Philip Dittmer Email and Phone Number
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A fundamental question in molecular neuroscience is: how the properties of dendritic spines and the adjoining shafts are tuned to support specialized function, e.g. synaptic plasticity? These plastic changes to synapses form the basis for cognitive learning and memory storage which are mostly triggered by transient rises in the cytosolic concentration of calcium ions [Ca2+]i. The precise signaling that supports architectural and functional tuning needs to be ascertained in order to identify irregularities in Ca2+ signaling that underlie etiologies of neurological disorders such as autism spectrum disorder (ASDs) and stroke. My research utilizes advanced imaging technologies and electrophysiology to examine the molecular signaling pathway(s) that underlie synaptic plasticity. In the lab, we induce synaptic plasticity in a single dendritic spine using laser uncaging of glutamate, while measuring Ca2+ and structural changes. From this, we discovered a mechanism implicating surface voltage-gated and ligand-gated Ca2+ channels to induce Ca2+ release from intracellular stores and activate the ER Ca2+ sensor, STIM. Ongoing research will test whether the shape of the Ca2+ signal and/or the physical interaction between activated STIM1 and LTCCs are required for support of homosynaptic plasticity, as well as other forms of plasticity like synaptic crosstalk, heterosynaptic plasticity or homeostatic scaling. In addition, my lab seeks to understand the molecular queues necessary for the long-term preservation of these functional and structural changes. It is reasonable to expect that an upsurge in local protein expression of nascent protein is required. Therefore, the obvious questions are; whether translation of local mRNA transcripts is sufficient to escalate synaptic proteins and support long-term potentiation (LTP) or whether new transcripts from the nucleus of synaptic genes are required for persistent LTP. Pharmacological and genetic manipulations are a few of the tools that my lab uses to intervene with the underlying mechanisms and synaptic circuitry.
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Research InstructorUniversity Of Colorado Anschutz Medical CampusLafayette, Co, Us -
Research InstructorUniversity Of Colorado Anschutz Medical Campus Mar 2021 - Present -
Research AssociateUniversity Of Colorado Anschutz Medical Campus Oct 2017 - Mar 2021Aurora, Colorado, United States -
Postdoctoral FellowUniversity Of Colorado Anschutz Medical Campus Oct 2010 - Oct 2017United StatesThe primary focus of my work is to understand how protein complexes are regulated and organize to form signaling networks involved in synaptic plasticity.
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Graduate Research AssistantUniversity Of Colorado At Boulder Aug 2004 - Jul 2010My graduate research aimed at engineering and using genetically encoded probes to understand how cells maintain a critical balance of metal ions and to identify the mechanisms by which dyshomeostasis lead to disease and degeneration. -
Analytical ChemistAbbott Laboratories Mar 1992 - Aug 2004
Philip Dittmer Skills
Philip Dittmer Education Details
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Biochemistry And Molecular Biophysics -
Chemistry -
Biochemistry
Frequently Asked Questions about Philip Dittmer
What company does Philip Dittmer work for?
Philip Dittmer works for University Of Colorado Anschutz Medical Campus
What is Philip Dittmer's role at the current company?
Philip Dittmer's current role is Research Instructor.
What is Philip Dittmer's email address?
Philip Dittmer's email address is ph****@****ado.edu
What schools did Philip Dittmer attend?
Philip Dittmer attended University Of Colorado At Boulder, Depaul University, Indiana University Bloomington.
What skills is Philip Dittmer known for?
Philip Dittmer has skills like Biochemistry, Molecular Biology, Protein Expression, Cell Culture, Protein Purification, Pcr, Protein Chemistry, Western Blotting, Hplc, Cell Biology, Fluorescence Microscopy, Chemistry.
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Phil Dittmer
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