Glycosylation defects and muscular dystrophy

Advances in Experimental Medicine and Biology

Volumn 564, Issue , 2005, Pages 97-98

  Blake, Derek J ^a   Esapa, Christopher T ^a   Martin Rendon, Enca ^b   McIlhinney, R A Jeffrey ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b NHS BLOOD AND TRANSPLANT   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

DYSTROGLYCAN; FUKUTIN; GLYCOSYLTRANSFERASE; LAMININ; PROTEASOME; FKRP PROTEIN, HUMAN; PROTEIN; CALNEXIN; FUKUTIN RELATED PROTEIN;

CONFERENCE PAPER; CONGENITAL DISORDER OF GLYCOSYLATION; ENDOPLASMIC RETICULUM; GENE MUTATION; GOLGI COMPLEX; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MISSENSE MUTATION; MUSCULAR DYSTROPHY; PRIORITY JOURNAL; PROTEIN DEFECT; PROTEIN GLYCOSYLATION; PROTEIN PROCESSING; ARTICLE; GENETICS; GLYCOSYLATION; METABOLISM; AMINO TERMINAL SEQUENCE; BRAIN MALFORMATION; CELL MIGRATION; CONGENITAL MUSCULAR DYSTROPHY TYPE 1C; FKRP GENE; GENETIC ASSOCIATION; LIMB GIRDLE MUSCULAR DYSTROPHY 2I; MENTAL DEFICIENCY; NOTE; PROTEIN DEGRADATION;

GLYCOSYLATION; HUMANS; MUSCULAR DYSTROPHIES; PROTEIN PROCESSING, POST-TRANSLATIONAL; PROTEINS;

EID: 33644848034     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/0-387-25515-X_15     Document Type: Conference Paper

References (3)

1. Brockington M et al., (2001) Am J. Hum. Genet. 69: 1198-209.
2. Esapa CT et al., (2002) Hum. Mol. Genet. 11: 3319-3331.
3. Martin-Rendon E and Blake DJ (2003) Trends Pharm. Sci. 24: 178-183.