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pro vyhledávání: '"T G, Krontiris"'
Autor:
T G, Krontiris
Publikováno v:
New England Journal of Medicine. 333:303-306
Autor:
J N, Weitzel, S, Ding, G P, Larson, R A, Nelson, A, Goodman, E C, Grendys, H G, Ball, T G, Krontiris
Publikováno v:
Cancer research. 60(2)
Approximately 10% of ovarian cancers are due to mutations in highly penetrant inherited cancer susceptibility genes. The highly polymorphic HRAS1 minisatellite locus, located just downstream from the proto-oncogene H-ras-1 on chromosome 11p, consists
Publikováno v:
American journal of human genetics. 47(5)
Three genetic markers within the promoter-exon 1 region of the HRAS1 locus have been employed to investigate lineage relationships among alleles of the highly polymorphic variable tandem repeat (VTR) immediately downstream of the HRAS1 gene. These ma
Autor:
H, Sugimura, N E, Caporaso, R V, Modali, R N, Hoover, J H, Resau, B F, Trump, J A, Longergan, T G, Krontiris, D L, Mann, A, Weston
Publikováno v:
Cancer research. 50(6)
The hypothesis that rare variable nucleotide tandem repeat alleles of the Ha-ras-1 polymorphism are an inherited predisposing factor in human lung carcinogenesis has been evaluated in an age, race, and smoking matched case-control study. Twenty-three
Autor:
T G, Krontiris
Publikováno v:
Birth defects original article series. 26(1)
Autor:
M, Colb, T G, Krontiris
Publikováno v:
Advances in internal medicine. 31
Many of the genes that are likely participants in the pathogenesis of human neoplasia have been identified. The major classes of events that activate these genes in tumors have also been described. We expect that continuing research on the function o
Publikováno v:
American journal of human genetics. 45(5)
We have detected a 6-bp deletion in the untranslated first exon of a unique HRAS1 gene cloned from lymphocyte DNA of a familial melanoma patient. The deletion is without apparent functional consequence. Using an RNase protection assay, we have demons
Publikováno v:
Cancer research. 48(22)
We have prospectively examined 66 consecutive initial diagnostic lymph node biopsies from unselected patients suspected of having malignant lymphoma for clonal immunophenotypic and immunogenotypic markers. By morphological and cell surface phenotypic