Year |
Citation |
Score |
2024 |
López-García I, Oh S, Chaney C, Tsunezumi J, Drummond I, Oxburgh L, Carroll T, Marciano DK. Epithelial tubule interconnection driven by HGF-Met signaling in the kidney. Biorxiv : the Preprint Server For Biology. PMID 38895378 DOI: 10.1101/2024.06.03.597185 |
0.31 |
|
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 |
0.335 |
|
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 |
0.361 |
|
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 |
0.329 |
|
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 |
0.385 |
|
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 |
0.341 |
|
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 |
0.32 |
|
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 |
0.301 |
|
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 |
0.307 |
|
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 |
0.305 |
|
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 |
0.316 |
|
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 |
0.325 |
|
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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