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Faculty Detail    
Name GIRISH MELKANI
Associate Professor of Pathology
Division of Molecular and Cellular Pathology, Department of Pathology, UAB Heersink School of Medicine		  
Campus Address BMR2 436 Zip 2186
Phone  (205)-996-0591
E-mail  gmelkani@uab.edu, girishmelkani@uabmc.edu
Other websites Circadian, Cardiometabolic, Myofibrillar, Aggregation, and Aging Disorders Research Lab
     

Education
Undergraduate  Kumaun University, Nainital, India    1993  B.S. 
Graduate  Kumaun University, Nainital, India    1995  M.S. 
Graduate  Central Drug Research Institute, Lucknow, India & Kumaun University, Nainital, India.    2001  Ph.D. 


Faculty Appointment(s)
Appointment Type Department Division Rank
Primary  Joint Pathology  Molecular & Cellular Pathology Associate Professor
Center  Comprehensive Cancer Center  Comprehensive Cancer Center Associate Professor
Center  Comprehensive Cardiovascular Ctr  Comprehensive Cardiovascular Ctr Associate Professor
Center  Comprehensive Diabetes Center  Comprehensive Diabetes Center Associate Professor
Center  Nutrition Sciences Research  Nutrition Obesity Res Ctr (NORC) Associate Professor
Center  UWIRC Microbiome Center  UWIRC Microbiome Center Associate Professor

Biographical Sketch 
Girish Melkani acquired a Ph.D. degree from Central Drug Research Institute, Lucknow, India (A CSIR premier Drug Institute) & Kumaun University, Nainital, India. For his Ph.D. dissertation, he studied lipoproteins under oxidative stress (in vitro and in vivo) and their cardiovascular implication in humans. After acquiring his Ph.D., he became interested in naturally occurring defense mechanisms involving heat shock proteins, which play a critical role in maintaining protein structure and function during cellular processes and stresses. He drew from his background in oxidative stress in lipoproteins for his postdoctoral position (at the Cal State San Marcos, CA) which focused on how GroEL (heat shock protein HSP-60 analog of E. coli) performs its chaperone function under multiple stress conditions. At the San Diego State University (SDSU), he then went on to further study the role of chaperones in vivo, particularly in the regulation of cardiac and skeletal muscle as well as in protein folding diseases. For these purposes, he used Drosophila as a model system using genetics, molecular biology, cell biology, cardiac physiology, and gene transfer techniques. For his Independent faculty career at SDSU, he used the Drosophila model to explore the mechanism of cardiac failure associated with amyloid accumulation in the cardiomyocytes (referred to as cardiac amyloidosis). He continued his faculty tenure at SDSU before joining the University of Alabama at Birmingham on Oct 1st, 2020, and with multiple collaborations over the years, his research projects are currently supported by three R01 grants. During this tenure, his research group has been at the forefront of developing and using clinically relevant Drosophila models to address the pathophysiological basis of human circadian/metabolic disorders linked to cardiometabolic disease, myofibrillar-myopathies, proteinopathies neuropathies, sleep, and aging disruptions. He also integrates physiological, cell-molecular, genetics, and nutritional approaches to understanding how lifestyle (including, chrono-nutrition, circadian rhythms, and eating/sleeping patterns) and genetic factors act to maintain the structural integrity of cells, tissues, and organs that in turn dictates organismal physiology. Additionally, using strategic collaborations, he applies the findings to higher mammals or even humans to develop therapies for human metabolic and myofibrillar and misfolding protein disorders. In addition to his research involvement, he is deeply committed to the academic excellence of undergraduate and graduate students with diverse backgrounds through classroom teaching and lab training. For his university and other services, he has served on various committees and grant review panels. He has also delivered invited talks at various national and international platforms including various universities, institutes, seminars, and conferences. He has reviewed scientific manuscripts for over 35 journals and served on the editorial board of three journals.



Research/Clinical Interest
Title
Circadian, Cardiometabolic, Myofibrillar, Aggregation, and Aging Disorders Research Lab
Description
My research group has been at the forefront of developing and using clinically relevant genetic models (Drosophila melanogaster) to address the pathophysiological basis of human circadian/metabolic disorders linked to cardiometabolic disease, myofibrillar-myopathies, proteinopathies neuropathies, sleep, and aging disruptions. I also integrate physiological, cell-molecular, genetics, genomics, and nutritional approaches to understand how lifestyle (including circadian rhythms and eating/sleeping patterns) and genetic factors act to maintain the structural integrity of cells, tissues, and organs that in turn dictates organismal physiology. Currently funded with three NIH R01 Grants (one PI and two MPI), our research findings have been published in Science, Nature Communications, Aging Cells, Human Molecular Genetics, Physiology, and PLoS Genetics. A summary of my main research projects is in the research section.

Keywords
Circadian Clock & Rhythm, Time-Restricted Feeding, Cardiometabolic Disorders, Cardiovascular Diseases, Skeletal Muscle Physiology, Laninopathy, Insomnia, Aging and Logitivity, Protein Misfolding & Aggregations, Drosophila Model