← Leaderboards
David D Moore
Baylor College Of Medicine
$17,888,087
Attributed
$20,160,062
Total exposure
13
Grants
9
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 $1.3M · FY2005–23$2M$1.5M$1M$500K$0
'05
'06
'07
'08
'09
'10
'11
'12
'13
'14
'15
'16
'17
'18
'19
'20
'21
'22
'23
Funding mix
By agency
NIH$24,499,091 · 14
By mechanism
R01$14,455,361 · 7
P01$8,410,834 · 4
U19$865,985 · 1
T32$736,911 · 1
R13$30,000 · 1
Top collaborators
- Loning None Fu10 shared
Most similar at Baylor College Of Medicine
Same institution · by research overlap
- Loning None Fu$3,948,648
- Kjersti Marie Aagaard-Tillery$19,552,738
- Bert W O'Malley$52,747,816
- Saul Joseph Karpen$21,015,108
- Wendong Huang$7,587,297
Others in their field
Top investigators on “Nuclear Receptors”
- Angela M. Gronenborn · Diabetes, Digestive, Kidney Diseases$48,244,951
- Bert W O'Malley · Baylor College Of Medicine$47,299,701
- Mitchell A. Lazar · University Of Pennsylvania$41,671,296
- Ronald M. Evans · Salk Institute For Biological Studies$41,421,070
- Michael G Rosenfeld · University Of California, San Diego$36,716,896
- John Didsbury · T3d Therapeutics, Inc.$25,150,614
Research focus
Nuclear ReceptorsMetabolicLiverHepaticBile AcidsResponseMolecularPathway InteractionsLigandsBaseAgonistGene TargetingHomeostasisReceptorMouse ModelMediatingInsightMetabolic SyndromeHepatocyteMetabolismNonalcoholic SteatohepatitisGene ExpressionPathologySignal Transduction
Grant awards (75)
Sympathetic circadian dysfunction in obesity-related hepatocarcinogenesis$424,987
R01 · FY2023 · CA
(PQ6)Nuclear receptor mechanisms in circadian disruption induced hepatocarcinogenesis$467,462
R01 · FY2022 · CA
Sympathetic circadian dysfunction in obesity-related hepatocarcinogenesis$426,448
R01 · FY2022 · CA
Project 2: Coordinate regulation of liver energy balance by PPARalpha/SRC-1 and FXR/SRC-2$356,625
P01 · FY2022 · DK · contact PI
(PQ6)Nuclear receptor mechanisms in circadian disruption induced hepatocarcinogenesis$500,441
R01 · FY2021 · CA
Sympathetic circadian dysfunction in obesity-related hepatocarcinogenesis$457,161
R01 · FY2021 · CA
Project 2: Coordinate regulation of liver energy balance by PPARalpha/SRC-1 and FXR/SRC-2$356,625
P01 · FY2021 · DK · contact PI
(PQ6)Nuclear receptor mechanisms in circadian disruption induced hepatocarcinogenesis$489,764
R01 · FY2020 · CA
Sympathetic circadian dysfunction in obesity-related hepatocarcinogenesis$445,069
R01 · FY2020 · CA
Project 2: Coordinate regulation of liver energy balance by PPARalpha/SRC-1 and FXR/SRC-2$356,625
P01 · FY2020 · DK · contact PI
Sympathetic circadian dysfunction in obesity-related hepatocarcinogenesis$446,883
R01 · FY2019 · CA
(PQ6)Nuclear receptor mechanisms in circadian disruption induced hepatocarcinogenesis$443,175
R01 · FY2019 · CA
Project 2: Coordinate regulation of liver energy balance by PPARalpha/SRC-1 and FXR/SRC-2$356,625
P01 · FY2019 · DK · contact PI
(PQ6)Nuclear receptor mechanisms in circadian disruption induced hepatocarcinogenesis$442,560
R01 · FY2018 · CA
Project 2: Coordinate regulation of liver energy balance by PPARalpha/SRC-1 and FXR/SRC-2$356,625
P01 · FY2018 · DK · contact PI
FASEB SRC on Fundamental Biology and Pathophysiology of the Liver$30,000
R13 · FY2018 · DK · contact PI
SRC-2 Mediates the Preventative Effects of LRH-1 for NASH in Metabolic Disease$353,529
P01 · FY2016 · DK · contact PI
SRC-2 Mediates the Preventative Effects of LRH-1 for NASH in Metabolic Disease$353,529
P01 · FY2015 · DK · contact PI
SRC-2 Mediates the Preventative Effects of LRH-1 for NASH in Metabolic Disease$353,529
P01 · FY2014 · DK · contact PI
Functions of the Nuclear Receptor CAR$340,388
R01 · FY2014 · DK · contact PI
SRC-2 Mediates the Preventative Effects of LRH-1 for NASH in Metabolic Disease$342,865
P01 · FY2013 · DK · contact PI
Functions of the Nuclear Receptor CAR$328,475
R01 · FY2013 · DK · contact PI
SRC-2 Mediates the Preventative Effects of LRH-1 for NASH in Metabolic Disease$353,529
P01 · FY2012 · DK · contact PI
Functions of the Nuclear Receptor CAR$340,388
R01 · FY2012 · DK · contact PI
Training Program in Molecular Endocrinology$256,475
T32 · FY2012 · DK · contact PI
Training Program in Molecular Endocrinology$24,488
T32 · FY2012 · DK · contact PI
Functions of the Nuclear Receptor CAR$340,388
R01 · FY2011 · DK · contact PI
Training Program in Molecular Endocrinology$153,883
T32 · FY2011 · DK · contact PI
Nuclear Receptor Function in Hepatic Pathology$129,757
U19 · FY2011 · DK · contact PI
Training Program in Molecular Endocrinology$24,138
T32 · FY2011 · DK · contact PI
Function of the Nuclear Receptor LRH-1$383,750
R01 · FY2010 · DK · contact PI
Metabolic Regulation by the Nuclear Receptor CAR$335,083
R01 · FY2010 · DK · contact PI
Training Program in Molecular Endocrinology$190,605
T32 · FY2010 · DK · contact PI
Nuclear Receptor Function in Hepatic Pathology$135,000
U19 · FY2010 · DK · contact PI
Training Program in Molecular Endocrinology$55,592
T32 · FY2010 · DK · contact PI
Training Program in Molecular Endocrinology$31,730
T32 · FY2010 · DK · contact PI
Function of the Nuclear Receptor LRH-1$383,750
R01 · FY2009 · DK · contact PI
Metabolic Regulation by the Nuclear Receptor CAR$338,468
R01 · FY2009 · DK · contact PI
Nuclear Receptor Function in Hepatic Pathology$135,000
U19 · FY2009 · DK · contact PI
Metabolic Regulation by the Nuclear Receptor CAR$2,914
R01 · FY2009 · DK · contact PI
Functions of the Nuclear Receptor SHP$445,409
R01 · FY2008 · DK · contact PI
Metabolic Regulation by the Nuclear Receptor CAR$338,468
R01 · FY2008 · DK · contact PI
Nuclear Receptor Function in Hepatic Pathology$135,000
U19 · FY2008 · DK · contact PI
Functions of the Nuclear Receptor SHP$441,263
R01 · FY2007 · DK · contact PI
Metabolic Regulation by the Nuclear Receptor CAR$345,375
R01 · FY2007 · DK · contact PI
Nuclear Receptor Function in Hepatic Pathology$331,228
U19 · FY2007 · DK · contact PI
Functions of the Nuclear Receptor SHP$441,209
R01 · FY2006 · DK · contact PI
Metabolic Regulation by the Nuclear Receptor CAR$315,972
R01 · FY2006 · DK · contact PI
Function of The Bile Acid Receptor FXR$301,275
R01 · FY2006 · DK · contact PI
Functions of the Nuclear Receptor SHP$438,666
R01 · FY2005 · DK
Metabolic Regulation by the Nuclear Receptor CAR$323,575
R01 · FY2005 · DK
Function of The Bile Acid Receptor FXR$308,525
R01 · FY2005 · DK
Metabolic Regulation by the Nuclear Receptor CAR$323,575
R01 · FY2004 · DK
Function of The Bile Acid Receptor FXR$308,525
R01 · FY2004 · DK
ORPHAN RECEPTORS IN ORGANOGENESIS$82,775
P01 · FY2004 · DK
ORPHAN RECEPTORS IN ORGANOGENESIS$1,064,286
P01 · FY2003 · DK
Metabolic Regulation by the Nuclear Receptor CAR$323,575
R01 · FY2003 · DK
Function of The Bile Acid Receptor FXR$308,525
R01 · FY2003 · DK
ORPHAN RECEPTORS IN ORGANOGENESIS$1,064,286
P01 · FY2002 · DK
FUNCTION OF CAR, A NEW ORPHAN NUCLEAR HORMONE RECEPTOR$286,039
R01 · FY2002 · DK
RETINOID SIGNALING BY A NEW NUCLEAR HORMONE RECEPTOR$249,744
R01 · FY2002 · DK
Function of SHP$177,233
P01 · FY2002 · DK
Genomic &Metabolic Profiling of Orphan Nuclear Receptors III$0
U19 · FY2002 · DK
Genomic &Metabolic Profiling of Orphan Nuclear Receptors III$0
U19 · FY2002 · DK
ORPHAN RECEPTORS IN ORGANOGENESIS$1,064,286
P01 · FY2001 · DK
FUNCTION OF CAR, A NEW ORPHAN NUCLEAR HORMONE RECEPTOR$297,195
R01 · FY2001 · DK
BIOCHEMISTRY AND GENETICS OF THYROID HORMONE RECEPTORS$277,097
R01 · FY2001 · DK
RETINOID SIGNALING BY A NEW NUCLEAR HORMONE RECEPTOR$244,586
R01 · FY2001 · DK
Function of SHP$177,233
P01 · FY2001 · DK
FUNCTION OF CAR, A NEW ORPHAN NUCLEAR HORMONE RECEPTOR$22,575
R01 · FY2001 · DK
ORPHAN RECEPTORS IN ORGANOGENESIS$1,063,396
P01 · FY2000 · DK
BIOCHEMISTRY AND GENETICS OF THYROID HORMONE RECEPTORS$270,964
R01 · FY2000 · DK
FUNCTION OF CAR, A NEW ORPHAN NUCLEAR HORMONE RECEPTOR$266,091
R01 · FY2000 · DK
RETINOID SIGNALING BY A NEW NUCLEAR HORMONE RECEPTOR$239,579
R01 · FY2000 · DK
Function of SHP$177,233
P01 · FY2000 · DK