Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors
Article
Rahner, Nils, Brockschmidt, Felix F., Steinke, Verena, Kahl, Philip, Becker, Tim, Vasen, Hans F. A.
, Wijnen, Juul T., Tops, Carli J. M., Holinski-Feder, Elke, Ligtenberg, Marjolijn J. L.
, Spruijt, Liesbeth, Görgens, Heike, Stemmler, Susanne, Kloor, Matthias, Dietmaier, Wolfgang, Schumacher, Johannes
, Nöthen, Markus M. and Propping, Peter
(2012)
Mutation and association analyses of the candidate genes ESR1, ESR2, MAX, PCNA, and KAT2A in patients with unexplained MSH2-deficient tumors.
Familial Cancer 11 (1), pp. 19-26.
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| Item type | Article | ||||
| Journal or Publication Title | Familial Cancer | ||||
| Publisher | SPRINGER | ||||
| Place of Publication | DORDRECHT | ||||
| Volume | 11 | ||||
| Number of Issue or Book Chapter | 1 | ||||
| Page Range | pp. 19-26 | ||||
| Date | 2012 | ||||
| Date of publication | 19 Dec 2024 09:42 | ||||
| Institutions | Medicine > Lehrstuhl für Pathologie | ||||
| Identification Number |
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| Keywords | NONPOLYPOSIS COLORECTAL-CANCER; DNA MISMATCH REPAIR; CELL NUCLEAR ANTIGEN; MICROSATELLITE INSTABILITY; CLINICAL-CRITERIA; LYNCH-SYNDROME; C-MYC; COMPLEX; MLH1; MSH2; Association study; ESR; HNPCC; KAT2A; Lynch syndrome; MAX; Mutation analysis; PCNA | ||||
| Dewey Decimal Classification | 600 Technology > 610 Medical sciences Medicine | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 63987 |
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