These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
252 related articles for article (PubMed ID: 33496382)
1. Aquatic models of human ciliary diseases. Corkins ME; Krneta-Stankic V; Kloc M; Miller RK Genesis; 2021 Feb; 59(1-2):e23410. PubMed ID: 33496382 [TBL] [Abstract][Full Text] [Related]
2. Zebrafish as a Model for Human Ciliopathies. Song Z; Zhang X; Jia S; Yelick PC; Zhao C J Genet Genomics; 2016 Mar; 43(3):107-20. PubMed ID: 27020031 [TBL] [Abstract][Full Text] [Related]
3. Xenopus to the rescue: A model to validate and characterize candidate ciliopathy genes. Rao VG; Kulkarni SS Genesis; 2021 Feb; 59(1-2):e23414. PubMed ID: 33576572 [TBL] [Abstract][Full Text] [Related]
4. Ttc30a affects tubulin modifications in a model for ciliary chondrodysplasia with polycystic kidney disease. Getwan M; Hoppmann A; Schlosser P; Grand K; Song W; Diehl R; Schroda S; Heeg F; Deutsch K; Hildebrandt F; Lausch E; Köttgen A; Lienkamp SS Proc Natl Acad Sci U S A; 2021 Sep; 118(39):. PubMed ID: 34548398 [TBL] [Abstract][Full Text] [Related]
5. Ciliopathy-associated proteins are involved in vesicle distribution in sensory cilia. Li M; He W; Li W; Ou G J Genet Genomics; 2019 May; 46(5):269-271. PubMed ID: 31176629 [No Abstract] [Full Text] [Related]
6. What we can learn from a tadpole about ciliopathies and airway diseases: Using systems biology in Xenopus to study cilia and mucociliary epithelia. Walentek P; Quigley IK Genesis; 2017 Jan; 55(1-2):. PubMed ID: 28095645 [TBL] [Abstract][Full Text] [Related]
7. Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish. Van De Weghe JC; Rusterholz TDS; Latour B; Grout ME; Aldinger KA; Shaheen R; Dempsey JC; Maddirevula S; Cheng YH; Phelps IG; Gesemann M; Goel H; Birk OS; Alanzi T; Rawashdeh R; Khan AO; ; Bamshad MJ; Nickerson DA; Neuhauss SCF; Dobyns WB; Alkuraya FS; Roepman R; Bachmann-Gagescu R; Doherty D Am J Hum Genet; 2017 Jul; 101(1):23-36. PubMed ID: 28625504 [TBL] [Abstract][Full Text] [Related]
9. CiliaMiner: an integrated database for ciliopathy genes and ciliopathies. Turan MG; Orhan ME; Cevik S; Kaplan OI Database (Oxford); 2023 Jul; 2023():. PubMed ID: 37542408 [TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of renal ciliopathies. Barroso-Gil M; Olinger E; Sayer JA Biochem Soc Trans; 2021 Jun; 49(3):1205-1220. PubMed ID: 33960378 [TBL] [Abstract][Full Text] [Related]
11. The nucleoside-diphosphate kinase NME3 associates with nephronophthisis proteins and is required for ciliary function during renal development. Hoff S; Epting D; Falk N; Schroda S; Braun DA; Halbritter J; Hildebrandt F; Kramer-Zucker A; Bergmann C; Walz G; Lienkamp SS J Biol Chem; 2018 Sep; 293(39):15243-15255. PubMed ID: 30111592 [TBL] [Abstract][Full Text] [Related]
12. Xenopus: An Undervalued Model Organism to Study and Model Human Genetic Disease. Blum M; Ott T Cells Tissues Organs; 2018; 205(5-6):303-313. PubMed ID: 30092565 [TBL] [Abstract][Full Text] [Related]
13. c21orf59/kurly Controls Both Cilia Motility and Polarization. Jaffe KM; Grimes DT; Schottenfeld-Roames J; Werner ME; Ku TS; Kim SK; Pelliccia JL; Morante NF; Mitchell BJ; Burdine RD Cell Rep; 2016 Mar; 14(8):1841-9. PubMed ID: 26904945 [TBL] [Abstract][Full Text] [Related]