White R, Viskochil D, O'Connell P
Howard Hughes Medical Institute, Salt Lake City, Utah.
Curr Opin Neurobiol. 1991 Oct;1(3):462-7. doi: 10.1016/0959-4388(91)90070-n.
Elucidation of the partial genomic structure and DNA sequence of the gene that is altered in neurofibromatosis type 1, and the discovery of clues to its function, have opened new opportunities not only for understanding this particular disease process but also for clarifying signal pathways involved in cellular growth and differentiation. (This review is an updated and modified version of a review first published in Current Opinion in Genetics and Development 1991, 1:15-19.)
对1型神经纤维瘤病中发生改变的基因的部分基因组结构和DNA序列的阐明,以及对其功能线索的发现,不仅为理解这一特定疾病过程,也为阐明细胞生长和分化所涉及的信号通路开辟了新的机遇。(本综述是首次发表于《遗传学与发育学当前观点》1991年第1卷第15 - 19页的一篇综述的更新和修订版。)