On protein solubility in organic solvent von Chin, Jennifer T., Wheeler, Sarah L., Klibanov, Alexander M.

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MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder von Heimer, Gali, Kerätär, Juha M., Riley, Lisa G., Balasubramaniam, Shanti, Eyal, Eran, Pietikäinen, Laura P., Hiltunen, J. Kalervo, Marek-Yagel, Dina, Hamada, Jeffrey, Gregory, Allison, Rogers, Caleb, Hogarth, Penelope, Nance, Martha A., Shalva, Nechama, Veber, Alvit, Tzadok, Michal, Nissenkorn, Andreea, Tonduti, Davide, Renaldo, Florence, Bamshad, Michael J., Leal, Suzanne M., Nickerson, Deborah A., Anderson, Peter, Annable, Marcus, Blue, Elizabeth Marchani, Buckingham, Kati J., Chin, Jennifer, Chong, Jessica X., Cornejo, Rodolfo, Davis, Colleen P., Frazar, Christopher, He, Zongxiao, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Kolar, Tom, Krauter, Stephanie A., Luksic, Daniel, Marvin, Colby T., McGee, Sean, McGoldrick, Daniel J., Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Robertson, Peggy D., Santos-Cortez, Regie, Shankar, Aditi, Slattery, Krystal, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Tackett, Monica, Wang, Gao, Wegener, Marc, Weiss, Jeffrey M., Wernick, Riana I., Wheeler, Marsha M., Yi, Qian, Kraoua, Ichraf, Panteghini, Celeste, Valletta, Lorella, Garavaglia, Barbara, Cowley, Mark J., Gayevskiy, Velimir, Roscioli, Tony, Silberstein, Jonathon M., Hoffmann, Chen, Raas-Rothschild, Annick, Tiranti, Valeria, Anikster, Yair, Christodoulou, John, Kastaniotis, Alexander J., Ben-Zeev, Bruria, Hayflick, Susan J.

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De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay von Chong, Jessica X., McMillin, Margaret J., Shively, Kathryn M., Beck, Anita E., Marvin, Colby T., Armenteros, Jose R., Buckingham, Kati J., Nkinsi, Naomi T., Boyle, Evan A., Berry, Margaret N., Bocian, Maureen, Foulds, Nicola, Uzielli, Maria Luisa Giovannucci, Haldeman-Englert, Chad, Hennekam, Raoul C.M., Kaplan, Paige, Kline, Antonie D., Mercer, Catherine L., Nowaczyk, Malgorzata J.M., Klein Wassink-Ruiter, Jolien S., McPherson, Elizabeth W., Moreno, Regina A., Scheuerle, Angela E., Shashi, Vandana, Stevens, Cathy A., Carey, John C., Monteil, Arnaud, Lory, Philippe, Tabor, Holly K., Smith, Joshua D., Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay, Nickerson, Deborah A., Abecasis, Gonçalo R., Anderson, Peter, Blue, Elizabeth Marchani, Annable, Marcus, Browning, Brian L., Buckingham, Kati J., Chen, Christina, Chin, Jennifer, Chong, Jessica X., Cooper, Gregory M., Davis, Colleen P., Frazar, Christopher, Harrell, Tanya M., He, Zongxiao, Jain, Preti, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Jun, Goo, Kircher, Martin, Kolar, Tom, Krauter, Stephanie A., Krumm, Niklas, Leal, Suzanne M., Luksic, Daniel, Marvin, Colby T., McMillin, Margaret J., McGee, Sean, O’Reilly, Patrick, Paeper, Bryan, Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Poel, Christa, Reinier, Frederic, Robertson, Peggy D., Santos-Cortez, Regie, Shaffer, Tristan, Shephard, Cindy, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Staples, Jeffrey C., Tabor, Holly K., Tackett, Monica, Underwood, Jason G., Wegener, Marc, Wang, Gao, Wheeler, Marsha M., Yi, Qian, Bamshad, Michael J.

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Mutation of ATF6 causes autosomal recessive achromatopsia von Ansar, Muhammad, Santos-Cortez, Regie Lyn P., Saqib, Muhammad Arif Nadeem, Zulfiqar, Fareeha, Lee, Kwanghyuk, Ashraf, Naeem Mahmood, Ullah, Ehsan, Wang, Xin, Sajid, Sundus, Khan, Falak Sher, Amin-ud-Din, Muhammad, Smith, Joshua D., Shendure, Jay, Bamshad, Michael J., Nickerson, Deborah A., Hameed, Abdul, Riazuddin, Saima, Ahmed, Zubair M., Ahmad, Wasim, Leal, Suzanne M.

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Rare A2ML1 variants confer susceptibility to otitis media von Santos-Cortez, Regie Lyn P, Chiong, Charlotte M, Reyes-Quintos, Ma Rina T, Tantoco, Ma Leah C, Wang, Xin, Acharya, Anushree, Abbe, Izoduwa, Giese, Arnaud P, Smith, Joshua D, Allen, E Kaitlynn, Li, Biao, Cutiongco-de la Paz, Eva Maria, Garcia, Marieflor Cristy, Llanes, Erasmo Gonzalo D V, Labra, Patrick John, Gloria-Cruz, Teresa Luisa I, Chan, Abner L, Wang, Gao T, Daly, Kathleen A, Shendure, Jay, Bamshad, Michael J, Nickerson, Deborah A, Patel, Janak A, Riazuddin, Saima, Sale, Michele M, Chonmaitree, Tasnee, Ahmed, Zubair M, Abes, Generoso T, Leal, Suzanne M

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Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3 von Chong, Jessica X., Burrage, Lindsay C., Beck, Anita E., Marvin, Colby T., McMillin, Margaret J., Shively, Kathryn M., Harrell, Tanya M., Buckingham, Kati J., Bacino, Carlos A., Jain, Mahim, Alanay, Yasemin, Berry, Susan A., Carey, John C., Gibbs, Richard A., Lee, Brendan H., Krakow, Deborah, Shendure, Jay, Nickerson, Deborah A., Bamshad, Michael J., Shendure, Jay, Nickerson, Deborah A., Abecasis, Gonçalo R., Anderson, Peter, Blue, Elizabeth Marchani, Annable, Marcus, Browning, Brian L., Buckingham, Kati J., Chen, Christina, Chin, Jennifer, Chong, Jessica X., Cooper, Gregory M., Davis, Colleen P., Frazar, Christopher, Harrell, Tanya M., He, Zongxiao, Jain, Preti, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Jun, Goo, Kircher, Martin, Kolar, Tom, Krauter, Stephanie A., Krumm, Niklas, Leal, Suzanne M., Luksic, Daniel, Marvin, Colby T., McMillin, Margaret J., McGee, Sean, O’Reilly, Patrick, Paeper, Bryan, Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Poel, Christa, Reinier, Frederic, Robertson, Peggy D., Santos-Cortez, Regie, Shaffer, Tristan, Shephard, Cindy, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Staples, Jeffrey C., Tabor, Holly K., Tackett, Monica, Underwood, Jason G., Wegener, Marc, Wang, Gao, Wheeler, Marsha M., Yi, Qian, Bamshad, Michael J.

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Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani population von Shahzad, Mohsin, Yousaf, Sairah, Waryah, Yar M., Gul, Hadia, Kausar, Tasleem, Tariq, Nabeela, Mahmood, Umair, Ali, Muhammad, Khan, Muzammil A., Waryah, Ali M., Shaikh, Rehan S., Riazuddin, Saima, Ahmed, Zubair M.

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Novel digenic inheritance of PCDH15 and USH1G underlies profound non-syndromic hearing impairment von Schrauwen, Isabelle, Chakchouk, Imen, Acharya, Anushree, Liaqat, Khurram, Irfanullah, Nickerson, Deborah A, Bamshad, Michael J, Shah, Khadim, Ahmad, Wasim, Leal, Suzanne M

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Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability von Ansar, Muhammad, Jan, Abid, Santos-Cortez, Regie Lyn P, Wang, Xin, Suliman, Muhammad, Acharya, Anushree, Habib, Rabia, Abbe, Izoduwa, Ali, Ghazanfar, Lee, Kwanghyuk, Smith, Joshua D, Nickerson, Deborah A, Shendure, Jay, Bamshad, Michael J, Ahmad, Wasim, Leal, Suzanne M

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On protein solubility in organic solvents von CHIN, J. T, WHEELER, S. L, KLIBANOV, A. M

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Structural basis for the modulation of voltage-gated sodium channels by animal toxins von Shen, Huaizong, Li, Zhangqiang, Jiang, Yan, Pan, Xiaojing, Wu, Jianping, Cristofori-Armstrong, Ben, Smith, Jennifer J, Chin, Yanni K Y, Lei, Jianlin, Zhou, Qiang, King, Glenn F, Yan, Nieng

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High-frequency dynamics of ocean pH: a multi-ecosystem comparison von Hofmann, Gretchen E, Smith, Jennifer E, Johnson, Kenneth S, Send, Uwe, Levin, Lisa A, Micheli, Fiorenza, Paytan, Adina, Price, Nichole N, Peterson, Brittany, Takeshita, Yuichiro, Matson, Paul G, Crook, Elizabeth Derse, Kroeker, Kristy J, Gambi, Maria Cristina, Rivest, Emily B, Frieder, Christina A, Yu, Pauline C, Martz, Todd R

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Pulmonary Embolism and Increased Levels of D-Dimer in Patients with Coronavirus Disease von Griffin, Daniel O., Jensen, Alexandra, Khan, Mushmoom, Chin, Jessica, Chin, Kelly, Saad, Jennifer, Parnell, Ryan, Awwad, Christopher, Patel, Darshan

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Markers of Focal and Diffuse Nonischemic Myocardial Fibrosis Are Associated With Adverse Cardiac Remodeling and Prognosis in Patients With Hypertension: The REMODEL Study von Iyer, Nithin R., Le, Thu-Thao, Kui, Michelle S.L., Tang, Hak-Chiaw, Chin, Chee-Tang, Phua, Soon-Kieng, Bryant, Jennifer A., Pua, Chee-Jian, Ang, Briana, Toh, Desiree-Faye, Aw, Tar-Choon, Lee, Chi-Hang, Cook, Stuart A., Ugander, Martin, Chin, Calvin W.L.

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Telomere Shortening in Familial and Sporadic Pulmonary Fibrosis von Cronkhite, Jennifer T, Xing, Chao, Raghu, Ganesh, Chin, Kelly M, Torres, Fernando, Rosenblatt, Randall L, Garcia, Christine Kim

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Effect of moist heat reprocessing of N95 respirators on SARS-CoV-2 inactivation and respirator function von Daeschler, Simeon C., Manson, Niclas, Joachim, Kariym, Chin, Alex W. H., Chan, Katelyn, Chen, Paul Z., Tajdaran, Kiana, Mirmoeini, Kaveh, Zhang, Jennifer J., Maynes, Jason T., Zhang, Libo, Science, Michelle, Darbandi, Ali, Stephens, Derek, Gu, Frank, Poon, Leo L. M., Borschel, Gregory H.

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Expert panel consensus recommendations for ambulatory blood pressure monitoring in Asia: The HOPE Asia Network von Kario, Kazuomi, Shin, Jinho, Chen, Chen‐Huan, Buranakitjaroen, Peera, Chia, Yook‐Chin, Divinagracia, Romeo, Nailes, Jennifer, Hoshide, Satoshi, Siddique, Saulat, Sison, Jorge, Soenarta, Arieska Ann, Sogunuru, Guru Prasad, Tay, Jam Chin, Teo, Boon Wee, Turana, Yuda, Zhang, Yuqing, Park, Sungha, Van Minh, Huynh, Wang, Ji‐Guang

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An Empirical Analysis of Triple Bottom-Line Reporting and its Determinants: Evidence from the United States and Japan von Jennifer Ho, Li-Chin, Taylor, Martin E.

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p97/VCP promotes degradation of CRBN substrate glutamine synthetase and neosubstrates von Van Nguyen, Thang, Li, Jing, Lu, Chin-Chun (Jean), Mamrosh, Jennifer L., Lu, Gang, Cathers, Brian E., Deshaies, Raymond J.

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MBNL1-mediated regulation of differentiation RNAs promotes myofibroblast transformation and the fibrotic response von Davis, Jennifer, Salomonis, Nathan, Ghearing, Natasha, Lin, Suh-Chin J., Kwong, Jennifer Q., Mohan, Apoorva, Swanson, Maurice S., Molkentin, Jeffery D.

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