锚原纤维缺陷是否具有特异性？就发病机制而言，这意味着什么？ - Suppr

Suppr

超能文献

Is there any specificity to defects of anchoring fibrils in epidermolysis bullosa dystrophica, and what does this mean in terms of pathogenesis?

作者信息

Briggaman R A

出版信息

J Invest Dermatol. 1985 May;84(5):371-3. doi: 10.1111/1523-1747.ep12265450.

DOI:10.1111/1523-1747.ep12265450

PMID:3889167

Abstract

摘要

相似文献

Is there any specificity to defects of anchoring fibrils in epidermolysis bullosa dystrophica, and what does this mean in terms of pathogenesis?在营养不良性大疱性表皮松解症中，锚原纤维缺陷是否具有特异性？就发病机制而言，这意味着什么？

J Invest Dermatol. 1985 May;84(5):371-3. doi: 10.1111/1523-1747.ep12265450.

[Immunofluorescence mapping for diagnosis of congenital epidermolysis bullosa].[免疫荧光定位用于先天性大疱性表皮松解症的诊断]

Actas Dermosifiliogr. 2010 Oct;101(8):673-82.

Epidermolysis bullosa dystrophica-recessive: a possible role of anchoring fibrils in the pathogenesis.隐性营养不良型大疱性表皮松解症：锚定原纤维在发病机制中的可能作用。

J Invest Dermatol. 1975 Aug;65(2):203-11. doi: 10.1111/1523-1747.ep12598208.

The carboxyl-terminal domain of type VII collagen is present at the basement membrane in recessive dystrophic epidermolysis bullosa.VII型胶原蛋白的羧基末端结构域存在于隐性营养不良性大疱性表皮松解症的基底膜中。

J Invest Dermatol. 1989 Apr;92(4):623-7. doi: 10.1111/1523-1747.ep12712167.

Ultrastructural findings in epidermolysis bullosa.大疱性表皮松解症的超微结构研究结果。

Arch Dermatol. 1993 Dec;129(12):1578-84.

Epidermolysis bullosa acquisita antigen and the carboxy terminus of type VII collagen have a common immunolocalization to anchoring fibrils and lamina densa of basement membrane.获得性大疱性表皮松解症抗原与VII型胶原的羧基末端在基底膜的锚定原纤维和致密板上具有共同的免疫定位。

Br J Dermatol. 1990 May;122(5):577-85. doi: 10.1111/j.1365-2133.1990.tb07278.x.

The basement membrane. Interface between the epithelium and the dermis: structural features.

Arch Dermatol. 1988 May;124(5):709-12. doi: 10.1001/archderm.124.5.709.

[Epidermolysis bullosa dystrophica dominans-a defect of the anchoring fibrils? (authors transl)].显性营养不良性大疱性表皮松解症——锚原纤维的一种缺陷？（作者译）

Dermatologica. 1973;147(5):289-98.

Comparative electron microscopic study between Mendes da Costa's disease and recessive epidermolysis bullosa dystrophica.

Br J Dermatol. 1978 May;98(5):529-36. doi: 10.1111/j.1365-2133.1978.tb01938.x.

Ultrastructure and molecular pathogenesis of epidermolysis bullosa.大疱性表皮松解症的超微结构与分子发病机制。

Clin Dermatol. 2011 Jul-Aug;29(4):412-9. doi: 10.1016/j.clindermatol.2011.01.010.

引用本文的文献

Autoantibodies to extracellular collagen matrix components in epidermolysis bullosa and other bullous diseases.大疱性表皮松解症及其他大疱性疾病中针对细胞外胶原基质成分的自身抗体。

Arch Dermatol Res. 1988;280(6):333-7. doi: 10.1007/BF00426610.

Mapping of epidermolysis bullosa simplex mutation to chromosome 12.

Am J Hum Genet. 1991 Nov;49(5):978-84.

Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa.人类VII型胶原蛋白：3号染色体上的基因（COL7A1）与显性营养不良型大疱性表皮松解症的遗传连锁关系。

Am J Hum Genet. 1991 Oct;49(4):797-803.

Exclusion of linkage between the collagenase gene and generalized recessive dystrophic epidermolysis bullosa phenotype.排除胶原酶基因与全身性隐性营养不良性大疱性表皮松解症表型之间的连锁关系。

J Clin Invest. 1991 Nov;88(5):1716-21. doi: 10.1172/JCI115489.

Genetic linkage of recessive dystrophic epidermolysis bullosa to the type VII collagen gene.隐性营养不良型大疱性表皮松解症与VII型胶原蛋白基因的遗传连锁。

J Clin Invest. 1992 Sep;90(3):1032-6. doi: 10.1172/JCI115916.

Genetic linkage of type VII collagen (COL7A1) to dominant dystrophic epidermolysis bullosa in families with abnormal anchoring fibrils.在具有异常锚定原纤维的家族中，VII型胶原蛋白（COL7A1）与显性营养不良性大疱性表皮松解症的遗传连锁关系。

J Clin Invest. 1992 Mar;89(3):974-80. doi: 10.1172/JCI115680.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验