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Volumn 661, Issue , 2010, Pages 433-447
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Mutational and functional analysis in human Ras/MAP kinase genetic syndromes.
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Author keywords
[No Author keywords available]
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Indexed keywords
B RAF KINASE;
COMPLEMENTARY DNA;
DNA;
MITOGEN ACTIVATED PROTEIN KINASE KINASE 1;
MITOGEN ACTIVATED PROTEIN KINASE KINASE 2;
PROTEIN SERINE THREONINE KINASE;
ARTICLE;
CARDIOFACIOCUTANEOUS SYNDROME;
CELL STRAIN HEK293;
CONGENITAL HEART MALFORMATION;
ECTODERMAL DYSPLASIA;
ENZYME ASSAY;
ENZYMOLOGY;
FACIES;
FAILURE TO THRIVE;
GENETIC TRANSFECTION;
GENETICS;
GENOME;
HUMAN;
ISOLATION AND PURIFICATION;
METABOLISM;
METHODOLOGY;
MOLECULAR CLONING;
NUCLEOTIDE SEQUENCE;
POINT MUTATION;
SIGNAL TRANSDUCTION;
SYNDROME;
WESTERN BLOTTING;
BASE SEQUENCE;
BLOTTING, WESTERN;
CLONING, MOLECULAR;
DNA;
DNA MUTATIONAL ANALYSIS;
DNA, COMPLEMENTARY;
ECTODERMAL DYSPLASIA;
ENZYME ASSAYS;
FACIES;
FAILURE TO THRIVE;
GENOME;
HEART DEFECTS, CONGENITAL;
HEK293 CELLS;
HUMANS;
MAP KINASE KINASE 1;
MAP KINASE KINASE 2;
MAP KINASE SIGNALING SYSTEM;
POINT MUTATION;
PROTEIN-SERINE-THREONINE KINASES;
PROTO-ONCOGENE PROTEINS B-RAF;
SYNDROME;
TRANSFECTION;
MLCS;
MLOWN;
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EID: 79952112081
PISSN: None
EISSN: 19406029
Source Type: Journal
DOI: 10.1007/978-1-60761-795-2_27 Document Type: Article |
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Times cited : (11)
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References (0)
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