Mutations in the cell adhesion molecule LI cause mental retardation
- 1 April 1995
- journal article
- review article
- Published by Elsevier in Trends in Neurosciences
- Vol. 18 (4) , 168-172
- https://doi.org/10.1016/0166-2236(95)93896-6
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Ankyrin binding activity shared by the neurofascin/L1/NrCAM family of nervous system cell adhesion molecules.Journal of Biological Chemistry, 1994
- X–linked spastic paraplegia (SPG1), MASA syndrome and X–linked hydrocephalus result from mutations in the L1 geneNature Genetics, 1994
- Sensitivity of neurite outgrowth to microfilament disruption varies with adhesion molecule substrateJournal of Neurobiology, 1993
- Modulation of growth cone morphology by substrate-bound adhesion moleculesCell Motility, 1992
- Assignment of X-linked hydrocephalus to Xq28 by linkage analysisGenomics, 1990
- The gene encoding L1, a neural adhesion molecule of the immunoglobulin family, is located on the X chromosome in mouse and manGenomics, 1990
- Distinct roles for adhesion molecules during innervation of embryonic chick muscleDevelopmental Biology, 1988
- Involvement of the nerve growth factor-inducible large external glycoprotein (NILE) in neurite fasciculation in primary cultures of rat brain.Proceedings of the National Academy of Sciences, 1985
- L1 mono- and polyclonal antibodies modify cell migration in early postnatal mouse cerebellumNature, 1983
- HEREDITARY STENOSIS OF THE AQUEDUCT OF SYLVIUS AS A CAUSE OF CONGENITAL HYDROCEPHALUSBrain, 1949