Brent R. Weil - Concepedia

Author

Brent R. Weil

Indiana University – Purdue University Indianapolis ORCID

Also Known As

B WEIL, B Weil, B. R. Weil, B. Weil, B.R. Weil, Brent R Weil, Brent R. Weil, Brent Weil, Edy Y. Kim, Mary Frances Wedekind Malone

148

Publications

3.3K

Citations

H-Index

102

Concepts

All Affiliations

Indiana University – Purdue University Indianapolis Indiana University School of Medicine Boston Children's Hospital Harvard University Brigham and Women's Hospital

About

Brent R. Weil is an author at Indiana University – Purdue University Indianapolis specializing in medicine, stem cells, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	38	1.7K
2	Cell Biology	17	17	919
3	Health Sciences	5	5	279
4	Biomedical Engineering	5	5	334
5	Blood Transplantation	1	1	14

Brent R. Weil

Publications

2.2K

Citations

H-Index

Page 1

	Year	Citations
PRECONDITIONING MESENCHYMAL STEM CELLS WITH TRANSFORMING GROWTH FACTOR-ALPHA IMPROVES MESENCHYMAL STEM CELL-MEDIATED CARDIOPROTECTION Jeremy L. Herrmann, Yue Wang, Aaron M. Abarbanell, Shock Bone Marrow MscsCardiac MuscleCell TherapyAdult Stem CellImmunology	2009	158
Estrogen receptor β mediates increased activation of PI3K/Akt signaling and improved myocardial function in female hearts following acute ischemia Meijing Wang, Yue Wang, Brent R. Weil, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology Heart FailureCell DeathFemale Reproductive FunctionCardiovascular FunctionMetabolic Syndrome	2009	152
High glucose concentration in cell culture medium does not acutely affect human mesenchymal stem cell growth factor production or proliferation Brent R. Weil, Aaron M. Abarbanell, Jeremy L. Herrmann, American Journal of Physiology-Regulatory, Integrative and Comparative Physiology High GlucoseHuman GrowthCell Culture MediumAdult Stem CellCell Culture	2009	96
Mesenchymal stem cells enhance the viability and proliferation of human fetal intestinal epithelial cells following hypoxic injury via paracrine mechanisms Brent R. Weil, Troy A. Markel, Jeremy L. Herrmann, Surgery Regenerative MedicineMesenchymal Stem CellsDevelopmental BiologyMedicineAdult Stem Cell	2009	88
Mesenchymal stem cells attenuate myocardial functional depression and reduce systemic and myocardial inflammation during endotoxemia Brent R. Weil, Mariuxi C. Manukyan, Jeremy L. Herrmann, Surgery Regenerative MedicineInflammationMesenchymal Stem CellsMyocardial Functional DepressionMedicine	2010	83
Signaling via GPR30 protects the myocardium from ischemia/reperfusion injury Brent R. Weil, Mariuxi C. Manukyan, Jeremy L. Herrmann, Surgery Molecular PhysiologyIschemia/reperfusion InjuryPhysiologyCardiologyVascular Biology	2010	83
Intravenous Infusion of Mesenchymal Stem Cells Is Associated With Improved Myocardial Function During Endotoxemia Brent R. Weil, Jeremy L. Herrmann, Aaron M. Abarbanell, Shock Adult Stem CellImmunologyCardiac RegenerationSystemic Inflammatory ResponseBiomedical Engineering	2011	66
Hernia recurrence following inguinal hernia repair in children Kathryn Taylor, Kristin Sonderman, Lindsey L. Wolf, Journal of Pediatric Surgery Hernia SurgeryHernia RecurrencePediatricsPediatric SurgerySurgery	2018	56
TNF RECEPTOR 2, NOT TNF RECEPTOR 1, ENHANCES MESENCHYMAL STEM CELL-MEDIATED CARDIAC PROTECTION FOLLOWING ACUTE ISCHEMIA Megan L. Kelly, Meijing Wang, Paul R. Crisostomo, Shock Cardiac MuscleHeart FailureTnf Receptor 2Adult Stem CellImmunology	2010	55
TLR4 Inhibits Mesenchymal Stem Cell (MSC) STAT3 Activation and Thereby Exerts Deleterious Effects on MSC–Mediated Cardioprotection Yue Wang, Aaron M. Abarbanell, Jeremy L. Herrmann, PLoS ONE	2010	54

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