Search Results - "Debrosse, M."

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  1. 1

    O029 Chromatin exchange in interferon induced transcription by Ozato, K., Sarai, N., Patel, M., Debrosse, M., Heightman, T., Tamura, T., Ura, K.

    Published in Cytokine (Philadelphia, Pa.) (01-09-2012)
    “…Type I interferons (IFNs) activate the JAK/STAT pathway and stimulate transcription from many IFN stimulated genes (ISGs). This process likely involves…”
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    Journal Article
  2. 2

    A novel conductive membrane sensor protection technique to mitigate redox-active interferences by DeBrosse, M.C., Suresh, S., Karajic, A., Kim, S., Hussain, S., Heikenfeld, J.

    Published in Biosensors and bioelectronics. X (01-09-2023)
    “…Due to their high specificity and selectivity, receptor-based biosensors play an important role in real-time health monitoring. However, maintaining an ideal…”
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    Journal Article
  3. 3

    Dimerization of FIR upon FUSE DNA binding suggests a mechanism of c-myc inhibition by Crichlow, Gregg V, Zhou, Hongwen, Hsiao, Hsin-hao, Frederick, Kendra B, Debrosse, Maxime, Yang, Yuande, Folta-Stogniew, Ewa J, Chung, Hye-Jung, Fan, Chengpeng, De La Cruz, Enrique M, Levens, David, Lolis, Elias, Braddock, Demetrios

    Published in The EMBO journal (09-01-2008)
    “…c‐myc is essential for cell homeostasis and growth but lethal if improperly regulated. Transcription of this oncogene is governed by the counterbalancing…”
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    Journal Article
  4. 4

    Chemical Exchange Saturation Transfer Imaging of Endogenous Metabolites for Monitoring Oxidative Phosphorylation and Glycolysis in Vivo by DeBrosse, Catherine M

    Published 01-01-2017
    “…Oxidative phosphorylation (OXPHOS) and glycolysis are two cellular metabolic pathways that play a crucial role in the functions of biological systems…”
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    Dissertation
  5. 5

    Neurologic Disorders Due to Mitochondrial DNA Mutations by DeBrosse, Suzanne, MD, Parikh, Sumit, MD

    Published in Seminars in pediatric neurology (01-12-2012)
    “…The mitochondrial DNA (mtDNA) is a compact genome inherited through the maternal lineage. Mutations in mtDNA lead to many of the earliest identified syndromic…”
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    Journal Article
  6. 6

    Fever-induced paroxysmal weakness and encephalopathy, a new phenotype of ATP1A3 mutation by Yano, Sho T., MD, PhD, Silver, Kenneth, MD, Young, Richard, MD, DeBrosse, Suzanne D., MD, Ebel, Roseànne S., MS, Swoboda, Kathryn J., MD, Acsadi, Gyula, MD, PhD

    Published in Pediatric neurology (01-08-2017)
    “…Structured Abstract Objectives We identified a group of patients with ATP1A3 mutations at residue 756 who display a new phenotype distinct from alternating…”
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    Journal Article
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    Steroid Induced Acne Secondary to Low Dose Inhaled Corticosteroids in a Pediatric Patient and Resolution with Every Other Day Ics Dosing by DeBrosse, Charles W., MD, Moncrief, Terri M., MD FAAAAI, Bonnin, Arturo J., MD, FAAAAI

    Published in Journal of allergy and clinical immunology (01-02-2017)
    “…Methods A 5-year-old male with mild persistent asthma, and a known history of food allergy presented with an erythematous papulopustular rash that began 10…”
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    Journal Article