Editing Reelin (section)

== Further reading ==
{{Commons category}}
{{refbegin}}
* {{cite journal | vauthors = Fatemi SH | title = Reelin glycoprotein: structure, biology and roles in health and disease | journal = Molecular Psychiatry | volume = 10 | issue = 3 | pages = 251–257 | date = March 2005 | pmid = 15583703 | doi = 10.1038/sj.mp.4001613 | publisher = Springer | isbn = 978-0-387-76760-4 | s2cid = 21206951 }}
* {{cite journal | vauthors = Förster E, Jossin Y, Zhao S, Chai X, Frotscher M, Goffinet AM | title = Recent progress in understanding the role of Reelin in radial neuronal migration, with specific emphasis on the dentate gyrus | journal = The European Journal of Neuroscience | volume = 23 | issue = 4 | pages = 901–9 | date = February 2006 | pmid = 16519655 | doi = 10.1111/j.1460-9568.2006.04612.x | s2cid = 25269492 }}
* {{cite journal | vauthors = Beffert U, Stolt PC, Herz J | title = Functions of lipoprotein receptors in neurons | journal = Journal of Lipid Research | volume = 45 | issue = 3 | pages = 403–9 | date = March 2004 | pmid = 14657206 | doi = 10.1194/jlr.R300017-JLR200 | doi-access = free }}
* {{cite journal | vauthors = Dong E, Agis-Balboa RC, Simonini MV, Grayson DR, Costa E, Guidotti A | title = Reelin and glutamic acid decarboxylase67 promoter remodeling in an epigenetic methionine-induced mouse model of schizophrenia | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 102 | issue = 35 | pages = 12578–83 | date = August 2005 | pmid = 16113080 | pmc = 1194936 | doi = 10.1073/pnas.0505394102 | bibcode = 2005PNAS..10212578D | doi-access = free }}
* {{cite journal | vauthors = Magdaleno SM, Curran T | title = Brain development: integrins and the Reelin pathway | journal = Current Biology | volume = 11 | issue = 24 | pages = R1032-5 | date = December 2001 | pmid = 11747842 | doi = 10.1016/S0960-9822(01)00618-2 | s2cid = 8790079 | doi-access = free | bibcode = 2001CBio...11R1032M }}
* {{cite journal | vauthors = Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA | title = Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations | journal = Nature Genetics | volume = 26 | issue = 1 | pages = 93–6 | date = September 2000 | pmid = 10973257 | doi = 10.1038/79246 | s2cid = 67748801 }}
{{refend}}