Clinical manifestations of mutations in RAS and related intracellular signal transduction factors von Zenker, Martin

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Genetic and Pathogenetic Aspects of Noonan Syndrome and Related Disorders von Zenker, Martin

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Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-Inhibition von Andelfinger, Gregor, Marquis, Christopher, Raboisson, Marie-Josée, Théoret, Yves, Waldmüller, Stephan, Wiegand, Gesa, Gelb, Bruce D., Zenker, Martin, Delrue, Marie-Ange, Hofbeck, Michael

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ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation von Gelb, Bruce D, Cavé, Hélène, Dillon, Mitchell W, Gripp, Karen W, Lee, Jennifer A, Mason-Suares, Heather, Rauen, Katherine A, Williams, Bradley, Zenker, Martin, Vincent, Lisa M

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Syndromic forms of congenital hyperinsulinism von Zenker, Martin, Mohnike, Klaus, Palm, Katja

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Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling von Motta, Marialetizia, Fidan, Miray, Bellacchio, Emanuele, Pantaleoni, Francesca, Schneider-Heieck, Konstantin, Coppola, Simona, Borck, Guntram, Salviati, Leonardo, Zenker, Martin, Cirstea, Ion C, Tartaglia, Marco

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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes von Endele, Sabine, Rosenberger, Georg, Geider, Kirsten, Popp, Bernt, Tamer, Ceyhun, Stefanova, Irina, Milh, Mathieu, Kortum, Fanny, Fritsch, Angela, Pientka, Friederike K, Hellenbroich, Yorck, Kalscheuer, Vera M, Kohlhase, Jurgen, Moog, Ute, Rappold, Gudrun, Rauch, Anita, Ropers, Hans-Hilger, von Spiczak, Sarah, Tonnies, Holger, Villeneuve, Nathalie, Villard, Laurent, Zabel, Bernhard, Zenker, Martin, Laube, Bodo, Reis, Andre, Wieczorek, Dagmar, Van Maldergem, Lionel, Kutsche, Kerstin

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Microbial composition of tumorous and adjacent gastric tissue is associated with prognosis of gastric cancer von Lehr, Konrad, Nikitina, Darja, Vilchez-Vargas, Ramiro, Steponaitiene, Ruta, Thon, Cosima, Skieceviciene, Jurgita, Schanze, Denny, Zenker, Martin, Malfertheiner, Peter, Kupcinskas, Juozas, Link, Alexander

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Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood von Vogel, Katrin, Arra, Aditya, Lingel, Holger, Bretschneider, Dirk, Prätsch, Florian, Schanze, Denny, Zenker, Martin, Balk, Silke, Bruder, Dunja, Geffers, Robert, Hachenberg, Thomas, Arens, Christoph, Brunner-Weinzierl, Monika C.

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Food‐Derived Xeno‐microRNAs: Influence of Diet and Detectability in Gastrointestinal Tract—Proof‐of‐Principle Study von Link, Jastin, Thon, Cosima, Schanze, Denny, Steponaitiene, Ruta, Kupcinskas, Juozas, Zenker, Martin, Canbay, Ali, Malfertheiner, Peter, Link, Alexander

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Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study von Lehr, Konrad, Lange, Undine Gabriele, Hipler, Noam Mathias, Vilchez-Vargas, Ramiro, Hoffmeister, Albrecht, Feisthammel, Jürgen, Buchloh, Dorina, Schanze, Denny, Zenker, Martin, Gockel, Ines, Link, Alexander, Jansen-Winkeln, Boris

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Editorial: Endocrine aspects of Noonan syndrome and related syndromes von Radetti, Giorgio, Edouard, Thomas, Mazzanti, Laura, Tartaglia, Marco, Zenker, Martin

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RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1 von Meyer Zum Büschenfelde, Uta, Brandenstein, Laura Isabel, von Elsner, Leonie, Flato, Kristina, Holling, Tess, Zenker, Martin, Rosenberger, Georg, Kutsche, Kerstin

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Nephrotic Syndrome in the First Year of Life: Two Thirds of Cases Are Caused by Mutations in 4 Genes (NPHS1, NPHS2, WT1, and LAMB2) von Hinkes, Bernward G, Mucha, Bettina, Vlangos, Christopher N, Gbadegesin, Rasheed, Liu, Jinhong, Hasselbacher, Katrin, Hangan, Daniela, Ozaltin, Fatih, Zenker, Martin, Hildebrandt, Friedhelm, members of Arbeitsgemeinschaft fur Paediatrische Nephrologie Study Group

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Developmental effect of RASopathy mutations on neuronal network activity on a chip von Weiss, Eva-Maria, Guhathakurta, Debarpan, Petrušková, Aneta, Hundrup, Verena, Zenker, Martin, Fejtová, Anna

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Correction to: Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA von Revencu, Nicole, Eijkelenboom, Astrid, Bracquemart, Claire, Alhopuro, Pia, Armstrong, Judith, Baselga, Eulalia, Cesario, Claudia, Dentici, Maria Lisa, Eyries, Melanie, Frisk, Sofia, Karstensen, Helena Gásdal, Gene-Olaciregui, Nagore, Kivirikko, Sirpa, Lavarino, Cinzia, Mero, Inger-Lise, Michiels, Rodolphe, Pisaneschi, Elisa, Schönewolf-Greulich, Bitten, Wieland, Ilse, Zenker, Martin, Vikkula, Miikka

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Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA von Revencu, Nicole, Eijkelenboom, Astrid, Bracquemart, Claire, Alhopuro, Pia, Armstrong, Judith, Baselga, Eulalia, Cesario, Claudia, Dentici, Maria Lisa, Eyries, Melanie, Frisk, Sofia, Karstensen, Helena Gásdal, Gene-Olaciregui, Nagore, Kivirikko, Sirpa, Lavarino, Cinzia, Mero, Inger-Lise, Michiels, Rodolphe, Pisaneschi, Elisa, Schönewolf-Greulich, Bitten, Wieland, Ilse, Zenker, Martin, Vikkula, Miikka

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Improvement of synaptic plasticity and cognitive function in RASopathies-a monocentre, randomized, double-blind, parallel-group, placebo-controlled, cross-over clinical trial (SynC... von Jung, Nikolai H, Egert-Schwender, Silvia, Schossow, Beate, Kehl, Victoria, Wahlländer, Ute, Brich, Louisa, Janke, Viktoria, Blankenstein, Christiane, Zenker, Martin, Mall, Volker

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Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1 von Uludağ Alkaya, Dilek, Lissewski, Christina, Yeşil, Gözde, Zenker, Martin, Tüysüz, Beyhan

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bFGF-mediated pluripotency maintenance in human induced pluripotent stem cells is associated with NRAS-MAPK signaling von Haghighi, Fereshteh, Dahlmann, Julia, Nakhaei-Rad, Saeideh, Lang, Alexander, Kutschka, Ingo, Zenker, Martin, Kensah, George, Piekorz, Roland P, Ahmadian, Mohammad Reza

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