Search Results - "Schackert, Konrad"
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Age‐dependent performance of BRAF mutation testing in Lynch syndrome diagnostics
Published in International journal of cancer (15-11-2020)“…BRAF V600E mutations have been reported as a marker of sporadic microsatellite instability (MSI) colorectal cancer (CRC). Current international diagnostic…”
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Biallelic MLH1 SNP cDNA expression or constitutional promoter methylation can hide genomic rearrangements causing Lynch syndrome
Published in Journal of medical genetics (01-08-2011)“…A positive family history, germline mutations in DNA mismatch repair genes, tumours with high microsatellite instability, and loss of mismatch repair protein…”
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3
Meta-analysis of microarray data on pancreatic cancer defines a set of commonly dysregulated genes
Published in Oncogene (28-07-2005)“…Pancreatic ductal adenocarcinoma is the eighth most common cancer with the lowest overall 5-year relative survival rate of any tumor type today. Expression…”
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4
Frequent loss of the CDKN2C (p18INK4c) gene product in pituitary adenomas
Published in Genes chromosomes & cancer (01-02-2009)“…Genomic alterations of cyclin‐dependent kinase inhibitors have been demonstrated in a variety of tumor types including brain tumors. Among them, the…”
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Gene Expression Profiling of Microdissected Pancreatic Ductal Carcinomas Using High-Density DNA Microarrays
Published in Neoplasia (New York, N.Y.) (01-09-2004)“…Pancreatic ductal adenocarcinoma (PDAC) remains an important cause of malignancy-related death and is the eighth most common cancer with the lowest overall…”
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6
Examination of apoptosis signaling in pancreatic cancer by computational signal transduction analysis
Published in PloS one (19-08-2010)“…Pancreatic ductal adenocarcinoma (PDAC) remains an important cause of cancer death. Changes in apoptosis signaling in pancreatic cancer result in chemotherapy…”
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Therapy of Hematogenous Melanoma Brain Metastases with Endostatin
Published in Clinical cancer research (01-02-2005)“…Purpose: Cerebral metastases represent the most common type of brain tumors. This study investigated the effects of endogenous endostatin on hematogenous…”
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Functional Cathepsin C mutations cause different Papillon-Lefèvre syndrome phenotypes
Published in Journal of clinical periodontology (01-04-2008)“…Aim: The autosomal‐recessive Papillon–Lefèvre syndrome (PLS) is characterized by severe aggressive periodontitis, combined with palmoplantar hyperkeratosis,…”
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Comparative genetic analysis of metachronous anaplastic oligoastrocytomas with extended recurrence-free interval
Published in Journal of neuro-oncology (01-04-2005)“…Two metachronous anaplastic oligoastrocytomas with different cerebral locations were analyzed in a 51-year-old patient with an extended recurrence-free…”
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10
Lack of association between Endoglin intron 7 insertion polymorphism and intracranial aneurysms in a white population : Evidence of racial/ethnic differences
Published in Stroke (1970) (01-11-2001)“…Endoglin is a component of the transforming growth factor-beta receptor complex and is predominantly expressed on cell surfaces of endothelial cells. A…”
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Microarray-based gene expression profiling in pancreatic ductal carcinoma: status quo and perspectives
Published in International journal of colorectal disease (01-09-2004)“…Pancreatic ductal adenocarcinoma has an extremely poor prognosis. To improve the prognosis, novel molecular markers and targets for earlier diagnosis and…”
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Missense variants in hMLH1 identified in patients from the German HNPCC consortium and functional studies
Published in Familial cancer (01-06-2011)“…Missense mutations of the DNA mismatch repair gene MLH1 are found in a significant fraction of patients with Lynch syndrome (hereditary nonpolyposis colorectal…”
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Cytosine deaminase gene as a potential tool for the genetic therapy of colorectal cancer
Published in Journal of surgical oncology (01-01-1996)“…The bacterial enzyme cytosine deaminase (CD) catalyzes the conversion of 5‐fluorocytosine (5‐FC) to the lethal 5‐fluorouracil (5‐FU) and so provides a useful…”
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14
Microsatellite instability analysis : A multicenter study for reliability and quality control
Published in Cancer research (Chicago, Ill.) (01-11-1997)“…The molecular biology section of the Hereditary Non-Polyposis Colorectal Cancer study group-Germany, instituted a multicenter study to test the reliability and…”
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Correspondence (reply): In reply
Published in Deutsches Ärzteblatt international (01-05-2013)Get full text
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Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome
Published in Deutsches Ärzteblatt international (01-01-2013)“…Hereditary nonpolyposis colorectal cancer HNPCC, Lynch syndrome) is a genetic disease of autosomal dominant inheritance. It is caused by a mutation in one of…”
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Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC
Published in European journal of human genetics : EJHG (01-07-2008)“…Germline mutations in mismatch repair (MMR) genes, tumours with high microsatellite instability (MSI-H) and loss of MMR protein expression are the hallmarks of…”
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TLR4 and IL-18 gene variants in aggressive periodontitis
Published in Journal of clinical periodontology (01-12-2008)“…Aim: We aimed to assess the association of different genotypes with increased aggressive periodontitis susceptibility by studying functional relevant variants…”
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Occult endometrial cancer and decision making for prophylactic hysterectomy in hereditary nonpolyposis colorectal cancer patients
Published in Gynecologic oncology (01-08-2006)“…Hereditary nonpolyposis colorectal cancer (HNPCC) is the most frequent form of hereditary colorectal cancer. In addition to the high lifetime risk for…”
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