Convergent Solid-Phase Synthesis of N-Glycopeptides Facilitated by Pseudoprolines at Consensus-Sequence Ser/Thr Residues von Ullmann, Vera, Rädisch, Marisa, Boos, Irene, Freund, Jutta, Pöhner, Claudia, Schwarzinger, Stefan, Unverzagt, Carlo

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Convergent Solid-Phase Synthesis of N-Glycopeptides Facilitated by Pseudoprolines at Consensus-Sequence Ser/Thr Residues von Ullmann, Vera, Rädisch, Marisa, Boos, Irene, Freund, Jutta, Pöhner, Claudia, Schwarzinger, Stefan, Unverzagt, Carlo

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Chemoselective coupling of sugar oximes and α-ketoacids to glycosyl amides and N-glycopeptides von Pöhner, Claudia, Ullmann, Vera, Hilpert, Ramona, Samain, Eric, Unverzagt, Carlo

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Convergent Solid-Phase Synthesis of N-Glycopeptides Facilitated by Pseudoprolines at Consensus-Sequence Ser/Thr Residues von Ullmann, Vera, Rädisch, Marisa, Boos, Irene, Freund, Jutta, Pöhner, Claudia, Schwarzinger, Stefan, Unverzagt, Carlo

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ChemInform Abstract: Chemoselective Coupling of Sugar Oximes and α-Ketoacids to Glycosyl Amides and N-Glycopeptides von Poehner, Claudia, Ullmann, Vera, Hilpert, Ramona, Samain, Eric, Unverzagt, Carlo

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ChemInform Abstract: Chemoselective Coupling of Sugar Oximes and [alpha]-Ketoacids to Glycosyl Amides and N-Glycopeptides von Poehner, Claudia, Ullmann, Vera, Hilpert, Ramona, Samain, Eric, Unverzagt, Carlo

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Deep sequencing reveals 50 novel genes for recessive cognitive disorders von Najmabadi, Hossein, Hu, Hao, Garshasbi, Masoud, Zemojtel, Tomasz, Abedini, Seyedeh Sedigheh, Chen, Wei, Hosseini, Masoumeh, Behjati, Farkhondeh, Haas, Stefan, Jamali, Payman, Zecha, Agnes, Mohseni, Marzieh, Püttmann, Lucia, Vahid, Leyla Nouri, Jensen, Corinna, Moheb, Lia Abbasi, Bienek, Melanie, Larti, Farzaneh, Mueller, Ines, Weissmann, Robert, Darvish, Hossein, Wrogemann, Klaus, Hadavi, Valeh, Lipkowitz, Bettina, Esmaeeli-Nieh, Sahar, Wieczorek, Dagmar, Kariminejad, Roxana, Firouzabadi, Saghar Ghasemi, Cohen, Monika, Fattahi, Zohreh, Rost, Imma, Mojahedi, Faezeh, Hertzberg, Christoph, Dehghan, Atefeh, Rajab, Anna, Banavandi, Mohammad Javad Soltani, Hoffer, Julia, Falah, Masoumeh, Musante, Luciana, Kalscheuer, Vera, Ullmann, Reinhard, Kuss, Andreas Walter, Tzschach, Andreas, Kahrizi, Kimia, Ropers, H. Hilger

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Mapping translocation breakpoints by next-generation sequencing von Chen, Wei, Kalscheuer, Vera, Tzschach, Andreas, Menzel, Corinna, Ullmann, Reinhard, Schulz, Marcel Holger, Erdogan, Fikret, Li, Na, Kijas, Zofia, Arkesteijn, Ger, Pajares, Isidora Lopez, Goetz-Sothmann, Margret, Heinrich, Uwe, Rost, Imma, Dufke, Andreas, Grasshoff, Ute, Glaeser, Birgitta, Vingron, Martin, Ropers, H Hilger

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Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients von Kunde, Stella-Amrei, Rademacher, Nils, Tzschach, Andreas, Wiedersberg, Eberhard, Ullmann, Reinhard, Kalscheuer, Vera M., Shoichet, Sarah A.

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WDR11, a WD Protein that Interacts with Transcription Factor EMX1, Is Mutated in Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome von Kim, Hyung-Goo, Ahn, Jang-Won, Kurth, Ingo, Ullmann, Reinhard, Kim, Hyun-Taek, Kulharya, Anita, Ha, Kyung-Soo, Itokawa, Yasuhide, Meliciani, Irene, Wenzel, Wolfgang, Lee, Deresa, Rosenberger, Georg, Ozata, Metin, Bick, David P., Sherins, Richard J., Nagase, Takahiro, Tekin, Mustafa, Kim, Soo-Hyun, Kim, Cheol-Hee, Ropers, Hans-Hilger, Gusella, James F., Kalscheuer, Vera, Choi, Cheol Yong, Layman, Lawrence C.

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balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation von Kalscheuer, Vera M, Musante, Luciana, Fang, Cheng, Hoffmann, Kirsten, Fuchs, Celine, Carta, Eloisa, Deas, Emma, Venkateswarlu, Kanamarlapudi, Menzel, Corinna, Ullmann, Reinhard, Tommerup, Niels, Dalprà, Leda, Tzschach, Andreas, Selicorni, Angelo, Lüscher, Bernhard, Ropers, Hans-Hilger, Harvey, Kirsten, Harvey, Robert J

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Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly von Møller, Rikke S., Kübart, Sabine, Hoeltzenbein, Maria, Heye, Babett, Vogel, Ida, Hansen, Christian P., Menzel, Corinna, Ullmann, Reinhard, Tommerup, Niels, Ropers, Hans-Hilger, Tümer, Zeynep, Kalscheuer, Vera M.

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Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation von KALSCHEUER, Vera M, FITZPATRICK, David, ARKESTEIJN, Ger, ROPERS, Hans-Hilger, ULLMANN, Reinhard, TOMMERUP, Niels, BUGGE, Merete, NIEBUHR, Erik, NEUMANN, Luitgard M, TZSCHACH, Andreas, SHOICHET, Sarah A, MENZEL, Corinna, ERDOGAN, Fikret

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Increased STAG2 dosage defines a novel cohesinopathy with intellectual disability and behavioral problems von Kumar, Raman, Corbett, Mark A, Van Bon, Bregje W M, Gardner, Alison, Woenig, Joshua A, Jolly, Lachlan A, Douglas, Evelyn, Friend, Kathryn, Tan, Chuan, Van Esch, Hilde, Holvoet, Maureen, Raynaud, Martine, Field, Michael, Leffler, Melanie, Budny, Bartłomiej, Wisniewska, Marzena, Badura-Stronka, Magdalena, Latos-Bieleńska, Anna, Batanian, Jacqueline, Rosenfeld, Jill A, Basel-Vanagaite, Lina, Jensen, Corinna, Bienek, Melanie, Froyen, Guy, Ullmann, Reinhard, Hu, Hao, Love, Michael I, Haas, Stefan A, Stankiewicz, Pawel, Cheung, Sau Wai, Baxendale, Anne, Nicholl, Jillian, Thompson, Elizabeth M, Haan, Eric, Kalscheuer, Vera M, Gecz, Jozef

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Mutations in SLC33A1 Cause a Lethal Autosomal-Recessive Disorder with Congenital Cataracts, Hearing Loss, and Low Serum Copper and Ceruloplasmin von Huppke, Peter, Brendel, Cornelia, Kalscheuer, Vera, Korenke, Georg Christoph, Marquardt, Iris, Freisinger, Peter, Christodoulou, John, Hillebrand, Merle, Pitelet, Gaele, Wilson, Callum, Gruber-Sedlmayr, Ursula, Ullmann, Reinhard, Haas, Stefan, Elpeleg, Orly, Nürnberg, Gudrun, Nürnberg, Peter, Dad, Shzeena, Møller, Lisbeth Birk, Kaler, Stephen G., Gärtner, Jutta

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Chromosome deletions in 13q33-34: Report of four patients and review of the literature von Walczak-Sztulpa, Joanna, Wisniewska, Marzena, Latos-Bielenska, Anna, Linné, Maja, Kelbova, Christina, Belitz, Britta, Pfeiffer, Lutz, Kalscheuer, Vera, Erdogan, Fikret, Kuss, Andreas W., Ropers, Hans-Hilger, Ullmann, Reinhard, Tzschach, Andreas

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Breakpoint analysis of balanced chromosome rearrangements by next-generation paired-end sequencing von WEI CHEN, ULLMANN, Reinhard, HOELTZENBEIN, Maria, NEITZEL, Heidemarie, MARKUS, Susanne, WIEDERSBERG, Eberhard, KISTNER, Gerd, VAN RAVENSWAAIJ-ARTS, Conny M. A, KLEEFSTRA, Tjitske, KALSCHEUER, Vera M, ROPERS, Hans-Hilger, LANGNICK, Claudia, MENZEL, Corinna, WOTSCHOFSKY, Zofia, HAO HU, DÖRING, Andreas, YUHUI HU, HUI KANG, TZSCHACH, Andreas

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Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders von Gilling, Mette, Rasmussen, Hanne B, Calloe, Kirstine, Sequeira, Ana F, Baretto, Marta, Oliveira, Guiomar, Almeida, Joana, Lauritsen, Marlene B, Ullmann, Reinhard, Boonen, Susanne E, Brondum-Nielsen, Karen, Kalscheuer, Vera M, Tümer, Zeynep, Vicente, Astrid M, Schmitt, Nicole, Tommerup, Niels

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Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11 von TZSCHACH, Andreas, BISGAARD, Anne-Marie, KALSCHEUER, Vera M, ULLMANN, Reinhard, KIRCHHOFF, Maria, GRAUL-NEUMANN, Luitgard M, NEITZEL, Heidemarie, PAGE, Stephanie, AHMED, Alischo, MÜLLER, Ines, ERDOGAN, Fikret, ROPERS, Hans-Hilger

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Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt-Hopkins syndrome von Kalscheuer, Vera M., Feenstra, Ilse, Van Ravenswaaij-Arts, Conny M.A., Smeets, Dominique F.C.M., Menzel, Corinna, Ullmann, Reinhard, Musante, Luciana, Ropers, Hans-Hilger

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