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Hai-Ying Jin

Researcher at Sapporo Medical University

Publications -  16
Citations -  465

Hai-Ying Jin is an academic researcher from Sapporo Medical University. The author has contributed to research in topics: Tyrosinase & Melanosome. The author has an hindex of 10, co-authored 14 publications receiving 432 citations.

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Combination of porous hydroxyapatite and cationic liposomes as a vector for BMP-2 gene therapy

TL;DR: The results confirm the clinical usefulness of gene therapy for bone formation, using the BMP-2 gene combined with cationic liposomes as a vector and it is possible that the effects of administering the B MP-2 genes will be improved by specializing the microstructure of scaffold for gene therapy.
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Local administration of hepatocyte growth factor gene enhances the regeneration of dermis in acute incisional wounds.

TL;DR: HGF supplementation through gene therapy may be an effective strategy for treating wounds, as it increases the regeneration of the dermis to allow for "scarless wound healing," according to its antifibrotic effect.
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Tyrosinase-related proteins suppress tyrosinase-mediated cell death of melanocytes and melanoma cells.

TL;DR: It is suggested that TYRP1 and DCT play an important role in suppressing TYR-mediated cytotoxicity in melanocytic cells without decreasing TYR expression and/or activity.
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Intracellular vesicular trafficking of tyrosinase gene family protein in eu- and pheomelanosome biogenesis.

TL;DR: The intracellular vesicular trafficking in the melanosome biogenesis (melanogenesis) is reviewed with the incorporation of the authors' own experimental findings and it is suggested that tyrosinase is involved in lysosomal degradation after forming dopaquinone.
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Tyrosinase and tyrosinase-related protein 1 require Rab7 for their intracellular transport.

TL;DR: The findings indicate that the dominant-negative mutant of Rab7 impairs vesicular transport of tyrosinase and TRP-1, suggesting that the transport of these melanogenic proteins from the trans-Golgi network to maturing melanosomes requires passage through endosome-delineated compartments.