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Frontiers in Genetics|May 25, 2023
Genetic diagnosis of fetal microcephaly at a single tertiary center in ChinaYou Wang, Fang Fu, Tingying Lei, et al.BMC Medical Genomics|April 22, 2024
Single-cell RNA sequencing reveals cellular and molecular landscape of fetal cystic hygromaFang Fu, Xin Yang, Ru Li, et al.Genes|December 23, 2022
The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective StudyFang Fu, Ru Li, Qiu-Xia Yu, et al.Human Genetics|April 24, 2023
Prenatal diagnosis in the fetal hyperechogenic kidneys: assessment using chromosomal microarray analysis and exome sequencingRuibin Huang, Fang Fu, Hang Zhou, et al.Science Advances|January 10, 2025
Flap endonuclease 1 repairs DNA-protein cross-links via ADP-ribosylation-dependent mechanismsYilun Sun, Lisa M Jenkins, Lara H El Touny, et al.Nature Communications|February 2, 2026
PRMT3-mediated post-translational adaptation to fasting regulates metabolic flexibilityZhengyun Huang, Xiangpeng Liu, Xiyue Chen, et al.Atherosclerosis|April 8, 2021
Aging-induced isoDGR-modified fibronectin activates monocytic and endothelial cells to promote atherosclerosisJung Eun Park, Gnanasekaran JebaMercy, Kalailingam Pazhanchamy, et al.Genome Medicine|October 29, 2022
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetusesFang Fu, Ru Li, Qiuxia Yu, et al.Cell Reports|March 14, 2019
Displacement of WDR5 from Chromatin by a WIN Site Inhibitor with Picomolar AffinityErin R Aho, Jing Wang, Rocco D Gogliotti, et al.ACS Central Science|January 17, 2019
Canvass: A Crowd-Sourced, Natural-Product Screening Library for Exploring Biological SpaceSara E Kearney, Gergely Zahoránszky-Kőhalmi, Kyle R Brimacombe, et al.Pageof 23