Desmin forms toxic, seeding-competent amyloid aggregates that persist in muscle fibers
Kedia, N., Arhzaouy, K., Pittman, S.K., (…), *Weihl, C.C., Bieschke, J., PNAS, Volume 116, Issue 34, 20 August 2019, Pages 16835-16840, 2019.
Single-Cell Analysis Reveals Regional Reprogramming During Adaptation to Massive Small Bowel Resection in Mice
Seiler, K.M., Waye, S.E., Kong, W., (…), Warner, B.W., *Morris, S.A., Cell Mol Gastroenterol Hepatol, Volume 8, Issue 3, 2019, Pages 407-426, 2019.
Macrophage Plasticity and Function in the Eye and Heart
Wang, Z., Koenig, A.L., *Lavine, K.J., *Apte, R.S., Trends Immunol, Volume 40, Issue 9, September 2019, Pages 825-841, 2019.
Immunomodulatory role of nonneuronal cholinergic signaling in myocardial injury
Rocha-Resende, C., Weinheimer, C., Bajpai, G., (…), *Lavine, K.J., Mann, D.L., JCI Insight, Volume 4, Issue 14, 25 July 2019, Article number e128961, 2019.
An endogenous peptide marker differentiates SOD1 stability and facilitates pharmacodynamic monitoring in SOD1 amyotrophic lateral sclerosis
Gertsman, I., Wuu, J., McAlonis-Downes, M., (…), *Miller, T.M., Da Cruz, S., JCI Insight, Volume 4, Issue 10, 2019, Article number e122768, 2019.
Zmym2 inhibits nanog-mediated reprogramming
Lawrence, M., *Theunissen, T.W., Lombard, P., Adams, D.J., Silva, J.C.R., Wellcome Open Res, Volume 4, 2019, Article number 88, 2019.
Sox2 and FGF20 interact to regulate organ of Corti hair cell and supporting cell development in a spatially-graded manner
Yang, L.M., Cheah, K.S.E., Huh, S.-H., *Ornitz, D.M., PLoS Genetics, Volume 15, Issue 7, July 2019, Article number e1008254, 2019.
VEGFA From Early Osteoblast Lineage Cells (Osterix+) Is Required in Mice for Fracture Healing
Buettmann, E.G., McKenzie, J.A., Migotsky, N., (…), Yoneda, S., Silva, M.J., J Bone Min Res, May 2019.
Transcriptional and Epigenetic Regulation of Cardiac Electrophysiology
Jimenez, J., Rentschler, S.L., Pediatric Cardiology, 2019
Generation and validation of novel conditional flox and inducible Cre alleles targeting fibroblast growth factor 18 (Fgf18)
Hagan, A.S., Boylan, M., Smith, C., (…), Lewandoski, M., Ornitz, D.M. Dev Dyn, 2019.
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
Undiagnosed Diseases Network (including *Schedl, TS, *Cole FF, and *Solnica-Krezel, L. Am J Hum Genet, 105:413-24, 2019.
Applications of RNA interference in the treatment of arthritis
*Rai, M.F., Pan, H., Yan, H., (…), Pham, C.T.N., Wickline, S.A. Translational Res, 2019.