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ZAR1 is a novel epigenetically inactivated tumour suppressor in lung cancer.
Clin Epigenetics. 2017 Jun 2;9:60. doi: 10.1186/s13148-017-0360-4. eCollection 2017.
Clin Epigenetics. 2017.
PMID: 28588743
Free PMC article.
Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants.
Köger N, Brieger A, Hinrichsen IM, Zeuzem S, Plotz G.
Köger N, et al.
Hum Mutat. 2019 Apr;40(4):472-482. doi: 10.1002/humu.23709. Epub 2019 Jan 24.
Hum Mutat. 2019.
PMID: 30653782
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Functional testing strategy for coding genetic variants of unclear significance in MLH1 in Lynch syndrome diagnosis.
Hinrichsen I, Schäfer D, Langer D, Köger N, Wittmann M, Aretz S, Steinke V, Holzapfel S, Trojan J, König R, Zeuzem S, Brieger A, Plotz G.
Hinrichsen I, et al. Among authors: koger n.
Carcinogenesis. 2015 Feb;36(2):202-11. doi: 10.1093/carcin/bgu239. Epub 2014 Dec 4.
Carcinogenesis. 2015.
PMID: 25477341
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Evaluation of MLH1 variants of unclear significance.
Köger N, Paulsen L, López-Kostner F, Della Valle A, Vaccaro CA, Palmero EI, Alvarez K, Sarroca C, Neffa F, Kalfayan PG, Gonzalez ML, Rossi BM, Reis RM, Brieger A, Zeuzem S, Hinrichsen I, Dominguez-Valentin M, Plotz G.
Köger N, et al.
Genes Chromosomes Cancer. 2018 Jul;57(7):350-358. doi: 10.1002/gcc.22536. Epub 2018 Apr 30.
Genes Chromosomes Cancer. 2018.
PMID: 29520894
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Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype.
Seguí N, Navarro M, Pineda M, Köger N, Bellido F, González S, Campos O, Iglesias S, Valdés-Mas R, López-Doriga A, Gut M, Blanco I, Lázaro C, Capellá G, Puente XS, Plotz G, Valle L.
Seguí N, et al. Among authors: koger n.
Gut. 2015 Feb;64(2):355-6. doi: 10.1136/gutjnl-2014-307084. Epub 2014 Apr 1.
Gut. 2015.
PMID: 24691292
No abstract available.
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