Synthesis and profile of SCH351591, a novel PDE4 inhibitor by Billah, Motasim, Cooper, Nicola, Cuss, Francis, Davenport, Richard J., Dyke, Hazel J., Egan, Robert, Ganguly, Ashit, Gowers, Lewis, Hannah, Duncan R., Haughan, Alan F., Kendall, Hannah J., Lowe, Christopher, Minnicozzi, Michael, Montana, John G., Naylor, Robert, Oxford, Janet, Peake, Joanna C., Piwinski, John J., Runcie, Karen A., Sabin, Verity, Sharpe, Andrew, Shih, Neng-Yang, Warneck, Julie B.H.

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8-Methoxyquinolines as PDE4 inhibitors by Billah, Motasim, Buckley, George M., Cooper, Nicola, Dyke, Hazel J., Egan, Robert, Ganguly, Ashit, Gowers, Lewis, Haughan, Alan F., Kendall, Hannah J., Lowe, Christopher, Minnicozzi, Michael, Montana, John G., Oxford, Janet, Peake, Joanna C., Picken, C.Louise, Piwinski, John J., Naylor, Robert, Sabin, Verity, Shih, Neng-Yang, Warneck, Julie B.H.

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7-Methoxyfuro[2,3- c]pyridine-4-carboxamides as PDE4 Inhibitors: A Potential Treatment for Asthma by Buckley, George M, Cooper, Nicola, Davenport, Richard J, Dyke, Hazel J, Galleway, Fiona P, Gowers, Lewis, Haughan, Alan F, Kendall, Hannah J, Lowe, Christopher, Montana, John G, Oxford, Janet, Peake, Joanna C, Picken, C.Louise, Richard, Marianna D, Sabin, Verity, Sharpe, Andrew, Warneck, Julie B.H

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8-Methoxyquinoline-5-carboxamides as PDE4 inhibitors: a potential treatment for asthma by Buckley, George M., Cooper, Nicola, Dyke, Hazel J., Galleway, Fiona P., Gowers, Lewis, Haughan, Alan F., Kendall, Hannah J., Lowe, Christopher, Maxey, Robert, Montana, John G., Naylor, Robert, Oxford, Janet, Peake, Joanna C., Picken, C.Louise, Runcie, Karen A., Sabin, Verity, Sharpe, Andrew, Warneck, Julie B.H.

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Effects of the neo‐X chromosome on genomic signatures of hybridization in Rumex hastatulus by Beaudry, Felix E. G., Rifkin, Joanna L., Peake, Amanda L., Kim, Deanna, Jarvis‐Cross, Madeline, Barrett, Spencer C. H., Wright, Stephen I., Richard, Abbott

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Epidemiologic and Clinical Characteristics of Monkeypox Cases - United States, May 17-July 22, 2022 by Philpott, David, Hughes, Christine M, Alroy, Karen A, Kerins, Janna L, Pavlick, Jessica, Asbel, Lenore, Crawley, Addie, Newman, Alexandra P, Spencer, Hillary, Feldpausch, Amanda, Cogswell, Kelly, Davis, Kenneth R, Chen, Jinlene, Henderson, Tiffany, Murphy, Katherine, Barnes, Meghan, Hopkins, Brandi, Fill, Mary-Margaret A, Mangla, Anil T, Perella, Dana, Barnes, Arti, Hughes, Scott, Griffith, Jayne, Berns, Abby L, Milroy, Lauren, Blake, Haley, Sievers, Maria M, Marzan-Rodriguez, Melissa, Tori, Marco, Black, Stephanie R, Kopping, Erik, Ruberto, Irene, Maxted, Angela, Sharma, Anuj, Tarter, Kara, Jones, Sydney A, White, Brooklyn, Chatelain, Ryan, Russo, Mia, Gillani, Sarah, Bornstein, Ethan, White, Stephen L, Johnson, Shannon A, Ortega, Emma, Saathoff-Huber, Lori, Syed, Anam, Wills, Aprielle, Anderson, Bridget J, Oster, Alexandra M, Christie, Athalia, McQuiston, Jennifer, McCollum, Andrea M, Rao, Agam K, Negrón, María E

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A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion by ALIEN, S, ABUZENADAH, A. M, HINKS, J, BLAGG, J. L, GURSEL, T, INGERSLEV, J, GOODEVE, A. C, PEAKE, L. R, DALY, M. E

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Two novel type 2N von Willebrand disease–causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factor by Allen, Simon, Abuzenadah, Adel M., Blagg, Joanna L., Hinks, Joanna, Nesbitt, I. Mandy, Goodeve, Anne C., Gursel, Turkiz, Ingerslev, Jørgen, Peake, Ian R., Daly, Martina E.

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A novel von Willebrand disease–causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretion by Allen, Simon, Abuzenadah, Adel M., Hinks, Joanna, Blagg, Joanna L., Gursel, Turkiz, Ingerslev, Jørgen, Goodeve, Anne C., Peake, Ian R., Daly, Martina E.

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