Publications by authors named "Christopher B Jackson"

21Publications

The impact of rapid diagnostic testing, surveillance software, and clinical pharmacist staffing at a large community hospital in the management of Gram-negative bloodstream infections.

Diagn Microbiol Infect Dis 2020 Sep 16;98(1):115084. Epub 2020 May 16.

Pharmacotherapy Education & Research Center, UT Health Science Center at San Antonio, 7703 Floyd Curl Drive, San Antonio, TX 78229; The University of Texas at Austin College of Pharmacy, 2409 University Ave., Austin, TX 78712. Electronic address:

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http://dx.doi.org/10.1016/j.diagmicrobio.2020.115084DOI Listing
September 2020

Therapeutic Manipulation of mtDNA Heteroplasmy: A Shifting Perspective.

Trends Mol Med 2020 07 26;26(7):698-709. Epub 2020 Mar 26.

CRUK Beatson Institute, Glasgow, UK; Institute of Cancer Sciences, University of Glasgow, Glasgow, UK. Electronic address:

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http://dx.doi.org/10.1016/j.molmed.2020.02.006DOI Listing
July 2020

Fibroblast Growth Factor 21 Drives Dynamics of Local and Systemic Stress Responses in Mitochondrial Myopathy with mtDNA Deletions.

Cell Metab 2019 12 12;30(6):1040-1054.e7. Epub 2019 Sep 12.

Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki, 00290 Helsinki, Finland; Department of Neurosciences, Helsinki University Central Hospital, 00290 Helsinki, Finland; Neuroscience Center, University of Helsinki, 00290 Helsinki, Finland. Electronic address:

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http://dx.doi.org/10.1016/j.cmet.2019.08.019DOI Listing
December 2019

Novel synonymous and missense variants in FGFR1 causing Hartsfield syndrome.

Am J Med Genet A 2019 12 11;179(12):2447-2453. Epub 2019 Sep 11.

Institute of Human Genetics, University of Leipzig Medical Center, Leipzig, Germany.

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http://dx.doi.org/10.1002/ajmg.a.61354DOI Listing
December 2019

Temozolomide Sensitizes MGMT-Deficient Tumor Cells to ATR Inhibitors.

Cancer Res 2019 09 4;79(17):4331-4338. Epub 2019 Jul 4.

Department of Therapeutic Radiology, Yale University School of Medicine, New Haven, Connecticut.

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http://dx.doi.org/10.1158/0008-5472.CAN-18-3394DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6810597PMC
September 2019

Reply to 'Letter to Editor by Finsterer J and Zarrouk-Mahjoub S: Phenotypic manifestations of the m.8969G>A variant'.

Neurogenetics 2018 05 26;19(2):133-134. Epub 2018 Feb 26.

Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.

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http://dx.doi.org/10.1007/s10048-018-0542-zDOI Listing
May 2018

Defective mitochondrial ATPase due to rare mtDNA m.8969G>A mutation-causing lactic acidosis, intellectual disability, and poor growth.

Neurogenetics 2018 01 19;19(1):49-53. Epub 2018 Jan 19.

Research Programs Unit, Molecular Neurology, Biomedicum-Helsinki, University of Helsinki, Helsinki, Finland.

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http://dx.doi.org/10.1007/s10048-018-0537-9DOI Listing
January 2018

Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy.

Nat Commun 2018 01 4;9(1):70. Epub 2018 Jan 4.

Research Programs Unit, Molecular Neurology, Biomedicum Helsinki, Haartmaninkatu 8, University of Helsinki, Helsinki, 00014, Finland.

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http://www.nature.com/articles/s41467-017-01859-9
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http://dx.doi.org/10.1038/s41467-017-01859-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754366PMC
January 2018

A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy.

Eur J Med Genet 2017 Jun 13;60(6):345-351. Epub 2017 Apr 13.

Division of Human Genetics, Bern, University Hospital Bern, Switzerland. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2017.04.006DOI Listing
June 2017

SDHA mutation with dominant transmission results in complex II deficiency with ocular, cardiac, and neurologic involvement.

Am J Med Genet A 2017 Jan 28;173(1):225-230. Epub 2016 Sep 28.

Division of Human Genetics, Department of Pediatrics, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1002/ajmg.a.37986DOI Listing
January 2017

Novel mitochondrial tRNA(Ile) m.4282A>G gene mutation leads to chronic progressive external ophthalmoplegia plus phenotype.

Br J Ophthalmol 2014 Oct 17;98(10):1453-9. Epub 2014 Jul 17.

Division of Human Genetics, Departments of Pediatrics and Clinical Research, Inselspital, University of Berne, Berne, Switzerland.

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http://dx.doi.org/10.1136/bjophthalmol-2014-305300DOI Listing
October 2014

qPCR-based mitochondrial DNA quantification: influence of template DNA fragmentation on accuracy.

Biochem Biophys Res Commun 2012 Jul 5;423(3):441-7. Epub 2012 Jun 5.

Division of Human Genetics, Departement of Pediatrics, Inselspital, University of Berne, Freiburgstrasse, CH-3010 Berne, Switzerland.

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http://dx.doi.org/10.1016/j.bbrc.2012.05.121DOI Listing
July 2012

Quantitative 1-step DNA methylation analysis with native genomic DNA as template.

Clin Chem 2010 Jul 14;56(7):1098-106. Epub 2010 May 14.

Division of Human Genetics, Department of Pediatrics, Inselspital, University of Bern, Bern, Switzerland.

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http://www.clinchem.org/content/56/7/1098.full.pdf
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http://www.clinchem.org/cgi/doi/10.1373/clinchem.2009.142828
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http://dx.doi.org/10.1373/clinchem.2009.142828DOI Listing
July 2010