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John David Symons

University Of Utah

$3,553,170
Attributed
$5,347,100
Total exposure
6
Grants
5
Lead (contact PI)

Attributed= this PI's even-split share of every grant they're on (the fair, additive number). Exposure = full size of all those grants.

Funding over time

peak $991K · FY200825
$1M$750K$500K$250K$0
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
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'25

Funding mix

By agency

NIH$5,347,100 · 6

By mechanism

R01$3,942,786 · 2
R15$660,844 · 1
R21$591,845 · 2
R03$151,625 · 1

Top collaborators

Most similar at University Of Utah

Same institution · by research overlap

Others in their field

Top investigators on “Endothelial Cells

Research focus

Endothelial CellsMediatingPreventNitric OxideFunctional DisorderIn VivoGenerationsBlood VesselsRepressionBlood FlowProceduresResponseAutophagocytosisAutophagosomeNos3 GeneGeneticKnockout MiceBaseHemodynamicsImpairmentEndotheliumDefectArteriesProduction

Grant awards (14)

Defining the contribution from endothelial cell sphingolipid metabolism to outcomes of acute ischemic stroke in mice$192,500
R21 · FY2025 · NS · contact PI
Autophagy and Arteriovenous Fistula Maturation$527,748
R01 · FY2024 · HL
Targeting endothelial cell metabolism to improve recovery from acute ischemic stroke in older mice.$399,345
R21 · FY2024 · AG · contact PI
Autophagy and Arteriovenous Fistula Maturation$538,518
R01 · FY2023 · HL
Autophagy and Arteriovenous Fistula Maturation$538,518
R01 · FY2022 · HL
Autophagy and Arteriovenous Fistula Maturation$594,103
R01 · FY2021 · HL
Autophagy maintains vascular function through a novel glycolysis-linked pathway regulating eNOS.$396,868
R01 · FY2021 · HL · contact PI
Autophagy maintains vascular function through a novel glycolysis-linked pathway regulating eNOS.$445,855
R01 · FY2020 · HL · contact PI
Autophagy maintains vascular function through a novel glycolysis-linked pathway regulating eNOS.$442,805
R01 · FY2019 · HL · contact PI
Autophagy maintains vascular function through a novel glycolysis-linked pathway regulating eNOS.$458,371
R01 · FY2018 · HL · contact PI
Characterizing the phenotype of young and old mice with disrupted vascular autophagy$76,000
R03 · FY2018 · AG · contact PI
Characterizing the phenotype of young and old mice with disrupted vascular autophagy$75,625
R03 · FY2017 · AG · contact PI
Mechanisms for Ceramide Mediated Vascular Dysfunction$436,594
R15 · FY2012 · HL · contact PI
The role of ceramide in obesity-related vascular dysfunction$224,250
R15 · FY2008 · HL · contact PI