M. Mathiak

发表

Standardized quantification of pulmonary fibrosis in histological samples.

H. Bolte, S. Freitag-Wolf, N. E. El Mokhtari, 2008, BioTechniques.

Stromal expression of invasion‐promoting, matrix‐degrading proteases MMP‐1 and ‐9 and the Ets 1 transcription factor in HNPCC carcinomas and sporadic colorectal cancers

A. Wellmann, F. Fogt, E. Mangold, 2003, International journal of cancer.

Endoscopic removal of a retained surgical sponge in a young Syrian refugee after Caesarean section: a case report with discussion of cultural and political consequences

I. Alkatout, N. Maass, M. Mathiak, 2016, Patient Safety in Surgery.

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.

PD-L1 is an independent prognostic predictor in gastric cancer of Western patients

H. Kalthoff, C. Röcken, M. Mathiak, 2016, Oncotarget.

Members of the EpCAM signalling pathway are expressed in gastric cancer tissue and are correlated with patient prognosis

C. Röcken, M. Ebert, M. Mathiak, 2013, British Journal of Cancer.

RNA based individualized drug selection in breast cancer patients without patient-matched normal tissue

F. Egberts, P. Rosenstiel, B. Leyland-Jones, 2018, Oncotarget.

Smoking-Induced SLPI Expression Hinders HPV Infections Also in Squamous Cell Carcinomas of the Vulva

I. Alkatout, C. Röcken, N. Maass, 2018, Translational oncology.

Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry.

J. Rüschoff, R. Buettner, T. Edmonston, 2004, The Journal of molecular diagnostics : JMD.

Frequency of microsatellite instability in unselected sebaceous gland neoplasias and hyperplasias.

P. Propping, M. Bisceglia, R. Kruse, 2003, The Journal of investigative dermatology.

Detection of APC and k-ras mutations in the serum of patients with colorectal cancer.

P. Propping, A. Hirner, R. Caspari, 2001, Cancer detection and prevention.

Investigation of the colorectal cancer susceptibility region on chromosome 8q24.21 in a large German case‐control sample

U. John, H. Völzke, J. Hampe, 2009, International journal of cancer.

A role for perlecan in the suppression of growth and invasion in fibrosarcoma cells.

R. Iozzo, D. Grant, Ç. Yenisey, 1997, Cancer research.

Clinicopathologic Characteristics of Microsatellite Instable Gastric Carcinomas Revisited: Urgent Need for Standardization

C. Röcken, M. Mathiak, C. Böger, 2016, Applied immunohistochemistry & molecular morphology : AIMM.

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.

Evaluation of two different vacuum-assisted breast biopsy systems: Mammotome® system 11G/8G vs. ATEC® system 12G/9G

W. Jonat, M. Heller, Alexander Strauss, 2013, Acta radiologica.

Serum cholesterol is elevated in patients with Achilles tendon ruptures

G. Mathiak, M. Mathiak, J. Wening, 1999, Archives of Orthopaedic and Trauma Surgery.

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.

Microsatellite instability—a useful diagnostic tool to select patients at high risk for hereditary non-polyposis colorectal cancer: a study in different groups of patients with colorectal cancer

T. Sauerbruch, P. Propping, R. Kruse, 1999, Gut.

[Diagnosis and therapy of cruciate ligament injuries in childhood. Clinical results].

G. Mathiak, M. Mathiak, J. Wening, 1995, Unfallchirurgie.

Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria.

P. Propping, M. Bisceglia, R. Kruse, 1998, American journal of human genetics.

Loss of DNA Mismatch Repair Proteins in Skin Tumors From Patients With Muir–Torre Syndrome and MSH2 or MLH1 Germline Mutations: Establishment of Immunohistochemical Analysis as a Screening Test

P. Propping, R. Kruse, T. Ruzicka, 2002, The American journal of surgical pathology.

E-cadherin expression is homogeneously reduced in adenoma from patients with familial adenomatous polyposis: an immunohistochemical study of E-cadherin, β-catenin and cyclooxygenase-2 expression

U. Spengler, R. Caspari, W. Friedl, 2004, International Journal of Colorectal Disease.

[Inflammatory pseudotumor of the liver--rare differential diagnosis of undetermined hepatic space-occupying lesion. Case report and review of the literature].

S. Schröder, D. Henne-Bruns, G. Mathiak, 1996, Langenbecks Archiv fur Chirurgie.

In situ localization of tumor cells associated with the epithelial-mesenchymal transition marker Snail and the prognostic impact of lymphocytes in the tumor microenvironment in invasive ductal breast cancer.

W. Klapper, I. Alkatout, C. Röcken, 2017, Experimental and molecular pathology.

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.

Reproducibility of Her2/neu scoring in gastric cancer and assessment of the 10% cut-off rule

Peter Hufnagl, Hans-Michael Behrens, Wolfram Klapper, 2014, Cancer medicine.

A Giant Mammary Hamartoma in a Young Breast Cancer Patient

A. Farrokh, M. van Mackelenbergh, F. Schäfer, 2020, Breast Care.

Rare Benign Entities of the Breast - Myoid Hamartoma and Capillary Hemangioma.

W. Jonat, A. Strauss, F. Schäfer, 2012, Geburtshilfe und Frauenheilkunde.

Morphological Evaluation of Tumor-Infiltrating Lymphocytes (TILs) to Investigate Invasive Breast Cancer Immunogenicity, Reveal Lymphocytic Networks and Help Relapse Prediction: A Retrospective Study

Wolfram Klapper, Ibrahim Alkatout, Gloria Romagnoli, 2017, International journal of molecular sciences.

Analysis of chromosomal instability in focal cortical dysplasia of Taylor’s balloon cell type

C. Elger, A. Becker, R. Lahl, 2004, Acta Neuropathologica.

[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)].

M. Kloor, D. Aust, C. Poremba, 2004, Der Pathologe.

Associations between polymorphisms in the thymidylate synthase gene, the expression of thymidylate synthase mRNA and the microsatellite instability phenotype of colorectal cancer.

V. Hans, J. Rüschoff, R. Büttner, 2004, Oncology reports.

The age-specific differences in histopathological tumor characteristics and TNM classification of breast carcinomas in Quality assured mamma diagnostic (QuaMaDi) program in the state of Schleswig–Holstein in Germany

C. Röcken, M. Mathiak, H. Behrens, 2021, Journal of Cancer Research and Clinical Oncology.

Intra-operative use of one-step nucleic acid amplification (OSNA) for detection of the tumor load of sentinel lymph nodes in breast cancer patients

M. Mackelenbergh, C. Schem, I. Alkatout, 2013, Journal of Cancer Research and Clinical Oncology.

Population-Based Registration of Unselected Colorectal Cancer Patients: Five-Year Survival in the Region of Bonn/Rhine-Sieg, Germany

R. Fimmers, T. Sauerbruch, M. Bollmann, 2005, Zeitschrift fur Gastroenterologie.

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 .

Molekularpathologische Diagnostik beim erblichen Dickdarmkarzinom

C. Poremba, W. Mueller, M. Mathiak, 2004, Der Pathologe.

Rare Benign Entities of the Breast - Myoid Hamartoma and Capillary Hemangioma.

W. Jonat, Alexander Strauss, F. Schäfer, 2012, Geburtshilfe und Frauenheilkunde.