Dynamic genetic regulation of gene expression during cellular differentiation von Strober, B J, Elorbany, R, Rhodes, K, Krishnan, N, Tayeb, K, Battle, A, Gilad, Y

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Chimerism, Graft Survival, and Withdrawal of Immunosuppressive Drugs in HLA Matched and Mismatched Patients After Living Donor Kidney and Hematopoietic Cell Transplantation von Scandling, J. D., Busque, S., Shizuru, J. A., Lowsky, R., Hoppe, R., Dejbakhsh‐Jones, S., Jensen, K., Shori, A., Strober, J. A., Lavori, P., Turnbull, B. B., Engleman, E. G., Strober, S.

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Single-cell sequencing reveals lineage-specific dynamic genetic regulation of gene expression during human cardiomyocyte differentiation von Elorbany, Reem, Popp, Joshua M, Rhodes, Katherine, Strober, Benjamin J, Barr, Kenneth, Qi, Guanghao, Gilad, Yoav, Battle, Alexis

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A method to predict the impact of regulatory variants from DNA sequence von Lee, Dongwon, Gorkin, David U, Baker, Maggie, Strober, Benjamin J, Asoni, Alessandro L, McCallion, Andrew S, Beer, Michael A

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Redefining tissue specificity of genetic regulation of gene expression in the presence of allelic heterogeneity von Arvanitis, Marios, Tayeb, Karl, Strober, Benjamin J., Battle, Alexis

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Single-cell allele-specific expression analysis reveals dynamic and cell-type-specific regulatory effects von Qi, Guanghao, Strober, Benjamin J., Popp, Joshua M., Keener, Rebecca, Ji, Hongkai, Battle, Alexis

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Younger children with MS have a distinct CSF inflammatory profile at disease onset von CHABAS, D, NESS, J, RODRIGUEZ, M, WEINSTOCK-GUTTMAN, B, KRUPP, L. B, WAUBANT, E, BELMAN, A, YEH, E. A, KUNTZ, N, GORMAN, M. P, STROBER, J. B, DE KOUCHKOVSKY, I, MCCULLOCH, C, CHITNIS, T

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SURGE: uncovering context-specific genetic-regulation of gene expression from single-cell RNA sequencing using latent-factor models von Strober, Benjamin J, Tayeb, Karl, Popp, Joshua, Qi, Guanghao, Gordon, M Grace, Perez, Richard, Ye, Chun Jimmie, Battle, Alexis

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Human embryoid bodies as a novel system for genomic studies of functionally diverse cell types von Rhodes, Katherine, Barr, Kenneth A, Popp, Joshua M, Strober, Benjamin J, Battle, Alexis, Gilad, Yoav

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Vanishing MS T2-bright lesions before puberty : A distinct MRI phenotype? von CHABAS, D, CASTILLO-TRIVINO, T, MOWRY, E. M, STROBER, J. B, GLENN, O. A, WAUBANT, E

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Common viruses associated with lower pediatric multiple sclerosis risk von WAUBANT, E, MOWRY, E. M, BELMAN, A, MILAZZO, M, GORMAN, M, WEINSTOCK-GUTTMAN, B, RODRIGUEZ, M, OKSENBERG, J. R, JAMES, J. A, KRUPP, L, CHITNIS, T, YEH, E. A, KUNTZ, N, NESS, J, CHABAS, D, STROBER, J, MCDONALD, J

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Antidepressant Exposure as a Predictor of Clinical Outcomes in the Treatment of Resistant Depression in Adolescents (TORDIA) Study von SAKOLSKY, Dara J, PEREL, James M, MCCRACKEN, James T, STROBER, Michael J, IYENGAR, Satish, PORTA, Giovanna, BRENT, David A, EMSLIE, Graham J, CLARKE, Gregory N, DINEEN WAGNER, Karen, VITIELLO, Benedetto, KELLER, Martin B, BIRMAHER, Boris, ROSENBAUM ASARNOW, Joan, RYAN, Neal D

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The functional impact of rare variation across the regulatory cascade von Li, Taibo, Ferraro, Nicole, Strober, Benjamin J., Aguet, Francois, Kasela, Silva, Arvanitis, Marios, Ni, Bohan, Wiel, Laurens, Hershberg, Elliot, Ardlie, Kristin, Arking, Dan E., Beer, Rebecca L., Brody, Jennifer, Blackwell, Thomas W., Clish, Clary, Gabriel, Stacey, Gerszten, Robert, Guo, Xiuqing, Gupta, Namrata, Johnson, W. Craig, Lappalainen, Tuuli, Lin, Henry J., Liu, Yongmei, Nickerson, Deborah A., Papanicolaou, George, Pritchard, Jonathan K., Qasba, Pankaj, Shojaie, Ali, Smith, Josh, Sotoodehnia, Nona, Taylor, Kent D., Tracy, Russell P., Van Den Berg, David, Wheeler, Matthew T., Rich, Stephen S., Rotter, Jerome I., Battle, Alexis, Montgomery, Stephen B.

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Eosinophilic infiltration related to CAPN3 mutations: a pathophysiological component of primary calpainopathy? von Krahn, M, Goicoechea, M, Hanisch, F, Groen, E, Bartoli, M, Pécheux, C, Garcia-Bragado, F, Leturcq, F, Jeannet, P-Y, Lobrinus, JA, Jacquemont, S, Strober, J, Urtizberea, JA, Saenz, A, Bushby, K, Lévy, N, Lopez de Munain, A

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332P Physician and caregiver concordance in Duchenne muscular dystrophy patients in Europe, Japan, and the USA: a multi-national survey von Talaga, A., Strober, J., Ishigaki, K., Posner, N., Cappelleri, J., Dukacz, S., Aslam, Z., Morton, E., Iqbal, H., Chatterton, E., DeCourcy, J.

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333P Real-World symptom progression in Duchenne muscular dystrophy patients in Europe, Japan, and the USA: results from a multi-national survey von Talaga, A., Strober, J., Ishigaki, K., Posner, N., Cappelleri, J., Dukacz, S., Aslam, Z., Morton, E., Iqbal, H., Chatterton, E., DeCourcy, J.

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PCR141 The Impact of Duchenne Muscular Dystrophy on Caregiver Employment: A Survey in Europe, Japan, and the United States von Strober, J., Ishigaki, K., Merla, V., Posner, N., Cappelleri, J., Xiao, S., Talaga, A.K., Brunner, S., Morton, E., Olsen, S., de Courcy, J.

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G.P.6.07 Mycophenolate mofetil’s beneficial effects on skeletal muscle in the mdx mouse von Strober, J, Rando, T

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RWD130 Healthcare Resource Utilization for Pediatric and Adolescent Duchenne Muscular Dystrophy Patients: Analysis of Real-World Data von Strober, J., Ishigaki, K., Merla, V., Posner, N., Cappelleri, J., Xiao, S., Talaga, A.K., Brunner, S., Iqbal, H., Chatterton, E., Hatchell, N.

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Prospectively ascertained mania and hypomania among young adults with child‐ and adolescent‐onset bipolar disorder von Hafeman, Danella M., Goldstein, Tina R., Strober, Michael, Merranko, John, Gill, Mary Kay, Liao, Fangzi, Diler, Rasim S., Ryan, Neal D., Goldstein, Benjamin I., Axelson, David A., Keller, Martin B., Hunt, Jeffrey I., Hower, Heather, Weinstock, Lauren M., Yen, Shirley, Birmaher, Boris

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