Publications by authors named "Jukyeong Jeong"

Article Synopsis
  • - This study focuses on creating an optimized method for cryopreserving the germ cells of an endangered snail species using vitrification, which is a new technique for preserving these organisms.
  • - Key reproductive organs like the ovotestis, which contains both male and female germ cells, were analyzed, revealing structures such as sperm and early germ cells through specific tissue staining methods.
  • - The results indicated that while cryopreservation using vitrification reduced cell viability (86.8%) compared to non-vitrification methods (96.6%), it provides a viable protocol for conserving the genetic resources of endangered snail species, potentially aiding broader biodiversity conservation efforts.
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This study aimed to develop a cryopreservation system for the reproductive organs of (oriental snail) to support the conservation of their species. The reproductive glands of are divided into numerous acini by acinar boundaries. Within each acinus, the presence of spermatogonia, spermatocytes, spermatids, and sperm were observed, indicating various stages of sperm development.

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During cementum formation, the key roles of osterix (Osx) and inorganic pyrophosphate (PPi), mainly controlled by nucleotide pyrophosphatase 1 (Npp1; encoded by the Enpp1 gene) and progressive ankylosis protein (Ank), have been demonstrated by animal models displaying altered cementum formation. In this study, we analyzed the relationship of Osx and local PPi during cementum formation using compound mutant mice with their wildtype and corresponding single gene mutants. Importantly, functional defects in PPi regulation led to the induction of Osx expression at the cervical cementum as demonstrated by Enpp1 mutant mice and cementoblasts with the retroviral transduction of small hairpin RNA for Enpp1 or Ank.

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Hutchinson-Gilford progeria syndrome (HGPS) is a rare accelerated senescence disease, manifesting dental abnormalities and several symptoms suggestive of premature aging. Although irregular secondary dentin formation in HGPS patients has been reported, pathological mechanisms underlying aberrant dentin formation remain undefined. In this study, we analyzed the mandibular molars of a tissue-specific mouse model that overexpresses the most common HGPS mutation (LMNA, c.

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