Seungbok相关文献与解析，生知库 | 链接生命科学的每一步

Lead-Free Tin-Based Perovskite LEDs Toward Rec. 2020: Organic Anion Coordination for Oxidation Suppression

面向 Rec. 2020 标准的无铅锡基钙钛矿 LED：有机阴离子配位抑制氧化

doi:10.1002/advs.202511006

Lee, Seungjae; Lee, Heeseung; Park, Joonho; Yeo, Hyeonwoo; Kim, Junho; Kim, Changjo; Kim, Hyojun; Lee, Seyun; Lee, Jihyung; Kim, Yun Hoo; Lee, Seungbok; Jeong, Seonju; Ying, Wu Bin; Lee, Ryong-Gyu; Kim, Yong-Hoon; Lee, Jung-Yong

发表日期：2026

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WWP1 gain-of-function drives developmental anoikis through TGFÎ² pathway during neurodevelopment.

WWP1 功能获得通过 TGFβ 通路在神经发育过程中驱动发育性失巢凋亡。

期刊:Cell Death Discovery

影响因子:7

doi:10.1038/s41420-026-02977-4

So Ki Hurn, Lee Seungbok, Wong Jiayi, Lee Hyunsik, Yun Eun-Jin, Jang Se Song, Choi Hee-Jung, Chae Jong-Hee, Baek Seung Tae

Drosophila Abi maintains blood cell homeostasis by promoting clathrin-mediated endocytosis of Notch.

果蝇 Abi 通过促进 Notch 的网格蛋白介导的内吞作用来维持血细胞稳态。

期刊:Journal of Cell Biology

影响因子:6.4

doi:10.1083/jcb.202505091

Park Hyun Gwan, Song Seunghwan, Kim Joohyung, Lee Seungbok

Another common genetic ataxia in South Korea: Spinocerebellar ataxia 36

韩国另一种常见的遗传性共济失调：脊髓小脑性共济失调36

期刊:European Journal of Human Genetics

影响因子:4.6

doi:10.1038/s41431-024-01783-9

Ahn, Jong Hyeon; Lee, Seungbok; Moon, Jangsup; Han, Yoojung; Chang, Hyeshik; Youn, Jinyoung; Cho, Jin Whan; Jang, Ja-Hyun

神经科学

发表日期：2026

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Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes

对R环形成区域的分析表明，RNU2-2和RNU5B-1是神经发育障碍基因。

期刊:Nature Genetics

影响因子:29

doi:10.1038/s41588-025-02209-y

Jackson, Adam; Thaker, Nishi; Blakes, Alexander; Rice, Gillian; Griffiths-Jones, Sam; Balasubramanian, Meena; Campbell, Jennifer; Shannon, Nora; Choi, Jungmin; Hong, Juhyeon; Hunt, David; de Burca, Anna; Kim, Soo Yeon; Kim, Taekeun; Lee, Seungbok; Redman, Melody; Rius, Rocio; Simons, Cas; Tan, Tiong Yang; Ellingford, Jamie; O'Keefe, Raymond T; Chae, Jong Hee; Banka, Siddharth

Publisher Correction: Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes

出版商更正：对R环形成区域的分析表明，RNU2-2和RNU5B-1是神经发育障碍基因。

期刊:Nature Genetics

影响因子:29

doi:10.1038/s41588-025-02274-3

Biallelic BRF2 mutations disrupt redox homeostasis as etiological factors in syndromic immunodeficiency and developmental disorders.

双等位基因 BRF2 突变破坏氧化还原稳态，是综合征性免疫缺陷和发育障碍的病因。

期刊:Molecular Therapy

影响因子:12

doi:10.1016/j.ymthe.2025.08.006

Yoon Seobin, Lee Seungbok, Kwon Haeyoon, Kim Hyo-Seung, Joo Jeong H, Hong Soogil, Kim Soo Yeon, Jang Sesong, Lee Hyunju, Choi Hyoung Soo, Cho Anna, Jeong Soyoung, Suh-Yun Joh Christine, Oh Hyeonseo, Choi Eui-Hwan, Choi Murim, Ahn Kangmo, Kim Hyun Je, Kim Keun Pil, Chae Jong-Hee

发育与干细胞

发表日期：2025

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Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders

罕见编码变异对神经发育障碍患者小头畸形的影响

期刊:Genome Medicine

影响因子:11.2

doi:10.1186/s13073-025-01513-w

Yoon, Jihoon G; Jang, Hyunsoo; Lee, Seungbok; Jang, Se Song; Park, Soojin; Cho, Jaeso; Kim, Minji; Han, Jiye; Yun, Hyounji; Kim, Man Jin; Kim, Soo Yeon; Kim, Woo Joong; Cho, Anna; Lee, Jin Sook; Choi, Murim; Fernandez-Jaen, Alberto; Silva, Sebastian; Uribe-San-Martín, Reinaldo; Cantillano, Christian; Miyake, Noriko; Lim, Byung Chan; Ko, Jung Min; Kim, Ki Joong; Yoon, Ki-Jun; Chae, Jong-Hee

Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approach.

采用综合诊断方法对感音神经性听力损失进行全面基因分析

期刊:Cell Reports Medicine

影响因子:10.6

doi:10.1016/j.xcrm.2025.102206

Lee Sang-Yeon, Lee Seungbok, Park Seongyeol, Jung Sung Ho, Yun Yejin, Choi Won Hoon, Cha Ju Hyuen, Yun Hongseok, Lee Sangmoon, Suh Myung-Whan, Park Moo Kyun, Song Jae-Jin, Choi Byung Yoon, Lee Jun Ho, Kang Tong Mook, Ju Young Seok, Koh June-Young, Chae Jong-Hee

神经科学

发表日期：2025

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Current Switching of Topological Spin Chirality in the van der Waals Antiferromagnet Co(1/3)TaS(2)

范德华反铁磁体Co(1/3)TaS(2)中拓扑自旋手性的电流切换

Lead-Free Tin-Based Perovskite LEDs Toward Rec. 2020: Organic Anion Coordination for Oxidation Suppression

面向 Rec. 2020 标准的无铅锡基钙钛矿 LED：有机阴离子配位抑制氧化

WWP1 gain-of-function drives developmental anoikis through TGFÎ² pathway during neurodevelopment.

WWP1 功能获得通过 TGFβ 通路在神经发育过程中驱动发育性失巢凋亡。

Drosophila Abi maintains blood cell homeostasis by promoting clathrin-mediated endocytosis of Notch.

果蝇 Abi 通过促进 Notch 的网格蛋白介导的内吞作用来维持血细胞稳态。

Another common genetic ataxia in South Korea: Spinocerebellar ataxia 36

韩国另一种常见的遗传性共济失调：脊髓小脑性共济失调36

Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes

对R环形成区域的分析表明，RNU2-2和RNU5B-1是神经发育障碍基因。

Publisher Correction: Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes

出版商更正：对R环形成区域的分析表明，RNU2-2和RNU5B-1是神经发育障碍基因。

Biallelic BRF2 mutations disrupt redox homeostasis as etiological factors in syndromic immunodeficiency and developmental disorders.

双等位基因 BRF2 突变破坏氧化还原稳态，是综合征性免疫缺陷和发育障碍的病因。

Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders

罕见编码变异对神经发育障碍患者小头畸形的影响

Comprehensive genetic profiling of sensorineural hearing loss using an integrative diagnostic approach.

采用综合诊断方法对感音神经性听力损失进行全面基因分析