Effect of Prior Infection with Virulent Shigella flexneri 2a on the Resistance of Monkeys to Subsequent Infection with Shigella sonnei von Formal, Samuel B., Oaks, Edwin V., Olsen, Raymond E., Wingfield-Eggleston, Michele, Snoy, Philip J., Cogan, John P.

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Oral vaccination of monkeys with an invasive Escherichia coli K-12 hybrid expressing Shigella flexneri 2a somatic antigen von Formal, S B, Hale, T L, Kapfer, C, Cogan, J P, Snoy, P J, Chung, R, Wingfield, M E, Elisberg, B L, Baron, L S

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Article trading among members of a community von COGAN JOHN P, BAIRD-SMITH ANSELM P, NGUYEN VU, ALVARADO CAROLE K, ALVARADO WILLIAM A

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ARTICLE TRADING PROCESS von COGAN JOHN P, BAIRD-SMITH ANSELM P, NGUYEN VU, ALVARADO CAROLE K, ALVARADO WILLIAM A

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ARTICLE TRADING PROCESS von COGAN JOHN P, BAIRD-SMITH ANSELM P, NGUYEN VU, ALVARADO CAROLE K, ALVARADO WILLIAM A

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ARTICLE TRADING PROCESS von NGUYEN, VU, ALVARADO, WILLIAM, A, COGAN, JOHN, P., III, ALVARADO, CAROLE, K, BAIRD-SMITH, ANSELM, P

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Are government bodies bound by arbitration agreements? an Eastman arbitration library prize-winning essay [problems and advantages related to the inclusion of arbitration agreement... von Cogan, John P

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ARTICLE TRADING PROCESS von COGAN JOHN P, BAIRD-SMITH ANSELM P, NGUYEN VU, ALVARADO CAROLE K, ALVARADO WILLIAM A

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ARTICLE TRADING PROCESS von NGUYEN, VU, ALVARADO, WILLIAM, A, COGAN, JOHN, P., III, ALVARADO, CAROLE, K, BAIRD-SMITH, ANSELM, P

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Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays von Ganapathi, Mythily, Matsuoka, Leticia S, March, Michael, Li, Dong, Brokamp, Elly, Benito-Sanz, Sara, White, Susan M, Lachlan, Katherine, Ahimaz, Priyanka, Sewda, Anshuman, Bastarache, Lisa, Thomas-Wilson, Amanda, Stoler, Joan M, Bramswig, Nuria C, Baptista, Julia, Stals, Karen, Demurger, Florence, Cogne, Benjamin, Isidor, Bertrand, Bedeschi, Maria Francesca, Peron, Angela, Amiel, Jeanne, Zackai, Elaine, Schacht, John P, Iglesias, Alejandro D, Morton, Jenny, Schmetz, Ariane, Seidel, Verónica, Lucia, Stephanie, Baskin, Stephanie M, Thiffault, Isabelle, Cogan, Joy D, Gordon, Christopher T, Chung, Wendy K, Bowdin, Sarah, Bhoj, Elizabeth

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Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease von Kropski, Jonathan A, Pritchett, Jason M, Zoz, Donald F, Crossno, Peter F, Markin, Cheryl, Garnett, Errine T, Degryse, Amber L, Mitchell, Daphne B, Polosukhin, Vasiliy V, Rickman, Otis B, Choi, Leena, Cheng, Dong-Sheng, McConaha, Melinda E, Jones, Brittany R, Gleaves, Linda A, McMahon, Frank B, Worrell, John A, Solus, Joseph F, Ware, Lorraine B, Lee, Jae Woo, Massion, Pierre P, Zaynagetdinov, Rinat, White, Eric S, Kurtis, Jonathan D, Johnson, Joyce E, Groshong, Steve D, Lancaster, Lisa H, Young, Lisa R, Steele, Mark P, Phillips Iii, John A, Cogan, Joy D, Loyd, James E, Lawson, William E, Blackwell, Timothy S

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High-throughput screening using patient-derived tumor xenografts to predict clinical trial drug response von Gao, Hui, Korn, Joshua M, Ferretti, Stéphane, Monahan, John E, Wang, Youzhen, Singh, Mallika, Zhang, Chao, Schnell, Christian, Yang, Guizhi, Zhang, Yun, Balbin, O Alejandro, Barbe, Stéphanie, Cai, Hongbo, Casey, Fergal, Chatterjee, Susmita, Chiang, Derek Y, Chuai, Shannon, Cogan, Shawn M, Collins, Scott D, Dammassa, Ernesta, Ebel, Nicolas, Embry, Millicent, Green, John, Kauffmann, Audrey, Kowal, Colleen, Leary, Rebecca J, Lehar, Joseph, Liang, Ying, Loo, Alice, Lorenzana, Edward, Robert McDonald, E, McLaughlin, Margaret E, Merkin, Jason, Meyer, Ronald, Naylor, Tara L, Patawaran, Montesa, Reddy, Anupama, Röelli, Claudia, Ruddy, David A, Salangsang, Fernando, Santacroce, Francesca, Singh, Angad P, Tang, Yan, Tinetto, Walter, Tobler, Sonja, Velazquez, Roberto, Venkatesan, Kavitha, Von Arx, Fabian, Wang, Hui Qin, Wang, Zongyao, Wiesmann, Marion, Wyss, Daniel, Xu, Fiona, Bitter, Hans, Atadja, Peter, Lees, Emma, Hofmann, Francesco, Li, En, Keen, Nicholas, Cozens, Robert, Jensen, Michael Rugaard, Pryer, Nancy K, Williams, Juliet A, Sellers, William R

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Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis von Armanios, Mary Y, Chen, Julian J.-L, Cogan, Joy D, Alder, Jonathan K, Ingersoll, Roxann G, Markin, Cheryl, Lawson, William E, Xie, Mingyi, Vulto, Irma, Phillips, John A, Lansdorp, Peter M, Greider, Carol W, Loyd, James E

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Genomic analysis of methanogenic archaea reveals a shift towards energy conservation von Gilmore, Sean P, Henske, John K, Sexton, Jessica A, Solomon, Kevin V, Seppälä, Susanna, Yoo, Justin I, Huyett, Lauren M, Pressman, Abe, Cogan, James Z, Kivenson, Veronika, Peng, Xuefeng, Tan, YerPeng, Valentine, David L, O'Malley, Michelle A

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Rare variants in RTEL1 are associated with familial interstitial pneumonia von Cogan, Joy D, Kropski, Jonathan A, Zhao, Min, Mitchell, Daphne B, Rives, Lynette, Markin, Cheryl, Garnett, Errine T, Montgomery, Keri H, Mason, Wendi R, McKean, David F, Powers, Julia, Murphy, Elissa, Olson, Lana M, Choi, Leena, Cheng, Dong-Sheng, Blue, Elizabeth Marchani, Young, Lisa R, Lancaster, Lisa H, Steele, Mark P, Brown, Kevin K, Schwarz, Marvin I, Fingerlin, Tasha E, Schwartz, David A, Lawson, William E, Loyd, James E, Zhao, Zhongming, Phillips, 3rd, John A, Blackwell, Timothy S

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Estrogen Metabolite 16α-Hydroxyestrone Exacerbates Bone Morphogenetic Protein Receptor Type II–Associated Pulmonary Arterial Hypertension Through MicroRNA-29–Mediated Modulation of... von Chen, Xinping, Talati, Megha, Fessel, Joshua P, Hemnes, Anna R, Gladson, Santhi, French, Jaketa, Shay, Sheila, Trammell, Aaron, Phillips, John A, Hamid, Rizwan, Cogan, Joy D, Dawson, Elliott P, Womble, Kristie E, Hedges, Lora K, Martinez, Elizabeth G, Wheeler, Lisa A, Loyd, James E, Majka, Susan J, West, James, Austin, Eric D

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Resequencing Study Confirms That Host Defense and Cell Senescence Gene Variants Contribute to the Risk of Idiopathic Pulmonary Fibrosis von Moore, Camille, Blumhagen, Rachel Z, Yang, Ivana V, Walts, Avram, Powers, Julie, Walker, Tarik, Bishop, Makenna, Russell, Pamela, Vestal, Brian, Cardwell, Jonathan, Markin, Cheryl R, Mathai, Susan K, Schwarz, Marvin I, Steele, Mark P, Lee, Joyce, Brown, Kevin K, Loyd, James E, Crapo, James D, Silverman, Edwin K, Cho, Michael H, James, Judith A, Guthridge, Joel M, Cogan, Joy D, Kropski, Jonathan A, Swigris, Jeffrey J, Bair, Carol, Kim, Dong Soon, Ji, Wonjun, Kim, Hocheol, Song, Jin Woo, Maier, Lisa A, Pacheco, Karin A, Hirani, Nikhil, Poon, Azin S, Li, Feng, Jenkins, R Gisli, Braybrooke, Rebecca, Saini, Gauri, Maher, Toby M, Molyneaux, Philip L, Saunders, Peter, Zhang, Yingze, Gibson, Kevin F, Kass, Daniel J, Rojas, Mauricio, Sembrat, John, Wolters, Paul J, Collard, Harold R, Sundy, John S, O'Riordan, Thomas, Strek, Mary E, Noth, Imre, Ma, Shwu-Fan, Porteous, Mary K, Kreider, Maryl E, Patel, Namrata B, Inoue, Yoshikazu, Hirose, Masaki, Arai, Toru, Akagawa, Shinobu, Eickelberg, Oliver, Fernandez, Isis Enlil, Behr, Jürgen, Mogulkoc, Nesrin, Corte, Tamera J, Glaspole, Ian, Tomassetti, Sara, Ravaglia, Claudia, Poletti, Venerino, Crestani, Bruno, Borie, Raphael, Kannengiesser, Caroline, Parfrey, Helen, Fiddler, Christine, Rassl, Doris, Molina-Molina, Maria, Machahua, Carlos, Worboys, Ana Montes, Gudmundsson, Gunnar, Isaksson, Helgi J, Lederer, David J, Podolanczuk, Anna J, Montesi, Sydney B, Bendstrup, Elisabeth, Danchel, Vivi, Selman, Moises, Pardo, Annie, Henry, Michael T, Keane, Michael P, Doran, Peter, Vašáková, Martina, Sterclova, Martina, Ryerson, Christopher J, Wilcox, Pearce G, Okamoto, Tsukasa, Furusawa, Haruhiko, Miyazaki, Yasunari, Laurent, Geoffrey, Baltic, Svetlana, Prele, Cecilia

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Effect of Genetic Diagnosis on Patients with Previously Undiagnosed Disease von Splinter, Kimberly, Adams, David R, Bacino, Carlos A, Bellen, Hugo J, Bernstein, Jonathan A, Cheatle-Jarvela, Alys M, Eng, Christine M, Esteves, Cecilia, Gahl, William A, Hamid, Rizwan, Jacob, Howard J, Kikani, Bijal, Koeller, David M, Kohane, Isaac S, Lee, Brendan H, Loscalzo, Joseph, Luo, Xi, McCray, Alexa T, Metz, Thomas O, Mulvihill, John J, Nelson, Stanley F, Palmer, Christina G.S, Phillips, John A, Pick, Leslie, Postlethwait, John H, Reuter, Chloe, Shashi, Vandana, Sweetser, David A, Tifft, Cynthia J, Walley, Nicole M, Wangler, Michael F, Westerfield, Monte, Wheeler, Matthew T, Wise, Anastasia L, Worthey, Elizabeth A, Yamamoto, Shinya, Ashley, Euan A

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High Frequency of BMPR2 Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension von Cogan, Joy D, Pauciulo, Michael W, Batchman, Amy P, Prince, Melissa A, Robbins, Ivan M, Hedges, Lora K, Stanton, Krista C, Wheeler, Lisa A, Phillips, John A., III, Loyd, James E, Nichols, William C

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Identification of rare-disease genes using blood transcriptome sequencing and large control cohorts von Frésard, Laure, Smail, Craig, Ferraro, Nicole M., Teran, Nicole A., Li, Xin, Smith, Kevin S., Bonner, Devon, Kernohan, Kristin D., Marwaha, Shruti, Zappala, Zachary, Balliu, Brunilda, Davis, Joe R., Liu, Boxiang, Prybol, Cameron J., Kohler, Jennefer N., Zastrow, Diane B., Reuter, Chloe M., Fisk, Dianna G., Grove, Megan E., Davidson, Jean M., Hartley, Taila, Joshi, Ruchi, Strober, Benjamin J., Utiramerur, Sowmithri, Lind, Lars, Ingelsson, Erik, Battle, Alexis, Bejerano, Gill, Bernstein, Jonathan A., Ashley, Euan A., Boycott, Kym M., Merker, Jason D., Wheeler, Matthew T., Montgomery, Stephen B.

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