Zobrazeno 1 - 10
of 256
pro vyhledávání: '"Katrin, Neumann"'
Autor:
Elisa Zanfrini, Manuj Bandral, Luka Jarc, Maria Alejandra Ramirez-Torres, Daniela Pezzolla, Vida Kufrin, Eva Rodriguez-Aznar, Ana Karen Mojica Avila, Christian Cohrs, Stephan Speier, Katrin Neumann, Anthony Gavalas
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-16 (2024)
Abstract The significant advances in the differentiation of human pluripotent stem (hPS) cells into pancreatic endocrine cells, including functional β-cells, have been based on a detailed understanding of the underlying developmental mechanisms. How
Externí odkaz:
https://doaj.org/article/29312b1f86b841f09af33ee6d30fc804
Autor:
Selina Wachtendorf, Fitriasari Jonin, Aaron Ochel, Fabian Heinrich, Astrid M. Westendorf, Gisa Tiegs, Katrin Neumann
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionThe alarmin IL-33 has been implicated in the pathology of immune-mediated liver diseases. IL-33 activates regulatory T cells (Tregs) and type 2 innate lymphoid cells (ILC2s) expressing the IL-33 receptor ST2. We have previously shown that
Externí odkaz:
https://doaj.org/article/fa6213fcf2124cacb771a89ecf01098d
Autor:
Luka Jarc, Manuj Bandral, Elisa Zanfrini, Mathias Lesche, Vida Kufrin, Raquel Sendra, Daniela Pezzolla, Ioannis Giannios, Shahryar Khattak, Katrin Neumann, Barbara Ludwig, Anthony Gavalas
Publikováno v:
eLife, Vol 12 (2024)
The unlimited expansion of human progenitor cells in vitro could unlock many prospects for regenerative medicine. However, it remains an important challenge as it requires the decoupling of the mechanisms supporting progenitor self-renewal and expans
Externí odkaz:
https://doaj.org/article/8328405f4f5f486284686d745152db17
Autor:
Leila Homami Totmaj, Arash Rasi, Katrin Neumann, Sepideh Pirouzi, Kammaledin Alizadeh, Hermann Behling
Publikováno v:
Acta Palaeobotanica, Vol 63, Iss 1, Pp 100-117 (2023)
We studied the modern pollen rain in two different landscapes from Hyrcanian lowland forests up to the slopes of the Alborz Mountains in Gilan province for the first time. Pollen traps were installed for one year and moss samples were collected along
Externí odkaz:
https://doaj.org/article/894e5f7c081f4fc5ae27456a20955f32
Autor:
Barbara Vona, Sabrina Regele, Aboulfazl Rad, Nicola Strenzke, Justin A. Pater, Katrin Neumann, Marc Sturm, Tobias B. Haack, Antoinette G. Am Zehnhoff-Dinnesen
Publikováno v:
Frontiers in Genetics, Vol 14 (2023)
Genetic heterogeneity makes it difficult to identify the causal genes for hearing loss. Studies from previous decades have mapped numerous genetic loci, providing critical supporting evidence for gene discovery studies. Despite widespread sequencing
Externí odkaz:
https://doaj.org/article/4ddb5e946428434ea3e9e48d7fcebbaf
Autor:
Philipp Gude, Thomas P. Weber, Stefan Dazert, Norbert Teig, Philipp Mathmann, Adrian I. Georgevici, Katrin Neumann
Publikováno v:
BMC Pediatrics, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background During pediatric general anesthesia (GA) and sedation, clinicians aim to maintain physiological parameters within normal ranges. Accordingly, regional cerebral oxygen saturation (rScO2) should not drop below preintervention baseli
Externí odkaz:
https://doaj.org/article/9ff01ea6a88447d58d7cd150367737c2
Autor:
Werner Brannath, Anja Neumann, Katharina Schwarze, Philipp Mathmann, Karolin Schäfer, Phillip-Hendrik Höhne, Sibel Altin, Lukas Prein, Awa Naghipour, Susanna Marie Zielonkowski, Susanne Wasmuth, Oliver Kanaan, Antoinette am Zehnhoff-Dinnesen, Anna Sophia Schwalen, Anna Schotenröhr, Martin Scharpenberg, Sarah Schlierenkamp, Nicole Stuhrmann, Ruth Lang-Roth, Muhittin Demir, Sandra Diekmann, Corinna Gietmann, Katrin Neumann
Publikováno v:
BMJ Open, Vol 13, Iss 5 (2023)
Introduction Individuals with intellectual disabilities (ID) often suffer from hearing loss, in most cases undiagnosed or inappropriately treated. The implementation of a programme of systematic hearing screening, diagnostics, therapy initiation or a
Externí odkaz:
https://doaj.org/article/857fc87e529b401aac882413f4b84fa4
Autor:
Carina Lüke, Christina Kauschke, Andrea Dohmen, Andrea Haid, Christina Leitinger, Claudia Männel, Tanja Penz, Steffi Sachse, Wiebke Scharff Rethfeldt, Julia Spranger, Susanne Vogt, Marlen Niederberger, Katrin Neumann
Publikováno v:
PLoS ONE, Vol 18, Iss 11, p e0293736 (2023)
In recent years, there have been intense international discussions about the definition and terminology of language disorders in childhood, such as those sparked by the publications of the CATALISE consortium. To address this ongoing debate, a Delphi
Externí odkaz:
https://doaj.org/article/23f28167544244f0a464dcc0224c3ac7
Autor:
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, Kerstin Engel, Shahryar Khattak, Katrin Neumann, Min Ae Lee-Kirsch
Publikováno v:
Stem Cell Research, Vol 64, Iss , Pp 102895- (2022)
Mutations in TREX1, encoding three prime repair exonuclease 1, cause Aicardi-Goutières syndrome (AGS) 1, an autoinflammatory disease characterized by neurodegeneration and constitutive activation of the antiviral cytokine type I interferon. Here, we
Externí odkaz:
https://doaj.org/article/fcb43ec64a754d08a33bdb8b8bbe2e94
Autor:
Vanessa Hänchen, Stefanie Kretschmer, Christine Wolf, Kerstin Engel, Shahryar Khattak, Katrin Neumann, Min Ae Lee-Kirsch
Publikováno v:
Stem Cell Research, Vol 64, Iss , Pp 102912- (2022)
Mutations in SAMHD1, encoding SAM and HD domain-containing protein 1, cause Aicardi-Goutières syndrome (AGS) 5, an infancy-onset autoinflammatory disease characterized by neurodegeneration and chronic activation of type I interferon. Here, we report
Externí odkaz:
https://doaj.org/article/3586418d6aa5442a809b8b1bdae9854d