Douglas A. Andres

Affiliations: 
1993- Molecular and Cellular Biochemistry University of Kentucky, Lexington, KY 
Area:
Biochemistry
Website:
https://biochemistry.med.uky.edu/users/dandres
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"Douglas A. Andres"
Bio:

https://biochemistry.med.uky.edu/sites/default/files/cv/Andres%20travel%20CV%202012%20July.pdf

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Parents

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Jack E. Dixon grad student 1985-1990 Purdue
 (Characterization of the Carboxyl-terminal Sequences Responsible for Protein Retention in the Endoplasmic Reticulum.)
Michael  Stuart Brown post-doc 1990-1993 UT Southwestern
Joseph L. Goldstein post-doc 1990-1993 UT Southwestern
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Publications

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Andres DA, Young LEA, Veeranki S, et al. (2020) Improved workflow for mass spectrometry-based metabolomics analysis of the heart. The Journal of Biological Chemistry
Ahern BM, Levitan BM, Veeranki S, et al. (2019) Myocardial-restricted ablation of the GTPase RAD results in a pro-adaptive heart response in mice. The Journal of Biological Chemistry
Mir S, Andres DA. (2018) Small GTPase RIT1 in Mouse Retina; Cellular and Functional Analysis. Current Eye Research
Manning JR, Chelvarajan L, Levitan BM, et al. (2018) Rad GTPase deletion attenuates post-ischemic cardiac dysfunction and remodeling. Jacc. Basic to Translational Science. 3: 83-96
Withers CN, Brown DM, Byiringiro I, et al. (2017) Rad GTPase is essential for the regulation of bone density and bone marrow adipose tissue in mice. Bone
Mir S, Cai W, Carlson SW, et al. (2017) IGF-1 mediated Neurogenesis Involves a Novel RIT1/Akt/Sox2 Cascade. Scientific Reports. 7: 3283
Mir S, Cai W, Andres DA. (2016) RIT1 GTPase Regulates Sox2 Transcriptional Activity and Hippocampal Neurogenesis. The Journal of Biological Chemistry
Levitan BM, Manning JR, Withers CN, et al. (2016) Rad-deletion Phenocopies Tonic Sympathetic Stimulation of the Heart. Journal of Cardiovascular Translational Research
Manning JR, Withers CN, Levitan B, et al. (2015) Loss of Rad-GTPase Produces a Novel Adaptive Cardiac Phenotype Resistant to Systolic decline with Aging. American Journal of Physiology. Heart and Circulatory Physiology. ajpheart.00389.2015
Koenighofer M, Hung CY, McCauley JL, et al. (2015) Mutations in RIT1 cause Noonan syndrome - additional functional evidence and expanding the clinical phenotype. Clinical Genetics
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