![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 2
2022
Harapas, Cassandra R.; Robinson, Kim S.; Lay, Kenneth; Wong, Jasmine; Traspas, Ricardo Moreno; Nabavizadeh, Nasrin; Rass-Rothschild, Annick; Boisson, Bertrand; Drutman, Scott B.; Laohamonthonkul, Pawat; Bonner, Devon; Xiong, Jingwei Rachel; Gorrell, Mark D.; Davidson, Sophia; Yu, Chien-Hsiung; Fleming, Mark D.; Gudera, Jonas; Stein, Jerry; Ben-Harosh, Miriam; Groopman, Emily; Shimamura, Akiko; Tamary, Hannah; Kayserili, Hulya; Hatipoglu, Nevin; Casanova, Jean-Laurent; Bernstein, Jonathan A.; Zhong, Franklin L.; Masters, Seth L. und Reversade, Bruno
(2022):
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling.
In: Science Immunology, Bd. 7, Nr. 75, eabi4611
2019
Ziaei, Amin; Xu, Xiaohong; Dehghani, Leila; Bonnard, Carine; Zellner, Andreas; Ng, Alvin Yu Jin; Tohari, Sumanty; Venkatesh, Byrappa; Haffner, Christof; Reversade, Bruno; Shaygannejad, Vahid und Pouladi, Mahmoud A.
(2019):
Novel mutation in HTRA1 in a family with diffuse white matter lesions and inflammatory features.
In: Neurology-Genetics, Bd. 5, Nr. 4, UNSP e345