High rate of autonomic neuropathy in Cornelia de Lange Syndrome von Pablo, M. J, Pamplona, P, Haddad, M, Benavente, I, Latorre-Pellicer, A, Arnedo, M, Trujillano, L, Bueno-Lozano, G, Kerr, L. M, Huisman, S. A, Kaiser, F. J, Ramos, F, Kline, A. D, Pie, J, Puisac, B

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Mutations in TWIST , a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome von Green, Eric D, Delgado, Costanza Garcia, Howard, Timothy D, Luna, Rosa Isela Ortiz De, Ma, Nancy, Gonzalez-Ramos, Mario, Jabs, Ethylin Wang, Chiang, Lydia C, Paznekas, William A, Kline, Antoine D

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Determination of the complete three-dimensional structure of the α-amylase inhibitor tendamistat in aqueous solution by nuclear magnetic resonance and distance geometry von Kline, Allen D., Braun, Werner, Wüthrich, Kurt

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Molecular analysis of the 18q- syndrome : and correlation with phenotype von KLINE, A. D, WHITE, M. E, WAPNER, R, ROJAS, K, BIESECKER, L. G, KAMHOLZ, J, ZACKAI, E. H, MUENKE, M, SCOTT, C. I, OVERHAUSER, J

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Non-Peptide RGD Surrogates Which Mimic a Gly-Asp β-Turn:  Potent Antagonists of Platelet Glycoprotein IIb−IIIa von Fisher, Matthew J, Gunn, Bruce, Harms, Cathy S, Kline, Allen D, Mullaney, Jeffrey T, Nunes, Anne, Scarborough, Robert M, Arfsten, Ann E, Skelton, Marshall A, Um, Suzane L, Utterback, Barbara G, Jakubowski, Joseph A

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Comparison of the high-resolution structures of the α-amylase inhibitor tendamistat determined by nuclear magnetic resonance in solution and by X-ray diffraction in single crystals... von Billeter, Martin, Kline, Allen D., Braun, Werner, Huber, Robert, Wüthrich, Kurt

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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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Clinical and molecular evaluation of four patients with partial duplications of the long arm of chromosome 18 von MEWAR, R, KLINE, A. D, HARRISON, W, ROJAS, K, GREENBERG, F, OVERHAUSER, J

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Somatic cell hybrid deletion map of human chromosome 18 von Kline, Antonie D., Rojas, Katherine, Mewar, Reema, Moshinsky, Deborah, Overhauser, Joan

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de Lange syndrome: A clinical review of 310 individuals von Jackson, L., Kline, A. D., Barr, M. A., Koch, S.

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NIPBL Mutational Analysis in 120 Individuals with Cornelia de Lange Syndrome and Evaluation of Genotype-Phenotype Correlations von Gillis, Lynette A., McCallum, Jennifer, Kaur, Maninder, DeScipio, Cheryl, Yaeger, Dinah, Mariani, Allison, Kline, Antonie D., Li, Hui-hua, Devoto, Marcella, Jackson, Laird G., Krantz, Ian D.

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Leptin is a four-helix bundle: secondary structure by NMR von Kline, Allen D, Becker, Gerald W, Churgay, Lisa M, Landen, Bryan E, Martin, Debra K, Muth, William L, Rathnachalam, Radhakrishnan, Richardson, John M, Schoner, Brigitte, Ulmer, Maverick, Hale, John E

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High discordance of chest x-ray and computed tomography for detection of pulmonary opacities in ED patients: implications for diagnosing pneumonia von Self, Wesley H., MD MPH, Courtney, D. Mark, MD MSCI, McNaughton, Candace D., MD MPH, Wunderink, Richard G., MD, Kline, Jeffrey A., MD

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Conformation of A82846B, a glycopeptide antibiotic, complexed with its cell wall fragment: An asymmetric homodimer determined using NMR spectroscopy von Prowse, Will G, Kline, Allen D, Skelton, Marshall A, Loncharich, Richard J

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Whole Blood Lactate Kinetics in Patients Undergoing Quantitative Resuscitation for Severe Sepsis and Septic Shock von Puskarich, Michael A., MD, Trzeciak, Stephen, MD, Shapiro, Nathan I., MD, Albers, Andrew B., MD, Heffner, Alan C., MD, Kline, Jeffrey A., MD, Jones, Alan E., MD

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Growth manifestations in the Brachmann-de Lange syndrome von Kline, Antonie D., Barr, Marie, Jackson, Laird G.

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Developmental data on individuals with the Brachmann-de Lange syndrome von Kline, Antonie D., Stanley, Christian, Belevich, Jacqueline, Brodsky, Karen, Barr, Marie, Jackson, Laird G.

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D-dimer Thresholds to Exclude Pulmonary Embolism among COVID-19 Patients in the Emergency Department: Derivation with Independent Validation von Bledsoe, Joseph R., Knox, Daniel, Peltan, Ithan D., Woller, Scott C., Lloyd, James F., Snow, Gregory L., Horne, Benjamin D., Connors, Jean M., Kline, Jeffrey A.

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The effect of relaxation on the epitope mapping by saturation transfer difference NMR von Yan, Jiangli, Kline, Allen D., Mo, Huaping, Shapiro, Michael J., Zartler, Edward R.

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Acceptability of Exercise in Urban Emergency Department Patients With Metabolic Syndrome, Including a Subset With Venous Thromboembolism von Stewart, Lauren K, Kline, Jeffrey A

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