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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. ; Propping, Peter

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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Details

Item typeArticle
Journal or Publication TitleFamilial Cancer
PublisherSPRINGER
Place of PublicationDORDRECHT
Volume11
Number of Issue or Book Chapter1
Page Rangepp. 19-26
Date2012
Date of publication19 Dec 2024 09:42
InstitutionsMedicine > Lehrstuhl für Pathologie
Identification Number
ValueType
10.1007/s10689-011-9489-zDOI
KeywordsNONPOLYPOSIS 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 Classification600 Technology > 610 Medical sciences Medicine
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgYes
Item ID63987

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