日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathy

RNU2-2基因的双等位基因变异会导致一种非常常见的发育性和癫痫性脑病。

Jackson, Adam; Blakes, Alexander J M; Alhaddad, Bader; Henry, Olivia J; Delgado-Vega, Angelica M; Wall, Elizabeth; Abdelhadi, Ola; Agrawal, Shakti; Bakur, Khadijah; Blair, Edward; Brady, Angela F; Brittain, Helen; Chandler, Kate E; Clarke, Natasha; Danelli, Miriana; Drinkall, Nicholas; Duba, Irene; Elmslie, Frances; Ellingford, Jamie; Ewans, Lisa J; Fennell, Andrew P; Gazdagh, Gabriella; Heller, Simon P; Hammarsjö, Anna; Karrman, Kristina; Kini, Usha; Lesko, Nicole; Lindstrand, Anna; Macintosh, Rebecca; Mansour, Sahar; Menzies, Lara; Metcalfe, Kay; Milhench, Alison; Nashef, Lina; O'Keefe, Raymond T; Pacheco, Nadja Pekkola; Palmer, Elizabeth E; Parida, Amitav; Prescott, Katrina; Redman, Melody; Renieri, Alessandra; Fallerini, Chiara; Rizzo, Caterina Lo; Sachdev, Rani; Simons, Cas; Sisodiya, Sanjay M; Stewart, Helen; Stödberg, Tommy; Banos-Pinero, Benito; Taylan, Fulya; Thomas, Huw B; Tinella, Flavia; Wiafe, Samuel; Wedell, Anna; Whiffin, Nicola; Walker, Susan; Rius, Rocio; Chae, Jong Hee; Nordgren, Ann; Alkuraya, Fowzan; Lord, Jenny; Banka, Siddharth

Reversibility and therapeutic feasibility of DNM1L-associated neurodevelopmental disorders.

DNM1L相关神经发育障碍的可逆性和治疗可行性。

So Ki Hurn, Kim Se Hee, Jang Shinyoung, Sang Hyeun Deok, Yun Eun-Jin, Choi Hee-Jung, Chae Jong-Hee, Baek Seung Tae

WWP1 gain-of-function drives developmental anoikis through TGFβ 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。

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

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。

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。

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

Inhibiting EZH2 complements steroid effects in Duchenne muscular dystrophy.

抑制 EZH2 可增强类固醇在杜氏肌营养不良症中的作用

Jeon Eun Young, Kwak Yejin, Kang Hyeji, Kim Hanbyeol, Jin Se Young, Park Soojin, Kim Ryeo Gyeong, Ko Dayoung, Won Jae-Kyung, Cho Anna, Jung Inkyung, Lee Chul-Hwan, Park Jeongbin, Kim Hyun-Young, Chae Jong-Hee, Choi Murim

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。

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

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

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

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

Effects of heterozygous SMG1 mutations on nonsense-mediated mRNA decay in human pluripotent stem cell model.

杂合SMG1突变对人类多能干细胞模型中无义介导的mRNA衰变的影响

Lee Chanyoung, Lee Jin Sook, Kwon Yejin, Shin Aeri, Jeong Tae Yeong, Yang Jiyun, Hwang Jung Woo, Kim Hyeong-In, Choi Hee-Jung, Kim Yoon Ki, Choi Murim, Kim Kyoungmi, Sun Woong, Chae Jong-Hee