Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-Inhibition
Andelfinger, Gregor, Marquis, Christopher, Raboisson, Marie-Josée, Théoret, Yves, Waldmüller, Stephan, Wiegand, Gesa, Gelb, Bruce D., Zenker, Martin, Delrue, Marie-Ange, Hofbeck, Michael
Published in Journal of the American College of Cardiology (07.05.2019)
Published in Journal of the American College of Cardiology (07.05.2019)
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Journal Article
ClinGen’s RASopathy Expert Panel consensus methods for variant interpretation
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
Published in Genetics in medicine (01.11.2018)
Published in Genetics in medicine (01.11.2018)
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Journal Article
Syndromic forms of congenital hyperinsulinism
Zenker, Martin, Mohnike, Klaus, Palm, Katja
Published in Frontiers in endocrinology (Lausanne) (30.03.2023)
Published in Frontiers in endocrinology (Lausanne) (30.03.2023)
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Journal Article
Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signaling
Motta, Marialetizia, Fidan, Miray, Bellacchio, Emanuele, Pantaleoni, Francesca, Schneider-Heieck, Konstantin, Coppola, Simona, Borck, Guntram, Salviati, Leonardo, Zenker, Martin, Cirstea, Ion C, Tartaglia, Marco
Published in Human molecular genetics (15.03.2019)
Published in Human molecular genetics (15.03.2019)
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Journal Article
Microbial composition of tumorous and adjacent gastric tissue is associated with prognosis of gastric cancer
Lehr, Konrad, Nikitina, Darja, Vilchez-Vargas, Ramiro, Steponaitiene, Ruta, Thon, Cosima, Skieceviciene, Jurgita, Schanze, Denny, Zenker, Martin, Malfertheiner, Peter, Kupcinskas, Juozas, Link, Alexander
Published in Scientific reports (21.03.2023)
Published in Scientific reports (21.03.2023)
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Journal Article
Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood
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.
Published in Nature communications (23.09.2023)
Published in Nature communications (23.09.2023)
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Journal Article
Food‐Derived Xeno‐microRNAs: Influence of Diet and Detectability in Gastrointestinal Tract—Proof‐of‐Principle Study
Link, Jastin, Thon, Cosima, Schanze, Denny, Steponaitiene, Ruta, Kupcinskas, Juozas, Zenker, Martin, Canbay, Ali, Malfertheiner, Peter, Link, Alexander
Published in Molecular nutrition & food research (01.01.2019)
Published in Molecular nutrition & food research (01.01.2019)
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Journal Article
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes
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
Published in Nature genetics (01.11.2010)
Published in Nature genetics (01.11.2010)
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Editorial: Endocrine aspects of Noonan syndrome and related syndromes
Radetti, Giorgio, Edouard, Thomas, Mazzanti, Laura, Tartaglia, Marco, Zenker, Martin
Published in Frontiers in endocrinology (Lausanne) (05.01.2023)
Published in Frontiers in endocrinology (Lausanne) (05.01.2023)
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Journal Article
Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study
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
Published in Scientific reports (03.07.2024)
Published in Scientific reports (03.07.2024)
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Journal Article
Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2)
Hinkes, Bernward G, Mucha, Bettina, Vlangos, Christopher N, Gbadegesin, Rasheed, Liu, Jinhong, Hasselbacher, Katrin, Hangan, Daniela, Ozaltin, Fatih, Zenker, Martin, Hildebrandt, Friedhelm
Published in Pediatrics (Evanston) (01.04.2007)
Published in Pediatrics (Evanston) (01.04.2007)
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Journal Article
Profiling of the Bacterial Microbiota along the Murine Alimentary Tract
Vilchez-Vargas, Ramiro, Salm, Franz, Znalesniak, Eva B, Haupenthal, Katharina, Schanze, Denny, Zenker, Martin, Link, Alexander, Hoffmann, Werner
Published in International journal of molecular sciences (04.02.2022)
Published in International journal of molecular sciences (04.02.2022)
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Journal Article
Expanding the clinical phenotype of RASopathies in 38 Turkish patients, including the rare LZTR1, RAF1, RIT1 variants, and large deletion in NF1
Uludağ Alkaya, Dilek, Lissewski, Christina, Yeşil, Gözde, Zenker, Martin, Tüysüz, Beyhan
Published in American journal of medical genetics. Part A (01.12.2021)
Published in American journal of medical genetics. Part A (01.12.2021)
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Journal Article
Variants in nuclear factor I genes influence growth and development
Zenker, Martin, Bunt, Jens, Schanze, Ina, Schanze, Denny, Piper, Michael, Priolo, Manuela, Gerkes, Erica H., Gronostajski, Richard M., Richards, Linda J., Vogt, Julie, Wessels, Marja W., Hennekam, Raoul C.
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.12.2019)
Published in American journal of medical genetics. Part C, Seminars in medical genetics (01.12.2019)
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Journal Article
Adams–Oliver syndrome caused by mutations of the EOGT gene
Schröder, Kim C., Duman, Duygu, Tekin, Mustafa, Schanze, Denny, Sukalo, Maja, Meester, Josephina, Wuyts, Wim, Zenker, Martin
Published in American journal of medical genetics. Part A (01.11.2019)
Published in American journal of medical genetics. Part A (01.11.2019)
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Journal Article
Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature
Hauer, Nadine N., Sticht, Heinrich, Boppudi, Sangamitra, Büttner, Christian, Kraus, Cornelia, Trautmann, Udo, Zenker, Martin, Zweier, Christiane, Wiesener, Antje, Jamra, Rami Abou, Wieczorek, Dagmar, Kelkel, Jaqueline, Jung, Anna-Maria, Uebe, Steffen, Ekici, Arif. B, Rohrer, Tilman, Reis, André, Dörr, Helmuth-Günther, Thiel, Christian T.
Published in Scientific reports (22.09.2017)
Published in Scientific reports (22.09.2017)
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Journal Article
RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1
Meyer Zum Büschenfelde, Uta, Brandenstein, Laura Isabel, von Elsner, Leonie, Flato, Kristina, Holling, Tess, Zenker, Martin, Rosenberger, Georg, Kutsche, Kerstin
Published in PLoS genetics (07.05.2018)
Published in PLoS genetics (07.05.2018)
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