Family Stability and Childhood Behavioral Outcomes: A Critical Review of the Literature von Baldridge, Stephen

Volltext

The Use of Mobility and Social Media to Improve Student Involvement von Baldridge, Stephen, Roberts, Amanda, Reed, Alexandra, Ellard, Amanda

Volltext bestellen

A Mobile Pedagogy Approach for Transforming Learners and Faculty von Hamm, Scott, Saltsman, George, Jones, Breana, Baldridge, Stephen, Perkins, Scott

Volltext

Mechanical Stimulation of Bone in Vivo Reduces Osteocyte Expression of Sost/Sclerostin von Robling, Alexander G., Niziolek, Paul J., Baldridge, Lee A., Condon, Keith W., Allen, Matthew R., Alam, Imranul, Mantila, Sara M., Gluhak-Heinrich, Jelica, Bellido, Teresita M., Harris, Stephen E., Turner, Charles H.

Volltext

Efficacy and safety of a quadruple ultra-low-dose treatment for hypertension (QUARTET USA): Rationale and design for a randomized controlled trial von Baldridge, Abigail S., Huffman, Mark D., Lazar, Danielle, Abbas, Hiba, Flowers, Fallon M., Quintana, Adriana, Jackson, Alema, Khan, Sadiya S., Chopra, Aashima, Vu, My, Tripathi, Priya, Jacobson, Tyler, Sanuade, Olutobi A., Kandula, Namratha R., Persell, Stephen D., Paparello, James J., Rosul, Linda L., Mejia, Jairo, Lloyd-Jones, Donald M., Chow, Clara K., Ciolino, Jody D.

Volltext

Relation of Biomarkers of Cardiac Injury, Stress, and Fibrosis With Cardiac Mechanics in Patients ≥ 65 Years of Age von Gottdiener, John S., Seliger, Stephen, deFilippi, Christopher, Christenson, Robert, Baldridge, Abigail S., Kizer, Jorge R., Psaty, Bruce M., Shah, Sanjiv J.

Volltext

Efficacy and safety of a four-drug, quarter-dose treatment for hypertension: the QUARTET USA randomized trial von Huffman, Mark D, Baldridge, Abigail S, Lazar, Danielle, Abbas, Hiba, Mejia, Jairo, Flowers, Fallon M, Quintana, Adriana, Jackson, Alema, Kandula, Namratha R, Lloyd-Jones, Donald M, Persell, Stephen D, Khan, Sadiya S, Paparello, James J, Chopra, Aashima, Tripathi, Priya, Vu, My H, Chow, Clara K, Ciolino, Jody D

Volltext

Dominant negative variants in KIF5B cause osteogenesis imperfecta via down regulation of mTOR signaling von Marom, Ronit, Zhang, Bo, Washington, Megan E, Song, I-Wen, Burrage, Lindsay C, Rossi, Vittoria C, Berrier, Ava S, Lindsey, Anika, Lesinski, Jacob, Nonet, Michael L, Chen, Jian, Baldridge, Dustin, Silverman, Gary A, Sutton, V Reid, Rosenfeld, Jill A, Tran, Alyssa A, Hicks, M John, Murdock, David R, Dai, Hongzheng, Weis, MaryAnn, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Caswell, Richard, Pottinger, Carrie, Cilliers, Deirdre, Stals, Karen, Eyre, David, Krakow, Deborah, Schedl, Tim, Pak, Stephen C, Lee, Brendan H

Volltext

1470-P: Modeling Familial Partial Lipodystropy Type 2 (LMNAp.R482W) Utilizing iPSC-Derived Adipocytes von BORREGO ALVAREZ, ALUET, LIU, KATIE, GOBBLE, MCKINLEE R.S., GRUPE, MICHAEL, MOHAMMED ALI, LINA, BUCHSER, WILLIAM J., BALDRIDGE, DUSTIN, STONE, STEPHEN I.

Volltext

The autophagy gene Epg5 promotes susceptibility to enteric viral infection von Kalugotla, Gowri, Lee, Sanghyun, Schriefer, Lawrence, Perez, Luis Alberto Casorla, Huang, Huiyan, Lu, Qun, Orvedahl, Anthony, Silverman, Gary, Pak, Stephen, Wang, David, Baldridge, Megan T

Volltext

Crust and upper mantle shear wave structure of the southwest United States: Implications for rifting and support for high elevation von West, Michael, Ni, James, Baldridge, W. Scott, Wilson, David, Aster, Richard, Gao, Wei, Grand, Stephen

Volltext

High-resolution receiver function imaging reveals Colorado Plateau lithospheric architecture and mantle-supported topography von Wilson, David C., Aster, Richard, Grand, Stephen, Ni, James, Baldridge, W. Scott

Volltext

Chemically Modulating the Photophysics of the GFP Chromophore von Conyard, Jamie, Kondo, Minako, Heisler, Ismael A, Jones, Garth, Baldridge, Anthony, Tolbert, Laren M, Solntsev, Kyril M, Meech, Stephen R

Volltext

A dominant negative variant of RAB5B disrupts maturation of surfactant protein B and surfactant protein C von Huang, Huiyan, Pan, Jiehong, Spielberg, David R., Hanchard, Neil A., Scott, Daryl A., Burrage, Lindsay C., Dai, Hongzheng, Murdock, David, Rosenfeld, Jill A., Mohammad, Ariz, Huang, Tao, Lindsey, Anika G., Kim, Hyori, Chen, Jian, Ramu, Avinash, Morrison, Stephanie A., Dawson, Zachary D., Hu, Alex Z., Tycksen, Eric, Silverman, Gary A., Baldridge, Dustin, Wambach, Jennifer A., Pak, Stephen C., Brody, Steven L., Schedl, Tim

Volltext

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling von Johnson, Brett V., Alexander, Suzy, Vega, Michelle Sanchez, Domingo, Deepti, Oh, Tracey, Lines, Matthew, Grønborg, Sabine, Mercier, Sandra, Küry, Sébastien, Billette de Villemeur, Thierry, Koolen, David A., Sa, Joaquim, Santiago-Fernández, Olaya, Fernández-Jaén, Alberto, Goldstein, Amy, Madan-Khetarpal, Suneeta, Sullivan, Jennifer A., Bacino, Carlos A., Baker, Eva, Bellen, Hugo J., Bernstein, Jonathan A., Bick, David P., Butte, Manish J., Davids, Mariska, Davidson, Jean M., Dayal, Jyoti G., Dhar, Shweta U., Douine, Emilie D., Draper, David D., Emrick, Lisa T., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Forghani, Irman, Friedman, Noah D., Gahl, William A., Godfrey, Rena A., Hanchard, Neil A., Jiang, Yong-hui, Karaviti, Lefkothea, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lanpher, Brendan C., LeBlanc, Kimberly, Lee, Brendan H., Liu, Xue Zhong, Marwaha, Shruti, McCauley, Jacob, Morimoto, Marie, Nath, Avi, Nelson, Stan F., Newman, John H., Oglesbee, Devin, Orengo, James P., Pak, Stephen, Parker, Neil H., Phillips, John A., Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Sampson, Jacinda B., Schedl, Timothy, Shakachite, Lisa, Sharma, Prashant, Signer, Rebecca, Silverman, Edwin K., Sinsheimer, Janet S., Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wang, Lee-kai, Wangler, Michael F., Worthey, Elizabeth A., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli, Gahl, William, Sullivan, Jennifer A., Barnett, Sarah S., Perry, M. Scott, Schuette, Jane L., Smith, Laurie D., Rosenfeld, Jill A., Bhoj, Elizabeth, Kaplan, Paige, Oegema, Renske, Armstrong, Martin, Lin, Angela E., Hollander, Nicolette den, Hoffer, Mariëtte J.V., Mosher, Theresa Mihalic, Tezcan, Kamer, Penzes, Peter, Piper, Michael

Volltext

De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia von Kanca, Oguz, Andrews, Jonathan C., Patel, Chirag, Slavotinek, Anne M., Williams, Judy, Indaram, Maanasa, Lau, C. Christopher, Adams, David R., Agrawal, Pankaj, Bademci, Guney, Baker, Eva, Baldridge, Dustin, Bale, Jim, Batzli, Gabriel F., Bayrak-Toydemir, Pinar, Bernstein, Jonathan A., Bick, David P., Bohnsack, John, Briere, Lauren C., Carey, John, Cogan, Joy D., Cole, F. Sessions, D'Souza, Precilla, Dayal, Jyoti G., Dorset, Daniel C., Douine, Emilie D., Draper, David D., Duncan, Laura, Fieg, Elizabeth L., Forghani, Irman, Fresard, Laure, Godfrey, Rena A., Goldman, Alica M., Groden, Catherine A., Haendel, Melissa, Hayes, Nichole, Huang, Alden, Huang, Yong, Jones, Angela L., Krasnewich, Donna M., Kyle, Jennifer E., Lalani, Seema R., Lau, C. Christopher, Levy, Shawn E., Liu, Xue Zhong, Loo, Sandra K., Loscalzo, Joseph, Markello, Thomas C., Marth, Gabor, McConkie-Rosell, Allyn, Might, Matthew, Morimoto, Marie, Nelson, Stan F., Newberry, J. Scott, Newman, John H., Orengo, James P., Pak, Stephen, Pallais, J. Carl, Palmer, Christina G.S., Papp, Jeanette C., Parker, Neil H., Pusey, Barbara N., Quinlan, Aaron, Raja, Archana N., Rosenfeld, Jill A., Ruzhnikov, Maura, Samson, Susan L., Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Shakachite, Lisa, Sharma, Prashant, Shashi, Vandana, Shields, Kathleen, Sillari, Catherine H., Sinsheimer, Janet S., Smith, Kevin S., Solnica-Krezel, Lilianna, Spillmann, Rebecca C., Stong, Nicholas, Sweetser, David A., Tekin, Mustafa, Telischi, Fred, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walley, Nicole M., Wang, Lee-kai, Wangler, Michael F., Wegner, Daniel, Wolfe, Lynne A., Worthey, Elizabeth A., Yu, Guoyun, Zhao, Chunli, Chung, Wendy K., Dobyns, William B., Adams, David R., Gahl, William A., Malicdan, May Christine V.

Volltext

Functional analysis of a de novo variant in the neurodevelopment and generalized epilepsy disease gene NBEA von Boulin, Thomas, Itani, Omar, El Mouridi, Sonia, Leclercq-Blondel, Alice, Gendrel, Marie, Macnamara, Ellen, Soldatos, Ariane, Murphy, Jennifer L., Gorman, Mark P., Lindsey, Anika, Shimada, Shino, Turner, Darian, Silverman, Gary A., Baldridge, Dustin, Malicdan, May C., Schedl, Tim, Pak, Stephen C.

Volltext

Brain malformations and seizures by impaired chaperonin function of TRiC von Kraft, Florian, Rodriguez-Aliaga, Piere, Yuan, Weimin, Franken, Lena, Zajt, Kamil, Hasan, Dimah, Lee, Ting-Ting, Flex, Elisabetta, Hentschel, Andreas, Innes, A Micheil, Zheng, Bixia, Julia Suh, Dong Sun, Knopp, Cordula, Lausberg, Eva, Krause, Jeremias, Zhang, Xiaomeng, Trapane, Pamela, Carroll, Riley, McClatchey, Martin, Fry, Andrew E, Wang, Lisa, Giesselmann, Sebastian, Hoang, Hieu, Baldridge, Dustin, Silverman, Gary A, Radio, Francesca Clementina, Bertini, Enrico, Ciolfi, Andrea, Blood, Katherine A, de Sainte Agathe, Jean-Madeleine, Charles, Perrine, Bergant, Gaber, Čuturilo, Goran, Peterlin, Borut, Diderich, Karin, Streff, Haley, Robak, Laurie, Oegema, Renske, van Binsbergen, Ellen, Herriges, John, Saunders, Carol J, Maier, Andrea, Wolking, Stefan, Weber, Yvonne, Lochmüller, Hanns, Meyer, Stefanie, Aleman, Alberto, Polavarapu, Kiran, Nicolas, Gael, Goldenberg, Alice, Guyant, Lucie, Pope, Kathleen, Hehmeyer, Katherine N, Monaghan, Kristin G, Quade, Annegret, Smol, Thomas, Caumes, Roseline, Duerinckx, Sarah, Depondt, Chantal, Van Paesschen, Wim, Rieubland, Claudine, Poloni, Claudia, Guipponi, Michel, Arcioni, Severine, Meuwissen, Marije, Jansen, Anna C, Rosenblum, Jessica, Haack, Tobias B, Bertrand, Miriam, Gerstner, Lea, Magg, Janine, Riess, Olaf, Schulz, Jörg B, Wagner, Norbert, Wiesmann, Martin, Weis, Joachim, Eggermann, Thomas, Begemann, Matthias, Roos, Andreas, Häusler, Martin, Schedl, Tim, Tartaglia, Marco, Bremer, Juliane, Pak, Stephen C, Frydman, Judith, Elbracht, Miriam, Kurth, Ingo

Volltext

De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation von Mao, Dongxue, Reuter, Chloe M., Farrow, Emily G., Rosenfeld, Jill A., Mackenzie, Katherine M., Küry, Sébastien, Genetti, Casie A., Alejandro, Mercedes, Agrawal, Pankaj B., Alvey, Justin, Ashley, Euan A., Balasubramanyam, Ashok, Beck, Anita, Bellen, Hugo J., Berg-Rood, Beverly, Bernier, Raphael, Bivona, Stephanie, Bohnsack, John, Briere, Lauren C., Burke, Elizabeth A., Butte, Manish J., Carrasquillo, Olveen, Cogan, Joy D., Cole, F. Sessions, Colley, Heather A., Cooper, Cynthia M., Craigen, William J., Cunningham, Michael, Dasari, Surendra, Dayal, Jyoti G., Dhar, Shweta U., Emrick, Lisa T., Estwick, Tyra, Ferreira, Carlos, Fieg, Elizabeth L., Fogel, Brent L., Forghani, Irman, Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Hahn, Sihoun, Hanchard, Neil A., Hing, Anne, Holm, Ingrid A., Huang, Yong, Jamal, Fariha, Jayadev, Suman, Karaviti, Lefkothea, Kelley, Emily G., Kohane, Isaac S., Kohler, Jennefer N., Krakow, Deborah, Korrick, Susan, Koziura, Mary, Krier, Joel B., Lam, Byron, Lanpher, Brendan C., Lanza, Ian R., Lee, Brendan H., Lewis, Richard A., Loo, Sandra K., Majcherska, Marta M., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., Martínez-Agosto, Julian A., McCormack, Colleen E., Merritt, J. Lawrence, Moretti, Paolo M., Mulvihill, John J., Murdock, David R., Nickerson, Deborah, Pallais, J. Carl, Posey, Jennifer E., Potocki, Lorraine, Raja, Archana N., Renteria, Genecee, Rosenfeld, Jill A., Samson, Susan L., Schedl, Timothy, Shakachite, Lisa, Signer, Rebecca, Silverman, Edwin K., Sybert, Virginia, Tekin, Mustafa, Thorson, Willa, Tran, Alyssa A., Urv, Tiina K., Wahl, Colleen E., Wegner, Daniel, Wheeler, Matthew T., Yamamoto, Shinya, Yang, John, Yoon, Amanda J., Yu, Guoyun, Zastrow, Diane B., Zhao, Chunli, Bernstein, Jonathan A., Chao, Hsiao-Tuan

Volltext

Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision von Baldridge, Dustin, Wangler, Michael F, Bowman, Angela N, Yamamoto, Shinya, Schedl, Tim, Pak, Stephen C, Postlethwait, John H, Shin, Jimann, Solnica-Krezel, Lilianna, Bellen, Hugo J, Westerfield, Monte

Volltext