Publications by authors named "Katharina Neumayer"

The BRAF gene and the TERT promoter are among the most frequently altered genomic loci in low-grade (LGG) and high-grade-glioma (HGG), respectively. The coexistence of BRAF and TERT promoter aberrations characterizes a subset of aggressive glioma. Therefore, we investigated interactions between those alterations in malignant glioma.

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  • Meningiomas are mostly non-cancerous tumors, but some can become more dangerous over time. Researchers studied how mutations in a specific gene (the TERT promoter) affect these tumors and patient survival.* -
  • They looked at 128 tissue samples from 110 patients, finding TERT promoter mutations in about 5.5% of those samples, which was linked to increased telomerase activity and poorer survival rates for patients.* -
  • The study suggests that while TERT promoter mutations make meningiomas more aggressive and shorten survival, they might also help develop new treatments for patients with these tumors.*
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  • - Ependymomas are a type of brain tumor in children that often reoccur even after complete surgical removal, and recent studies have identified different molecular subgroups of these tumors, though their aggressive behavior is not fully understood.
  • - This study investigated the role of telomerase reactivation, a common cancer mechanism for avoiding aging, in specific pediatric ependymoma subgroups by analyzing various molecular markers like telomerase activity and genetic variations in a patient cohort.
  • - Results showed that certain subgroups (particularly PF-EPN-A and ST-EPN-RELA) experienced significant telomerase activation linked to poorer survival rates, highlighting the importance of telomerase in disease progression and revealing potential molecular pathways influencing this process.
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Purpose: The purpose of the present study is the comparison of acute ACL reconstruction with or without meniscus repair within 48 h after injury and a delayed surgery during the inflammation-free interval. It was hypothesized that acute ACL reconstruction results in inferior patient reported outcomes and higher frequency of range of motion deficits.

Methods: The effect of acute (within 48 h) and delayed (during the inflammation-free interval) ACL surgery was prospectively studied on 160 consecutive patients with ACL injury between January 2010 and December 2011.

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The use of mesenchymal stromal cells (MSCs) differentiated toward a smooth muscle cell (SMC) phenotype may provide an alternative for investigators interested in regenerating urinary tract organs such as the bladder where autologous smooth muscle cells cannot be used or are unavailable. In this study we measured the effects of good manufacturing practice (GMP)-compliant expansion followed by myogenic differentiation of human MSCs on the expression of a range of contractile (from early to late) myogenic markers in relation to the electrophysiological parameters to assess the functional role of the differentiated MSCs and found that differentiation of MSCs associated with electrophysiological competence comparable to bladder SMCs. Within 1-2 weeks of myogenic differentiation, differentiating MSCs significantly expressed alpha smooth muscle actin (αSMA; ACTA2), transgelin (TAGLN), calponin (CNN1), and smooth muscle myosin heavy chain (SM-MHC; MYH11) according to qRT-PCR and/or immunofluorescence and Western blot.

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When sterile culture techniques of mammalian cells first became state of the art, there was tremendous anticipation that such cells could be eventually applied for therapeutic purposes. The discovery of adult human stem or progenitor cells further motivated scientists to pursue research in cell-based therapies. Although evidence from animal studies suggests that application of cells yields measurable benefits, in urology and many other disciplines, progenitor-cell-based therapies are not yet routinely clinically available.

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