Lori Wallrath

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"Lori Wallrath"
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Chandran S, Suggs JA, Wang BJ, et al. (2018) Suppression of myopathic lamin mutations by muscle-specific activation of AMPK and modulation of downstream signaling. Human Molecular Genetics
Bhide S, Trujillo AS, O'Connor MT, et al. (2018) Increasing autophagy and blocking Nrf2 suppress laminopathy-induced age-dependent cardiac dysfunction and shortened lifespan. Aging Cell. e12747
Bohnekamp J, Cryderman DE, Thiemann DA, et al. (2016) Using Drosophila for Studies of Intermediate Filaments. Methods in Enzymology. 568: 707-26
Dialynas G, Shrestha OK, Ponce JM, et al. (2015) Myopathic lamin mutations cause reductive stress and activate the nrf2/keap-1 pathway. Plos Genetics. 11: e1005231
Bohnekamp J, Cryderman DE, Paululat A, et al. (2015) A Drosophila Model of Epidermolysis Bullosa Simplex. The Journal of Investigative Dermatology. 135: 2031-9
Azzaz AM, Vitalini MW, Thomas AS, et al. (2014) Human heterochromatin protein 1α promotes nucleosome associations that drive chromatin condensation. The Journal of Biological Chemistry. 289: 6850-61
Wallrath LL, Vitalini MW, Elgin SCR. (2014) Heterochromatin: A critical part of the genome Fundamentals of Chromatin. 529-552
Fagan RL, Cryderman DE, Kopelovich L, et al. (2013) Laccaic acid A is a direct, DNA-competitive inhibitor of DNA methyltransferase 1. The Journal of Biological Chemistry. 288: 23858-67
Zwerger M, Jaalouk DE, Lombardi ML, et al. (2013) Myopathic lamin mutations impair nuclear stability in cells and tissue and disrupt nucleo-cytoskeletal coupling. Human Molecular Genetics. 22: 2335-49
Wallrath LL, Elgin SC. (2012) Enforcing silencing: dynamic HP1 complexes in Neurospora. Nature Structural & Molecular Biology. 19: 465-7
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