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

Nanobody-Based CAR NK Cells for Possible Immunotherapy of Mesothelin(+) Tumors.

基于纳米抗体的 CAR NK 细胞用于间皮素(+)肿瘤的潜在免疫治疗

Jung Dana, Choi Eunjeong, Jeoung Young-Hee, Lee Juheon, Gong Eun-Yeung, Jo Seo-Gyeong, Noh Kyunghee, Ha Kyungsoo, Wee Gabbine, Kim Hyeran, Jung Juyeon, Kim Seokho

Assessing the predictive ability of computational epitope prediction methods on Fel d 1 and other allergens

评估计算表位预测方法对Fel d 1和其他过敏原的预测能力

Kwon, Hyeji; Ko, Soobon; Ha, Kyungsoo; Lee, Jungjoon K; Choi, Yoonjoo

Pan-cancer analysis reveals multifaceted roles of retrotransposon-fusion RNAs

泛癌分析揭示逆转录转座子融合RNA的多方面作用

Lee, Boram; Park, Junseok; Voshall, Adam; Maury, Eduardo; Kang, Yeeok; Kim, Yoen Jeong; Lee, Jin-Young; Shim, Hye-Ran; Kim, Hyo-Ju; Lee, Jung-Woo; Jung, Min-Hyeok; Kim, Si-Cho; Chu, Hoang Bao Khanh; Kim, Da-Won; Kim, Minjeong; Choi, Eun-Ji; Hwang, Ok Kyung; Lee, Ho Won; Ha, Kyungsoo; Choi, Jung Kyoon; Kim, Yongjoon; Choi, Yoonjoo; Park, Woong-Yang; Lee, Eunjung Alice

Acetylation of TIP60 at K104 is essential for metabolic stress-induced apoptosis in cells of hepatocellular cancer

TIP60 K104 位点的乙酰化对于肝细胞癌细胞代谢应激诱导的细胞凋亡至关重要。

Fang, Xiao; Lu, Guojun; Ha, Kyungsoo; Lin, Han; Du, Ye; Zuo, Qiuhong; Fu, Yi; Zou, Chaoxia; Zhang, Pumin

The presence of two rare genomic syndromes, 1q21 deletion and Xq28 duplication, segregating independently in a family with intellectual disability

在一个智力障碍家族中,存在两种罕见的基因组综合征:1q21缺失和Xq28重复,且二者独立分离。

Ha, Kyungsoo; Shen, Yiping; Graves, Tyler; Kim, Cheol-Hee; Kim, Hyung-Goo

Familial 46,XY sex reversal without campomelic dysplasia caused by a deletion upstream of the SOX9 gene

由SOX9基因上游缺失引起的家族性46,XY性逆转,不伴有弯曲骨发育不良

Bhagavath, Bala; Layman, Lawrence C; Ullmann, Reinhard; Shen, Yiping; Ha, Kyungsoo; Rehman, Khurram; Looney, Stephen; McDonough, Paul G; Kim, Hyung-Goo; Carr, Bruce R

MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis

MYBPC1 突变会损害斑马鱼关节挛缩症模型中的骨骼肌功能。

Ha, Kyungsoo; Buchan, Jillian G; Alvarado, David M; McCall, Kevin; Vydyanath, Anupama; Luther, Pradeep K; Goldsmith, Matthew I; Dobbs, Matthew B; Gurnett, Christina A

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries

染色体异常测序揭示了跨越诊断界限的神经发育风险基因位点。

Talkowski, Michael E; Rosenfeld, Jill A; Blumenthal, Ian; Pillalamarri, Vamsee; Chiang, Colby; Heilbut, Adrian; Ernst, Carl; Hanscom, Carrie; Rossin, Elizabeth; Lindgren, Amelia M; Pereira, Shahrin; Ruderfer, Douglas; Kirby, Andrew; Ripke, Stephan; Harris, David J; Lee, Ji-Hyun; Ha, Kyungsoo; Kim, Hyung-Goo; Solomon, Benjamin D; Gropman, Andrea L; Lucente, Diane; Sims, Katherine; Ohsumi, Toshiro K; Borowsky, Mark L; Loranger, Stephanie; Quade, Bradley; Lage, Kasper; Miles, Judith; Wu, Bai-Lin; Shen, Yiping; Neale, Benjamin; Shaffer, Lisa G; Daly, Mark J; Morton, Cynthia C; Gusella, James F

Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome

鼻内胚胎促性腺激素释放激素因子(NELF)突变与正常嗅觉低促性腺激素性性腺功能减退症和卡尔曼综合征患者相关

Xu, Ning; Kim, Hyung-Goo; Bhagavath, Balasubramanian; Cho, Sung-Gyu; Lee, Jae Ho; Ha, Kyungsoo; Meliciani, Irene; Wenzel, Wolfgang; Podolsky, Robert H; Chorich, Lynn P; Stackhouse, Kathryn A; Grove, Anna M H; Odom, Lawrence N; Ozata, Metin; Bick, David P; Sherins, Richard J; Kim, Soo-Hyun; Cameron, Richard S; Layman, Lawrence C

Rapid and transient recruitment of DNMT1 to DNA double-strand breaks is mediated by its interaction with multiple components of the DNA damage response machinery

DNMT1 与 DNA 损伤反应机制的多个组分相互作用,介导其快速且短暂地募集到 DNA 双链断裂位点。

Ha, Kyungsoo; Lee, Gun Eui; Palii, Stela S; Brown, Kevin D; Takeda, Yoshihiko; Liu, Kebin; Bhalla, Kapil N; Robertson, Keith D