Proteolysis of latent transforming growth factor-beta (TGF-beta )-binding protein-1 by osteoclasts. A cellular mechanism for release of TGF-beta from bone matrix von Dallas, Sarah L, Rosser, Jennifer L, Mundy, Gregory R, Bonewald, Lynda F

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Time Lapse Imaging Techniques for Comparison of Mineralization Dynamics in Primary Murine Osteoblasts and the Late Osteoblast/Early Osteocyte-Like Cell Line MLO-A5 von Dallas, Sarah L., Veno, Patricia A., Rosser, Jennifer L., Barragan-Adjemian, Cielo, Rowe, David W., Kalajzic, Ivo, Bonewald, Lynda F.

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Proteolysis of Latent Transforming Growth Factor-β (TGF-β)-binding Protein-1 by Osteoclasts von Sarah L. Dallas, Jennifer L. Rosser, Gregory R. Mundy, Lynda F. Bonewald

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Proteolysis of Latent Transforming Growth Factor-β (TGF-β)-binding Protein-1 by Osteoclasts von Dallas, Sarah L., Rosser, Jennifer L., Mundy, Gregory R., Bonewald, Lynda F.

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Hypertension Across a Woman’s Life Cycle von Wenger, Nanette K., Arnold, Anita, Bairey Merz, C. Noel, Cooper-DeHoff, Rhonda M., Ferdinand, Keith C., Fleg, Jerome L., Gulati, Martha, Isiadinso, Ijeoma, Itchhaporia, Dipti, Light-McGroary, KellyAnn, Lindley, Kathryn J., Mieres, Jennifer H., Rosser, Mary L., Saade, George R., Walsh, Mary Norine, Pepine, Carl J.

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Oral hymecromone decreases hyaluronan in human study participants von Rosser, Joelle I, Nagy, Nadine, Goel, Riya, Kaber, Gernot, Demirdjian, Sally, Saxena, Jamie, Bollyky, Jennifer B, Frymoyer, Adam R, Pacheco-Navarro, Ana E, Burgener, Elizabeth B, Rajadas, Jayakumar, Wang, Zhe, Arbach, Olga, Dunn, Colleen E, Kalinowski, Anissa, Milla, Carlos E, Bollyky, Paul L

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Cell line IDG‐SW3 replicates osteoblast‐to‐late‐osteocyte differentiation in vitro and accelerates bone formation in vivo von Woo, Stacey M, Rosser, Jennifer, Dusevich, Vladimir, Kalajzic, Ivo, Bonewald, Lynda F

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The need for and acceptability of a curriculum to train nursing and medical students in the sexual healthcare of clients with female genital mutilation/cutting in Tanzania von Mwakawanga, Dorkasi L, Massae, Agnes F, Kohli, Nidhi, Lukumay, Gift Gadiel, Rohloff, Corissa T, Mushy, Stella Emmanuel, Mgopa, Lucy R, Mkoka, Dickson Ally, Mkonyi, Ever, Trent, Maria, Ross, Michael W, Rosser, B R Simon, Connor, Jennifer

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Whole exome sequencing in patients with white matter abnormalities von Vanderver, Adeline, Simons, Cas, Helman, Guy, Crawford, Joanna, Wolf, Nicole I., Bernard, Geneviève, Pizzino, Amy, Schmidt, Johanna L., Takanohashi, Asako, Miller, David, Khouzam, Amirah, Rajan, Vani, Ramos, Erica, Chowdhury, Shimul, Hambuch, Tina, Ru, Kelin, Baillie, Gregory J., Grimmond, Sean M., Caldovic, Ljubica, Devaney, Joseph, Bloom, Miriam, Evans, Sarah H., Murphy, Jennifer L. P., McNeill, Nathan, Fogel, Brent L., Schiffmann, Raphael, van der Knaap, Marjo S., Taft, Ryan J.

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Cardiovascular Health After Preeclampsia: Patient and Provider Perspective von Seely, Ellen W, Celi, Ann C, Chausmer, Jaimie, Graves, Cornelia, Kilpatrick, Sarah, Nicklas, Jacinda M, Rosser, Mary L, Rexrode, Kathryn M, Stuart, Jennifer J, Tsigas, Eleni, Voelker, Jennifer, Zelop, Carolyn, Rich-Edwards, Janet W

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Multicenter experience using telaprevir or boceprevir with peginterferon and ribavirin to treat hepatitis C genotype 1 after liver transplantation von Pungpapong, Surakit, Aqel, Bashar A., Koning, Ludi, Murphy, Jennifer L., Henry, Tanisha M., Ryland, Kristen L., Yataco, Maria L., Satyanarayana, Raj, Rosser, Barry G., Vargas, Hugo E., Charlton, Michael R., Keaveny, Andrew P.

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Contribution of copy-number variation to Down syndrome–associated atrioventricular septal defects von Ramachandran, Dhanya, Mulle, Jennifer G., Locke, Adam E., Bean, Lora J.H., Rosser, Tracie C., Bose, Promita, Dooley, Kenneth J., Cua, Clifford L., Capone, George T., Reeves, Roger H., Maslen, Cheryl L., Cutler, David J., Sherman, Stephanie L., Zwick, Michael E.

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A Randomized Trial of Epinephrine in Out-of-Hospital Cardiac Arrest von Perkins, Gavin D, Ji, Chen, Deakin, Charles D, Quinn, Tom, Nolan, Jerry P, Scomparin, Charlotte, Regan, Scott, Long, John, Slowther, Anne, Pocock, Helen, Black, John J.M, Moore, Fionna, Fothergill, Rachael T, Rees, Nigel, O’Shea, Lyndsey, Docherty, Mark, Gunson, Imogen, Han, Kyee, Charlton, Karl, Finn, Judith, Petrou, Stavros, Stallard, Nigel, Gates, Simon, Lall, Ranjit

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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A.J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.

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Screening for Memory Concerns at the Well‐Woman Visit von Joyce, Jillian L., Caes, Dorota, Chapman, Silvia, Gottesman, Reena T., Haque, Hoosna, Manly, Jennifer J, Waltrip, Leah H., Rizer, Sandra, Marder, Karen, Rosser, Mary L., Cosentino, Stephanie

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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects von Rambo-Martin, Benjamin L, Mulle, Jennifer G, Cutler, David J, Bean, Lora J H, Rosser, Tracie C, Dooley, Kenneth J, Cua, Clifford, Capone, George, Maslen, Cheryl L, Reeves, Roger H, Sherman, Stephanie L, Zwick, Michael E

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Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects von Ramachandran, Dhanya, Zeng, Zhen, Locke, Adam E, Mulle, Jennifer G, Bean, Lora J H, Rosser, Tracie C, Dooley, Kenneth J, Cua, Clifford L, Capone, George T, Reeves, Roger H, Maslen, Cheryl L, Cutler, David J, Feingold, Eleanor, Sherman, Stephanie L, Zwick, Michael E

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Recommendations for Social Skills End Points for Clinical Trials in Neurofibromatosis Type 1 von Janusz, Jennifer A., Klein-Tasman, Bonita P., Payne, Jonathan M., Wolters, Pamela L., Thompson, Heather L., Martin, Staci, de Blank, Peter, Ullrich, Nicole, del Castillo, Allison, Hussey, Maureen, Hardy, Kristina K., Haebich, Kristina, Rosser, Tena, Toledo-Tamula, Mary Anne, Walsh, Karin S.

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Cross-Sectional Exploration of Plasma Biomarkers of Alzheimer's Disease in Down Syndrome: Early Data from the Longitudinal Investigation for Enhancing Down Syndrome Research (LIFE-... von Hendrix, James A, Airey, David C, Britton, Angela, Burke, Anna D, Capone, George T, Chavez, Ronelyn, Chen, Jacqueline, Chicoine, Brian, Costa, Alberto C S, Dage, Jeffrey L, Doran, Eric, Esbensen, Anna, Evans, Casey L, Faber, Kelley M, Foroud, Tatiana M, Hart, Sarah, Haugen, Kelsey, Head, Elizabeth, Hendrix, Suzanne, Hillerstrom, Hampus, Kishnani, Priya S, Krell, Kavita, Ledesma, Duvia Lara, Lai, Florence, Lott, Ira, Ochoa-Lubinoff, Cesar, Mason, Jennifer, Nicodemus-Johnson, Jessie, Proctor, Nicholas Kyle, Pulsifer, Margaret B, Revta, Carolyn, Rosas, H Diana, Rosser, Tracie C, Santoro, Stephanie, Schafer, Kim, Scheidemantel, Thomas, Schmitt, Frederick, Skotko, Brian G, Stasko, Melissa R, Talboy, Amy, Torres, Amy, Wilmes, Kristi, Woodward, Jason, Zimmer, Jennifer A, Feldman, Howard H, Mobley, William

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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A. J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.

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