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Journal Article
Bartsch, Yannic C., Eschweiler, Simon ORCID: 0000-0002-6379-8588, Leliavski, Alexei, Lunding, Hanna B., Wagt, Sander, Petry, Janina, Lilienthal, Gina-Maria, Rahmoller, Johann, de Haan, Noortje, Holscher, Alexandra, Erapaneedi, Raghu, Giannou, Anastasios D., Aly, Lilian, Sato, Ryota, de Neef, Louise A., Winkler, Andre, Braumann, Dominique, Hobusch, Juliane, Kuhnigk, Kyra, Kremer, Vanessa, Steinhaus, Moritz, Blanchard, Veronique, Gemoll, Timo, Habermann, Jens K., Collin, Mattias
ORCID: 0000-0002-6166-7410, Salinas, Gabriela, Manz, Rudolf A., Fukuyama, Hidehiro
ORCID: 0000-0002-6457-0630, Korn, Thomas, Waisman, Ari, Yogev, Nir, Huber, Samuel, Rabe, Bjorn, Rose-John, Stefan, Busch, Hauke
ORCID: 0000-0003-4763-4521, Berberich-Siebelt, Friederike, Holscher, Christoph, Wuhrer, Manfred
ORCID: 0000-0002-0814-4995 and Ehlers, Marc
ORCID: 0000-0002-5383-8603
(2020).
IgG Fc sialylation is regulated during the germinal center reaction following immunization with different adjuvants.
J. Allergy Clin. Immunol., 146 (3).
S. 652 - 678.
NEW YORK:
MOSBY-ELSEVIER.
ISSN 1097-6825
Hanses, Ulrich, Kleinsorge, Mandy, Roos, Lennart, Yigit, Goekhan, Li, Yun, Barbarics, Boris, El-Battrawy, Ibrahim, Lan, Huan, Tiburcy, Malte, Hindmarsh, Robin, Lenz, Christof, Salinas, Gabriela, Diecke, Sebastian, Mueller, Christian, Adham, Ibrahim, Altmueller, Janine, Nuernberg, Peter, Paul, Thomas, Zimmermann, Wolfram-Hubertus, Hasenfuss, Gerd, Wollnik, Bernd and Cyganek, Lukas ORCID: 0000-0001-9120-1382
(2020).
Intronic CRISPR Repair in a Preclinical Model of Noonan Syndrome-Associated Cardiomyopathy.
Circulation, 142 (11).
S. 1059 - 1077.
PHILADELPHIA:
LIPPINCOTT WILLIAMS & WILKINS.
ISSN 1524-4539
Schmidt, Julia ORCID: 0000-0002-5942-2924, Goergens, Jonas, Pochechueva, Tatiana, Kotter, Annika, Schwenzer, Niko, Sitte, Maren, Werner, Gesa, Altmueller, Janine, Thiele, Holger, Nuernberg, Peter, Isensee, Joerg, Li, Yun, Mueller, Christian, Leube, Barbara, Reinhardt, H. Christian, Hucho, Tim
ORCID: 0000-0002-4147-9308, Salinas, Gabriela, Helm, Mark, Jachimowicz, Ron D., Wieczorek, Dagmar, Kohl, Tobias, Lehnart, Stephan E., Yigit, Goekhan and Wollnik, Bernd
ORCID: 0000-0003-2589-0364
(2021).
Biallelic variants in YRDC cause a developmental disorder with progeroid features.
Hum. Genet., 140 (12).
S. 1679 - 1694.
NEW YORK:
SPRINGER.
ISSN 1432-1203
Ufartes, Roser, Berger, Hanna, Till, Katharina, Salinas, Gabriela, Sturm, Marc ORCID: 0000-0002-6552-8362, Altmueller, Janine, Nuernberg, Peter, Thiele, Holger
ORCID: 0000-0002-0169-998X, Funke, Rudolf, Apeshiotis, Neophytos, Langen, Hendrik, Wollnik, Bernd, Borchers, Annette and Pauli, Silke
(2020).
De novo mutations in FBRSL1 cause a novel recognizable malformation and intellectual disability syndrome.
Hum. Genet., 139 (11).
S. 1363 - 1380.
NEW YORK:
SPRINGER.
ISSN 1432-1203