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.
25. Epb41l5 interacts with Iqcb1 and regulates ciliary function in zebrafish embryos. Yu T; Matsuda M J Cell Sci; 2020 Jun; 133(12):. PubMed ID: 32501287 [TBL] [Abstract][Full Text] [Related]
26. A function for the Joubert syndrome protein Arl13b in ciliary membrane extension and ciliary length regulation. Lu H; Toh MT; Narasimhan V; Thamilselvam SK; Choksi SP; Roy S Dev Biol; 2015 Jan; 397(2):225-36. PubMed ID: 25448689 [TBL] [Abstract][Full Text] [Related]
28. DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia. Li Y; Yagi H; Onuoha EO; Damerla RR; Francis R; Furutani Y; Tariq M; King SM; Hendricks G; Cui C; Saydmohammed M; Lee DM; Zahid M; Sami I; Leatherbury L; Pazour GJ; Ware SM; Nakanishi T; Goldmuntz E; Tsang M; Lo CW PLoS Genet; 2016 Feb; 12(2):e1005821. PubMed ID: 26918822 [TBL] [Abstract][Full Text] [Related]
29. Using zebrafish to study the function of nephronophthisis and related ciliopathy genes. Molinari E; Ramsbottom SA; Sammut V; Hughes FEP; Sayer JA F1000Res; 2018; 7():1133. PubMed ID: 30254740 [TBL] [Abstract][Full Text] [Related]
30. Turning the Curve Into Straight: Phenogenetics of the Spine Morphology and Coordinate Maintenance in the Zebrafish. Muñoz-Montecinos C; Romero A; Sepúlveda V; Vira MÁ; Fehrmann-Cartes K; Marcellini S; Aguilera F; Caprile T; Fuentes R Front Cell Dev Biol; 2021; 9():801652. PubMed ID: 35155449 [TBL] [Abstract][Full Text] [Related]
31. The Meckel syndrome protein meckelin (TMEM67) is a key regulator of cilia function but is not required for tissue planar polarity. Leightner AC; Hommerding CJ; Peng Y; Salisbury JL; Gainullin VG; Czarnecki PG; Sussman CR; Harris PC Hum Mol Genet; 2013 May; 22(10):2024-40. PubMed ID: 23393159 [TBL] [Abstract][Full Text] [Related]
32. Resolving primary pathomechanisms driving idiopathic-like spinal curvature using a new Meyer-Miner A; Van Gennip JLM; Henke K; Harris MP; Ciruna B iScience; 2022 Sep; 25(9):105028. PubMed ID: 36105588 [TBL] [Abstract][Full Text] [Related]
33. Could genetic determinants of inner ear anomalies be a factor for the development of idiopathic scoliosis? Patten SA; Moldovan F Med Hypotheses; 2011 Mar; 76(3):438-40. PubMed ID: 21146321 [TBL] [Abstract][Full Text] [Related]
34. Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis. Justice CM; Bishop K; Carrington B; Mullikin JC; Swindle K; Marosy B; Sood R; Miller NH; Wilson AF G3 (Bethesda); 2016 Jun; 6(6):1707-12. PubMed ID: 27172222 [TBL] [Abstract][Full Text] [Related]
35. Etiology of idiopathic scoliosis: current trends in research. Lowe TG; Edgar M; Margulies JY; Miller NH; Raso VJ; Reinker KA; Rivard CH J Bone Joint Surg Am; 2000 Aug; 82(8):1157-68. PubMed ID: 10954107 [TBL] [Abstract][Full Text] [Related]
36. Idiopathic-type scoliosis is not exclusive to bipedalism. Gorman KF; Breden F Med Hypotheses; 2009 Mar; 72(3):348-52. PubMed ID: 19070438 [TBL] [Abstract][Full Text] [Related]
37. Generation and Validation of a Complete Knockout Model of abcc6a in Zebrafish. Van Gils M; Willaert A; De Vilder EYG; Coucke PJ; Vanakker OM J Invest Dermatol; 2018 Nov; 138(11):2333-2342. PubMed ID: 30030150 [TBL] [Abstract][Full Text] [Related]
38. Centrin depletion causes cyst formation and other ciliopathy-related phenotypes in zebrafish. Delaval B; Covassin L; Lawson ND; Doxsey S Cell Cycle; 2011 Nov; 10(22):3964-72. PubMed ID: 22142866 [TBL] [Abstract][Full Text] [Related]
39. Zebrafish Motile Cilia as a Model for Primary Ciliary Dyskinesia. Pinto AL; Rasteiro M; Bota C; Pestana S; Sampaio P; Hogg C; Burgoyne T; Lopes SS Int J Mol Sci; 2021 Aug; 22(16):. PubMed ID: 34445067 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]