I have a background in Nursing as well as Computer Science. With more than 16 years of experience in biomedical research, I am very passionate about designing and executing experiments to address scientific questions. I like to accept new challenges, discover and solve problems, and love to work with a diverse group of people. A wide spectrum of experiences, including nursing, computer science and lab research, allow me to contribute to scientific endeavors with a unique perspective.
I love cooking, gardeingn, hiking and aerobic dancing. I have a son and a daughter, and live with my husband in beautiful Crozet, Virginia.
Phone: (434)982-4473, Fax: (434)982-3139, e-mail: email@example.com
Kim YK, Yadava RS, Mandal M, Mahadevan K, Yu Q, Leitges M, Mahadevan MS (2016). Disease Phenotypes in a Mouse Model of RNA Toxicity Are Independent of Protein Kinase Cα and Protein Kinase Cβ. Published 22 Sep 2016 PLoS ONE http://dx.doi.org/10.1371/journal.pone.0163325.
Yadava RS, Foff EP, Yu Q, Gladman JT, Zheng TS, Mahadevan MS (2016). TWEAK Regulates Muscle Functions in a Mouse Model of RNA Toxicity. PLoS ONE. 2016 Feb 22; 11(2):e0150192. doi: 10.1371/journal.pone.0150192. eCollection 2016.
Yadava RS, Foff EP, Yu Q, Gladman JT,Kim YK, Bhatt KS, Thornton CA, Zheng TS and Mahadevan MS (2014).TWEAK/Fn14,a pathway and novel therapeutic target in myotonic dystrophy. Hum Mol Genet First published online: December 11, 2014, doi: 10.1093/hmg/ddu617.
Gladman GT, Yadava RS, Mandal M, Yu Q, Kim YK and Mahadevan MS (2014). NKX2-5, a Modifier of Skeletal Muscle Pathology due to RNA Toxicity. Hum. Mol. Genet. First published online August 28, 2014 doi: 10.1093/hmg/ddu443.
Yadava RS, Frenzel-McCardell CD, Yu Q, Srinivasan V, Tucker AL, Puymirat J, Thornton CA, Prall OW, Harvey RP & Mahadevan MS (2008).Induced NKX2-5 expression resulting from RNA toxicity in myotonic muscular dystrophy. Nat Genet. Jan; 40(1): 61-8.
Mahadevan MS, Yadava RS, Yu Q, Balijepalli S, Frenzel-McCardell CD, Bourne TD, Phillips LH (2006). Reversible model of RNA toxicity and cardiac conduction defects in myotonic dystrophy. Nat Genet. Sep; 38(9):1066-70.