Fine J D, Johnson L B, Suchindran C M
Department of Dermatology, School of Medicine, University of North Carolina at Chapel Hill 27514.
J Invest Dermatol. 1994 Jun;102(6):54S-56S. doi: 10.1111/1523-1747.ep12388622.
Since its inception in 1986, the NEBR has proved to be an excellent example of how a relatively small allocation of federal research funds for the development of a registry of cases of a single rare disease can have a major impact on the rapid expansion in the depth of knowledge of not only the disease itself but of a number of associated biologic principles, including keratinization and epithelial cell-extracellular matrix interactions. At present, the NEBR is generating extensive clinical, laboratory, and demographic data, both from cross-sectional and longitudinal perspectives, as well as establishing a centralized cell and tissue bank that will serve the scientific community at large as a valuable resource for future basic research on this oftentimes devastating genetic disease.
自1986年成立以来,国家表皮松解性大疱病注册库(NEBR)已证明是一个绝佳范例,表明联邦政府为单一罕见病病例注册库的开发所拨出的相对少量研究资金,不仅能对该疾病本身的知识深度迅速拓展产生重大影响,还能对包括角质化和上皮细胞与细胞外基质相互作用在内的一些相关生物学原理的知识深度迅速拓展产生重大影响。目前,NEBR正在从横断面和纵向角度生成广泛的临床、实验室和人口统计学数据,同时还在建立一个集中的细胞和组织库,该库将作为这一常常具有毁灭性的遗传病未来基础研究的宝贵资源,为广大科学界服务。