Cho JL, Ling MF, Adams DC, et al. Allergic asthma is distinguished by sensitivity of allergen-specific CD4+ T cells and airway structural cells to type 2 inflammation. Sci Transl Med. 2016;8(359):359ra132. doi:10.1126/scitranslmed.aag1370
Publications
O’Grady GL, Verschuuren C, Yuen M, et al. Variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. Neurology. 2016;87(14):1442-1448. doi:10.1212/WNL.0000000000003179
Santeford A, Wiley LA, Park S, et al. Impaired autophagy in macrophages promotes inflammatory eye disease. Autophagy. 2016;12(10):1876-1885. doi:10.1080/15548627.2016.1207857
Sharma G, Lian CG, Lin WM, et al. Distinct genetic profiles of extracranial and intracranial acral melanoma metastases. J Cutan Pathol. 2016;43(10):884-91. doi:10.1111/cup.12746
McMorran BJ, McCarthy FE, Gibbs EM, et al. Differentiation-related glycan epitopes identify discrete domains of the muscle glycocalyx. Glycobiology. 2016;26(10):1120-1132. doi:10.1093/glycob/cww061
Trotta L, Hautala T, Hämäläinen S, et al. Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland. Eur J Hum Genet. 2016;24(10):1473-8. doi:10.1038/ejhg.2016.37
Braff D, Shis D, Collins JJ. Synthetic biology platform technologies for antimicrobial applications. Adv Drug Deliv Rev. 2016;105(Pt A):35-43. doi:10.1016/j.addr.2016.04.006
Cade BE, Chen H, Stilp AM, et al. Genetic Associations with Obstructive Sleep Apnea Traits in Hispanic/Latino Americans. Am J Respir Crit Care Med. 2016;194(7):886-897. doi:10.1164/rccm.201512-2431OC
Reddy HM, Hamed SA, Lek M, et al. Homozygous nonsense mutation in SGCA is a common cause of limb-girdle muscular dystrophy in Assiut, Egypt. Muscle Nerve. 2016;54(4):690-5. doi:10.1002/mus.25094
Gray SW, Park ER, Najita J, et al. Oncologists’ and cancer patients’ views on whole-exome sequencing and incidental findings: results from the CanSeq study. Genet Med. 2016;18(10):1011-9. doi:10.1038/gim.2015.207