C. Pagenstecher

发表

MUTYH‐associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype

P. Propping, S. Aretz, R. Caspari, 2006, International journal of cancer.

A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome

P. Propping, R. Kruse, A. Rütten, 2004, Journal of Medical Genetics.

N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC).

M. von Knebel Doeberitz, C. Engel, J. Rüschoff, 2006, Cancer letters.

Microsatellite stable colorectal cancers in clinically suspected hereditary nonpolyposis colorectal cancer patients without vertical transmission of disease are unlikely to be caused by biallelic germline mutations in MYH.

H. Schackert, S. Krüger, H. Görgens, 2006, The Journal of molecular diagnostics : JMD.

Tumours from MSH2 mutation carriers show loss of MSH2 expression but many tumours from MLH1 mutation carriers exhibit weak positive MLH1 staining

P. Propping, R. Buettner, N. Friedrichs, 2005, The Journal of pathology.

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study.

M. von Knebel Doeberitz, C. Engel, J. Rüschoff, 2005, The Lancet. Oncology.

Arg 462 Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer : a case-control study

C. Engel, J. Rüschoff, S. Krüger, 2022 .

A complex rearrangement in the APC gene uncovered by multiplex ligation-dependent probe amplification.

P. Propping, S. Aretz, D. Gadzicki, 2007, The Journal of molecular diagnostics : JMD.

Consultations in Molecular Diagnostics A Complex Rearrangement in the APC Gene Uncovered by Multiplex Ligation-Dependent Probe Amplification

P. Propping, S. Aretz, D. Gadzicki, 2007 .

HNPCC-associated small bowel cancer: clinical and molecular characteristics.

K. Schulmann, W. Schmiegel, C. Engel, 2005, Gastroenterology.

Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium.

M. Kloor, M. Loeffler, J. Gebert, 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer

M. Kloor, M. Loeffler, P. Kienle, 2006, International journal of cancer.

Cirrhotic Patients With or Without Hepatocellular Carcinoma Harbour AFP-Specific T-Lymphocytes That Can Be Activated in vitro by Human Alpha-Fetoprotein

T. Sauerbruch, W. Caselmann, C. Rabe, 2002, Scandinavian journal of gastroenterology.

Hereditary nonpolyposis colorectal cancer: Frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

P. Propping, E. Mangold, W. Friedl, 2003, International journal of cancer.

Frequency of Hereditary Non-Polyposis Colorectal Cancer among Unselected Patients with Colorectal Cancer in Germany

T. Sauerbruch, R. Büttner, P. Propping, 2006, Digestion.

MSH6 mutation in Muir–Torre syndrome: could this be a rare finding?

P. Propping, R. Buettner, N. Friedrichs, 2007, The British journal of dermatology.

Large submicroscopic genomic APC deletions are a common cause of typical familial adenomatous polyposis

P. Propping, R. Caspari, E. Mangold, 2005, Journal of Medical Genetics.

Microsatellite instability of selective target genes in HNPCC-associated colon adenomas

Holger Vogelsang, Matthias Kloor, M. Kloor, 2005, Oncogene.

Microsatellite instability did not predict individual survival of unselected patients with colorectal cancer

T. Sauerbruch, R. Büttner, N. Friedrichs, 2006, International Journal of Colorectal Disease.

High proportion of large genomic STK11 deletions in Peutz‐Jeghers syndrome

P. Propping, S. Aretz, R. Santer, 2005, Human mutation.

Frequency and parental origin of de novo APC mutations in familial adenomatous polyposis

P. Propping, S. Aretz, R. Caspari, 2004, European Journal of Human Genetics.

Eight novel MSH6 germline mutations in patients with familial and nonfamilial colorectal cancer selected by loss of protein expression in tumor tissue

C. Sutter, G. Evans, J. Gebert, 2004, Human mutation.

Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer

M. Kloor, M. Loeffler, J. Gebert, 2005, International journal of cancer.

Familial adenomatous polyposis: Aberrant splicing due to missense or silent mutations in the APC gene

K. Schulmann, P. Propping, S. Aretz, 2004, Human mutation.

The p53 codon 72 variation is associated with the age of onset of hereditary non-polyposis colorectal cancer (HNPCC)

M. von Knebel Doeberitz, K. Schulmann, C. Engel, 2005, Journal of Medical Genetics.

Aberrant splicing in MLH1 and MSH2 due to exonic and intronic variants

W. Henn, P. Propping, R. Buettner, 2006, Human Genetics.

Lower incidence of colorectal cancer and later age of disease onset in 27 families with pathogenic MSH6 germline mutations compared with families with MLH1 or MSH2 mutations: the German Hereditary Nonpolyposis Colorectal Cancer Consortium.

M. von Knebel Doeberitz, M. Loeffler, J. Gebert, 2004, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Hypothesis: Possible role of retinoic acid therapy in patients with biallelic mismatch repair gene defects

G. Plotz, W. Henn, R. Buettner, 2008, European Journal of Pediatrics.

The additive effect of p53 Arg72Pro and RNASEL Arg462Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH2 or MLH1.

M. von Knebel Doeberitz, C. Engel, H. Schackert, 2007, Cancer letters.

Hereditary nonpolyposis colorectal cancer: pitfalls in deletion screening in MSH2 and MLH1 genes

P. Propping, N. Friedrichs, S. Aretz, 2005, European Journal of Human Genetics.

The additive effect of p 53 Arg 72 Pro and RNASEL Arg 462 Gln genotypes on age of disease onset in Lynch syndrome patients with pathogenic germline mutations in MSH 2 or MLH 1

C. Engel, H. Schackert, S. Krüger, 2007 .

Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer.

C. Engel, J. Rüschoff, H. Schackert, 2006, Cancer letters.

TO JMG A genotype-phenotype correlation in HNPCC : strong predominance of msh 2 mutations in 41 patients with Muir-Torre syndrome

P. Propping, R. Kruse, T. Ruzicka, 2004 .