Whole Genome Sequencing Reveals a Chromosome 9p Deletion Causing DOCK8 Deficiency in an Adult Diagnosed with Hyper IgE Syndrome Who Developed Progressive Multifocal Leukoencephalop...

por G. Day-Williams, Aaron, Sun, Chao, Jelcic, Ilijas, McLaughlin, Helen, Harris, Tim, Martin, Roland, Carulli, John P.
Publicado 2014

Genetic Study of Severe Prolonged Lymphopenia in Multiple Sclerosis Patients Treated With Dimethyl Fumarate

por Sangurdekar, Dipen, Sun, Chao, McLaughlin, Helen, Ayling-Rouse, Katherine, Allaire, Normand E., Penny, Michelle A., Bronson, Paola G.
Publicado 2019

Systems Analysis of Transcriptomic and Proteomic Profiles Identifies Novel Regulation of Fibrotic Programs by miRNAs in Pulmonary Fibrosis Fibroblasts

por Mullenbrock, Steven, Liu, Fei, Szak, Suzanne, Hronowski, Xiaoping, Gao, Benbo, Juhasz, Peter, Sun, Chao, Liu, Mei, McLaughlin, Helen, Xiao, Qiurong, Feghali-Bostwick, Carol, Zheng, Timothy S.
Publicado 2018

Highly efficient neuronal gene knockout in vivo by CRISPR-Cas9 via neonatal intracerebroventricular injection of AAV in mice

por Hana, Sam, Peterson, Michael, McLaughlin, Helen, Marshall, Eric, Fabian, Attila J., McKissick, Olivia, Koszka, Kathryn, Marsh, Galina, Craft, Michael, Xu, Shanqin, Sorets, Alexander, Torregrosa, Tess, Sun, Chao, Henderson, Chris E., Lo, Shih-Ching
Publicado 2021

In vivo genome editing using novel AAV-PHP variants rescues motor function deficits and extends survival in a SOD1-ALS mouse model

por Chen, Yi A., Kankel, Mark W., Hana, Sam, Lau, Shukkwan Kelly, Zavodszky, Maria I., McKissick, Olivia, Mastrangelo, Nicole, Dion, Jessica, Wang, Bin, Ferretti, Daniel, Koske, David, Lehman, Sydney, Koszka, Kathryn, McLaughlin, Helen, Liu, Mei, Marshall, Eric, Fabian, Attila J., Cullen, Patrick, Marsh, Galina, Hamann, Stefan, Craft, Michael, Sebalusky, Jennifer, Arnold, H. Moore, Driscoll, Rachelle, Sheehy, Adam, Luo, Yi, Manca, Sonia, Carlile, Thomas, Sun, Chao, Sigrist, Kirsten, McCampbell, Alexander, Henderson, Christopher E., Lo, Shih-Ching
Publicado 2022