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The EMBO Journal|November 26, 2005
Phosphorylation by casein kinase 2 induces PACS-1 binding of nephrocystin and targeting to ciliaBernhard Schermer, Katja Höpker, Heymut Omran, et al.Pediatric Pulmonology|August 14, 2012
RPGR mutations might cause reduced orientation of respiratory ciliaZuzanna Bukowy-Bieryłło, Ewa Ziętkiewicz, Niki Tomas Loges, et al.European Journal of Medical Genetics|January 24, 2021
Recurrent necrotizing cellulitis, multi-organ autoimmune disease and humoral immunodeficiency due to a novel NFKB1 frameshift mutationAstrid Bergbreiter, Teresa Jaeger, Antje Karle, et al.Nature Genetics|July 23, 2003
Mutations in a novel gene, NPHP3, cause adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosisHeike Olbrich, Manfred Fliegauf, Julia Hoefele, et al.Human Mutation|November 21, 2007
Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutationsGeorg C Schwabe, Katrin Hoffmann, Niki Tomas Loges, et al.American Journal of Respiratory and Critical Care Medicine|April 22, 2006
DNAH5 mutations are a common cause of primary ciliary dyskinesia with outer dynein arm defectsNada Hornef, Heike Olbrich, Judit Horvath, et al.American Journal of Human Genetics|October 28, 2008
DNAI2 mutations cause primary ciliary dyskinesia with defects in the outer dynein armNiki Tomas Loges, Heike Olbrich, Lale Fenske, et al.Nature|December 5, 2008
Ktu/PF13 is required for cytoplasmic pre-assembly of axonemal dyneinsHeymut Omran, Daisuke Kobayashi, Heike Olbrich, et al.Nature Genetics|December 7, 2010
The coiled-coil domain containing protein CCDC40 is essential for motile cilia function and left-right axis formationAnita Becker-Heck, Irene E Zohn, Noriko Okabe, et al.Frontiers in Immunology|April 4, 2019
Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in <i>NFKB2</i>Christian Klemann, Nadezhda Camacho-Ordonez, Linlin Yang, et al.Pageof 7