Zobrazeno 1 - 8
of 8
pro vyhledávání: '"P T Reissmann"'
Publikováno v:
Journal of Cancer Research and Clinical Oncology. 125:61-70
Purpose: To study the structure and expression of the cyclin D1 and the epidermal growth factor receptor (EGFR) genes in a cohort of 298 non-small-cell lung cancer (NSCLC) specimens. Methods: Gene structure was studied by Southern analysis, and gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3907c78472a60e865eadcee2eb144802
https://doi.org/10.1007/s004320050243
https://doi.org/10.1007/s004320050243
Autor:
Graham Casey, P T Reissmann, Dennis J. Slamon, Wendy J. Levin, Juan Carlos Ramos, M. Jane Arboleda
Publikováno v:
Chest. 106:372S-376S
Non-small lung cancer (NSCLC) is a disease that exhibits multiple genetic lesions. Lung Cancer Study Group (LCSG) 871 was designed to analyze this group of malignancies for alterations in growth factors and/or their receptors, oncogenes, tumor suppre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7c1b8568ea9c8736fc318ae0e37e1ca2
https://doi.org/10.1378/chest.106.6_supplement.372s
https://doi.org/10.1378/chest.106.6_supplement.372s
Publikováno v:
Chest. 106:372S-376
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f30823fd7340a5b20d6ac4a021e549db
https://doi.org/10.1378/chest.106.6.372s
https://doi.org/10.1378/chest.106.6.372s
Publikováno v:
Journal of cancer research and clinical oncology. 125(2)
To study the structure and expression of the cyclin D1 and the epidermal growth factor receptor (EGFR) genes in a cohort of 298 non-small-cell lung cancer (NSCLC) specimens.Gene structure was studied by Southern analysis, and gene expression was stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::baffb2ea9cf0a86a91c3036fc4d0d3e7
https://pubmed.ncbi.nlm.nih.gov/10190311
https://pubmed.ncbi.nlm.nih.gov/10190311
Autor:
W J, Levin, M F, Press, R B, Gaynor, V P, Sukhatme, T C, Boone, P T, Reissmann, R A, Figlin, E C, Holmes, L M, Souza, D J, Slamon
Publikováno v:
Oncogene. 11(7)
In 1995, there will be 172,000 new cases of lung cancer diagnosed and 153,000 deaths from this disease in the United States. While the pathogenesis of the disease process is poorly understood, a growing body of evidence suggests that abnormalities in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::683588ff9d2940d2dd74d7ea0dccf8f8
https://pubmed.ncbi.nlm.nih.gov/7478546
https://pubmed.ncbi.nlm.nih.gov/7478546
Autor:
P T, Reissmann, H, Koga, R, Takahashi, R A, Figlin, E C, Holmes, S, Piantadosi, C, Cordon-Cardo, D J, Slamon
Publikováno v:
Oncogene. 8(7)
Mutations that prevent the normal expression of the retinoblastoma susceptibility gene (RB) have been linked to the pathogenesis of several human malignancies. Mutational inactivation of this tumor-suppressor gene appears to initiate the development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::72d36f8a905d73b8ca9e035cc6e0a49f
https://pubmed.ncbi.nlm.nih.gov/8390038
https://pubmed.ncbi.nlm.nih.gov/8390038
Autor:
Torsten Strohmeyer, Carlos Cordon-Cardo, Rolf Ackermann, Michael Hartmann, Dennis J. Slamon, P T Reissmann
Inactivation of the retinoblastoma gene (RB gene) is associated with the development of several human malignancies including retinoblastomas, some osteo- and soft tissue sarcomas, small cell lung cancer, and possibly breast and bladder cancers. To ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b20a26fcc0e3a44af7e5f80f415c21b
https://europepmc.org/articles/PMC52148/
https://europepmc.org/articles/PMC52148/
Publikováno v:
Oncogene. 4(7)
The retinoblastoma susceptibility gene, (RB), is a tumor suppressor gene which, when deleted is associated with the development of retinoblastoma. The observation that children with heritable retinoblastoma frequently develop second malignancies, pri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7194d5fa2413bea1e962024a10be1ba
https://pubmed.ncbi.nlm.nih.gov/2755701
https://pubmed.ncbi.nlm.nih.gov/2755701