1. Hildebrandt, Friedhelm 美国 Harvard Medical School 2015美国医学院院士 Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney ..
2. Anderson, Kathryn V. 美国 SLOAN KETTERING Institute 2002美国科学院院士 Spinocerebellar ataxia type 11-associated alleles of Ttbk2 dominantly interfere with ciliogenesis an..
3. 徐峰 中国 西安交通大学 Matrix Nonlinear Viscoelasticity Regulates Skeletal Myogenesis through MRTF Nuclear Localization and..
4. Jeremy W,Tomlinson 英国 University of Oxford Bardet-Biedl syndrome: A focus on genetics, mechanisms and metabolic dysfunction
5. 马旭 中国 国家计划生育委员会 所长 Novel compound heterozygous variants in ARL13B lead to Joubert syndrome
6. 周军 中国 南开大学 Peripheral and central control of obesity by primary cilia
7. 陳基湘 中国 香港中文大学 Convergent dysbiosis of upper aerodigestive microbiota between patients with esophageal and oral cav..
8. Petra,Van Damme 比利时 University of Ghent Proximity Mapping of CCP6 Reveals Its Association with Centrosome Organization and Cilium Assembly
9. Patrice,Codogno 法国 University of PARIS 05 Autophagy and the primary cilium in cell metabolism: What's upstream?
10. Roberto,Vettor 意大利 University of PADUA ASCs and their role in obesity and metabolic diseases
11. Leonid L,Moroz 美国 University of Florida Evolution of glutamatergic signaling and synapses
12. Tim,Stearns 美国 Stanford University Hedgehog signaling and the primary cilium: implications for spatial and temporal constraints on sign..
13. Laurence,Pelletier 加拿大 University of Toronto Charting the complex composite nature of centrosomes, primary cilia and centriolar satellites
14. Derya,Unutmaz 美国 New York University Whole-genome screen identifies diverse pathways that negatively regulate ciliogenesis
15. Francisco J,Esteva 美国 New York University Whole-genome screen identifies diverse pathways that negatively regulate ciliogenesis
16. Brian David,Dynlacht 美国 New York University Whole-genome screen identifies diverse pathways that negatively regulate ciliogenesis
17. Russell C,Dale 澳大利亚 University of Sydney Mutations in the exocyst component EXOC2 cause severe defects in human brain development
18. Marcel E,Dinger 澳大利亚 University of New South Wales Mutations in the exocyst component EXOC2 cause severe defects in human brain development
19. Renzo,Guerrini 意大利 University of Florence Mutations in the exocyst component EXOC2 cause severe defects in human brain development
20. Ian G,Macara 美国 VANDERBILT University Mutations in the exocyst component EXOC2 cause severe defects in human brain development