Adverse outcomes and an immunosuppressed endotype in septic patients with reduced IFN-γ ELISpot von Barrios, Evan L, Mazer, Monty B, McGonagill, Patrick W, Bergmann, Christian B, Goodman, Michael D, Gould, Robert W, Rao, Mahil, Polcz, Valerie E, Davis, Ruth J, Del Toro, Drew E, Dirain, Marvin Ls, Dram, Alexandra, Hale, Lucas O, Heidarian, Mohammad, Kim, Caleb Y, Kucaba, Tamara A, Lanz, Jennifer P, McCray, Ashley E, Meszaros, Sandra, Miles, Sydney, Nelson, Candace R, Rocha, Ivanna L, Silva, Elvia E, Ungaro, Ricardo F, Walton, Andrew H, Xu, Julie, Zeumer-Spataro, Leilani, Drewry, Anne M, Liang, Muxuan, Bible, Letitia E, Loftus, Tyler J, Turnbull, Isaiah R, Efron, Philip A, Remy, Kenneth E, Brakenridge, Scott C, Badovinac, Vladimir P, Griffith, Thomas S, Moldawer, Lyle L, Hotchkiss, Richard S, Caldwell, Charles C

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Widespread airway distribution and short-term phenotypic correction of cystic fibrosis pigs following aerosol delivery of piggyBac/adenovirus von Cooney, Ashley L, Singh, Brajesh K, Loza, Laura Marquez, Thornell, Ian M, Hippee, Camilla E, Powers, Linda S, Ostedgaard, Lynda S, Meyerholz, David K, Wohlford-Lenane, Chris, Stoltz, David A, B. McCray, Paul, Sinn, Patrick L

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microRNA network regulates expression and biosynthesis of wild-type and ΔF508 mutant cystic fibrosis transmembrane conductance regulator von Ramachandran, Shyam, Karp, Philip H, Jiang, Peng, Ostedgaard, Lynda S, Walz, Amy E, Fisher, John T, Keshavjee, Shaf, Lennox, Kim A, Jacobi, Ashley M, Rose, Scott D, Behlke, Mark A, Welsh, Michael J, Xing, Yi, McCray, Paul B

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes von Cortese, Andrea, Zhu, Yi, Rebelo, Adriana P., Negri, Sara, Courel, Steve, Abreu, Lisa, Bacon, Chelsea J., Bai, Yunhong, Bis-Brewer, Dana M., Bugiardini, Enrico, Buglo, Elena, Danzi, Matt C., Feely, Shawna M. E., Athanasiou-Fragkouli, Alkyoni, Haridy, Nourelhoda A., Isasi, Rosario, Khan, Alaa, Laurà, Matilde, Magri, Stefania, Pipis, Menelaos, Pisciotta, Chiara, Powell, Eric, Rossor, Alexander M., Saveri, Paola, Sowden, Janet E., Tozza, Stefano, Vandrovcova, Jana, Dallman, Julia, Grignani, Elena, Marchioni, Enrico, Scherer, Steven S., Tang, Beisha, Lin, Zhiqiang, Al-Ajmi, Abdullah, Schüle, Rebecca, Synofzik, Matthis, Maisonobe, Thierry, Stojkovic, Tanya, Auer-Grumbach, Michaela, Abdelhamed, Mohamed A., Hamed, Sherifa A., Zhang, Ruxu, Manganelli, Fiore, Santoro, Lucio, Taroni, Franco, Pareyson, Davide, Houlden, Henry, Herrmann, David N., Reilly, Mary M., Shy, Michael E., Zhai, R. Grace, Zuchner, Stephan

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Lentiviral Vector Gene Transfer to Porcine Airways von Sinn, Patrick L, Cooney, Ashley L, Oakland, Mayumi, Dylla, Douglas E, Wallen, Tanner J, Pezzulo, Alejandro A, Chang, Eugene H, McCray, Paul B

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Conceptualizing Indigenous strengths-based health and wellness research using group concept mapping von O'Keefe, Victoria M, Maudrie, Tara L, Cole, Ashley B, Ullrich, Jessica S, Fish, Jillian, Hill, Kyle X, White, Lauren A, Redvers, Nicole, Jernigan, Valarie Blue Bird, Lewis, Jordan P, West, Amy E, Apok, Charlene Aqpik, White, Evan J, Ivanich, Jerreed D, Schultz, Katie, Lewis, Melissa E, Sarche, Michelle C, Gonzalez, Miigis B, Parker, Myra, Neuner Weinstein, Sophie E, McCray, Celena J, Warne, Donald, Black, Jessica C, Richards, Jennifer R, Walls, Melissa L

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Assessing non-Mendelian inheritance in inherited axonopathies von Bis-Brewer, Dana M., Gan-Or, Ziv, Sleiman, Patrick, Hakonarson, Hakon, Fazal, Sarah, Courel, Steve, Cintra, Vivian, Tao, Feifei, Estiar, Mehrdad A., Tarnopolsky, Mark, Boycott, Kym M., Yoon, Grace, Suchowersky, Oksana, Dupré, Nicolas, Cheng, Andrew, Lloyd, Thomas E., Rouleau, Guy, Schüle, Rebecca, Züchner, Stephan

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Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort von Nagar, Shashwat Deepali, Pemu, Priscilla, Qian, Jun, Boerwinkle, Eric, Cicek, Mine, Clark, Cheryl R., Cohn, Elizabeth, Gebo, Kelly, Loperena, Roxana, Mayo, Kelsey, Mockrin, Stephen, Ohno-Machado, Lucila, Ramirez, Andrea H., Schully, Sheri, Able, Ashley, Green, Ashley, Zuchner, Stephan, Jordan, I. King, Meller, Robert

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Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes von Cortese, Andrea, Zhu, Yi, Rebelo, Adriana P., Negri, Sara, Courel, Steve, Abreu, Lisa, Bacon, Chelsea J., Bai, Yunhong, Bis-Brewer, Dana M., Bugiardini, Enrico, Buglo, Elena, Danzi, Matt C., Feely, Shawna M. E., Athanasiou-Fragkouli, Alkyoni, Haridy, Nourelhoda A., Isasi, Rosario, Khan, Alaa, Laurà, Matilde, Magri, Stefania, Pipis, Menelaos, Pisciotta, Chiara, Powell, Eric, Rossor, Alexander M., Saveri, Paola, Sowden, Janet E., Tozza, Stefano, Vandrovcova, Jana, Dallman, Julia, Grignani, Elena, Marchioni, Enrico, Scherer, Steven S., Tang, Beisha, Lin, Zhiqiang, Al-Ajmi, Abdullah, Schüle, Rebecca, Synofzik, Matthis, Maisonobe, Thierry, Stojkovic, Tanya, Auer-Grumbach, Michaela, Abdelhamed, Mohamed A., Hamed, Sherifa A., Zhang, Ruxu, Manganelli, Fiore, Santoro, Lucio, Taroni, Franco, Pareyson, Davide, Houlden, Henry, Herrmann, David N., Reilly, Mary M., Shy, Michael E., Zhai, R. Grace, Zuchner, Stephan

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A microRNA network regulates expression and biosynthesis of wild-type and ∆F508 mutant cystic fibrosis transmembrane conductance regulator von Ramachandran, Shyam, Karp, Philip H., Jiang, Peng, Ostedgaard, Lynda S., Walz, Amy E., Fisher, John T., Keshavjee, Shaf, Lennox, Kim A., Jacobi, Ashley M., Rose, Scott D., Behlke, Mark A., Welsh, Michael J., Xing, Yi, McCray, Paul B.

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A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulator von Ramachandran, Shyam, Karp, Philip H, Jiang, Peng, Ostedgaard, Lynda S, Walz, Amy E, Fisher, John T, Keshavjee, Shaf, Lennox, Kim A, Jacobi, Ashley M, Rose, Scott D, Behlke, Mark A, Welsh, Michael J, Xing, Yi, McCray, Jr, Paul B

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