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Trueb, Beat; Zhuang, Lei; Keller, Irene; von Köckritz, Leona; Kuchen, Stefan; Dufour, Jean-François; Villiger, Peter (2021). Coincidence of NOD2-Associated Autoinflammatory Disease (Yao Syndrome) and HCV Infection With Fatal Consequences: Interaction Between Genes and Environment. Journal of clinical rheumatology, 27(8S), S592-S594. Wolters Kluwer Health 10.1097/RHU.0000000000000963
Zhuang, Lei; Vogel, Monique; Villiger, Peter M.; Trueb, Beat (2020). Dissecting the Interaction of FGF8 with Receptor FGFRL1. Biomolecules, 10(10) MDPI 10.3390/biom10101399
Trueb, Beat; Zhuang, Lei; Villiger, Peter M. (2020). A Novel Mutation in the IL6R Gene Identified in a Family with Asthma Patients. Genetic testing and molecular biomarkers, 24(10), pp. 658-664. Mary Ann Liebert 10.1089/gtmb.2020.0081
Gerber, Simon D; Beauchamp, Philippe; Zhuang, Lei; Villiger, Peter M.; Trueb, Beat (2020). Functional domains of the FgfrL1 receptor. Developmental biology, 461(1), pp. 43-54. Elsevier 10.1016/j.ydbio.2020.01.003
Zhuang, Lei; Trueb, Beat (2017). Evolution of the fusogenic activity of the receptor FGFRL1. Archives of biochemistry and biophysics, 625-626, pp. 54-64. Elsevier 10.1016/j.abb.2017.06.002
Zhuang, Lei; Adler, Sabine; Aeberli, Daniel; Villiger, Peter; Trueb, Beat (2017). Identification of a MAFB mutation in a patient with multicentric carpotarsal osteolysis. Swiss medical weekly, 147(4344), w14529. EMH Schweizerischer Ärzteverlag 10.4414/smw.2017.14529
Zhuang, Lei; Steinberg, Florian; Trueb, Beat (2016). Receptor FGFRL1 acts as a tumor suppressor in nude mice when overexpressed in HEK 293 Tet-On cells. Oncology letters, 12(6), pp. 4524-4530. Spandidos Publications 10.3892/ol.2016.5245
Yang, Xiaochen; Steinberg, Florian; Zhuang, Lei; Bessey, Ralph; Trueb, Beat (2016). Receptor FGFRL1 does not promote cell proliferation but induces cell adhesion. International journal of molecular medicine, 38(1), pp. 30-38. Spandidos Publications 10.3892/ijmm.2016.2601
Zhuang, Lei; Gerber, Simon D; Kuchen, Stefan; Villiger, Peter; Trueb, Beat (2016). Deletion of exon 8 from the EXT1 gene causes multiple osteochondromas (MO) in a family with three affected members. SpringerPlus, 5(71), p. 71. Springer 10.1186/s40064-016-1695-6
Zhuang, Lei; Pandey, Amit Vikram; Villiger, Peter; Trueb, Beat (2015). Cell-cell fusion induced by the Ig3 domain of receptor FGFRL1 in CHO cells. Biochimica et biophysica acta - molecular cell research, 1853(10 Pt A), pp. 2273-2285. Elsevier 10.1016/j.bbamcr.2015.05.027
Zhuang, Lei; Bluteau, Gilles; Trueb, Beat (2015). Phylogenetic analysis of receptor FgfrL1 shows divergence of the C-terminal end in rodents. Comparative biochemistry and physiology. Part B - biochemistry & molecular biology, 186, pp. 43-50. Elsevier 10.1016/j.cbpb.2015.04.009
Amann, Ruth; Wyder, Stefan; Slavotinek, Anne M; Trueb, Beat (2014). The FgfrL1 receptor is required for development of slow muscle fibers. Developmental biology, 394(2), pp. 228-241. Elsevier 10.1016/j.ydbio.2014.08.016
Bluteau, Gilles; Zhuang, Lei; Amann, Ruth; Trueb, Beat (2014). Targeted disruption of the intracellular domain of receptor FgfrL1 in mice. PLoS ONE, 9(8), e105210. Public Library of Science 10.1371/journal.pone.0105210
Amann, Ruth; Trueb, Beat (2013). Evidence that the novel receptor FGFRL1 signals indirectly via FGFR1. International journal of molecular medicine, 32(5), pp. 983-988. Spandidos Publications 10.3892/ijmm.2013.1484
Balmer, Maria L.; Trueb, Beat; Zhuang, Lei; Slack, Emma; Beltraminelli, Helmut; Villiger, Peter Matthias (2013). Splicing defect of CD33 and inflammatory syndrome associated with occult bacterial infection. Journal of allergy and clinical immunology, 132(2), 490-493.e2. Mosby 10.1016/j.jaci.2013.03.027
Trueb, Beat; Amann, Ruth; Gerber, Simon D (2013). Role of FGFRL1 and other FGF signaling proteins in early kidney development. Cellular and molecular life sciences, 70(14), pp. 2505-18. Basel: SP Birkhäuser Verlag Basel 10.1007/s00018-012-1189-9
Gerber, Simon D.; Amann, Ruth; Wyder, Stefan; Trueb, Beat (2012). Comparison of the gene expression profiles from normal and Fgfrl1 deficient mouse kidneys reveals downstream targets of Fgfrl1 signaling. PLoS ONE, 7(3), e33457. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0033457
Trueb, Beat (2011). Biology of FGFRL1, the fifth fibroblast growth factor receptor. Cellular and molecular life sciences, 68(6), pp. 951-64. Basel: SP Birkhäuser Verlag Basel 10.1007/s00018-010-0576-3
LopezJimenez, Nelson; Gerber, Simon; Popovici, Vlad; Mirza, Sonia; Copren, Kirsten; Ta, Linda; Shaw, Gary M; Trueb, Beat; Slavotinek, Anne M (2010). Examination of FGFRL1 as a candidate gene for diaphragmatic defects at chromosome 4p16.3 shows that Fgfrl1 null mice have reduced expression of Tpm3, sarcomere genes and Lrtm1 in the diaphragm. Human genetics, 127(3), pp. 325-36. Berlin: Springer 10.1007/s00439-009-0777-8
Zhuang, Lei; Karotki, Andrei V; Bruecker, Philip; Trueb, Beat (2009). Comparison of the receptor FGFRL1 from sea urchins and humans illustrates evolution of a zinc binding motif in the intracellular domain. BMC biochemistry, 10, p. 33. London: BioMed Central 10.1186/1471-2091-10-33
