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Antibiotics (Basel, Switzerland)|February 25, 2023
Molecular Rapid Diagnostics Improve Time to Effective Therapy and Survival in Patients with Vancomycin-Resistant <i>Enterococcus</i> Bloodstream InfectionsSarah M Bandy, Christopher B Jackson, Cody A Black, et al.
Cellular and Molecular Life Sciences : CMLS|November 16, 2023
GTPBP8 is required for mitoribosomal biogenesis and mitochondrial translationLiang Wang, Taru Hilander, Xiaonan Liu, et al.
Diagnostic Microbiology and Infectious Disease|July 1, 2020
The impact of rapid diagnostic testing, surveillance software, and clinical pharmacist staffing at a large community hospital in the management of Gram-negative bloodstream infectionsGerard W Gawrys, Khine Tun, Christopher B Jackson, et al.
BMC Neurology|January 18, 2011
Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndromeAndré Schaller, Dagmar Hahn, Christopher B Jackson, et al.
Frontiers in Molecular Biosciences|March 3, 2020
3D Co-culture of hiPSC-Derived Cardiomyocytes With Cardiac Fibroblasts Improves Tissue-Like Features of Cardiac SpheroidsPhilippe Beauchamp, Christopher B Jackson, Lijo Cherian Ozhathil, et al.
Clinical Chemistry|May 18, 2010
Quantitative 1-step DNA methylation analysis with native genomic DNA as templateThomas von Kanel, Dominik Gerber, André Schaller, et al.
Nature Communications|January 6, 2018
Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathyOlesia Ignatenko, Dmitri Chilov, Ilse Paetau, et al.
European Journal of Medical Genetics|April 17, 2017
A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathyChristopher B Jackson, Dagmar Hahn, Barbara Schröter, et al.
Neuropediatrics|January 8, 2025
Intravitreal Enzyme Replacement Therapy Slows Retinopathy in Late Infantile Ceroid Lipofuscinosis Type 2Claudia S Priglinger, Carolina Courage, Amelie S Lotz-Havla, et al.
American Journal of Medical Genetics. Part A|September 13, 2019
Novel synonymous and missense variants in FGFR1 causing Hartsfield syndromeCarolina Courage, Christopher B Jackson, Marta Owczarek-Lipska, et al.
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