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

Quantifying cell traction forces at the single-fiber scale in 3D: An approach based on deformable photopolymerized fiber arrays

在三维空间中量化单纤维尺度上的细胞牵引力:一种基于可变形光聚合纤维阵列的方法

Ucla, Pierre; Lê-Chesnais, Joanne; Ver Hulst, Henri; Ju, Xingming; Calvente, Isabel; Nematollahi, Elnaz; Leconte, Ludovic; Salamero, Jean; Bonnet, Isabelle; Monnot, Catherine; Moreau, Hélène D; Landoulsi, Jessem; Semetey, Vincent; Coscoy, Sylvie

Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects

全外显子组测序发现右侧先天性心脏缺陷中存在新的GATA5/6变异

Zodanu, Gloria K E; Hwang, John H; Mudery, Jordan; Sisniega, Carlos; Kang, Xuedong; Wang, Lee-Kai; Barsegian, Alexander; Biniwale, Reshma M; Si, Ming-Sing; Halnon, Nancy J; Ucla Congenital Heart Defects-BioCore Faculty; Grody, Wayne W; Satou, Gary M; Van Arsdell, Glen S; Nelson, Stanly F; Touma, Marlin

High-Throughput Genomics Identify Novel FBN1/2 Variants in Severe Neonatal Marfan Syndrome and Congenital Heart Defects

高通量基因组学鉴定出与严重新生儿马凡综合征和先天性心脏缺陷相关的新型FBN1/2变异

Zodanu, Gloria K E; Hwang, John H; Mehta, Zubin; Sisniega, Carlos; Barsegian, Alexander; Kang, Xuedong; Biniwale, Reshma; Si, Ming-Sing; Satou, Gary M; Halnon, Nancy; Ucla Congenital Heart Defect BioCore Faculty; Grody, Wayne W; Van Arsdell, Glen S; Nelson, Stanley F; Touma, Marlin

Whole-Exome Sequencing Identifies Homozygote Nonsense Variants in LMOD2 Gene Causing Infantile Dilated Cardiomyopathy

全外显子组测序鉴定出导致婴儿扩张型心肌病的 LMOD2 基因纯合无义变异

Reiri Sono, Tania M Larrinaga, Alden Huang, Frank Makhlouf, Xuedong Kang, Jonathan Su, Ryan Lau, Valerie A Arboleda, Reshma Biniwale, Gregory A Fishbein, Negar Khanlou, Ming-Sing Si, Gary M Satou, Nancy Halnon, Ucla Congenital Heart Defects-BioCore Faculty, Glen S Van Arsdell, Carol C Gregorio, Stan

Kinetics of mRNA nuclear export regulate innate immune response gene expression

mRNA 核输出动力学调节先天免疫反应基因表达

Diane Lefaudeux, Supriya Sen, Kevin Jiang, Alexander Hoffmann; UCLA Ribonomics Group

Dynamics of Endothelial Engagement and Filopodia Formation in Complex 3D Microscaffolds

复杂 3D 微支架中内皮细胞参与和丝状伪足形成的动力学

Pierre Ucla, Xingming Ju, Melisa Demircioglu, Sarah Baiz, Laurent Muller, Stéphane Germain, Catherine Monnot, Vincent Semetey, Sylvie Coscoy

De novo loss-of-function variants in STAG2 are associated with developmental delay, microcephaly, and congenital anomalies

STAG2 的新生功能丧失变异与发育迟缓、小头畸形和先天性异常有关

Sureni V Mullegama, Steven D Klein, Milene V Mulatinho, Tharanga Niroshini Senaratne, Kathryn Singh; UCLA Clinical Genomics Center; Dzung C Nguyen, Natalie M Gallant, Samuel P Strom, Shahnaz Ghahremani, Nagesh P Rao, Julian A Martinez-Agosto

Truncating mutations in APP cause a distinct neurological phenotype

APP 截短突变导致独特的神经表型

Steven Klein, Alexander Goldman, Hane Lee, Shahnaz Ghahremani, Viraj Bhakta; UCLA Clinical Genomics Center; Stanley F Nelson, Julian A Martinez-Agosto

De novo nonsense mutations in KAT6A, a lysine acetyl-transferase gene, cause a syndrome including microcephaly and global developmental delay

赖氨酸乙酰转移酶基因 KAT6A 的新生无义突变可导致包括小头畸形和整体发育迟缓在内的综合征

Valerie A Arboleda, Hane Lee, Naghmeh Dorrani, Neda Zadeh, Mary Willis, Colleen Forsyth Macmurdo, Melanie A Manning, Andrea Kwan, Louanne Hudgins, Florian Barthelemy, M Carrie Miceli, Fabiola Quintero-Rivera, Sibel Kantarci, Samuel P Strom, Joshua L Deignan; UCLA Clinical Genomics Center; Wayne W Gr

Evidence for transcript networks composed of chimeric RNAs in human cells

人类细胞中嵌合RNA组成的转录组网络的证据

Djebali, Sarah; Lagarde, Julien; Kapranov, Philipp; Lacroix, Vincent; Borel, Christelle; Mudge, Jonathan M; Howald, Cédric; Foissac, Sylvain; Ucla, Catherine; Chrast, Jacqueline; Ribeca, Paolo; Martin, David; Murray, Ryan R; Yang, Xinping; Ghamsari, Lila; Lin, Chenwei; Bell, Ian; Dumais, Erica; Drenkow, Jorg; Tress, Michael L; Gelpí, Josep Lluís; Orozco, Modesto; Valencia, Alfonso; van Berkum, Nynke L; Lajoie, Bryan R; Vidal, Marc; Stamatoyannopoulos, John; Batut, Philippe; Dobin, Alex; Harrow, Jennifer; Hubbard, Tim; Dekker, Job; Frankish, Adam; Salehi-Ashtiani, Kourosh; Reymond, Alexandre; Antonarakis, Stylianos E; Guigó, Roderic; Gingeras, Thomas R