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Journal Articles

Abstract 4156: Multiple rare germline variants in a thyroid cancer family

Taina T. Nieminen, Daniel F. Comiskey, Yanqiang Wang, Sandya Liyanarachchi, Pamela Brock, Paivi Peltomaki, Huiling He, Albert de la Chapelle

Cancer Res (2019) 79 (13_Supplement): 4156.

https://doi.org/10.1158/1538-7445.AM2019-4156

Published: 01 July 2019

View articletitled, Abstract 4156: Multiple rare germline variants in a thyroid cancer family

Journal Articles

Abstract 3081: Methylation changes and somatic mutations as early events in Lynch syndrome-associated colorectal cancer

Satu Mäki-Nevala, Satu Valo, Ari Ristimäki, Laura Renkonen-Sinisalo, Anna Lepistö, Jukka-Pekka Mecklin, Päivi Peltomäki

Cancer Res (2018) 78 (13_Supplement): 3081.

https://doi.org/10.1158/1538-7445.AM2018-3081

Published: 01 July 2018

View articletitled, Abstract 3081: Methylation changes and somatic mutations as early events in Lynch syndrome-associated colorectal cancer

Journal Articles

Abstract 5369: Tumorigenesis in Lynch syndrome: Somatic mutation profiles compared to sporadic counterparts

Noora Porkka, Alisa Olkinuora, Satu Mäki-Nevala, Samuli Eldfors, Päivi Peltomäki

Cancer Res (2018) 78 (13_Supplement): 5369.

https://doi.org/10.1158/1538-7445.AM2018-5369

Published: 01 July 2018

View articletitled, Abstract 5369: Tumorigenesis in Lynch syndrome: Somatic mutation profiles compared to sporadic counterparts

Journal Articles

Abstract 4491: Pseudoexons may underlie unbalanced expression of APC alleles in familial adenomatous polyposis

Taina Tuulikki Nieminen, Walter Pavicic, Noora Porkka, Heikki J. Jarvinen, Anna Lepisto, Paivi Peltomaki

Cancer Res (2016) 76 (14_Supplement): 4491.

https://doi.org/10.1158/1538-7445.AM2016-4491

Published: 15 July 2016

View articletitled, Abstract 4491: Pseudoexons may underlie unbalanced expression of APC alleles in familial adenomatous polyposis

Journal Articles

Abstract 4766: DNA methylation changes in Lynch syndrome associated colorectal adenomas and carcinomas

Satu Valo, Sippy Kaur, Ari Ristimäki, Laura Renkonen-Sinisalo, Heikki Järvinen, Jukka-Pekka Mecklin, Minna Nyström, Päivi Peltomäki

Cancer Res (2015) 75 (15_Supplement): 4766.

https://doi.org/10.1158/1538-7445.AM2015-4766

Published: 01 August 2015

View articletitled, Abstract 4766: DNA methylation changes in Lynch syndrome associated colorectal adenomas and carcinomas

Journal Articles

Abstract 2964: Histology-specific patterns of DNA methylation in Lynch-associated and sporadic ovarian cancer

Anni Niskakoski, Sippy Kaur, Synnove Staff, Laura Renkonen-Sinisalo, Heini Lassus, Heikki J. Järvinen, Jukka-Pekka Mecklin, Ralf Bützow, Päivi Peltomäki

Cancer Res (2015) 75 (15_Supplement): 2964.

https://doi.org/10.1158/1538-7445.AM2015-2964

Published: 01 August 2015

View articletitled, Abstract 2964: Histology-specific patterns of DNA methylation in Lynch-associated and sporadic ovarian cancer

Journal Articles

Abstract 417: DNA methylation changes in Lynch syndrome and FAP-associated colorectal tumorigenesis

Satu Valo, Sippy Kaur, Ari Ristimäki, Laura Renkonen-Sinisalo, Heikki Järvinen, Jukka-Pekka Mecklin, Minna Nyström, Päivi Peltomäki

Cancer Res (2014) 74 (19_Supplement): 417.

https://doi.org/10.1158/1538-7445.AM2014-417

Published: 01 October 2014

View articletitled, Abstract 417: DNA methylation changes in Lynch syndrome and FAP-associated colorectal tumorigenesis

Journal Articles

3′-UTR Poly(T/U) Tract Deletions and Altered Expression of EWSR1 Are a Hallmark of Mismatch Repair–Deficient Cancers

Shivendra Kishore, Salvatore Piscuoglio, Michal B. Kovac, Annette Gylling, Friedel Wenzel, Francesca Trapani, Hans Joerg Altermatt, Valentina Mele, Giancarlo Marra, Päivi Peltomäki, Luigi Terracciano, Mihaela Zavolan, Karl Heinimann

Cancer Res (2014) 74 (1): 224–234.

https://doi.org/10.1158/0008-5472.CAN-13-2100

Published: 05 January 2014

View articletitled, 3′-UTR Poly(T/U) Tract Deletions and Altered Expression of EWSR1 Are a Hallmark of Mismatch Repair–Deficient Cancers

Includes: Supplementary data

Journal Articles

Abstract 5018: Genetic and epigenetic investigation of breast carcinoma arising in Lynch syndrome families

Johanna E. Lotsari, Annette Gylling, Wael M. Abdel-Rahman, Marjukka Friman, Markku Aarnio, Heikki J. Jarvinen, Jukka-Pekka Mecklin, Teijo Kuopio, Paivi Peltomaki

Cancer Res (2012) 72 (8_Supplement): 5018.

https://doi.org/10.1158/1538-7445.AM2012-5018

Published: 15 April 2012

View articletitled, Abstract 5018: Genetic and epigenetic investigation of breast carcinoma arising in Lynch syndrome families

Journal Articles

Molecular pathogenesis of different tumors arising in Lynch syndrome

Taina Nieminen, Annette Gylling, Wael Abdel-Rahman, M Juhola, K Nuorva, Emmi Joensuu, J-P Mecklin, M Aarnio, Paivi Peltomaki

Cancer Res (2008) 68 (9_Supplement): 5502.

Published: 01 May 2008

View articletitled, Molecular pathogenesis of different tumors arising in Lynch syndrome

Journal Articles

Gene Conversion Is a Frequent Mechanism of Inactivation of the Wild-Type Allele in Cancers from MLH1/MSH2 Deletion Carriers

Jian Zhang, Annette Lindroos, Saara Ollila, Anna Russell, Giancarlo Marra, Hansjakob Mueller, Paivi Peltomaki, Martina Plasilova, Karl Heinimann

Cancer Res (2006) 66 (2): 659–664.

https://doi.org/10.1158/0008-5472.CAN-05-4043

Published: 19 January 2006

View articletitled, Gene Conversion Is a Frequent Mechanism of Inactivation of the Wild-Type Allele in Cancers from MLH1/MSH2 Deletion Carriers

Includes: Supplementary data

Journal Articles

Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number

Wael M. Abdel-Rahman, Hannes Lohi, Sakari Knuutila, Paivi Peltomaki

Cancer Res (2004) 64 (7_Supplement): 610.

Published: 01 April 2004

View articletitled, Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number

Journal Articles

Expression of the Human Mismatch Repair Gene hMSH2 in Normal and Neoplastic Tissues

Fredrick S. Leach, Kornelia Polyak, Marilee Burrell, Karen A. Johnson, David Hill, Malcolm G. Dunlop, Andrew H. Wyllie, Paivi Peltomaki, Albert de la Chapelle, Stanley R. Hamilton, Kenneth W. Kinzler, Bert Vogelstein

Cancer Res (1996) 56 (2): 235–240.

Published: 01 January 1996

View articletitled, Expression of the Human Mismatch Repair Gene hMSH2 in Normal and Neoplastic Tissues

Journal Articles

Replication Errors in Benign and Malignant Tumors from Hereditary Nonpolyposis Colorectal Cancer Patients

Lauri A. Aaltonen, Päivi Peltomäki, Jukka-Pekka Mecklin, Heikki Järvinen, Jeremy R. Jass, Jane S. Green, Henry T. Lynch, Patrice Watson, Gustav Tallqvist, Matti Juhola, Pertti Sistonen, Stanley R. Hamilton, Kenneth W. Kinzler, Bert Vogelstein, Albert de la Chapelle

Cancer Res (1994) 54 (7): 1645–1648.

Published: 01 April 1994

View articletitled, Replication Errors in Benign and Malignant Tumors from Hereditary Nonpolyposis Colorectal Cancer Patients

Journal Articles

Genomic Instability in Colorectal Cancer: Relationship to Clinicopathological Variables and Family History

Ragnhild A. Lothe, Päivi Peltomäki, Gunn Iren Meling, Lauri A. Aaltonen, Minna Nyström-Lahti, Lea Pylkkänen, Ketil Heimdal, Tone I. Andersen, Pål Møller, Torleiv O. Rognum, Sophie D. Fosså, Tor Haldorsen, Frøydis Langmark, Anton Brøgger, Albert de la Chapelle, Anne-Lise Børresen

Cancer Res (1993) 53 (24): 5849–5852.

Published: 01 December 1993

View articletitled, Genomic Instability in Colorectal Cancer: Relationship to Clinicopathological Variables and Family History

Journal Articles

Microsatellite Instability Is Associated with Tumors That Characterize the Hereditary Non-Polyposis Colorectal Carcinoma Syndrome

Päivi Peltomäki, Ragnhild A. Lothe, Lauri A. Aaltonen, Lea Pylkkänen, Minna Nyström-Lahti, Raquel Seruca, Leonor David, Ruth Holm, David Ryberg, Aage Haugen, Anton Brøgger, Anne-Lise Børresen, Albert de la Chapelle

Cancer Res (1993) 53 (24): 5853–5855.

Published: 01 December 1993

View articletitled, Microsatellite Instability Is Associated with Tumors That Characterize the Hereditary Non-Polyposis Colorectal Carcinoma Syndrome

Journal Articles

Evidence that the MCC-APC Gene Region in 5q21 Is Not the Site for Susceptibility to Hereditary Nonpolyposis Colorectal Carcinoma

Päivi Peltomäki, Pertti Sistonen, Jukka-Pekka Mecklin, Lea Pylkkänen, Lauri Aaltonen, Stig Nordling, Juha Kere, Heikki Järvinen, Stanley R. Hamilton, Gloria Petersen, Kenneth W. Kinzler, Bert Vogelstein, Albert de la Chapelle

Cancer Res (1992) 52 (16): 4530–4533.

Published: 01 August 1992

View articletitled, Evidence that the MCC-APC Gene Region in 5q21 Is Not the Site for Susceptibility to Hereditary Nonpolyposis Colorectal Carcinoma

Journal Articles

Evidence Supporting Exclusion of the DCC Gene and a Portion of Chromosome 18q as the Locus for Susceptibility to Hereditary Nonpolyposis Colorectal Carcinoma in Five Kindreds

Päivi Peltomäki, Pertti Sistonen, Jukka-Pekka Mecklin, Lea Pylkkänen, Heikki Järvinen, Jonathan W. Simons, Kathleen R. Cho, Bert Vogelstein, Albert de la Chapelle

Cancer Res (1991) 51 (16): 4135–4140.

Published: 01 August 1991

View articletitled, Evidence Supporting Exclusion of the DCC Gene and a Portion of Chromosome 18q as the Locus for Susceptibility to Hereditary Nonpolyposis Colorectal Carcinoma in Five Kindreds

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Abstract 4156: Multiple rare germline variants in a thyroid cancer family

Abstract 3081: Methylation changes and somatic mutations as early events in Lynch syndrome-associated colorectal cancer

Abstract 5369: Tumorigenesis in Lynch syndrome: Somatic mutation profiles compared to sporadic counterparts

Abstract 4491: Pseudoexons may underlie unbalanced expression of APC alleles in familial adenomatous polyposis

Abstract 4766: DNA methylation changes in Lynch syndrome associated colorectal adenomas and carcinomas

Abstract 2964: Histology-specific patterns of DNA methylation in Lynch-associated and sporadic ovarian cancer

Abstract 417: DNA methylation changes in Lynch syndrome and FAP-associated colorectal tumorigenesis

3′-UTR Poly(T/U) Tract Deletions and Altered Expression of EWSR1 Are a Hallmark of Mismatch Repair–Deficient Cancers

Abstract 5018: Genetic and epigenetic investigation of breast carcinoma arising in Lynch syndrome families

Molecular pathogenesis of different tumors arising in Lynch syndrome

Gene Conversion Is a Frequent Mechanism of Inactivation of the Wild-Type Allele in Cancers from MLH1/MSH2 Deletion Carriers

Restoring mismatch repair does not stop the formation of reciprocal translocations in the colon cancer cell line HCA7 but further destabilizes chromosome number

Expression of the Human Mismatch Repair Gene hMSH2 in Normal and Neoplastic Tissues

Replication Errors in Benign and Malignant Tumors from Hereditary Nonpolyposis Colorectal Cancer Patients

Genomic Instability in Colorectal Cancer: Relationship to Clinicopathological Variables and Family History

Microsatellite Instability Is Associated with Tumors That Characterize the Hereditary Non-Polyposis Colorectal Carcinoma Syndrome

Evidence that the MCC-APC Gene Region in 5q21 Is Not the Site for Susceptibility to Hereditary Nonpolyposis Colorectal Carcinoma

Evidence Supporting Exclusion of the DCC Gene and a Portion of Chromosome 18q as the Locus for Susceptibility to Hereditary Nonpolyposis Colorectal Carcinoma in Five Kindreds

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