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American Journal of Medical Genetics. Part A|May 5, 2016
A novel de novo dominant negative mutation in DNM1L impairs mitochondrial fission and presents as childhood epileptic encephalopathyJill A Fahrner, Raymond Liu, Michael Scott Perry, et al.Cancer Research|June 5, 2007
DNA methylation and complete transcriptional silencing of cancer genes persist after depletion of EZH2Kelly M McGarvey, Eriko Greene, Jill A Fahrner, et al.Journal of Molecular Biology|April 29, 1994
A mutant hook-associated protein (HAP3) facilitates torsionally induced transformations of the flagellar filament of Escherichia coliK A Fahrner, S M Block, S Krishnaswamy, et al.Journal of Neural Transmission (Vienna, Austria : 1996)|June 18, 2003
Pronounced arterial collateralization was induced after permanent rat cerebral four-vessel occlusion. Relation to neuropathology and capillary ultrastructureK Plaschke, C Sommer, A Fahrner, et al.Cancer Research|April 6, 2006
Silenced tumor suppressor genes reactivated by DNA demethylation do not return to a fully euchromatic chromatin stateKelly M McGarvey, Jill A Fahrner, Eriko Greene, et al.Journal of Virology|June 14, 2000
Retargeting the coxsackievirus and adenovirus receptor to the apical surface of polarized epithelial cells reveals the glycocalyx as a barrier to adenovirus-mediated gene transferR J Pickles, J A Fahrner, J M Petrella, et al.Pituitary|December 21, 2019
Acromegaly in the setting of Tatton-Brown-Rahman SyndromeC Hage, E Sabini, H Alsharhan, et al.Human Genetics|March 23, 2023
Five years of experience in the Epigenetics and Chromatin Clinic: what have we learned and where do we go from here?Jacqueline R Harris, Christine W Gao, Jacquelyn F Britton, et al.Biorxiv : the Preprint Server for Biology|July 10, 2023
Novel mouse model of Weaver syndrome displays overgrowth and excess osteogenesis reversible with KDM6A/6B inhibitionChristine W Gao, WanYing Lin, Ryan C Riddle, et al.JIMD Reports|October 24, 2018
Severe Neonatal Manifestations of Infantile Liver Failure Syndrome Type 1 Caused by Cytosolic Leucine-tRNA Synthetase DeficiencyChristina Peroutka, Jacqueline Salas, Jacquelyn Britton, et al.Pageof 5