IN SITU EXPLORATION OF CHARACTERISTICS OF MACROPINOCYTOSIS AND SIZE RANGE OF INTERNALIZED SUBSTANCES IN CELLS BY 3D-STRUCTURED ILLUMINATION MICROSCOPY

In situ exploration of characteristics of macropinocytosis and size range of internalized substances in cells by 3D-structured illumination microscopy

Jing Jin,1 Yanting Shen,2 Biao Zhang,1 Rong Deng,3 Dianshuai Huang,1 Tianqi Lu,1 Fei Sun,1,* Shuping Xu,2,* Chongyang Liang1,*1Institute of Frontier Medical Science, Jilin University, Changchun 130021, Jilin, People’s Republic of RCA Cable China; 2State Key Lab of Supramolecular Structure and Materials, Jilin University, Changchun 130021, Jil

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Comparing Reforms of Juvenile Justice in Bangladesh and Malaysia

The article attempts to Baby Bib critically compare juvenile justice reforms in both jurisdictions of Bangladesh and Malaysia.It explores legal reforms in line with the international standards to ensure the effective juvenile justice system as well as child well-being in the respective legal systems.The juvenile justice practice of Bangladesh and M

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Does anime, idol culture bring depression? Structural analysis and deep learning on subcultural identity and various psychological outcomes

Subculture, includes animation, comics, games (ACG), and idol fan culture, is popular among young generations in Japan.Previous studies have shown different psychological outcomes within different subcultural groups; however, underlying mechanisms remain unclear.This study proposes that subcultural identity may play a crucial role in mental health

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A study protocol for evaluating the efficacy and safety of skin electrical stimulation for Leber hereditary optic neuropathy: a single-arm, open-label, non-randomized prospective exploratory study

Takuji Kurimoto, Kaori Ueda, Sotaro Mori, Mari Sakamoto, Yuko Yamada-Nakanishi, Wataru Matsumiya, Makoto NakamuraDivision of Ophthalmology, Department of Surgery, Kobe University Graduate School of Medicine, Kobe, JapanBackground: Leber hereditary optic neuropathy (LHON) is a maternally inherited disease caused by three missense mutations of mitoch

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