Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Lucas Wahl"'
Autor:
Lucas Wahl, Arun Karim, Amy R. Hassett, Max van der Doe, Stephanie Dijkhuizen, Aleksandra Badura
Publikováno v:
Biological Psychiatry Global Open Science, Vol 4, Iss 6, Pp 100366- (2024)
Background: Current phenotyping approaches for murine autism models often focus on one selected behavioral feature, making the translation onto a spectrum of autistic characteristics in humans challenging. Furthermore, sex and environmental factors a
Externí odkaz:
https://doaj.org/article/2cecd1b0a7fa473383f1e12ccdec50fb
Autor:
Ines Serra, Olivia R. Manusama, Fabian M.P. Kaiser, Izi Izumi Floriano, Lucas Wahl, Christian van der Zalm, Hanna IJspeert, P. Martin van Hagen, Nico J.M. van Beveren, Sandra M. Arend, Klaus Okkenhaug, Johan J.M. Pel, Virgil A.S.H. Dalm, Aleksandra Badura
Publikováno v:
Brain, Behavior, & Immunity - Health, Vol 18, Iss , Pp 100377- (2021)
The phosphoinositide-3-kinase (PI3K) family plays a major role in cell signaling and is predominant in leukocytes. Gain-of-function (GOF) mutations in the PIK3CD gene lead to the development of activated PI3Kδ syndrome (APDS), a rare primary immunod
Externí odkaz:
https://doaj.org/article/27d8b652350244c4b767f51c4c9d81e3
Autor:
Fabian M.P. Kaiser, Sarah Gruenbacher, Maria Roa Oyaga, Enzo Nio, Markus Jaritz, Qiong Sun, Wietske van der Zwaag, Emanuel Kreidl, Lydia M. Zopf, Virgil A.S.H. Dalm, Johan Pel, Carolin Gaiser, Rick van der Vliet, Lucas Wahl, André Rietman, Louisa Hill, Ines Leca, Gertjan Driessen, Charlie Laffeber, Alice Brooks, Peter D. Katsikis, Joyce H.G. Lebbink, Kikuë Tachibana, Mirjam van der Burg, Chris I. De Zeeuw, Aleksandra Badura, Meinrad Busslinger
Publikováno v:
Journal of Experimental Medicine. 220
Autor:
Fabian M.P. Kaiser, Sarah Gruenbacher, Maria Roa Oyaga, Enzo Nio, Markus Jaritz, Qiong Sun, Wietske van der Zwaag, Emanuel Kreidl, Lydia M. Zopf, Virgil A.S.H. Dalm, Johan Pel, Carolin Gaiser, Rick van der Vliet, Lucas Wahl, André Rietman, Louisa Hill, Ines Leca, Gertjan Driessen, Charlie Laffeber, Alice Brooks, Peter D. Katsikis, Joyce H.G. Lebbink, Kikuë Tachibana, Mirjam van der Burg, Chris I. De Zeeuw, Aleksandra Badura, Meinrad Busslinger
Publikováno v:
Journal of Experimental Medicine, 219(9). ROCKEFELLER UNIV PRESS
Journal of Experimental Medicine, 219(9). Rockefeller University Press
Journal of Experimental Medicine, 219(9):e20220498. Rockefeller University Press
Journal of Experimental Medicine, 219(9). Rockefeller University Press
Journal of Experimental Medicine, 219(9):e20220498. Rockefeller University Press
The genetic causes of primary antibody deficiencies and autism spectrum disorder (ASD) are largely unknown. Here, we report a patient with hypogammaglobulinemia and ASD who carries biallelic mutations in the transcription factor PAX5. A patient-speci
Autor:
Sandra M. Arend, Izi Izumi Floriano, P. Martin van Hagen, Aleksandra Badura, Ines Serra, Johan J.M. Pel, Olivia R. Manusama, Virgil A. S. H. Dalm, Fabian M.P. Kaiser, Christian van der Zalm, Klaus Okkenhaug, Nico J.M. van Beveren, Hanna IJspeert, Lucas Wahl
Publikováno v:
Brain, Behavior, & Immunity-Health, Vol 18, Iss, Pp 100377-(2021)
Brain, behavior, & immunity-health, 18:100377. Elsevier Inc.
Brain, Behavior, & Immunity-Health
Brain, behavior, & immunity-health, 18:100377. Elsevier Inc.
Brain, Behavior, & Immunity-Health
The phosphoinositide-3-kinase (PI3K) family plays a major role in cell signalling and is predominant in leukocytes. Gain-of-function (GOF) mutations in the PIK3CD gene lead to the development of activated PI3Kδ syndrome (APDS), a rare primary immuno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef066d6af7eda61a9ddca19fb022ef35
Publikováno v:
As Ciências Exatas e da Terra no Século XXI
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dbe29b480f6e5f6aca9feba5919b7004
https://doi.org/10.22533/at.ed.51419240519
https://doi.org/10.22533/at.ed.51419240519