Risk and Protective Factors for Unprotected Intercourse Among Rural African American Young Adults von Kogan, Steven M., Brody, Gene H., Chen, Yi-fu, Grange, Christina M., Slater, LaTrina M., DiClemente, Ralph J.

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The Strong African American Families–Teen Trial: Rationale, Design, Engagement Processes, and Family-Specific Effects von Kogan, Steven M., Brody, Gene H., Molgaard, Virginia K., Grange, Christina M., Oliver, Desirée A. H., Anderson, Tracy N., DiClemente, Ralph J., Wingood, Gina M., Chen, Yi-fu, Sperr, Megan C.

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Mechanisms of Family Impact on African American Adolescents' HIV-Related Behavior von Kogan, Steven M., Brody, Gene H., Gibbons, Frederick X., Chen, Yi-fu, Grange, Christina M., Simons, Ronald L., Gerrard, Meg, Cutrona, Carolyn E.

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Direct and Indirect Messages African American Women Receive From Their Familial Networks About Intimate Relationships and Sex: The Intersecting Influence of Race, Gender, and Class von Grange, Christina M., Brubaker, Sarah Jane, Corneille, Maya A.

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Mechanisms of Family Impact on African American Adolescents' HIV-Related Behavior: FAMILY IMPACT ON HIV-RELATED BEHAVIOR von Kogan, Steven M., Brody, Gene H., Gibbons, Frederick X., Chen, Yi-fu, Grange, Christina M., Simons, Ronald L., Gerrard, Meg, Cutrona, Carolyn E.

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Familial and Self Systems as Contributors to Sexual Decision-making Patterns of Young African American Women von Grange, Christina M

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Contribution of GATA6 to homeostasis of the human upper pilosebaceous unit and acne pathogenesis von Oulès, Bénédicte, Philippeos, Christina, Segal, Joe, Tihy, Matthieu, Vietri Rudan, Matteo, Cujba, Ana-Maria, Grange, Philippe A., Quist, Sven, Natsuga, Ken, Deschamps, Lydia, Dupin, Nicolas, Donati, Giacomo, Watt, Fiona M.

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Microplastics in European sea salts – An example of exposure through consumer choice and of interstudy methodological discrepancies von Thiele, Christina J., Grange, Laura J., Haggett, Emily, Hudson, Malcolm D., Hudson, Philippa, Russell, Andrea E., Zapata-Restrepo, Lina M.

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Enhanced MAPK1 Function Causes a Neurodevelopmental Disorder within the RASopathy Clinical Spectrum von Motta, Marialetizia, Pannone, Luca, Pantaleoni, Francesca, Bocchinfuso, Gianfranco, Radio, Francesca Clementina, Cecchetti, Serena, Ciolfi, Andrea, Di Rocco, Martina, Elting, Mariet W., Brilstra, Eva H., Boni, Stefania, Mazzanti, Laura, Tamburrino, Federica, Walsh, Larry, Payne, Katelyn, Fernández-Jaén, Alberto, Ganapathi, Mythily, Chung, Wendy K., Grange, Dorothy K., Dave-Wala, Ashita, Reshmi, Shalini C., Bartholomew, Dennis W., Mouhlas, Danielle, Carpentieri, Giovanna, Bruselles, Alessandro, Pizzi, Simone, Bellacchio, Emanuele, Piceci-Sparascio, Francesca, Lißewski, Christina, Brinkmann, Julia, Waclaw, Ronald R., Waisfisz, Quinten, van Gassen, Koen, Wentzensen, Ingrid M., Morrow, Michelle M., Álvarez, Sara, Martínez-García, Mónica, De Luca, Alessandro, Memo, Luigi, Zampino, Giuseppe, Rossi, Cesare, Seri, Marco, Gelb, Bruce D., Zenker, Martin, Dallapiccola, Bruno, Stella, Lorenzo, Prada, Carlos E., Martinelli, Simone, Flex, Elisabetta, Tartaglia, Marco

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Küry, Sébastien, van Woerden, Geeske M., Besnard, Thomas, Proietti Onori, Martina, Latypova, Xénia, Towne, Meghan C., Cho, Megan T., Ploeg, Melissa A., Sanders, Stephan, Stessman, Holly A.F., Pujol, Aurora, Distel, Ben, Robak, Laurie A., Bernstein, Jonathan A., Denommé-Pichon, Anne-Sophie, Lesca, Gaëtan, Sellars, Elizabeth A., Berg, Jonathan, Carré, Wilfrid, Busk, Øyvind Løvold, van Bon, Bregje W.M., Waugh, Jeff L., Deardorff, Matthew, Hoganson, George E., Bosanko, Katherine B., Johnson, Diana S., Dabir, Tabib, Holla, Øystein Lunde, Sarkar, Ajoy, Tveten, Kristian, de Bellescize, Julitta, Braathen, Geir J., Terhal, Paulien A., Grange, Dorothy K., van Haeringen, Arie, Lam, Christina, Mirzaa, Ghayda, Burton, Jennifer, Bhoj, Elizabeth J., Douglas, Jessica, Santani, Avni B., Nesbitt, Addie I., Helbig, Katherine L., Andrews, Marisa V., Begtrup, Amber, Tang, Sha, van Gassen, Koen L.I., Juusola, Jane, Foss, Kimberly, Enns, Gregory M., Moog, Ute, Hinderhofer, Katrin, Paramasivam, Nagarajan, Lincoln, Sharyn, Kusako, Brandon H., Lindenbaum, Pierre, Charpentier, Eric, Nowak, Catherine B., Cherot, Elouan, Simonet, Thomas, Ruivenkamp, Claudia A.L., Hahn, Sihoun, Brownstein, Catherine A., Xia, Fan, Schmitt, Sébastien, Deb, Wallid, Bonneau, Dominique, Nizon, Mathilde, Chelly, Jamel, Rudolf, Gabrielle, Sanlaville, Damien, Parent, Philippe, Gilbert-Dussardier, Brigitte, Toutain, Annick, Sutton, Vernon R., Thies, Jenny, Peart-Vissers, Lisenka E.L.M., Boisseau, Pierre, Vincent, Marie, Grabrucker, Andreas M., Dubourg, Christèle, Tan, Wen-Hann, Verbeek, Nienke E., Granzow, Martin, Santen, Gijs W.E., Shendure, Jay, Pasquier, Laurent, Redon, Richard, Yang, Yaping, State, Matthew W., Kleefstra, Tjitske, Cogné, Benjamin, Petrovski, Slavé, Retterer, Kyle, Eichler, Evan E., Rosenfeld, Jill A., Agrawal, Pankaj B., Bézieau, Stéphane, Odent, Sylvie, Mercier, Sandra

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Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis von Buchan, Jillian G, Alvarado, David M, Haller, Gabe E, Cruchaga, Carlos, Harms, Matthew B, Zhang, Tianxiao, Willing, Marcia C, Grange, Dorothy K, Braverman, Alan C, Miller, Nancy H, Morcuende, Jose A, Tang, Nelson Leung-Sang, Lam, Tsz-Ping, Ng, Bobby Kin-Wah, Cheng, Jack Chun-Yiu, Dobbs, Matthew B, Gurnett, Christina A

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The Contribution of Community and Family Contexts to African American Young Adults’ Romantic Relationship Health: A Prospective Analysis von Kogan, Steven M., Lei, Man-Kit, Grange, Christina R., Simons, Ronald L., Brody, Gene H., Gibbons, Frederick X., Chen, Yi-fu

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Controversies in the management of patients with soft tissue sarcoma: Recommendations of the Conference on State of Science in Sarcoma 2022 von Rothermundt, Christian, Andreou, Dimosthenis, Blay, Jean-Yves, Brodowicz, Thomas, Desar, Ingrid M.E., Dileo, Palma, Gelderblom, Hans, Haas, Rick, Jakob, Jens, Jones, Robin L., Judson, Ian, Kunz, Wolfgang G., Liegl-Atzwanger, Berndadette, Lindner, Lars H., Messiou, Christina, Miah, Aisha B., Reichardt, Peter, Szkandera, Joanna, van der Graaf, Winette T.A., van Houdt, Winan J., Wardelmann, Eva, Hofer, Silvia, Andreou, Dimosthenis, Barth, Thomas, Bauer, Sebastian, Blay, Jean-Yves, Blum, Veronika, Bode, Beata, Bonvalot, Sylvie, Bovee, Judith, Braam, Petra, Brodowicz, Thomas, Broto, Jean Martin, Dei Tos, Angelo, Denschlag, Dominik, Desar, Ingrid, Digklia, Antonia, Dileo, Palma, Dirksen, Uta, Douchy, Thomas, Duffaud, Florence, Eriksson, Mikael, Fröhling, Stefan, Gelderblom, Hans, Gronchi, Alessandro, Haas, Rick, Hardes, Jenrik, Hartmann, Wolfgang, Hofer, Silvia, Hohenberger, Peter, Hompes, Daphne, Huang, Paul, Italiano, Antoine, Jakob, Jens, Jones, Robin, Judson, Ian, Köhler, Günter, Kollàr, Attila, Krasniqi, Fatime, Krol, Stijn, Kunz, Wolfgang, Le Grange, Franel, Le Pechoux, Cécile, LeCesne, Alexandre, Leithner, Andreas, Liegl-Atzwanger, Bernadette, Lindner, Lars, Mechtersheimer, Gunhild, Messiou, Christina, Miah, Aisha, Pink, Daniel, Reichardt, Peter, Romagosa, Cleo, Rothermundt, Christian, Rutkowski, Piotr, Safwat, Akmel, Sangalli, Claudia, Szkandera, Joanna, Thway, Khin, Tunn, Per-Ulf, Van der Graaf, Winette, Van Houdt, Winan, Wardelmann, Eva, Zachariah, Ralph, Botter, Sander, Cerny, Thomas

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F-BAR protein CIP4 promotes GLUT4 endocytosis through bidirectional interactions with N-WASp and Dynamin-2 von Hartig, Sean M, Ishikura, Shuhei, Hicklen, Rachel S, Feng, Yanming, Blanchard, Elisabeth G, Voelker, Kevin A, Pichot, Christina S, Grange, Robert W, Raphael, Robert M, Klip, Amira, Corey, Seth J

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Is childhood trauma associated with lifetime suicide attempts in women with bulimia nervosa? von Smith, Christina E., Pisetsky, Emily M., Wonderlich, Stephen A., Crosby, Ross D., Mitchell, James E., Joiner, Thomas E., Bardone-Cone, Anna, Le Grange, Daniel, Klein, Marjorie H., Crow, Scott J., Peterson, Carol B.

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Pilocytic astrocytoma in a child with Noonan syndrome von Schuettpelz, Laura G., McDonald, Sharon, Whitesell, Kristina, Desruisseau, David M., Grange, Dorothy K., Gurnett, Christina A., Wilson, David B.

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De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability von Küry, Sébastien, van Woerden, Geeske M, Besnard, Thomas, Onori, Martina Proietti, Latypova, Xénia, Towne, Meghan C, Cho, Megan T, Prescott, Trine E, Ploeg, Melissa A, Sanders, Stephan J., Stessman, Holly A.F., Pujol, Aurora, Distel, Ben, Robak, Laurie A, Bernstein, Jonathan A., Denommé-Pichon, Anne-Sophie, Lesca, Gaëtan, Sellars, Elizabeth A, Berg, Jonathan, Carré, Wilfrid, Busk, Øyvind Løvold, van Bon, Bregje W.M., Waugh, Jeff L, Deardorff, Matthew A., Hoganson, George E, Bosanko, Katherine B, Johnson, Diana S., Dabir, Tabib, Lunde Holla, Øystein, Sarkar, Ajoy, Tveten, Kristian, de Bellescize, Julitta, Braathen, Geir J., Terhal, Paulien A, Grange, Dorothy K, van Haeringen, Arie, Lam, Christina, Mirzaa, Ghayda, Burton, Jennifer, Bhoj, Elizabeth J., Douglas, Jessica, Santani, Avni B., Nesbitt, Addie I., Helbig, Katherine L., Andrews, Marisa V., Begtrup, Amber, Tang, Sha, van Gassen, Koen L.I., Juusola, Jane, Foss, Kimberly, Enns, Gregory M., Moog, Ute, Hinderhofer, Katrin, Paramasivam, Nagarajan, Lincoln, Sharyn, Kusako, Brandon H., Lindenbaum, Pierre, Charpentier, Eric, Nowak, Catherine B., Cherot, Elouan, Simonet, Thomas, Ruivenkamp, Claudia A.L., Hahn, Sihoun, Brownstein, Catherine A., Xia, Fan, Schmitt, Sébastien, Deb, Wallid, Bonneau, Dominique, Nizon, Mathilde, Quinquis, Delphine, Chelly, Jamel, Rudolf, Gabrielle, Sanlaville, Damien, Parent, Philippe, Gilbert-Dussardier, Brigitte, Toutain, Annick, Sutton, Vernon R., Thies, Jenny, Peart-Vissers, Lisenka E.L.M., Boisseau, Pierre, Vincent, Marie, Grabrucker, Andreas M., Dubourg, Christèle, Diseases Network, Undiagnosed, Tan, Wen-Hann, Verbeek, Nienke E., Granzow, Martin, Santen, Gijs W.E., Shendure, Jay, Isidor, Bertrand, Pasquier, Laurent, Redon, Richard, Yang, Yaping, State, Matthew W., Kleefstra, Tjitske, Cogné, Benjamin, Hugo, Gem, Study, Deciphering Developmental Disorders, Petrovski, Slavé, Retterer, Kyle

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Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase von MACMULLEN, Courtney, JIE FANG, HSU, Betty Y. L, KELLY, Andrea, DE LONLAY-DEBENEY, Pascale, SAUDUBRAY, Jean-Marie, GANGULY, Arupa, SMITH, Thomas J, STANLEY, Charles A

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Molecular and clinical analyses of greig cephalopolysyndactyly and pallister-hall syndromes : Robust phenotype prediction from the type and position of GL13 mutations von JOHNSTON, Jennifer J, OLIVOS-GLANDER, Isabelle, BOOTH, Carol, CURRY, Cynthia J, DAVID, Albert, DINULOS, Mary Beth, FLANNERY, David B, FOX, Michelle A, GRAHAM, John M, GRANGE, Dorothy K, GUTTMACHER, Alan E, HANNIBAL, Mark C, KILLORAN, Christina, HENN, Wolfram, HENNEKAM, Raoul C. M, HOLMES, Lewis B, EUGENE HOYME, H, LEPPIG, Kathleen A, LIN, Angela E, MACLEOD, Patrick, MANCHESTER, David K, MARCELIS, Carlo, MAZZANTI, Laura, ELSON, Emma, MCCANN, Emma, MCDONALD, Marie T, MENDELSOHN, Nancy J, MOESCHLER, John B, MOGHADDAM, Billur, NERI, Giovanni, NEWBURY-ECOB, Ruth, PAGON, Roberta A, PHILLIPS, John A, SADLER, Laurie S, TURNER, Joyce T, STOLER, Joan M, TILSTRA, David, WALSH VOCKLEY, Catherine M, ZACKAI, Elaine H, ZADEH, Touran M, BRUETON, Louise, BLACK, Graeme Charles M, BIESECKER, Leslie G, PETERS, Kathryn F, ABBOTT, Margaret H, AUGHTON, David J, AYLSWORTH, Arthur S, BAMSHAD, Michael J

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