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

Functional analysis of NPR2 variants supports the therapeutic rationale for CNP in short stature

NPR2 变异体的功能分析支持了矮小症 CNP 的治疗理论依据

Jeong, Raehoon; Covarrubias, Sergio; Shanghavi, Devanshi; Ruhrmund, Donald; Estrada, Karol; Zhou, Dejie; Marom, Nofar; Bauer, Christopher R; Froelich, Steven

Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity

人类叉头转录因子中的错义变异揭示了叉头DNA双特异性的决定因素

King, Jessica; Gisselbrecht, Stephen S; Dias, Julie-Alexia; Jeong, Raehoon; Rothman, Elisabeth; Bulyk, Martha L

Chromatin accessibility variation provides insights into missing regulation underlying immune-mediated diseases

染色质可及性变异为免疫介导疾病中缺失的调控机制提供了新的见解

Jeong, Raehoon; Bulyk, Martha L

Meta-analysis reveals transcription factors and DNA binding domain variants associated with congenital heart defect and orofacial cleft

荟萃分析揭示了与先天性心脏缺陷和唇腭裂相关的转录因子和DNA结合域变异

Jeong, Raehoon; Bulyk, Martha L

Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays

利用人类测序、斑马鱼筛选和蛋白质结合微阵列技术鉴定眼部先天性颅神经运动神经元疾病的致病基因

Jurgens, Julie A; Matos Ruiz, Paola M; King, Jessica; Foster, Emma E; Berube, Lindsay; Chan, Wai-Man; Barry, Brenda J; Jeong, Raehoon; Rothman, Elisabeth; Whitman, Mary C; MacKinnon, Sarah; Rivera-Quiles, Cristina; Pratt, Brandon M; Easterbrooks, Teresa; Mensching, Fiona M; Di Gioia, Silvio Alessandro; Pais, Lynn; England, Eleina M; de Berardinis, Teresa; Magli, Adriano; Koc, Feray; Asakawa, Kazuhide; Kawakami, Koichi; O'Donnell-Luria, Anne; Hunter, David G; Robson, Caroline D; Bulyk, Martha L; Engle, Elizabeth C

Meta-analysis reveals transcription factors and DNA binding domain variants associated with congenital heart defect and orofacial cleft

荟萃分析揭示了与先天性心脏缺陷和唇腭裂相关的转录因子和DNA结合域变异

Jeong, Raehoon; Bulyk, Martha L

Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity

人类叉头转录因子中的错义变异揭示了叉头DNA双特异性的决定因素

King, Jessica; Gisselbrecht, Stephen S; Dias, Julie-Alexia; Jeong, Raehoon; Rothman, Elisabeth; Bulyk, Martha L

Chromatin accessibility variation provides insights into missing regulation underlying immune-mediated diseases

染色质可及性变异为免疫介导疾病中缺失的调控机制提供了新的见解

Jeong, Raehoon; Bulyk, Martha L

DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues.

对同源域中罕见变异体的DNA结合分析揭示了决定同源域特异性的残基

Kock Kian Hong, Kimes Patrick K, Gisselbrecht Stephen S, Inukai Sachi, Phanor Sabrina K, Anderson James T, Ramakrishnan Gayatri, Lipper Colin H, Song Dongyuan, Kurland Jesse V, Rogers Julia M, Jeong Raehoon, Blacklow Stephen C, Irizarry Rafael A, Bulyk Martha L

Pharmacokinetic Comparison Between a Fixed-Dose Combination of Atorvastatin/Omega-3-Acid Ethyl Esters and the Corresponding Loose Combination in Healthy Korean Male Subjects

在健康韩国男性受试者中,阿托伐他汀/ω-3脂肪酸乙酯固定剂量复方制剂与相应松散复方制剂的药代动力学比较

Khwarg, Juyoung; Lee, Soyoung; Jang, In-Jin; Kang, Won-Ho; Lee, Hye Jung; Kim, Kyu Yeon; Jeong, Ki-Sun; Won, Chongho; Choi, Youn Woong; Ha, Dae Chul; Jung, RaeHoon; Han, Min-Gu; Jung, Won Tae; Nam, Kyu-Yeol; Kim, YeSeul; Yu, Kyung-Sang; Oh, Jaeseong