Publications by authors named "K K KRUEGER"

Off-label hypomethylating agents and venetoclax (HMA/VEN) are often used for relapsed and refractory (R/R) AML patients. However, predictors of outcome are elusive. The objective of the current retrospective observational multicenter study of 240 adult patients (median age 68.

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The activation of progenitor cells near wound sites is a common feature of regeneration across species, but the conserved signaling mechanisms responsible for this step in whole-body regeneration are still incompletely understood. The acoel undergoes whole-body regeneration using Piwi+ pluripotent adult stem cells (neoblasts) that accumulate at amputation sites early in the regeneration process. The EGFR signaling pathway has broad roles in controlling proliferation, migration, differentiation, and cell survival across metazoans.

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Twenty years ago, Rotundo et al. (2001) meta-analyzed the gender differences in sexual harassment (SH) perception. They found an overall d of 0.

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Article Synopsis
  • - Individuals with subjective memory complaints (SMCs) have higher levels of neurodegeneration biomarkers like neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP), indicating increased neurodegenerative processes.
  • - The study involved 1,096 older adults and found that those with more memory complaints experienced a 12% increase in NfL and a 9.4% increase in GFAP compared to those with fewer complaints.
  • - Participants reporting more memory issues also showed a faster cognitive decline, suggesting that SMCs could help identify individuals at higher risk for neurodegenerative conditions.
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Most cancers present with mutations or amplifications in distinctive tumor promoter genes that activate principal cell-signaling cascades promoting cell proliferation, dedifferentiation, cell survival, and replicative immortality. Somatic mutations found in this these driver proto-oncogenes invariably result in constitutive activation of the encoded protein. A salient feature of the activating mutations observed throughout many thousands of clinical tumor specimens reveals these driver missense mutations are recurrent and restricted to just one or very few codons of the entire gene, suggesting they have been positively selected during the course of tumor development.

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