Iain A. Drummond - Publications

Affiliations: 
Medicine Massachusetts General Hospital & Harvard Medical School, Boston, MA, United States 

17 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Gallegos TF, Kamei CN, Rohly M, Drummond IA. Fibroblast growth factor signaling mediates progenitor cell aggregation and nephron regeneration in the adult zebrafish kidney. Developmental Biology. PMID 31220433 DOI: 10.1016/J.Ydbio.2019.06.011  0.324
2019 Grainger S, Nguyen N, Richter J, Setayesh J, Lonquich B, Oon CH, Wozniak JM, Barahona R, Kamei CN, Houston J, Carrillo-Terrazas M, Drummond IA, Gonzalez D, Willert K, Traver D. EGFR is required for Wnt9a-Fzd9b signalling specificity in haematopoietic stem cells. Nature Cell Biology. PMID 31110287 DOI: 10.1038/S41556-019-0330-5  0.338
2019 Kamei CN, Gallegos TF, Liu Y, Hukriede N, Drummond IA. Wnt signaling mediates new nephron formation during zebrafish kidney regeneration. Development (Cambridge, England). 146. PMID 31036548 DOI: 10.1242/Dev.168294  0.362
2018 Bergboer JGM, Wyatt C, Austin-Tse C, Yaksi E, Drummond IA. Assaying sensory ciliopathies using calcium biosensor expression in zebrafish ciliated olfactory neurons. Cilia. 7: 2. PMID 29568513 DOI: 10.1186/s13630-018-0056-1  0.333
2016 Lewis WR, Malarkey EB, Tritschler D, Bower R, Pasek RC, Porath JD, Birket SE, Saunier S, Antignac C, Knowles MR, Leigh MW, Zariwala MA, Challa AK, Kesterson RA, Rowe SM, ... Drummond IA, et al. Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease. Plos Genetics. 12: e1006220. PMID 27472056 DOI: 10.1371/Journal.Pgen.1006220  0.388
2015 Oltrabella F, Pietka G, Ramirez IB, Mironov A, Starborg T, Drummond IA, Hinchliffe KA, Lowe M. The Lowe syndrome protein OCRL1 is required for endocytosis in the zebrafish pronephric tubule. Plos Genetics. 11: e1005058. PMID 25838181 DOI: 10.1371/journal.pgen.1005058  0.306
2014 Jin D, Ni TT, Sun J, Wan H, Amack JD, Yu G, Fleming J, Chiang C, Li W, Papierniak A, Cheepala S, Conseil G, Cole SP, Zhou B, Drummond IA, et al. Prostaglandin signalling regulates ciliogenesis by modulating intraflagellar transport. Nature Cell Biology. 16: 841-51. PMID 25173977 DOI: 10.1038/Ncb3029  0.344
2014 Le Corre S, Eyre D, Drummond IA. Modulation of the secretory pathway rescues zebrafish polycystic kidney disease pathology. Journal of the American Society of Nephrology : Jasn. 25: 1749-59. PMID 24627348 DOI: 10.1681/ASN.2013101060  0.321
2013 Manning DK, Sergeev M, van Heesbeen RG, Wong MD, Oh JH, Liu Y, Henkelman RM, Drummond I, Shah JV, Beier DR. Loss of the ciliary kinase Nek8 causes left-right asymmetry defects. Journal of the American Society of Nephrology : Jasn. 24: 100-12. PMID 23274954 DOI: 10.1681/Asn.2012050490  0.307
2012 Vasilyev A, Liu Y, Hellman N, Pathak N, Drummond IA. Mechanical stretch and PI3K signaling link cell migration and proliferation to coordinate epithelial tubule morphogenesis in the zebrafish pronephros. Plos One. 7: e39992. PMID 22815719 DOI: 10.1371/journal.pone.0039992  0.303
2012 Drummond IA. Cilia functions in development. Current Opinion in Cell Biology. 24: 24-30. PMID 22226236 DOI: 10.1016/j.ceb.2011.12.007  0.309
2010 Mangos S, Lam PY, Zhao A, Liu Y, Mudumana S, Vasilyev A, Liu A, Drummond IA. The ADPKD genes pkd1a/b and pkd2 regulate extracellular matrix formation. Disease Models & Mechanisms. 3: 354-65. PMID 20335443 DOI: 10.1242/dmm.003194  0.306
2007 Liu Y, Pathak N, Kramer-Zucker A, Drummond IA. Notch signaling controls the differentiation of transporting epithelia and multiciliated cells in the zebrafish pronephros. Development (Cambridge, England). 134: 1111-22. PMID 17287248 DOI: 10.1242/dev.02806  0.317
2006 Hinkes B, Wiggins RC, Gbadegesin R, Vlangos CN, Seelow D, Nürnberg G, Garg P, Verma R, Chaib H, Hoskins BE, Ashraf S, Becker C, Hennies HC, Goyal M, Wharram BL, ... ... Drummond I, et al. Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible. Nature Genetics. 38: 1397-405. PMID 17086182 DOI: 10.1038/Ng1918  0.326
2006 Sayer JA, Otto EA, O'Toole JF, Nurnberg G, Kennedy MA, Becker C, Hennies HC, Helou J, Attanasio M, Fausett BV, Utsch B, Khanna H, Liu Y, Drummond I, Kawakami I, et al. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4. Nature Genetics. 38: 674-81. PMID 16682973 DOI: 10.1038/Ng1786  0.308
2003 Otto EA, Schermer B, Obara T, O'Toole JF, Hiller KS, Mueller AM, Ruf RG, Hoefele J, Beekmann F, Landau D, Foreman JW, Goodship JA, Strachan T, Kispert A, Wolf MT, ... ... Drummond IA, et al. Mutations in INVS encoding inversin cause nephronophthisis type 2, linking renal cystic disease to the function of primary cilia and left-right axis determination. Nature Genetics. 34: 413-20. PMID 12872123 DOI: 10.1038/ng1217  0.314
2002 Liu S, Lu W, Obara T, Kuida S, Lehoczky J, Dewar K, Drummond IA, Beier DR. A defect in a novel Nek-family kinase causes cystic kidney disease in the mouse and in zebrafish. Development (Cambridge, England). 129: 5839-46. PMID 12421721 DOI: 10.1242/Dev.00173  0.307
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