Publications by authors named "Dongyoon Yoo"

Article Synopsis
  • The aggregation of α-synuclein in the nervous system leads to α-synucleinopathies, with Lewy body dementia (LBD) being a primary form of dementia characterized by Lewy bodies and neurites.
  • Despite being the second leading cause of dementia after Alzheimer's, there is limited understanding of LBD’s pathological mechanisms and diagnostic criteria.
  • The study used mass spectrometry to identify 179 proteins with significant changes post α-synuclein injection, linking several neurodegenerative pathways and suggesting a potential framework for distinguishing LBD from other dementias based on later cortical proteome changes.
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Gut barrier dysfunction occurs commonly in patients with critical disorders, leading to the translocation of luminal toxic substances and bacteria to the bloodstream. Connexin 43 (Cx43) acts as a gap junction protein and is crucial for intercellular communication and the diffusion of nutrients. The levels of cellular Cx43 are tightly regulated by multiple factors, including polyamines, but the exact mechanism underlying the control of Cx43 expression remains largely unknown.

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Purpose: Pubertal gonadotropin secretion shows circadian pattern and the luteinizing hormone (LH) levels tend to rise in later stages of puberty in girls. We studied the usefulness of basal LH in the evaluation of central precocious puberty with emphasis on the influence of sampling time.

Methods: Medical records of 334 girls that underwent gonadotropin-releasing hormone stimulation test (GnRHST) were reviewed.

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Purpose: The triglyceride-to-high-density lipoprotein cholesterol (TG/HDL-C) ratio has recently been reported as a biomarker of cardiometabolic risk in obese children and adolescents. The purpose of this study is to describe the TG/HDL-C ratio and related factors in overweight and normal weight Korean children and to evaluate whether the high TG/HDL-C ratio is associated with insulin resistance in overweight children and adolescents.

Methods: Data from 255 overweight (aged 8.

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Neonatal hypocalcemia and congenital heart defects has been known as the first clinical manifestation of the chromosome 22q11.2 deletion syndrome (22q11DS). However, because of its wide clinical spectrum, diagnosis of 22q11DS can be delayed in children without classic symptoms.

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