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Journal of Molecular and Cellular Cardiology|September 23, 2015
p63RhoGEF regulates auto- and paracrine signaling in cardiac fibroblastsAnita Ongherth, Sebastian Pasch, Christina M Wuertz, et al.Nature Communications|November 5, 2022
Lamin A/C-dependent chromatin architecture safeguards naïve pluripotency to prevent aberrant cardiovascular cell fate and functionYinuo Wang, Adel Elsherbiny, Linda Kessler, et al.Scientific Reports|September 13, 2016
Sequence variation between 462 human individuals fine-tunes functional sites of RNA processingPedro G Ferreira, Martin Oti, Matthias Barann, et al.Nature Cardiovascular Research|September 25, 2024
RNF20-mediated transcriptional pausing and VEGFA splicing orchestrate vessel growthNalan Tetik-Elsherbiny, Adel Elsherbiny, Aadhyaa Setya, et al.European Journal of Medical Genetics|March 5, 2013
Mutations at Ser331 in the HSN type I gene SPTLC1 are associated with a distinct syndromic phenotypeMichaela Auer-Grumbach, Heiko Bode, Thomas R Pieber, et al.Journal of Neurology|March 15, 2014
Whole-exome sequencing in patients with inherited neuropathies: outcome and challengesMaria Schabhüttl, Thomas Wieland, Jan Senderek, et al.Scientific Reports|June 9, 2017
Lipopolysaccharides induced inflammatory responses and electrophysiological dysfunctions in human-induced pluripotent stem cell derived cardiomyocytesGökhan Yücel, Zhihan Zhao, Ibrahim El-Battrawy, et al.American Journal of Human Genetics|November 13, 2012
DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduriaKatharina Danhauser, Sven W Sauer, Tobias B Haack, et al.American Journal of Human Genetics|May 26, 2015
Recessive mutations in the α3 (VI) collagen gene COL6A3 cause early-onset isolated dystoniaMichael Zech, Daniel D Lam, Ludmila Francescatto, et al.Clinical Pharmacology and Therapeutics|April 5, 2019
Drug Testing in Human-Induced Pluripotent Stem Cell-Derived Cardiomyocytes From a Patient With Short QT Syndrome Type 1Zhihan Zhao, Xin Li, Ibrahim El-Battrawy, et al.Pageof 22