Zobrazeno 1 - 10
of 17
pro vyhledávání: '"G E, Tomlinson"'
Publikováno v:
Cancer research. 61(21)
Gamma-radiation results in cell cycle arrest and apoptosis in a wide variety of cells. Cell cycle arrest provides time for the cell to repair damaged DNA before entering the next phase of the cycle. If the damage is severe and cannot be repaired, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::585a345fd928b6311ffe6f7abd182e67
https://pubmed.ncbi.nlm.nih.gov/11691798
https://pubmed.ncbi.nlm.nih.gov/11691798
Publikováno v:
The Journal of family practice. 49(12)
Primary care physicians will be providing longitudinal health care for long-term survivors of childhood acute lymphoblastic leukemia (ALL) with increasing frequency. Late effects (sequelae) secondary to treatment with radiation or chemotherapeutic ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b427b87ffb9db22beeb4254ee821d2b
https://pubmed.ncbi.nlm.nih.gov/11132063
https://pubmed.ncbi.nlm.nih.gov/11132063
Autor:
I I, Wistuba, G E, Tomlinson, C, Behrens, A, Virmani, J, Geradts, J L, Blum, J D, Minna, A F, Gazdar
Publikováno v:
Genes, chromosomescancer. 28(4)
Monozygotic twins, each of whom has breast cancer, offer a natural study population for gene-environmental interactions as causation of cancer, because they are genetically identical. If heritable factors play a large role in the origin of a neoplasm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2a839c2ecfedae4bd35e104f3dd80808
https://pubmed.ncbi.nlm.nih.gov/10862044
https://pubmed.ncbi.nlm.nih.gov/10862044
Publikováno v:
Cancer. 88(7)
The objective of the current study was to describe a multidisciplinary transition program for following young adult survivors of childhood cancer in an adult-based ambulatory medical setting and to report the late effects with grades of toxicity diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fceeff519af95d57362c6b49e6b9a59e
https://pubmed.ncbi.nlm.nih.gov/10738228
https://pubmed.ncbi.nlm.nih.gov/10738228
Publikováno v:
Cancer research. 59(15)
Mutations in BRCA1 and BRCA2 account for the majority of familial breast cancers. Cells with mutated BRCA1 or BRCA2 are hypersensitive to ionizing radiation (IR) and exhibit defective DNA repair. Both BRCA1 and BRCA2 have been reported to bind Rad51,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8f0064eb30f391d00489c3065b2efc17
https://pubmed.ncbi.nlm.nih.gov/10446958
https://pubmed.ncbi.nlm.nih.gov/10446958
Autor:
G E, Tomlinson, T T, Chen, V A, Stastny, A K, Virmani, M A, Spillman, V, Tonk, J L, Blum, N R, Schneider, I I, Wistuba, J W, Shay, J D, Minna, A F, Gazdar
Publikováno v:
Cancer research. 58(15)
A tumor cell line, HCC1937, was established from a primary breast carcinoma from a 24-year-old patient with a germ-line BRCA1 mutation. A corresponding B-lymphoblastoid cell line was established from the patient's peripheral blood lymphocytes. BRCA1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::184b4f0c8cdd250736b04f6cd1fa46a2
https://pubmed.ncbi.nlm.nih.gov/9699648
https://pubmed.ncbi.nlm.nih.gov/9699648
Publikováno v:
Cancer research. 58(8)
3p deletion, a common chromosome defect in lung cancer, occurs more frequently in the lung tumor tissues of smoking patients than it does in those of nonsmoking patients. This pilot study evaluated whether 3p aberrations induced by benzo[a]pyrene dio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1371a4cce8c0e51e97d4100545ac2488
https://pubmed.ncbi.nlm.nih.gov/9563468
https://pubmed.ncbi.nlm.nih.gov/9563468
Autor:
M, Ahmadian, I I, Wistuba, K M, Fong, C, Behrens, D R, Kodagoda, M H, Saboorian, J, Shay, G E, Tomlinson, J, Blum, J D, Minna, A F, Gazdar
Publikováno v:
Cancer research. 57(17)
The FHIT gene, which spans the FRA3B fragile site at chromosome 3p14.2, is a candidate tumor suppressor gene in breast and other cancers. We investigated FHIT and FRA3B for loss of heterozygosity (LOH); homozygous deletions; abnormal transcripts; and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4e5719b8ff6c1ac02b257c6f1c778cd9
https://pubmed.ncbi.nlm.nih.gov/9288768
https://pubmed.ncbi.nlm.nih.gov/9288768
Publikováno v:
Genes, chromosomescancer. 19(4)
We report four cases of hepatoblastoma with a derivative chromosome 4 from an unbalanced translocation between the long arms of chromosomes 1 and 4, an aberration reported only rarely in isolated cases of other types of neoplasms. The abnormality in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::63f9fd133063449575ae9a131f719010
https://pubmed.ncbi.nlm.nih.gov/9258666
https://pubmed.ncbi.nlm.nih.gov/9258666
Autor:
G E, Tomlinson
Publikováno v:
Cancer treatment and research. 92
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::148e361ea222bb0ff399b81841a40277
https://pubmed.ncbi.nlm.nih.gov/9494758
https://pubmed.ncbi.nlm.nih.gov/9494758