← Leaderboards
Paul A Janmey
Thomas Jefferson University
$17,822,534
Attributed
$24,390,599
Total exposure
15
Grants
10
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 $3M · FY2005–25$5M$3.8M$2.5M$1.3M$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
'24
'25
Funding mix
By agency
NIH$31,557,547 · 16
By mechanism
R01$19,434,232 · 8
P01$8,625,624 · 4
R35$2,576,612 · 1
R21$487,729 · 1
U54$313,338 · 1
R03$120,012 · 1
Top collaborators
- Vivek Shenoy12 shared
- Rebecca G Wells12 shared
- Gaudenz Danuser4 shared
- Vladimir I Gelfand4 shared
- Robert D Goldman4 shared
- Richard Tyler Miller4 shared
- Martin R. Pollak4 shared
- Karen M Ridge4 shared
Most similar at Thomas Jefferson University
Same institution · by research overlap
- Robert Rogers$1,539,725
Others in their field
Top investigators on “Property”
- Mitchell J Malone · Texas A&M Research Foundation$344,583,004
- Gary D Acton · University Of California-Davis$320,373,312
- Everette D Joseph · Howard University$250,079,293
- Valerie Koch · University Corporation For Atmospheric Res$247,762,266
- Antonio J Busalacchi · University Of Maryland, College Park$243,972,016
- Eric J Barron · Pennsylvania State Univ University Park$243,972,016
Research focus
PropertyMechanicsCellsStructureCytoskeletonTissuesResponseActinsSignal TransductionProteinsViscoelasticityPolymersStressMechanical StressIn VitroCrosslinkAffectFibrosisCell PhysiologyExtracellular MatrixDesignCell TypeLeadPhenotype
Grant awards (71)
Pathological consequences of altered tissue mechanics in fibrosis$652,816
R01 · FY2025 · EB
Molecular function of extracellular vimentin in regulating the response to lens wounding$451,480
R01 · FY2025 · EY
Pathological consequences of altered tissue mechanics in fibrosis$639,759
R01 · FY2024 · EB
Regulation of cell function by mechanical properties of biopolymer networks and lipid bilayers$626,644
R35 · FY2024 · GM · contact PI
Molecular function of extracellular vimentin in regulating the response to lens wounding$480,805
R01 · FY2024 · EY
Pathological consequences of altered tissue mechanics in fibrosis$652,816
R01 · FY2023 · EB
Regulation of cell function by mechanical properties of biopolymer networks and lipid bilayers$626,644
R35 · FY2023 · GM · contact PI
Regulation of cell function by mechanical properties of biopolymer networks and lipid bilayers$55,251
R35 · FY2023 · GM · contact PI
Pathological consequences of altered tissue mechanics in fibrosis$652,816
R01 · FY2022 · EB
Regulation of cell function by mechanical properties of biopolymer networks and lipid bilayers$539,437
R35 · FY2022 · GM · contact PI
Regulation and Function of Intermediate Filaments in Cell Mechanics$1,771,186
P01 · FY2021 · GM
Pathological consequences of altered tissue mechanics in fibrosis$491,086
R01 · FY2021 · EB
Regulation of cell function by mechanical properties of biopolymer networks and lipid bilayers$364,739
R35 · FY2021 · GM · contact PI
Regulation of the Micromechanical Properties of Cells by Intermediate Filaments$245,797
P01 · FY2021 · GM · contact PI
Regulation and Function of Intermediate Filaments in Cell Mechanics$1,771,683
P01 · FY2020 · GM
Pathological consequences of altered tissue mechanics in fibrosis$501,109
R01 · FY2020 · EB
Regulation of cell function by mechanical properties of biopolymer networks and lipid bilayers$363,897
R35 · FY2020 · GM · contact PI
Regulation of the Micromechanical Properties of Cells by Intermediate Filaments$247,851
P01 · FY2020 · GM · contact PI
Regulation and Function of Intermediate Filaments in Cell Mechanics$1,810,628
P01 · FY2019 · GM
Pathological consequences of altered tissue mechanics in fibrosis$501,109
R01 · FY2019 · EB
Project 1: Mechanisms of Stiffening in Liver Cancer$313,338
U54 · FY2019 · CA · contact PI
Regulation of the Micromechanical Properties of Cells by Intermediate Filaments$250,597
P01 · FY2019 · GM · contact PI
Regulation and Function of Intermediate Filaments in Cell Mechanics$1,813,451
P01 · FY2018 · GM
Pathological consequences of altered tissue mechanics in fibrosis$501,109
R01 · FY2018 · EB
Spatial control of actin assembly by phosphoinositides$443,541
R01 · FY2018 · GM · contact PI
Regulation of the Micromechanical Properties of Cells by Intermediate Filaments$259,296
P01 · FY2018 · GM · contact PI
Spatial control of actin assembly by phosphoinositides$443,541
R01 · FY2017 · GM · contact PI
Pathological consequences of altered tissue mechanics in fibrosis$432,811
R01 · FY2017 · EB
Spatial control of actin assembly by phosphoinositides$443,541
R01 · FY2016 · GM · contact PI
Pathological consequences of altered tissue mechanics in fibrosis$432,811
R01 · FY2016 · EB
Spatial control of actin assembly by phosphoinositides$443,541
R01 · FY2015 · GM · contact PI
Pathological consequences of altered tissue mechanics in fibrosis$424,155
R01 · FY2015 · EB
Pathological consequences of altered tissue mechanics in fibrosis$432,811
R01 · FY2014 · EB
Biophysical Properties of Renal Glomeruli and Podocytes$501,982
R01 · FY2013 · DK
Biophysical Properties of Renal Glomeruli and Podocytes$528,287
R01 · FY2012 · DK
Biophysical Properties of Renal Glomeruli and Podocytes$529,068
R01 · FY2011 · DK
Mechanical control of cell growth and differentiation$472,344
R01 · FY2011 · GM · contact PI
Regulation of the Micromechanical Properties of Cells by Intermediate Filaments$272,286
P01 · FY2011 · GM · contact PI
Biophysical Properties of Renal Glomeruli and Podocytes$679,471
R01 · FY2010 · DK
Mechanical control of cell growth and differentiation$477,379
R01 · FY2010 · GM · contact PI
Novel antibacterial agents resistant to inactivation by polyelectrolytes$451,390
R01 · FY2010 · HL · contact PI
Novel antibacterial agents resistant to inactivation by polyelectrolytes$438,243
R01 · FY2009 · HL · contact PI
Mechanical control of cell growth and differentiation$346,500
R01 · FY2009 · GM · contact PI
Mechanical control of cell growth and differentiation$223,416
R01 · FY2009 · GM · contact PI
Signal Initiation from the T-cell Antigen Receptor by Mechanical Force$210,244
R21 · FY2009 · AI
Mechanical control of cell growth and differentiation$150,299
R01 · FY2009 · GM · contact PI
Signal Initiation from the T-cell Antigen Receptor by Mechanical Force$20,661
R21 · FY2009 · AI
Mechanical control of cell growth and differentiation$346,500
R01 · FY2008 · GM · contact PI
Signal Initiation from the T-cell Antigen Receptor by Mechanical Force$256,824
R21 · FY2008 · AI
Dynamic Light Scattering (DLS) and Atomic Force Microscopy (AFM)$80,208
P01 · FY2008 · AR · contact PI
Dynamic Light Scattering (DLS) and Atomic Force Microscopy (AFM)$102,641
P01 · FY2007 · AR · contact PI
Effects of phosphoinositidies on cytoskeletal structure$295,183
R01 · FY2006 · AR · contact PI
Effects of phosphoinositides on cytoskeletal structure$39,372
R03 · FY2006 · TW · contact PI
Dissolution of polyelectrolyte bundles in airway fluids$315,675
R01 · FY2005 · HL
Effects of phosphoinositidies on cytoskeletal structure$302,286
R01 · FY2005 · AR
Effects of phosphoinositides on cytoskeletal structure$40,320
R03 · FY2005 · TW
MECHANISMS OF NEUROFILAMENT TRANSLOCATION$435,875
R01 · FY2004 · GM
Effects of phosphoinositidies on cytoskeletal structure$327,618
R01 · FY2004 · AR
Dissolution of polyelectrolyte bundles in airway fluids$315,675
R01 · FY2004 · HL
Effects of phosphoinositides on cytoskeletal structure$40,320
R03 · FY2004 · TW
Effects of phosphoinositidies on cytoskeletal structure$327,618
R01 · FY2003 · AR
MECHANISMS OF NEUROFILAMENT TRANSLOCATION$317,000
R01 · FY2003 · GM
Dissolution of polyelectrolyte bundles in airway fluids$315,675
R01 · FY2003 · HL
MECHANISMS OF NEUROFILAMENT TRANSLOCATION$39,625
R01 · FY2003 · GM
Effects of phosphoinositidies on cytoskeletal structure$341,804
R01 · FY2002 · AR
MECHANISMS OF NEUROFILAMENT TRANSLOCATION$317,000
R01 · FY2002 · GM
Dissolution of polyelectrolyte bundles in airway fluids$315,675
R01 · FY2002 · HL
MECHANISMS OF NEUROFILAMENT TRANSLOCATION$367,000
R01 · FY2001 · GM
Dissolution of polyelectrolyte bundles in airway fluids$355,300
R01 · FY2001 · HL
REVERSIBLE FORMATION AND STRUCTURE OF ACTIN NETWORKS$293,620
R01 · FY2001 · AR
REVERSIBLE FORMATION AND STRUCTURE OF ACTIN NETWORKS$285,067
R01 · FY2000 · AR