Matthew Gorr Email & Phone Number
@osu.edu
4 phones found area 858 and 614
LinkedIn matched
Who is Matthew Gorr? Overview
A concise factual answer block for searchers comparing this professional profile.
Matthew Gorr is listed as Assistant Professor at The Ohio State University, based in Columbus, Ohio, United States. AeroLeads shows a work email signal at osu.edu, phone signal with area code 858, 614, and a matched LinkedIn profile for Matthew Gorr.
Matthew Gorr previously worked as Research Assistant Professor at The Ohio State University and Postdoctoral Fellow at University Of California, San Diego. Matthew Gorr holds Phd, Molecular, Cellular And Developmental Biology from The Ohio State University.
Email format at The Ohio State University
This section adds company-level context without repeating Matthew Gorr's masked contact details.
AeroLeads found 2 current-domain work email signals for Matthew Gorr. Compare company email patterns before reaching out.
About Matthew Gorr
I am an Assistant Professor at The Ohio State University, where I am utilizing patient-derived samples and animal models of disease to uncover novel biology in heart and lung disease and environmental exposures. I am implementing this through my expertise in molecular biology, animal models, pharmacology and cardiovascular physiology.
Listed skills include Statistics, Research, Microsoft Office, Writing, and 30 others.
Matthew Gorr's current company
Company context helps verify the profile and gives searchers a useful next step.
Matthew Gorr work experience
A career timeline built from the work history available for this profile.
Assistant Professor
Current• Examining the biology of the right ventricle to characterize right ventricle biology in search of novel therapeutic strategies for right heart disease. This is completed by molecular and cellular experiments isolated from disease tissue.• Examining the novel biology of exposure during pregnancy including to e-cigarettes (vaping) using rodent exposure paradigms.• Using patient-derived primary cell culture to study the expression of relevant genes in lung diseases including pulmonary hypertension, idiopathic pulmonary fibrosis, and chronic obstructive pulmonary disease.
Research Assistant Professor
• Upon discovery of unique features of the right ventricle of the heart compared to the left ventricle, I utilized RNA-sequencing, immunohistochemistry, molecular biology, flow cytometry and cell culture to examine the biology of the right ventricle to characterize right ventricle biology in search of novel therapeutic strategies for right heart disease.• Tested novel drug targets on right ventricular fibrosis and function using animal models of pulmonary hypertension.•Utilized patient-derived primary cell culture of smooth muscle cells and fibroblasts to study the expression of relevant genes in lung diseases including pulmonary hypertension, idiopathic pulmonary fibrosis, and chronic obstructive pulmonary disease.• Worked toward the discovery of novel biology of e-cigarette (vaping) use using rodent exposure paradigms, and cell culture.
Postdoctoral Fellow
• Identified novel G protein-coupled receptors as potential drug targets in pulmonary hypertension using patient-derived samples and RNA-seq. Validating targets with in vitro assays including second messengers.• Collaborated with pharmaceutical industry partners to further validate targets in vitro and in a mouse model of pulmonary hypertension. Resulted in new and maintained drug discovery funding from industry partners.• Recruited, trained, and directed three undergraduates and one Ph.D. student. Three of these students have presented research at conferences and all are pursuing graduate school or scientific positions.• Presented findings at two national meetings with two oral presentations, one resulted in a postdoc speaking award from the American Society for Pharmacology and Experimental Therapeutics (ASPET).Membrane receptors known as G protein coupled receptors (GPCRs) make up a large number of currently approved drug targets, though many that are expressed in human tissue remain undefined. GPCRs are capable of receiving a signal and modifying a myriad of downstream cellular processes. My work in Dr. Paul Insel's lab utilized an unbiased approach to screen for GPCRs expressed in human cells collected from patients with disease. I applied this approach to pulmonary arterial hypertension, a progressive heart and lung disease, to identify and characterize functional GPCRs that could be used as future therapy.
Graduate Student
- Utilized rodent echocardiography, cardiomyocyte function (contractility) and calcium measurements, and molecular biology to characterize heart failure-like phenotype in mice exposed to air pollution.- Developed a cellular model using lung epithelial cells and cardiomyocytes to study the toxicity of pollutants across the air-blood interface using measurement of cardiomyocyte calcium flux and contractility.- Research resulted in publication of 13 articles in peer-reviewed journals, a pre-doctoral fellowship from the American Heart Association, and presentations at multiple national conferences.- Served as laboratory manager of a diverse staff of technicians, undergraduate and medical students, volunteers, and peers by guiding operations, developing experiments, and collaborating with labs at multiple institutions.
Adjunct Faculty
Taught Human Nutrition to undergraduates. Designed lectures, activities, quizzes and exams based on developed curriculum.
Research Assistant
- Performed daily experiments involving isolation of cardiomyocytes and examining cellular physiology and function in response to drugs and pollutants. Collected, analyzed, and interpreted data for publication.- Presented research at laboratory meetings and provided valuable input towards other experiments, including utilization of a rat model of diabetes and an animal model of air pollution exposure.
Graduate Research Associate
- Spearheaded project with industrial collaborator to develop biological treatment wetland for contaminant remediation. Utilized computer modeling combined with data collected from mesoscale system.- Taught recitation section for undergraduate biology and developed material for presentations.
Matthew Gorr education
Phd, Molecular, Cellular And Developmental Biology
Master Of Science, Ecology
Bachelor Of Science, Biology
Frequently asked questions about Matthew Gorr
Quick answers generated from the profile data available on this page.
What company does Matthew Gorr work for?
Matthew Gorr works for The Ohio State University.
What is Matthew Gorr's role at The Ohio State University?
Matthew Gorr is listed as Assistant Professor at The Ohio State University.
What is Matthew Gorr's email address?
AeroLeads has found 2 work email signals at @osu.edu for Matthew Gorr at The Ohio State University.
What is Matthew Gorr's phone number?
AeroLeads has found 4 phone signal(s) with area code 858, 614 for Matthew Gorr at The Ohio State University.
Where is Matthew Gorr based?
Matthew Gorr is based in Columbus, Ohio, United States while working with The Ohio State University.
What companies has Matthew Gorr worked for?
Matthew Gorr has worked for The Ohio State University, University Of California, San Diego, Central Ohio Technical College, The Research Institute At Nationwide Children'S Hospital, and The University Of Toledo.
How can I contact Matthew Gorr?
You can use AeroLeads to view verified contact signals for Matthew Gorr at The Ohio State University, including work email, phone, and LinkedIn data when available.
What schools did Matthew Gorr attend?
Matthew Gorr holds Phd, Molecular, Cellular And Developmental Biology from The Ohio State University.
What skills is Matthew Gorr known for?
Matthew Gorr is listed with skills including Statistics, Research, Microsoft Office, Writing, Molecular Biology, Echocardiography, Cell Culture, and Cell Biology.
Search by job title, company, industry, location, and seniority. Export verified B2B contact data when you need it.
Start free trialCheck these profiles if this is not the Matthew Gorr you were looking for.
View similar profiles