Publications by authors named "W David Mauck"

We combined mitochondrial DNA sequence data and paleoclimatic distribution models to document phylogeographic patterns and investigate the historical demography of two manakins, and , as well as to explore connections between Amazonia and the Atlantic Forest. ND2 sequences of (75 individuals, 24 sites) and (196, 77) were used in Bayesian inference and maximum likelihood analyses. We estimated mitochondrial nucleotide diversity, employed statistical tests to detect deviations from neutral evolution and constant population sizes, and used species distribution modeling to infer the location of suitable climate for both species under present-day conditions, the Last Glacial Maximum (LGM), and the Last Interglacial Maximum (LIG).

View Article and Find Full Text PDF

Introduction: Chronic axial low back pain (CLBP) that is not responsive to medication management or physical therapy often requires significant clinical intervention. Several interventional pain management options exist, including a 60-day peripheral nerve stimulation (PNS) treatment. This economic evaluation investigated the potential for projected cost savings associated with prioritizing 60-day PNS treatment relative to a 'standard of care' (SOC) approach (where patients do not have access to 60-day PNS).

View Article and Find Full Text PDF
Article Synopsis
  • The study investigated the relationship between patient response to a diagnostic peripheral nerve block before receiving a peripheral nerve stimulator (PNS) and the effectiveness of the PNS in reducing pain.
  • Researchers analyzed medical records from the Mayo Clinic, focusing on patients who received PNS implantation between January 2014 and January 2023, examining pain relief at three and six months post-implantation.
  • Out of 173 patients examined, results showed no significant differences in pain relief outcomes for those who had the diagnostic block compared to those who did not, both in temporary and permanent PNS groups.
View Article and Find Full Text PDF

Pooled CRISPR screens coupled with single-cell RNA-sequencing have enabled systematic interrogation of gene function and regulatory networks. Here, we introduce Cas13 RNA Perturb-seq (CaRPool-seq), which leverages the RNA-targeting CRISPR-Cas13d system and enables efficient combinatorial perturbations alongside multimodal single-cell profiling. CaRPool-seq encodes multiple perturbations on a cleavable CRISPR array that is associated with a detectable barcode sequence, allowing for the simultaneous targeting of multiple genes.

View Article and Find Full Text PDF