Showing results (1-10 of 17) with videos related to
Sort By:
Pageof 2
Science (New York, N.Y.)|April 6, 2013
Nuclear actin network assembly by formins regulates the SRF coactivator MALChristian Baarlink, Haicui Wang, Robert GrosseMaterials (Basel, Switzerland)|October 27, 2022
Influence of Inertia on the Dynamic Compressive Strength of ConcreteZhangchen Qin, Dan Zheng, Xinxin Li, et al.International Journal of Molecular Sciences|December 23, 2022
LMNA Co-Regulated Gene Expression as a Suitable Readout after Precise Gene CorrectionHaicui Wang, Anne Krause, Helena Escobar, et al.Journal of Human Genetics|February 19, 2016
Homozygous mutation in Atlastin GTPase 1 causes recessive hereditary spastic paraplegiaLena Willkomm, Raul Heredia, Katrin Hoffmann, et al.Molecular Therapy. Nucleic Acids|November 6, 2018
Shorter Phosphorodiamidate Morpholino Splice-Switching Oligonucleotides May Increase Exon-Skipping Efficacy in DMDUgur Akpulat, Haicui Wang, Kerstin Becker, et al.Cell Research|December 21, 2011
Differing and isoform-specific roles for the formin DIAPH3 in plasma membrane blebbing and filopodia formationJana Stastna, Xiaoyu Pan, Haicui Wang, et al.The Turkish Journal of Pediatrics|March 6, 2020
Bi-allelic mutations in PRUNE lead to neurodegeneration with spinal motor neuron involvement and hyperCKaemiaDerya Okur, Hülya Sevcan Daimagüler, Ayça Ersen Danyeli, et al.Human Genome Variation|May 25, 2019
Clinical outcomes of two patients with a novel pathogenic variant in ASNS: response to asparagine supplementation and review of the literatureRosanne Sprute, Didem Ardicli, Kader Karli Oguz, et al.Iscience|June 30, 2026
Neuronal differentiation of neuroblastoma cell lines for neurological disease modelingClaudia Pommerenke, Vivien Hauer, Sonja Eberth, et al.Brain & Development|November 24, 2016
Dropped head congenital muscular dystrophy caused by de novo mutations in LMNAPakize Karaoglu, Nicolas Quizon, Matthias Pergande, et al.Pageof 2