Novel Formulations of Vitamins and Insulin by Nanoengineering of Polyelectrolyte Multilayers around Microcrystals von Dai, Zhifei, Heilig, Anne, Zastrow, Heidi, Donath, Edwin, Möhwald, Helmuth

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Single particle light scattering method for studying aging properties of Pickering emulsions stabilized by catanionic crystals von Schelero, Natascha, Lichtenfeld, Heinz, Zastrow, Heidi, Möhwald, Helmuth, Dubois, Monique, Zemb, Thomas

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Characterization of structure and mechanism of transfection-active peptide–DNA complexes von Dallüge, Roman, Haberland, Annekathrin, Zaitsev, Sergei, Schneider, Marc, Zastrow, Heidi, Sukhorukov, Gleb, Böttger, Michael

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Preparation and use of dna-polyelectrolyte nanoparticles for gene transfer von SERGEI ZAITSEV, ANNEKATHRIN HABERLAND, GLEB SUKHORUKOV, MICHAEL BOTTGER, REGIS CARTIER, HEIDI ZASTROW, MARC SCHNEIDER, HELMUTH MOHWALD

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PREPARATION AND USE OF DNA-POLYELECTROLYTE NANOPARTICLES FOR GENE TRANSFER von SERGEI ZAITSEV, ANNEKATHRIN HABERLAND, GLEB SUKHORUKOV, MICHAEL BOTTGER, REGIS CARTIER, HEIDI ZASTROW, MARC SCHNEIDER, HELMUTH MOHWALD

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PREPARATION AND USE OF DNA-POLYELECTROLYTE NANOPARTICLES FOR GENE TRANSFER von SUKHORUKOV, GLEB, ZAITSEV, SERGEI, MOEHWALD, HELMUTH, CARTIER, REGIS, HABERLAND, ANNEKATHRIN, BOETTGER, MICHAEL, ZASTROW, HEIDI, SCHNEIDER, MARC

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Gene transfer to animal cells, useful in vitro or for gene therapy, using vector DNA treated sequentially in water with oppositely charged polyelectrolytes von SUKHORUKOV, GLEB, ZAITSEV, SERGEI, MOEHWALD, HELMUTH, HABERLAND, ANNEKATHRIN, SCHNEIDER, MARK, BOETTGER, MICHAEL, ZASTROW, HEIDI, DALLUEGE, ROMAN

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Preparation and use of DNA-polyelectrolyte nanoparticles for gene transfer von SUKHORUKOV, GLEB, ZAITSEV, SERGEI, CARTIER, REGIS, HABERLAND, ANNEKATHRIN, BOETTGER, MICHAEL, ZASTROW, HEIDI, SCHNEIDER, MARC, MOEHWALD, HELMUT, DR

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ClinGen Variant Curation Interface: a variant classification platform for the application of evidence criteria from ACMG/AMP guidelines von Preston, Christine G, Wright, Matt W, Madhavrao, Rao, Harrison, Steven M, Goldstein, Jennifer L, Luo, Xi, Wand, Hannah, Wulf, Bryan, Cheung, Gloria, Mandell, Mark E, Tong, Howard, Cheng, Shaung, Iacocca, Michael A, Pineda, Arturo Lopez, Popejoy, Alice B, Dalton, Karen, Zhen, Jimmy, Dwight, Selina S, Babb, Lawrence, DiStefano, Marina, O'Daniel, Julianne M, Lee, Kristy, Riggs, Erin R, Zastrow, Diane B, Mester, Jessica L, Ritter, Deborah I, Patel, Ronak Y, Subramanian, Sai Lakshmi, Milosavljevic, Aleksander, Berg, Jonathan S, Rehm, Heidi L, Plon, Sharon E, Cherry, J Michael, Bustamante, Carlos D, Costa, Helio A

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SPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia von Srivastava, Siddharth, Shaked, Hagar Mor, Gable, Kenneth, Gupta, Sita D, Pan, Xueyang, Somashekarappa, Niranjanakumari, Han, Gongshe, Mohassel, Payam, Gotkine, Marc, Doney, Elizabeth, Goldenberg, Paula, Tan, Queenie K G, Gong, Yi, Kleinstiver, Benjamin, Wishart, Brian, Cope, Heidi, Pires, Claudia Brito, Stutzman, Hannah, Spillmann, Rebecca C, Sadjadi, Reza, Elpeleg, Orly, Lee, Chia-Hsueh, Bellen, Hugo J, Edvardson, Simon, Eichler, Florian, Dunn, Teresa M

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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

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A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative von Schoch, Kelly, Spillmann, Rebecca, Tan, Queenie K.-G., McConkie-Rosell, Allyn, Jiang, Yong-Hui, Goldstein, David B., Adams, David R., Allard, Patrick, Ashley, Euan A., Bacino, Carlos A., Beggs, Alan H., Birch, Camille L., Bonner, Devon, Boone, Braden E., Brown, Donna M., Chen, Shan, Coakley, Terra R., Cogan, Joy D., Cooper, Cynthia M., Cope, Heidi, Craigen, William J., Davidson, Jean M., Dayal, Jyoti G., Dell’Angelica, Esteban C., Dipple, Katrina M., Donnell-Fink, Laurel A., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Fernandez, Liliana, Ferreira, Carlos, Fisher, Paul G., Fogel, Brent L., Friedman, Noah D., Gahl, William A., Goldstein, David B., Gourdine, Jean-Philippe F., Haendel, Melissa, Handley, Lori H., Krasnewich, Donna M., Krier, Joel B., Lazar, Jozef, Levy, Shawn E., Lincoln, Sharyn A., Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., MacRae, Calum A., Majcherska, Marta M., Mamounas, Laura A., Manolio, Teri A., Markello, Thomas C., Marom, Ronit, Martin, Martin G., McConkie-Rosell, Allyn, McCormack, Colleen E., Might, Matthew, Morimoto, Marie, Mulvihill, John J., Murphy, Jennifer L., Muzny, Donna M., Nehrebecky, Michele E., Nelson, Stan F., Newberry, J. Scott, Newman, John H., Nicholas, Sarah K., Pallais, J. Carl, Palmer, Christina GS, Parker, Neil H., Phillips, John A., Postlethwait, John H., Reuter, Chloe M., Sampson, Jacinda B., Scott, Daryl A., Sharma, Prashant, Shashi, Vandana, Silverman, Edwin K., Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Urv, Tiina K., Vogel, Tiphanie P., Wahl, Colleen E., Walsh, Chris A., Wan, Jijun, Wangler, Michael F., Ward, Patricia A., Wheeler, Matthew T., Wolfe, Lynne A., Worthey, Elizabeth A., Yamamoto, Shinya, Yang, Yaping, Yu, Guoyun, Zhao, Chunli, Zheng, Allison

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Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder von Schneeberger, Pauline E, Kortüm, Fanny, Korenke, Georg Christoph, Alawi, Malik, Santer, René, Woidy, Mathias, Buhas, Daniela, Fox, Stephanie, Juusola, Jane, Alfadhel, Majid, Webb, Bryn D, Coci, Emanuele G, Abou Jamra, Rami, Siekmeyer, Manuela, Biskup, Saskia, Heller, Corina, Maier, Esther M, Javaher-Haghighi, Poupak, Bedeschi, Maria F, Ajmone, Paola F, Iascone, Maria, Peeters, Hilde, Ballon, Katleen, Jaeken, Jaak, Rodríguez Alonso, Aroa, Palomares-Bralo, María, Santos-Simarro, Fernando, Meuwissen, Marije E C, Beysen, Diane, Kooy, R Frank, Houlden, Henry, Murphy, David, Doosti, Mohammad, Karimiani, Ehsan G, Mojarrad, Majid, Maroofian, Reza, Noskova, Lenka, Kmoch, Stanislav, Honzik, Tomas, Cope, Heidi, Sanchez-Valle, Amarilis, Gelb, Bruce D, Kurth, Ingo, Hempel, Maja, Kutsche, Kerstin

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Continuing a search for a diagnosis: the impact of adolescence and family dynamics von Miller, Ilana M, Yashar, Beverly M, Macnamara, Ellen F

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VarSight: prioritizing clinically reported variants with binary classification algorithms von Holt, James M, Wilk, Brandon, Birch, Camille L, Brown, Donna M, Gajapathy, Manavalan, Moss, Alexander C, Sosonkina, Nadiya, Wilk, Melissa A, Anderson, Julie A, Harris, Jeremy M, Kelly, Jacob M, Shaterferdosian, Fariba, Uno-Antonison, Angelina E, Weborg, Arthur, Worthey, Elizabeth A

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Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review von Kumar, Akash, Zastrow, Diane B., Kravets, Elijah J., Beleford, Daniah, Ruzhnikov, Maura R. Z., Grove, Megan E., Dries, Annika M., Kohler, Jennefer N., Waggott, Daryl M., Yang, Yaping, Huang, Yong, Mackenzie, Katherine M., Eng, Christine M., Fisher, Paul G., Ashley, Euan A., Teng, Joyce M., Stevenson, David A., Shieh, Joseph T., Wheeler, Matthew T., Bernstein, Jonathan A.

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Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation von Kelley, Emily G., Boyd, Brenna M., Acosta, Maria T, Adams, David R, Amendola, Laura, Andrews, Ashley, Baker, Eva, Bale, Jim, Beggs, Alan H, Behrens, Edward, Bejerano, Gill, Bennet, Jimmy, Berry, Gerard T, Blue, Elizabeth, Bonnenmann, Carsten, Bonner, Devon, Brokamp, Elly, Brown, Gabrielle, Burrage, Lindsay C, Carrasquillo, Olveen, Chao, Hsiao‐Tuan, Sessions Cole, F, Cooper, Cynthia M, Crouse, Andrew B, Dai, Hongzheng, Davis, Joie, Dayal, Jyoti G, Deardorff, Matthew, Dhar, Shweta U, Doherty, Daniel, Duncan, Laura, Eckstein, David J, Emrick, Lisa T, Eng, Christine M, Esteves, Cecilia, Falk, Marni, Fisher, Paul G, Fogel, Brent L, Forghani, Irman, Fresard, Laure, Gahl, William A, Glass, Ian, Godfrey, Rena A, Golden‐Grant, Katie, Goldrich, Madison P, Groden, Catherine A, Gutierrez, Irma, Hahn, Sihoun, Hayes, Nichole, Hing, Anne, Isasi, Rosario, Karaviti, Lefkothea, Kiley, Dana, Kobren, Shilpa N, Kohler, Jennefer N, Krasnewich, Donna M, Krier, Joel B, Latham, Lea, Lee, Hane, Liu, Xue Zhong, Maas, Richard L, Mak, Bryan C, Maclidan, May Christine V., Martínez‐Agosto, Julian A, McGee, Elisabeth, Might, Matthew, Moretti, Paolo M, Nicholas, Sarah K, Novacic, Donna, Pace, Laura, Papp, Jeanette C, Phillips, John A, Posey, Jennifer E, Potocki, Lorraine, Quinlan, Aaron, Rao, Deepak A, Rives, Lynette, Rosenfeld, Jill A, Smith, Edward C, Spillmann, Rebecca C, Stoler, Joan M, Sybert, Virginia, Tekin, Mustafa, Thorson, Willa, Thurm, Audrey, Toro, Camilo, Tucker, Brianna M, Vanderver, Adeline, Velinder, Matt, Vogel, Tiphanie P, Wallace, Stephanie, Walley, Nicole M, Walker, Melissa, Wambach, Jennifer, Wan, Jijun, Wangler, Michael F, Wener, Mark, Wenger, Tara, Yang, John, Yousef, Muhammad

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A resource of lipidomics and metabolomics data from individuals with undiagnosed diseases von Kyle, Jennifer E., Stratton, Kelly G., Zink, Erika M., Kim, Young-Mo, Bloodsworth, Kent J., Monroe, Matthew E., Waters, Katrina M., Webb-Robertson, Bobbie-Jo M., Koeller, David M., Metz, Thomas O.

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A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing von Zastrow, Diane B., Bonner, Devon, Reuter, Chloe M., Fisk, Dianna G., Yang, Yaping, Eng, Christine M., Fisher, Paul G., Merker, Jason, Schelley, Susan, Zappala, Zach, Prybol, Cameron, Olahova, Monika, Allard, Patrick, Bacino, Carlos A., Beggs, Alan H., Behnam, Babak, Bick, David P., Birch, Camille L., Bostwick, Bret L., Brokamp, Elly, Brown, Donna M., Chen, Shan, Coakley, Terra R., Cogan, Joy D., Cope, Heidi, Craigen, William J., Dayal, Jyoti G., Dell'Angelica, Esteban C., Dipple, Katrina M., Dorrani, Naghmeh, Draper, David D., Dries, Annika M., Eckstein, David J., Emrick, Lisa T., Enns, Gregory M., Esteves, Cecilia, Estwick, Tyra, Ferreira, Carlos, Fieg, Elizabeth L., Fogel, Brent L., Godfrey, Rena A., Goldstein, David B., Hamid, Rizwan, Holm, Ingrid A., Howerton, Ellen M., Huang, Yong, Jones, Angela L., Karaviti, Lefkothea, Krasnewich, Donna M., Korrick, Susan, Koziura, Mary, Krier, Joel B., Kyle, Jennifer E., Lau, C. Christopher, Lazar, Jozef, LeBlanc, Kimberly, Lee, Hane, Lewis, Richard A., Lincoln, Sharyn A., Loo, Sandra K., Malicdan, May Christine V., Mamounas, Laura A., Markello, Thomas C., Martin, Martin G., Martínez‐Agosto, Julian A., May, Thomas, McConkie‐Rosell, Allyn, McCray, Alexa T., Merker, Jason D., Metz, Thomas O., Moretti, Paolo M., Mulvihill, John J., Muzny, Donna M., Nelson, Stan F., Newberry, J. Scott, Nicholas, Sarah K., Orengo, James P., Pallais, J. Carl, Papp, Jeanette C., Phillips, John A., Posey, Jennifer E., Postlethwait, John H., Rosenfeld, Jill A., Sampson, Jacinda B., Shakachite, Lisa, Sharma, Prashant, Stoler, Joan M., Sweetser, David A., Toro, Camilo, Tran, Alyssa A., Urv, Tiina K., Vilain, Eric, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Webb‐Robertson, Bobbie‐Jo M., Westerfield, Monte, Wolfe, Lynne A., Yu, Guoyun, Zheng, Allison

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Progressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum von Macnamara, Ellen F., McGuire, Peter, Adam, Margaret, Alejandro, Mercedes E, Alvey, Justin, Ashley, Euan A, Balasubramanyam, Ashok, Bayrak‐Toydemir, Pinar, Beck, Anita, Beggs, Alan H, Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Butte, Manish J, Chanprasert, Sirisak, Coakley, Terra R, Coggins, Matthew, Cope, Heidi, Craigen, William J, Crouse, Andrew B, Davids, Mariska, Dayal, Jyoti G, Dell'Angelica, Esteban C, Dorrani, Naghmeh, Draper, David D, Earl, Dawn, Eckstein, David J, Emrick, Lisa T, Eng, Christine M, Ferreira, Carlos, Findley, Laurie C, Goldman, Alica M, Groden, Catherine A, Gropman, Andrea L, Gutierrez, Irma, Hanchard, Neil A, Hassey, Kelly, Hayes, Nichole, Hisama, Fuki M, Holm, Ingrid A, Hom, Jason, Horike‐Pyne, Martha, Huang, Alden, Isasi, Rosario, Johnston, Jean M, Kennedy, Jennifer, Kiley, Dana, Kohane, Isaac S, Krier, Joel B, Lee, Hane, Liu, Xue Zhong, Maas, Richard L, Macnamara, Ellen F., MacRae, Calum A, Mak, Bryan, Manolio, Teri A, Marom, Ronit, Marth, Gabor, Martínez‐Agosto, Julian A, McConkie‐Rosell, Allyn, McCormack, Colleen E, McCray, Alexa T, McGee, Elisabeth, Might, Matthew, Mirzaa, Ghayda, Mulvihill, John J, Nelson, Stan F, Nickerson, Deborah, Nieves‐Rodriguez, Shirley, Phillips, John A., Pusey, Barbara N, Raskind, Wendy, Raja, Archana N, Robertson, Amy K, Rodan, Lance H, Ruzhnikov, Maura, Sampson, Jacinda B, Scott, C. Ron, Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Scott, Daryl A, Shin, Jimann, Signer, Rebecca, Sinsheimer, Janet S, Solem, Emily, Sullivan, Jennifer A, Sun, Angela, Telischi, Fred, Toro, Camilo, Tran, Alyssa A, Wang, Lee‐kai, Wangler, Michael F, Ward, Patricia A, Perry, Katherine Wesseling, Westerfield, Monte, Whitlock, Jordan, Woods, Jeremy D, Yamamoto, Shinya, Yu, Guoyun

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