络丝蛋白 (英语:Reelin )是一种分泌于细胞外基质 的大型糖蛋白 ,用于在大脑 的发育中通过细胞-细胞相互作用 调控神经元的迁移和定位。
Articles, publications, webpages[ 编辑 ]
Reelin gene expression in mice . Brain Gene Expression Map. St. Jude Children’s Research Hospital. [2008-08-23 ] . (原始内容 存档于2005-01-23).
Schematic representation of signaling through the LDLR family members apoER2 and VLDL receptor . [2008-08-23 ] . [永久失效链接 ] – A figure from Beffert U, Stolt PC, Herz J. Functions of lipoprotein receptors in neurons . J. Lipid Res. March 2004, 45 (3): 403–9. PMID 14657206 . doi:10.1194/jlr.R300017-JLR200 .
Proposed mechanism by which mouse RELN promoter regulate reelin gene expression . Proc. Natl. Acad. Sci. USA. [2008-08-23 ] . (原始内容存档 于2007-12-25). – A figure from Dong E, Agis-Balboa RC, Simonini MV, Grayson DR, Costa E, Guidotti A. Reelin and glutamic acid decarboxylase67 promoter remodeling in an epigenetic methionine-induced mouse model of schizophrenia . Proc. Natl. Acad. Sci. U.S.A. August 2005, 102 (35): 12578–83. PMC 1194936 . PMID 16113080 . doi:10.1073/pnas.0505394102 .
Corticogenesis in wild-type, reeler mutant and β1 deficient mice . [2008-08-23 ] . (原始内容 存档于2007-12-24). Pictorial rendition of the difference that the lack of reelin brings to the cortical structure – A figure from Magdaleno SM, Curran T. Brain development: integrins and the Reelin pathway. Curr. Biol. December 2001, 11 (24): R1032–5. PMID 11747842 . doi:10.1016/S0960-9822(01)00618-2 .
Effects of human and naturally occurring mouse RELN mutations on the predicted protein . Nature Genetics. [2008-08-23 ] . (原始内容存档 于2007-12-15). A figure from Hong SE; Shugart YY; Huang DT; et al. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat. Genet. September 2000, 26 (1): 93–6. PMID 10973257 . doi:10.1038/79246 .
MRI analysis of chromosome 7q22-linked lissencephaly with cerebellar hypoplasia . Nature Genetics. [2008-08-23 ] . (原始内容存档 于2007-12-15). – A figure from Hong et al.