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The recurring features of molecular subtypes in distinct gastrointestinal malignancies—A systematic review

Critical reviews in oncology/hematology, 2021-08, Vol.164, p.103428-103428, Article 103428

2021

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Development of a miRNA‐based classifier for detection of colorectal cancer molecular subtypes

Molecular oncology, 2022-07, Vol.16 (14), p.2693-2709

2022

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Intestinal region-specific Wnt signalling profiles reveal interrelation between cell identity and oncogenic pathway activity in cancer development

Cancer cell international, 2020-12, Vol.20 (1), p.578-578, Article 578

2020

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Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis

PloS one, 2021-11, Vol.16 (11), p.e0259185

2021

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Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes

Hereditary cancer in clinical practice, 2019-01, Vol.17 (1), p.5-5, Article 5

2019

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C-terminal fluorescent labeling impairs functionality of DNA mismatch repair proteins

PloS one, 2012-02, Vol.7 (2), p.e31863

2012

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Chromoendoscopy in combination with random biopsies does not improve detection of gastric cancer foci in CDH1 mutation positive patients

Endoscopy International Open, 2016-12, Vol.4 (12), p.E1305-E1310

2016

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

American journal of human genetics, 2016-08, Vol.99 (2), p.337-351

2016

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Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas

International journal of cancer, 2015-07, Vol.137 (2), p.320-331

2015

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Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

Journal of medical genetics, 2016-03, Vol.53 (3), p.172-179

2016

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Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

Familial cancer, 2016-04, Vol.15 (2), p.281-288

2016

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Prophylactic total gastrectomy in the management of hereditary tumor syndromes

International journal of colorectal disease, 2016-12, Vol.31 (12), p.1825-1833

2016

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A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization

Genes chromosomes & cancer, 2011-02, Vol.50 (2), p.59-70

2011

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De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis

Molecular cytogenetics, 2014-01, Vol.7 (1), p.7-7

2014

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De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis

Molecular cytogenetics, 2014, Vol.7 (1), p.7-7

2014

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In Situ Spectroscopic Detection of Large‐Scale Reorientations of Transmembrane Helices During Influenza A M2 Channel Opening

Angewandte Chemie International Edition, 2023-11, Vol.62 (47), p.e202309069-n/a

International ed. in English, 2023

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A vibrational spectroscopic approach to elucidate the molecular mechanism behind the channel activity of viroporins

Biophysical journal, 2023-02, Vol.122 (3), p.44a-44a

2023

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In situ‐spektroskopische Detektion der weitreichenden Reorientierung von Transmembranhelices während der Öffnung des Influenza A M2‐Kanals

Angewandte Chemie, 2023-11, Vol.135 (47), p.n/a

2023

Volltextzugriff (PDF)

In situ‐spektroskopische Detektion der weitreichenden Reorientierung von Transmembranhelices während der Öffnung des Influenza A M2‐Kanals

Angewandte Chemie, 2023-11, Vol.135 (47)

2023

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Tourette syndrome as a motor disorder revisited – Evidence from action coding

NeuroImage clinical, 2021-01, Vol.30, p.102611-102611, Article 102611

2021

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Prompt-gamma emission in GEANT4 revisited and confronted with experiment

Physica medica, 2021-08, Vol.88, p.250-261

2021

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Macro Talent Management: A Global Perspective on Managing Talent in Developed Markets

1st, 2018

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The recurring features of molecular subtypes in distinct gastrointestinal malignancies—A systematic review

Stem cell functionality is microenvironmentally defined during tumour expansion and therapy response in colon cancer

Development of a miRNA‐based classifier for detection of colorectal cancer molecular subtypes

Intestinal region-specific Wnt signalling profiles reveal interrelation between cell identity and oncogenic pathway activity in cancer development

Variant profiling of colorectal adenomas from three patients of two families with MSH3-related adenomatous polyposis

Genome‐wide CNV analysis in 221 unrelated patients and targeted high‐throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

Diagnostic yield and clinical utility of a comprehensive gene panel for hereditary tumor syndromes

C-terminal fluorescent labeling impairs functionality of DNA mismatch repair proteins

Chromoendoscopy in combination with random biopsies does not improve detection of gastric cancer foci in CDH1 mutation positive patients

Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis

Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas

Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases

Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposis

Prophylactic total gastrectomy in the management of hereditary tumor syndromes

A CRM1-dependent nuclear export pathway is involved in the regulation of MutLα subcellular localization

De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis

De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis

In Situ Spectroscopic Detection of Large‐Scale Reorientations of Transmembrane Helices During Influenza A M2 Channel Opening

A vibrational spectroscopic approach to elucidate the molecular mechanism behind the channel activity of viroporins

In situ‐spektroskopische Detektion der weitreichenden Reorientierung von Transmembranhelices während der Öffnung des Influenza A M2‐Kanals

In situ‐spektroskopische Detektion der weitreichenden Reorientierung von Transmembranhelices während der Öffnung des Influenza A M2‐Kanals

Tourette syndrome as a motor disorder revisited – Evidence from action coding

Prompt-gamma emission in GEANT4 revisited and confronted with experiment

Macro Talent Management: A Global Perspective on Managing Talent in Developed Markets

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