1. Analysis of MUTYH alternative transcript expression, promoter function, and the effect of human genetic variants. Issue 4 (24th January 2019) Authors: Köger, Nicole; Brieger, Angela; Hinrichsen, Inga M.; Zeuzem, Stefan; Plotz, Guido Journal: Human mutation Issue: Volume 40:Issue 4(2019) Page Start: 472 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Comprehensive Functional Assessment of MLH1 Variants of Unknown Significance. Issue 1 (27th November 2012) Authors: Borràs, Ester; Pineda, Marta; Brieger, Angela; Hinrichsen, Inga; Gómez, Carolina; Navarro, Matilde; Balmaña, Judit; Ramón y Cajal, Teresa; Torres, Asunción; Brunet, Joan; Blanco, Ignacio; Plotz, Guido; Lázaro, Conxi; Capellá, Gabriel Journal: Human mutation Issue: Volume 34:Issue 1(2013:Jan.) Page Start: 274 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. DNA mismatch repair activity of MutLα is regulated by CK2‐dependent phosphorylation of MLH1 (S477). Issue 12 (5th September 2018) Authors: Weßbecher, Isabel M.; Hinrichsen, Inga; Funke, Sebastian; Oellerich, Thomas; Plotz, Guido; Zeuzem, Stefan; Grus, Franz H.; Biondi, Ricardo M.; Brieger, Angela Journal: Molecular carcinogenesis Issue: Volume 57:Issue 12(2018) Page Start: 1723 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evaluation of MLH1 variants of unclear significance. Issue 7 (30th April 2018) Authors: Köger, Nicole; Paulsen, Lea; López‐Kostner, Francisco; Della Valle, Adriana; Vaccaro, Carlos Alberto; Palmero, Edenir Inêz; Alvarez, Karin; Sarroca, Carlos; Neffa, Florencia; Kalfayan, Pablo German; Gonzalez, Maria Laura; Rossi, Benedito Mauro; Reis, Rui Manuel; Brieger, Angela; Zeuzem, Stefan; H... Journal: Genes, chromosomes & cancer Issue: Volume 57:Issue 7(2018) Page Start: 350 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Exome sequencing identifies MUTYH mutations in a family with colorectal cancer and an atypical phenotype. Issue 2 (1st April 2014) Authors: Seguí, Nuria; Navarro, Matilde; Pineda, Marta; Köger, Nicole; Bellido, Fernando; González, Sara; Campos, Olga; Iglesias, Silvia; Valdés-Mas, Rafael; López-Doriga, Adriana; Gut, Marta; Blanco, Ignacio; Lázaro, Conxi; Capellá, Gabriel; Puente, Xose S; Plotz, Guido; Valle, Laura Journal: Gut Issue: Volume 64:Issue 2(2015) Page Start: 355 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas. Issue 2 (20th January 2015) Authors: Spier, Isabel; Holzapfel, Stefanie; Altmüller, Janine; Zhao, Bixiao; Horpaopan, Sukanya; Vogt, Stefanie; Chen, Sophia; Morak, Monika; Raeder, Susanne; Kayser, Katrin; Stienen, Dietlinde; Adam, Ronja; Nürnberg, Peter; Plotz, Guido; Holinski‐Feder, Elke; Lifton, Richard P.; Thiele, Holger; Hoffmann... Journal: International journal of cancer Issue: Volume 137:Issue 2(2015:Jul. 15) Page Start: 320 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Loss of MLH1 sensitizes colon cancer cells to DNA‐PKcs inhibitor KU60648. Issue 7 (10th March 2017) Authors: Hinrichsen, Inga; Ackermann, Anne; Düding, Tonja; Graband, Annika; Filmann, Natalie; Plotz, Guido; Zeuzem, Stefan; Brieger, Angela Journal: Molecular carcinogenesis Issue: Volume 56:Issue 7(2017) Page Start: 1816 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Phosphorylation‐dependent signaling controls degradation of DNA mismatch repair protein PMS2. Issue 12 (7th September 2017) Authors: Hinrichsen, Inga; Weßbecher, Isabel M.; Huhn, Meik; Passmann, Sandra; Zeuzem, Stefan; Plotz, Guido; Biondi, Ricardo M.; Brieger, Angela Journal: Molecular carcinogenesis Issue: Volume 56:Issue 12(2017) Page Start: 2663 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Refining the role of pms2 in Lynch syndrome: germline mutational analysis improved by comprehensive assessment of variants. Issue 8 (24th May 2013) Authors: Borràs, Ester; Pineda, Marta; Cadiñanos, Juan; del Valle, Jesús; Brieger, Angela; Hinrichsen, Inga; Cabanillas, Ruben; Navarro, Matilde; Brunet, Joan; Sanjuan, Xavier; Musulen, Eva; van der Klift, Helen; Lázaro, Conxi; Plotz, Guido; Blanco, Ignacio; Capellá, Gabriel Journal: Journal of medical genetics Issue: Volume 50:Issue 8(2013) Page Start: 552 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗