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Volumn 275, Issue 47, 2000, Pages 36920-36926

The human synaptotagmin IV gene defines an evolutionary break point between syntenic mouse and human chromosome regions but retains ligand inducibility and tissue specificity

(4) Ferguson, Gregory D a,c Chen, Xiao Ning b Korenberg, Julie R b Herschman, Harvey R a,b

a UNIVERSITY OF CALIFORNIA (United States)

b UNIVERSITY OF CALIFORNIA (United States)

c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LIGAND; SYNAPTOTAGMIN;

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME; CHROMOSOME 18Q; CHROMOSOME MAP; CONTROLLED STUDY; EVOLUTION; GENE; GENETIC ANALYSIS; HIPPOCAMPUS; HUMAN; HUMAN CELL; MEMORY; NEUROBLASTOMA CELL; NONHUMAN; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SYNAPSE VESICLE; SYNTENY; TISSUE SPECIFICITY;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CALCIUM-BINDING PROTEINS; CHROMOSOME BANDING; CHROMOSOMES; EVOLUTION, MOLECULAR; HUMANS; IN SITU HYBRIDIZATION; LIGANDS; MEMBRANE GLYCOPROTEINS; MICE; MOLECULAR SEQUENCE DATA; NERVE TISSUE PROTEINS; NEUROBLASTOMA; RATS; SYNAPTOTAGMINS; TUMOR CELLS, CULTURED;

CAENORHABDITIS ELEGANS; RODENTIA; STAPHYLOCOCCUS PHAGE 3A;

EID: 0034711269 PISSN: 00219258 EISSN: None Source Type: Journal
DOI: 10.1074/jbc.M005801200 Document Type: Article

Times cited : (9)

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