Multiple forms of BRMS1 are differentially expressed in the MCF10 isogenic breast cancer progression model

Clinical and Experimental Metastasis

Volumn 26, Issue 2, 2009, Pages 89-96

  Hurst, Douglas R ^a   Xie, Yi ^a   Edmonds, Mick D ^a   Welch, Danny R ^a,b,c,d  

^a University of Alabama at Birmingham   (United States)

^b UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

^c University of Alabama at Birmingham   (United States)

^d UNIVERSITY OF ALABAMA AT BIRMINGHAM   (United States)

Author keywords

Breast cancer progression; Co immunoprecipitation; Metastasis; Splice variant; Synonymous transition

Indexed keywords

BRMS1 PROTEIN; EPITOPE; GENOMIC DNA; MESSENGER RNA; PROTEIN; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BREAST CANCER; CANCER CELL; CONTROLLED STUDY; HUMAN; HUMAN CELL; LUNG METASTASIS; METASTASIS; METASTASIS SUPPRESOR GENE BRMS1; METASTASIS SUPPRESSOR GENE; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; NUDE MOUSE; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TUMOR SUPPRESSOR GENE; WESTERN BLOTTING;

ALTERNATIVE SPLICING; AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BREAST NEOPLASMS; CELL LINE; CELL TRANSFORMATION, NEOPLASTIC; FEMALE; HUMANS; LUNG NEOPLASMS; MICE; MICE, NUDE; MOLECULAR SEQUENCE DATA; NEOPLASM INVASIVENESS; NEOPLASM PROTEINS; NEOPLASM TRANSPLANTATION; PROTEIN ISOFORMS; RNA, MESSENGER; TRANSPLANTATION, HETEROLOGOUS;

EID: 60449091248     PISSN: 02620898     EISSN: 15737276     Source Type: Journal    
DOI: 10.1007/s10585-008-9216-9     Document Type: Article

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