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

Base editing rescues seizures and sudden death in a SCN8A mutation-associated developmental epileptic encephalopathy model.

碱基编辑可挽救 SCN8A 突变相关发育性癫痫性脑病模型中的癫痫发作和猝死。

Reever Caeley M, Boscia Alexis R, Deutsch Tyler Cj, Patel Mansi P, Miralles Raquel M, Kittur Shrinidhi, Fleischel Erik J, Buo Atum Ml, Yorek Matthew S, Meisler Miriam H, Farber Charles R, Patel Manoj K

Identification of target genes and regulatory networks for bone mineral density GWAS loci through systematic targeting and inhibition

通过系统靶向和抑制,鉴定骨矿物质密度 GWAS 位点的目标基因和调控网络

Kahlani, Mohammadjavad; Mesner, Larry; Madhu, Vedavathi; Wagner, Lucia; Kupkova, Kristyna; Pitas, Hannah J; Mello, Ana C; Ghatan, Samuel; Lappalainen, Tuuli; Sanjana, Neville E; Morris, John A; Farber, Charles R

Author Correction: RhoA determines lineage fate of mesenchymal stem cells by modulating CTGF-VEGF complex in extracellular matrix

作者更正:RhoA通过调节细胞外基质中的CTGF-VEGF复合物来决定间充质干细胞的谱系命运

Li, Changjun; Zhen, Gehua; Chai, Yu; Xie, Liang; Crane, Janet L; Farber, Emily; Farber, Charles R; Luo, Xianghang; Gao, Peisong; Cao, Xu; Wan, Mei

[Mechanisms and intervention strategies of angiogenesis disorders in diabetic foot ulcers]

【糖尿病足溃疡血管生成障碍的机制及干预策略】

Wang, Tao; Yang, Liang; Yuan, Mingjie; Farber, Charles R; Spolski, Rosanne; Leonard, Warren J; Ganta, Vijay C; Annex, Brian H; 陶, 克; 曹, 涛; 郝, 彤

Osteoporosis Associated with SCN8A Mutation

与SCN8A基因突变相关的骨质疏松症

Khurram, Daniyeh; Kupkova, Kristyna; Mesner, Larry D; Kraftson, Andrew T; Farber, Charles R; Clines, Gregory A

Long-read proteogenomics to connect disease-associated sQTLs to the protein isoform effectors of disease.

利用长读长蛋白质基因组学将疾病相关的 sQTL 与疾病的蛋白质亚型效应因子联系起来

Abood Abdullah, Mesner Larry D, Jeffery Erin D, Murali Mayank, Lehe Micah D, Saquing Jamie, Farber Charles R, Sheynkman Gloria M

Multi-scale cortical bone traits vary in females and males from two mouse models of genetic diversity

来自两种遗传多样性小鼠模型的雌性和雄性小鼠的多尺度皮质骨特征存在差异

Migotsky, Nicole; Kumar, Surabhi; Shuster, John T; Coulombe, Jennifer C; Senwar, Bhavya; Gestos, Adrian A; Farber, Charles R; Ferguson, Virginia L; Silva, Matthew J

Systems genetics approaches for understanding complex traits with relevance for human disease

系统遗传学方法在理解与人类疾病相关的复杂性状方面的应用

Allayee, Hooman; Farber, Charles R; Seldin, Marcus M; Williams, Evan Graehl; James, David E; Lusis, Aldons J

Single-Cell Transcriptomics of Bone Marrow Stromal Cells in Diversity Outbred Mice: A Model for Population-Level scRNA-Seq Studies

多样性近交系小鼠骨髓基质细胞的单细胞转录组学:群体水平单细胞RNA测序研究模型

Dillard, Luke J; Rosenow, Will T; Calabrese, Gina M; Mesner, Larry D; Al-Barghouthi, Basel M; Abood, Abdullah; Farber, Emily A; Onengut-Gumuscu, Suna; Tommasini, Steven M; Horowitz, Mark A; Rosen, Clifford J; Yao, Lutian; Qin, Ling; Farber, Charles R

Multi-Scale Cortical Bone Traits Vary in Two Mouse Models of Genetic Diversity

两种遗传多样性小鼠模型中多尺度皮质骨性状存在差异

Migotsky, Nicole; Kumar, Surabhi; Shuster, John T; Coulombe, Jennifer C; Senwar, Bhavya; Gestos, Adrian A; Farber, Charles R; Ferguson, Virginia L; Silva, Matthew J