Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Katrin Hübscher"'
Autor:
Christina Nöltner, Alla Bulashevska, Katrin Hübscher, Hanna Haberstroh, Bodo Grimbacher, Michele Proietti
Publikováno v:
Journal of Clinical Immunology.
Objective Common variable immunodeficiency (CVID) is the most common clinically relevant entity of inborn errors of immunity. In these patients, an altered gut microbiome composition with reduced diversity has been described. We sought to investigate
Autor:
Peter Lunt, Mary Buchta, Laura Gámez-Díaz, Roya Sherkat, Pere Soler-Palacín, Desa Lilic, Christoph Klein, Turkan Patiroglu, Fulya Bektas Kut, Natalie Frede, Sara Sebnem Kilic, Katrin Hübscher, T. Prescott Atkinson, Jessica Rojas-Restrepo, Zahra Chavoshzadeh, Zineb Jouhadi, Ekrem Unal, Ömür Ardenyz, Moudjahed Saleh Al-Ddafari, Bodo Grimbacher, Niten Makwana, Fatih Celmeli, Nermeen Galal, Horst von Bernuth, Mehdi Adeli, Rainer Doffinger, Ilija Kirovski, Anne-Sophie Korganow, Margo L. Whiteford, Ayşe Akman Karakaş, Michele Proietti, Shiva Saghafi, V. Wahn, Andrés Caballero Garcia de Oteyza, Helen Rees, Robin Kobbe, Tuba Turul Özgür, Ana Berta Sousa, Juan Carlos Aldave-Becerra, Ayse Metin, Suranjith L. Seneviratne
Publikováno v:
Journal of Clinical Immunology
Hyper-IgE syndromes and chronic mucocutaneous candidiasis constitute rare primary immunodeficiency syndromes with an overlapping clinical phenotype. In recent years, a growing number of underlying genetic defects have been identified. To characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::254537c26d9bb02ee348c67f73dcaeb4
https://avesis.erciyes.edu.tr/publication/details/c6046c8d-ff93-4b70-862c-47a8222980b9/oai
https://avesis.erciyes.edu.tr/publication/details/c6046c8d-ff93-4b70-862c-47a8222980b9/oai
Autor:
Katrin Hübscher, Eirini Trompouki, Danilo Guerini, Roger Geiger, Ole K. Greiner-Tollersrud, Honnappa Srinivas, Sebastian Baasch, Eva Bartok, Hilmar Ebersbach, Salvatore Raieli, Jan Ole Olsen, Martine Marchant, Bodo Grimbacher, Vincent Boehler, Georg Kochs, Aikaterini Polyzou, Regina Link, Cristian R. Smulski, Gunther Hartmann, Máté Krausz, Michele Proietti, Dieter Staab, Maximilian Seidl, Johanna Schepp, Philipp Henneke, Max Warncke
Deficiency of adenosine deaminase 2 (DADA2) is a severe, congenital syndrome, which manifests with hematologic, immunologic and inflammatory pathologies. DADA2 is caused by biallelic mutations in ADA2, but the function of ADA2, and the mechanistic li
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::26a38fc6bbd8be9ab969f0fdbf4f90d2
https://doi.org/10.1101/2020.06.21.162990
https://doi.org/10.1101/2020.06.21.162990
Autor:
Sigune Goldacker, Jessica Rojas Restrepo, Michele Proietti, Vassilios Lougaris, Johanna Schepp, Ignacio Uriarte, Mary Buchta, Jana Pachlopnik Schmid, Katrin Hübscher, Andrea Duppenthaler, Klaus Warnatz, Michael S. Hershfield, Bodo Grimbacher, Susan J. Kelly, Natalie Frede
Publikováno v:
Arthritis & Rheumatology. 69:1689-1700
Objective: We aimed to test the relevance of Deficiency of Adenosine Deaminase 2 in patients with antibody deficiency and describe the clinical picture of the disease in adulthood. Methods: We screened for DADA2 in a cohort of 181 patients with antib
Autor:
Erik-Oliver Glocker, Jan Rohr, Nadia Saleh, Mehrnaz Mesdaghi, Christian Klemann, Robin Kobbe, Natalie Frede, Renate Abt, Peter Hasselblatt, Sigune Goldacker, Ronnie Chee, Naghi Dara, Mary Buchta, Florian Brinkert, Alla Bulashevska, Aisha Elmarsafy, Birol Öztürk, Paul Thankam, Nermeen Galal, Patrick Gerner, Jutta Hammermann, Mahboubeh M. Kharaghani, Katrin Hübscher, Gunda Ruzaike, Jutte Van Der Werff Ten Bosch, Lida Atarod, Safa Baris, Suranjith L. Seneviratne, Ana Cordeiro, Daniel Kotlarz, Sebastian Zeissig, Horst von Bernuth, Britt-Sabina Petersen, Yvonne Zeissig, Milos Jesenak, Gregor Dückers, Andre Franke, João Farela Neves, Sara Sebnem Kilic, Sally G. Mitton, Dietrich August, Zuzana Havlíčeková, Neslihan Edeer Karaca, T. Ronan Leahy, Bodo Grimbacher, Christoph Klein, Hemant Bhavsar, Moudjahed Saleh Al-Ddafari, Ebru Senol, Carsten Speckmann, Jessica L.R. Restrepo, Daniel Tegtmeyer, Ayca Kiykim, Martin W. Laass, Luis F. Pereira, Elif Karakoc-Aydiner
"Çalışmada 57 yazar bulunmaktadır. Bu yazarlardan sadece Bursa Uludağ Üniversitesi mensuplarının girişleri yapılmıştır.” Background: In contrast to adult-onset inflammatory bowel disease (IBD), where many genetic loci have been shown t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1410e31a1932bf36de7f66bbd5614be0
https://hdl.handle.net/20.500.14017/226c4e28-a237-4494-bfb9-0233866baed5
https://hdl.handle.net/20.500.14017/226c4e28-a237-4494-bfb9-0233866baed5
Publikováno v:
Development. 140:93-106
Precise spatiotemporal control of axon guidance factor expression is a prerequisite for formation of functional neuronal connections. Although Netrin/Dcc- and Robo/Slit-mediated attractive and repulsive guidance of commissural axons have been extensi