The Genetic Basis of a Craniofacial Disease Provides Insight into COPII Coat Assembly

Developmental Cell

Volumn 13, Issue 5, 2007, Pages 623-634

  Fromme, J Christopher ^a   Ravazzola, Mariella ^b   Hamamoto, Susan ^a   Al Balwi, Mohammed ^c   Eyaid, Wafaa ^d   Boyadjiev, Simeon A ^e   Cosson, Pierre ^b   Schekman, Randy ^a   Orci, Lelio ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF GENEVA MEDICAL SCHOOL   (Switzerland)

^c KING SAUD BIN ABDULAZIZ UNIVERSITY FOR HEALTH SCIENCES   (Saudi Arabia)

^d KING FAHAD MEDICAL CITY   (Saudi Arabia)

^e UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

CELLBIO; HUMDISEASE

Indexed keywords

COAT PROTEIN COMPLEX II; CYTOPLASM PROTEIN; PROTEIN SAR1; PROTEIN SEC13; PROTEIN SEC31; PROTEIN SEC324; UNCLASSIFIED DRUG;

ARTICLE; BINDING AFFINITY; CELL MEMBRANE; CELL VACUOLE; COMPLEX FORMATION; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; CRANIOLENTICULOSUTURAL DYSPLASIA; ENDOPLASMIC RETICULUM; HUMAN; HUMAN CELL; HUMAN TISSUE; IN VITRO STUDY; IN VIVO STUDY; MISSENSE MUTATION; MUTANT; PARALOGY; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN ASSEMBLY;

AMINO ACID SEQUENCE; CARRIER PROTEINS; CELL MEMBRANE; CELLS, CULTURED; COP-COATED VESICLES; CRANIOFACIAL ABNORMALITIES; ENDOPLASMIC RETICULUM; FIBROBLASTS; HUMANS; MEMBRANE FUSION; MODELS, MOLECULAR; MOLECULAR SEQUENCE DATA; MONOMERIC GTP-BINDING PROTEINS; MUTATION; OSTEOBLASTS; PROTEIN TRANSPORT; VESICULAR TRANSPORT PROTEINS;

EID: 35548961813     PISSN: 15345807     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.devcel.2007.10.005     Document Type: Article

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