March 15th, 2024
Another grad from the Wende Lab: Congratulations to Dr. Luke Potter for a successful thesis defense! And best of luck in your future endeavors!
March 15th, 2024
Another grad from the Wende Lab: Congratulations to Dr. Luke Potter for a successful thesis defense! And best of luck in your future endeavors!
10/27/2023
Samuel wins 2nd place for his poster at the 10th Annual UAB Comprehensive Cardiovascular Center Symposium
09/12/2023
Mahima R. wins a Trainee Research Competition Award for her poster at the UCEM/UABNSC/BHM&ATL GRECC/UABICAR “Exercise and Aging” Research Symposium
08/17/2023
Adam Wende, Ph.D., UCEM Scientist and co-leader of UCEM Pre-Clinical Research Team has been appointed as the Associate Director of the UCEM T32 Interdisciplinary Training in Pathobiology and Rehabilitation Medicine Program. The goal of the training program is to develop burgeoning pre- and post-doctoral candidates into future leaders in translational rehabilitation research—scientists who are equipped to test and disseminate novel rehabilitative strategies that will alleviate impairment and compromised life quality in the face of chronic disease management. |
08/2023
The Wende Lab attends the 2023 AHA Basic Cardiovascular Sciences Sessions in Boston MA. Dr. Ha and trainees, Sayan and Samuel, present their latest work (https://bcvs.apprisor.org/epsSearchBCVS.cfm).
7/30/2023
Sayan wins the 3rd place pre-doctoral trainee award for his oral presentation at the 2023 pre-BCVS Asian Cardiovascular Symposium.
5/25/2023
Samuel was selected from a highly competitive applicant pool for one of three predoctoral traineeship positions in the NIH funded UAB Center for Exercise Medicine (UCEM) T32 program. T32 HD071866 “Interdisciplinary Training in Pathobiology and Rehabilitation Medicine“.
April 11th, 2023
Dr. Wende honored with a 2023 UAB Graduate School Dean’s Excellence in Mentorship Award!
Date: Mar. 9th 2023
Wende was awarded an R01 from NHLBI of the NIH entitled, “Novel roles of PDK2 in heart failure: Regulation of mitochondrial nuclear crosstalk via metabolic regulation and histone acetylation” (1R01HL167872-01). A brief introduction to the project: Cardiovascular disease is the number one cause of mortality in the United States, with different etiologies of heart failure associated with distinct changes in mitochondrial substrate selection, utilization, and gene expression mediating these differences. Here we test the hypothesis that one family of kinases that regulate this process (i.e., PDKs) play distinct roles in mortality, cardiac hypertrophy, mitochondrial oxidative metabolism, and signaling to transcriptional pathways in the nucleus mediated by epigenetics (i.e., histone acetylation). We have developed new animal model systems of inducible and cardiomyocyte specific loss-of-function mice of the two cardiac enriched isoforms of this pathway (i.e., PDK2 and PDK4) to determine the mechanism of this regulation and test the potential of their isoform-specific impact on pressure-overload induced heart failure.
01/10/2023
Bakshi receives an AHA 23PRE1022560 fellowship entitled: “Epigenetic regulation of gene expression in ischemic heart failure via EZH2 methyltransferase”