Focal Defects in Single-Celled Tubes Mutant for Cerebral Cavernous Malformation 3, GCKIII, or NSF2

Developmental Cell

Volumn 25, Issue 5, 2013, Pages 507-519

  Song, Yanjun ^a   Eng, Melissa ^a   Ghabrial, Amin S ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CEREBRAL CARVERNOUS MALFORMATION 3; GERMINAL CENTER KINASE III; N ETHYLMALEIMIDE SENSITIVE FACTOR; N ETHYLMALEIMIDE SENSITIVE FACTOR 2; PROTEIN; PROTEIN CRUMBS; PROTEIN VARICOSE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CCM3 GENE; CONTROLLED STUDY; DROSOPHILA; GENE; GENETIC ANALYSIS; LOSS OF FUNCTION MUTATION; LOTUS GENE; MORPHOLOGY; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RNA INTERFERENCE; TRACHEA; WHEEZY GENE;

ALLELES; AMINO ACID SEQUENCE; ANIMALS; APOPTOSIS REGULATORY PROTEINS; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; GENETIC COMPLEMENTATION TEST; GENOTYPE; MEMBRANE PROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; N-ETHYLMALEIMIDE-SENSITIVE PROTEINS; PHENOTYPE; PROTEIN-SERINE-THREONINE KINASES; PROTO-ONCOGENE PROTEINS; SEQUENCE HOMOLOGY, AMINO ACID; TRACHEA;

EID: 84878963613     PISSN: 15345807     EISSN: 18781551     Source Type: Journal    
DOI: 10.1016/j.devcel.2013.05.002     Document Type: Article

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