Publications by authors named "J W Mickelson"

Objective: The tendency to linguistically synchronize is an adaptive and prosocial process observed in verbal and written communication. Research in therapeutic contexts has primarily conceptualized reciprocal language style matching (rLSM; i.e.

View Article and Find Full Text PDF
Article Synopsis
  • Chronic posttraumatic pain (CPTP) is prevalent after traumatic stress exposure (TSE), especially in women, and higher levels of 17β-estradiol (E2) during the traumatic event are linked to lower CPTP risks in women.
  • In a study involving 543 samples, researchers found a significant negative relationship between peritraumatic E2 levels and subsequent CPTP in women but not in men.
  • An animal study revealed that administering E2 immediately after TSE in female rats helped prevent mechanical hypersensitivity, suggesting that timely E2 treatment could be a potential therapeutic approach for women at risk of developing CPTP.
View Article and Find Full Text PDF

(1) Background: An adult dog was presented to a board-certified veterinary neurologist for evaluation of chronic weakness, exercise intolerance and lactic acidemia. (2) Methods: A mitochondrial myopathy was diagnosed based on the histological and histochemical phenotype of numerous COX-negative muscle fibers. Whole-genome sequencing established the presence of multiple extended deletions in the mitochondrial DNA (mtDNA), with the highest prevalence between the 1-11 kb positions of the approximately 16 kb mitochondrial chromosome.

View Article and Find Full Text PDF

Disease-causing variants have been identified for less than 20% of suspected equine genetic diseases. Whole genome sequencing (WGS) allows rapid identification of rare disease causal variants. However, interpreting the clinical variant consequence is confounded by the number of predicted deleterious variants that healthy individuals carry (predicted genetic burden).

View Article and Find Full Text PDF

(1) Background: Muscle hypertrophy, swallowing disorders, and gait abnormalities are clinical signs common to many muscle diseases, including muscular dystrophies, non-dystrophic myotonias, genetic myopathies associated with deficiency of myostatin, and acquired inflammatory myopathies. Here, we investigated underlying causes of this triad of clinical signs in four young French bulldogs via muscle histopathology coupled with whole genome and Sanger sequencing. (2) Methods: Dogs were evaluated by veterinary clinical internists and neurologists, and biopsies were obtained for histopathological diagnosis.

View Article and Find Full Text PDF