Is loss of heterozygosity at 9q22.3 (PTCH gene) and 19p13.3 (STK11 gene) involved in the pathogenesis of ovarian stromal tumors?

Human Pathology

Volumn 36, Issue 7, 2005, Pages 792-796

  Tsuji, Takahiro ^a   Catasus, Lluis ^a   Prat, Jaime ^a  

^a UNIVERSITAT AUTÒNOMA DE BARCELONA   (Spain)

Author keywords

19p13.3; 9q22.3; Cellular fibroma; Gorlin syndrome; Human homologue of Drosophila patched (PTCH) gene; Loss of heterozygosity; Luteinized thecoma

Indexed keywords

PROTEIN KINASE LKB1; PROTEIN PATCHED;

ADULT; AGED; ALLELE; ARTICLE; CONTROLLED STUDY; FEMALE; FIBROMA; FIBROSARCOMA; GENETIC ASSOCIATION; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; MICROSATELLITE MARKER; OVARY TUMOR; PATHOGENESIS; THECOMA;

ADULT; AGED; BASAL CELL NEVUS SYNDROME; CHROMOSOMES, HUMAN, PAIR 19; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; FIBROMA; GENETIC MARKERS; HUMANS; LOSS OF HETEROZYGOSITY; LUTEAL CELLS; LUTEIN; MICROSATELLITE REPEATS; MIDDLE AGED; OVARIAN NEOPLASMS; POLYMERASE CHAIN REACTION; PROTEIN-SERINE-THREONINE KINASES; RECEPTORS, CELL SURFACE; STROMAL CELLS; THECOMA;

EID: 23444445658     PISSN: 00468177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.humpath.2005.05.009     Document Type: Article

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