Unrestrained ESCRT-III drives micronuclear catastrophe and chromosome fragmentation von Vietri, Marina, Schultz, Sebastian W., Bellanger, Aurélie, Jones, Carl M., Petersen, Louise I., Raiborg, Camilla, Skarpen, Ellen, Pedurupillay, Christeen Ramane J., Kjos, Ingrid, Kip, Eline, Timmer, Romy, Jain, Ashish, Collas, Philippe, Knorr, Roland L., Grellscheid, Sushma N., Kusumaatmaja, Halim, Brech, Andreas, Micci, Francesca, Stenmark, Harald, Campsteijn, Coen

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Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy von Lemke, Johannes R, Geider, Kirsten, Helbig, Katherine L, Heyne, Henrike O, Schütz, Hannah, Hentschel, Julia, Courage, Carolina, Depienne, Christel, Nava, Caroline, Heron, Delphine, Møller, Rikke S, Hjalgrim, Helle, Lal, Dennis, Neubauer, Bernd A, Nürnberg, Peter, Thiele, Holger, Kurlemann, Gerhard, Arnold, Georgianne L, Bhambhani, Vikas, Bartholdi, Deborah, Pedurupillay, Christeen Ramane J, Misceo, Doriana, Frengen, Eirik, Strømme, Petter, Dlugos, Dennis J, Doherty, Emily S, Bijlsma, Emilia K, Ruivenkamp, Claudia A, Hoffer, Mariette J.V, Goldstein, Amy, Rajan, Deepa S, Narayanan, Vinodh, Ramsey, Keri, Belnap, Newell, Schrauwen, Isabelle, Richholt, Ryan, Koeleman, Bobby P.C, Sá, Joaquim, Mendonça, Carla, de Kovel, Carolien G.F, Weckhuysen, Sarah, Hardies, Katia, De Jonghe, Peter, De Meirleir, Linda, Milh, Mathieu, Badens, Catherine, Lebrun, Marine, Busa, Tiffany, Francannet, Christine, Piton, Amélie, Riesch, Erik, Biskup, Saskia, Vogt, Heinrich, Dorn, Thomas, Helbig, Ingo, Michaud, Jacques L, Laube, Bodo, Syrbe, Steffen

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Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2 von Pedurupillay, Christeen Ramane J, Amundsen, Silja S, Barøy, Tuva, Rasmussen, Magnhild, Blomhoff, Anne, Stadheim, Barbro Fossøy, Ørstavik, Kristin, Holmgren, Asbjørn, Iqbal, Tahir, Frengen, Eirik, Misceo, Doriana, Strømme, Petter

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Kaufman oculocerebrofacial syndrome in sisters with novel compound heterozygous mutation in UBE3B von Pedurupillay, Christeen Ramane J., Barøy, Tuva, Holmgren, Asbjørn, Blomhoff, Anne, Vigeland, Magnus D., Sheng, Ying, Frengen, Eirik, Strømme, Petter, Misceo, Doriana

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Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan von Pedurupillay, Christeen Ramane J, Landsend, Erlend Christoffer Sommer, Vigeland, Magnus Dehli, Ansar, Muhammad, Frengen, Eirik, Misceo, Doriana, Strømme, Petter

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A novel mutation in FBXL4 in a Norwegian child with encephalomyopathic mitochondrial DNA depletion syndrome 13 von Barøy, Tuva, Pedurupillay, Christeen Ramane J, Bliksrud, Yngve T, Rasmussen, Magnhild, Holmgren, Asbjørn, Vigeland, Magnus D, Hughes, Timothy, Brink, Maaike, Richard, Nedregaard, Bård, Strømme, Petter, Frengen, Eirik, Misceo, Doriana

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction von Gabriele, Michele, Vulto-van Silfhout, Anneke T., Germain, Pierre-Luc, Vitriolo, Alessandro, Kumar, Raman, Douglas, Evelyn, Haan, Eric, Kosaki, Kenjiro, Takenouchi, Toshiki, Rauch, Anita, Steindl, Katharina, Frengen, Eirik, Misceo, Doriana, Pedurupillay, Christeen Ramane J., Stromme, Petter, Rosenfeld, Jill A., Shao, Yunru, Craigen, William J., Schaaf, Christian P., Rodriguez-Buritica, David, Farach, Laura, Friedman, Jennifer, Thulin, Perla, McLean, Scott D., Nugent, Kimberly M., Morton, Jenny, Nicholl, Jillian, Andrieux, Joris, Stray-Pedersen, Asbjørg, Chambon, Pascal, Patrier, Sophie, Lynch, Sally A., Kjaergaard, Susanne, Tørring, Pernille M., Brasch-Andersen, Charlotte, Ronan, Anne, van Haeringen, Arie, Anderson, Peter J., Powis, Zöe, Brunner, Han G., Pfundt, Rolph, Schuurs-Hoeijmakers, Janneke H.M., van Bon, Bregje W.M., Lelieveld, Stefan, Gilissen, Christian, Nillesen, Willy M., Vissers, Lisenka E.L.M., Gecz, Jozef, Koolen, David A., Testa, Giuseppe, de Vries, Bert B.A.

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Products obtained from decomposition of glass fibre-reinforced composites using microwave pyrolysis von AKESSON, DAN, FOLTYNOWICZ, ZENON, CHRISTEEN, JONAS, SKRIFVARS, MIKAEL

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A Sri Lankan child with 49,XXXXY syndrome von Dissanayake, Vajira H W, Bandarage, Palinda, Pedurupillay, Christeen R J, Jayasekara, Rohan W

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YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction von Gabriele, Michele, Vulto-van Silfhout, Anneke T, Germain, Pierre-Luc, Vitriolo, Alessandro, Kumar, Raman, Douglas, Evelyn, Haan, Eric, Kosaki, Kenjiro, Takenouchi, Toshiki, Rauch, Anita, Steindl, Katharina, Frengen, Eirik, Misceo, Doriana, Pedurupillay, Christeen Ramane J, Stromme, Petter, Rosenfeld, Jill A, Shao, Yunru, Craigen, William J, Schaaf, Christian P, Rodriguez-Buritica, David, Farach, Laura, Friedman, Jennifer, Thulin, Perla, McLean, Scott D, Nugent, Kimberly M, Morton, Jenny, Nicholl, Jillian, Andrieux, Joris, Stray-Pedersen, Asbjørg, Chambon, Pascal

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Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy von Lemke, Johannes R, Geider, Kirsten, Helbig, Katherine L, Heyne, Henrike O, Schütz, Hannah, Hentschel, Julia, Courage, Carolina, Depienne, Christel, Nava, Caroline, Heron, Delphine, Møller, Rikke S, Hjalgrim, Helle, Lal, Dennis, Neubauer, Bernd A, Nürnberg, Peter, Thiele, Holger, Kurlemann, Gerhard, Arnold, Georgianne L, Bhambhani, Vikas, Bartholdi, Deborah, Pedurupillay, Christeen Ramane J, Misceo, Doriana, Frengen, Eirik, Strømme, Petter, Dlugos, Dennis J, Doherty, Emily S, Bijlsma, Emilia K, Ruivenkamp, Claudia A, Hoffer, Mariette J.V, Goldstein, Amy, Rajan, Deepa S, Narayanan, Vinodh, Ramsey, Keri, Belnap, Newell, Schrauwen, Isabelle, Richholt, Ryan, Koeleman, Bobby P.C, Sá, Joaquim, Mendoncą, Carla, de Kovel, Carolien G F, Weckhuysen, Sarah, Hardies, Katia, De Jonghe, Peter, Meirleir, Linda De, Milh, Mathieu, Badens, Catherine, Lebrun, Marine, Busa, Tiffany, Francannet, Christine, Piton, Amélie, Riesch, Erik, Biskup, Saskia, Vogt, Heinrich, Dorn, Thomas, Helbig, Ingo, Michaud, Jacques L, Laube, Bodo, Syrbe, Steffen

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Products obtained from decomposition of glass fiber-reinforced composites using microwave pyrolysis von Aakesson, D, Foltynowicz, Z, Christeen, J, Skrifvars, M

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Chromosomal abnormalities in patients with recurrent spontaneous pregnancy loss and sub-fertility von Dissanayake, Vajira HW, Athapaththu, AM Maheshi H, Opanayake, D Jeewani S, Hidellage, Nethra T, Wijetunge, Kalpani, Pedurupillay, Christeen RJ

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Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan von Pedurupillay, Christeen Ramane J, Landsend, Erlend Christoffer Sommer, Vigeland, Magnus Dehli, Ansar, Muhammad, Frengen, Eirik, Misceo, Doriana, Strømme, Petter

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A Sri Lankan child with 49,XXXXY syndrome von Dissanayake, Vajira H W, Bandarage, Palinda, Pedurupillay, Christeen R J, Jayasekara, Rohan W

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Process Evaluation of an Early-Intervention Program for Mood and Anxiety Disorders Among Older Adolescents and Young Adults von Osuch, Elizabeth A, Vingilis, Evelyn, Summerhurst, Carolyn, Forster, Christeen I, Ross, Erin E, Wrath, Andrew J

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T63. Neurocognitive Correlates of Resilience in Youth With a History of Traumatic Stress Exposure von Barzilay, Ran, Samuel, Christeen, Calkins, Monica, Moore, Tyler, Scott, J. Cobb, Gur, Raquel, Gur, Ruben

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Optical diffraction tomography and image reconstruction to measure host cell alterations caused by divergent Plasmodium species von Ong, Jessica J.Y., Oh, Jeonghun, Yong Ang, Xiang, Naidu, Renugah, Chu, Trang T.T., Hyoung Im, Jae, Manzoor, Umar, Kha Nguyen, Tuyet, Na, Seok-Won, Han, Eun-Taek, Davis, Christeen, Sun Park, Won, Chun, Wanjoo, Jun, Hojong, Jin Lee, Se, Na, Sunghun, Chan, Jerry K.Y., Park, YongKeun, Russell, Bruce, Chandramohanadas, Rajesh, Han, Jin-Hee

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Identification of two haplotypes of cytochrome oxidase subunit II (COII) gene of the Formosan subterranean termite, Coptotermes formosanus Shiraki (Isoptera: Rhinotermitidae), in s... von Zhu, Yu Cheng, Sun, Jian-Zhong, Luo, Lily Li, Liu, Xiaofen Fanny, Lee, Karmen Christeen, Mallette, Eldon J, Abel, Craig A

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The representation of female athletes in textual and visual media von George, Christeen, Hartley, Andrew, Paris, Jenny

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