Adhesion molecules and inherited diseases of the human nervous system

Annual Review of Neuroscience

Volumn 21, Issue , 1998, Pages 97-125

  Kamiguchi, H ^a   Hlavin, M L ^b   Yamasaki, M ^a,c   Lemmon, V ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b CASE WESTERN RESERVE UNIVERSITY   (United States)

^c OSAKA NATIONAL HOSPITAL   (Japan)

Author keywords

Charcot Marie Tooth disease; Muscular dystrophy; X linked hydrocephalus

Indexed keywords

CELL ADHESION MOLECULE; MEROSIN;

CORPUS CALLOSUM; GENE MUTATION; MUSCULAR DYSTROPHY; MYELINATION; PRIORITY JOURNAL; PYRAMIDAL TRACT; REVIEW; SYNDROME;

CELL ADHESION MOLECULES, NEURONAL; HUMANS; MUTATION; NERVOUS SYSTEM DISEASES;

EID: 0031948880     PISSN: 0147006X     EISSN: None     Source Type: Book Series    
DOI: 10.1146/annurev.neuro.21.1.97     Document Type: Review

References (6)

1. Anton ES, Sandrock AW, Matthew WD. 1994. Merosin promotes neurite growth and Schwann cell migration in vitro and nerve regeneration in vivo: evidence using an antibody to merosin, ARM-1. Dev. Biol. 164:133-16
2. Barami K, Kirschenbaum B, Lemmon V, Goldman SA. 1994. N-cadherin and NgCAM/8D9 are involved serially in the migration of newly generated neurons into the adult songbird brain. Neuron 13:567-82
3. Batemann A, Jouet M, MacFarlane J, Du J-S, Kenwrick S, Chothia C. 1996. Outline structure of the human L1 cell adhesion molecule and the sites where mutations cause neurological disorders. EMBO J 15:6050-59
4. Bianchine JW, Lewis RC. 1974. The MASA syndrome: a new heritable mental retardation syndrome. Clin. Genet. 5:298-306
5. Zhao X, Siu CH. 1995. Colocalization of the homophilic binding site and the neuritogenic activity of the cell adhesion molecule L1 to its second Ig-like domain. J. Biol. Chem. 270:29413-21
6. Zhao X, Siu CH. 1996. Differential effects of two hydrocephalus/MASA syndrome-related mutations on the homophilic binding and neuritogenic activities of the cell adhesion molecule L1. J. Biol. Chem. 271:6563-66