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C Niessen

Showing results (91-100 of 100) with videos related to

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Carcinogenesis|March 31, 2009
Promoter CpG island hypermethylation- and H3K9me3 and H3K27me3-mediated epigenetic silencing targets the deleted in colon cancer (DCC) gene in colorectal carcinogenesis without affecting neighboring genes on chromosomal region 18q21Sarah Derks, Linda J W Bosch, Hanneke E C Niessen, et al.
Familial Cancer|September 26, 2012
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature reviewA P Knopperts, M Nielsen, R C Niessen, et al.
European Journal of Cancer (Oxford, England : 1990)|March 8, 2011
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelinesJohanna C Herkert, Renée C Niessen, Maria J W Olderode-Berends, et al.
Human Genetics|January 13, 2006
MUTYH and the mismatch repair system: partners in crime?Renée C Niessen, Rolf H Sijmons, J Ou, et al.
Cancer Prevention Research (Philadelphia, Pa.)|December 25, 2014
Spectrin repeat containing nuclear envelope 1 and forkhead box protein E1 are promising markers for the detection of colorectal cancer in bloodVeerle Melotte, Joo Mi Yi, Marjolein H F M Lentjes, et al.
Gut|April 26, 2006
Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancerR C Niessen, M J W Berends, Y Wu, et al.
Genes, Chromosomes & Cancer|April 27, 2005
Colorectal cancer and the CHEK2 1100delC mutationMirjam M de Jong, Ilja M Nolte, Gerard J Te Meerman, et al.
Oncogene|July 5, 2006
High EPHB2 mutation rate in gastric but not endometrial tumors with microsatellite instabilityV Davalos, H Dopeso, S Velho, et al.
Human Mutation|February 11, 2011
Recurrence and variability of germline EPCAM deletions in Lynch syndromeRoland P Kuiper, Lisenka E L M Vissers, Ramprasath Venkatachalam, et al.
The Lancet. Oncology|December 15, 2010
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort studyMarlies J E Kempers, Roland P Kuiper, Charlotte W Ockeloen, et al.
Pageof 10

Showing results (91-100 of 100) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 100 results.
Carcinogenesis|March 31, 2009
Promoter CpG island hypermethylation- and H3K9me3 and H3K27me3-mediated epigenetic silencing targets the deleted in colon cancer (DCC) gene in colorectal carcinogenesis without affecting neighboring genes on chromosomal region 18q21Sarah Derks, Linda J W Bosch, Hanneke E C Niessen, et al.
Familial Cancer|September 26, 2012
Contribution of bi-allelic germline MUTYH mutations to early-onset and familial colorectal cancer and to low number of adenomatous polyps: case-series and literature reviewA P Knopperts, M Nielsen, R C Niessen, et al.
European Journal of Cancer (Oxford, England : 1990)|March 8, 2011
Paediatric intestinal cancer and polyposis due to bi-allelic PMS2 mutations: case series, review and follow-up guidelinesJohanna C Herkert, Renée C Niessen, Maria J W Olderode-Berends, et al.
Human Genetics|January 13, 2006
MUTYH and the mismatch repair system: partners in crime?Renée C Niessen, Rolf H Sijmons, J Ou, et al.
Cancer Prevention Research (Philadelphia, Pa.)|December 25, 2014
Spectrin repeat containing nuclear envelope 1 and forkhead box protein E1 are promising markers for the detection of colorectal cancer in bloodVeerle Melotte, Joo Mi Yi, Marjolein H F M Lentjes, et al.
Gut|April 26, 2006
Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancerR C Niessen, M J W Berends, Y Wu, et al.
Genes, Chromosomes & Cancer|April 27, 2005
Colorectal cancer and the CHEK2 1100delC mutationMirjam M de Jong, Ilja M Nolte, Gerard J Te Meerman, et al.
Oncogene|July 5, 2006
High EPHB2 mutation rate in gastric but not endometrial tumors with microsatellite instabilityV Davalos, H Dopeso, S Velho, et al.
Human Mutation|February 11, 2011
Recurrence and variability of germline EPCAM deletions in Lynch syndromeRoland P Kuiper, Lisenka E L M Vissers, Ramprasath Venkatachalam, et al.
The Lancet. Oncology|December 15, 2010
Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: a cohort studyMarlies J E Kempers, Roland P Kuiper, Charlotte W Ockeloen, et al.
Pageof 10