Publication Listing for the MeSH term frequent loss. Found 4 abstracts

Dong XY, Guo P, Boyd J, Sun XD, Li QN, Zhou W, Dong JT. Implication of snoRNA U50 in human breast cancer. Journal of Genetics and Genomics. 2009 Aug;36(8):447-54.   PMCID: PMCID: PMC2854654

Hamilton TC, Berek JS, Kaye SB. Basic research: how much do we know, and what are we likely to learn about ovarian cancer in the near future?. Annals of Oncology. 1999 Jan;10:69-73.

Boente MP, Godwin AK, Hogan WM. Screening, Imaging, and Early Diagnosis of Ovarian-Cancer. Clinical obstetrics and gynecology. 1994 Jun;37(2):377-91.

Godwin AK, Vanderveer L, Schultz DC, Lynch HT, Altomare DA, Buetow KH, Daly M, Getts LA, Masny A, Rosenblum N, Hogan M, Ozols RF, Hamilton TC. A Common Region of Deletion on Chromosome 17q in Both Sporadic and Familial Epithelial Ovarian-Tumors Distal to Brcai. American journal of human genetics. 1994 Oct;55(4):666-77.

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heterozygosity frequent loss p53 gene carcinomas serum markers rna spontaneous transformation identification prostate-cancer regions 6q receptor gene familial breast losses tumor-suppressor gene U50 allele loss dinucleotide repeat polymorphism linkage genes ca 125 suppressor tumor suppressor gene ROSE incessant ovulation surface epithelial-cells allelic loss snoRNA benign oral-contraceptives BRCA1 low-grade deletion unit breast cancer tumors distal ovarian tumours experimental mod candidate breast-cancer risk