| Year |
Citation |
Score |
| 2023 |
Sharma Y, Jacobs JS, Sivan-Loukianova E, Lee E, Kernan MJ, Eberl DF. The retrograde IFT dynein is required for normal function of diverse mechanosensory cilia in . Frontiers in Molecular Neuroscience. 16: 1263411. PMID 37808471 DOI: 10.3389/fnmol.2023.1263411 |
0.73 |
|
| 2015 |
Karak S, Jacobs JS, Kittelmann M, Spalthoff C, Katana R, Sivan-Loukianova E, Schon MA, Kernan MJ, Eberl DF, Göpfert MC. Diverse Roles of Axonemal Dyneins in Drosophila Auditory Neuron Function and Mechanical Amplification in Hearing. Scientific Reports. 5: 17085. PMID 26608786 DOI: 10.1038/srep17085 |
0.681 |
|
| 2012 |
Enjolras C, Thomas J, Chhin B, Cortier E, Duteyrat JL, Soulavie F, Kernan MJ, Laurençon A, Durand B. Drosophila chibby is required for basal body formation and ciliogenesis but not for Wg signaling. The Journal of Cell Biology. 197: 313-25. PMID 22508513 DOI: 10.1083/jcb.201109148 |
0.333 |
|
| 2011 |
Eberl DF, Kernan MJ. Recording sound-evoked potentials from the Drosophila antennal nerve. Cold Spring Harbor Protocols. 2011: prot5576. PMID 21363940 DOI: 10.1101/pdb.prot5576 |
0.583 |
|
| 2010 |
Kavlie RG, Kernan MJ, Eberl DF. Hearing in Drosophila requires TilB, a conserved protein associated with ciliary motility. Genetics. 185: 177-88. PMID 20215474 DOI: 10.1534/genetics.110.114009 |
0.608 |
|
| 2008 |
Lee E, Sivan-Loukianova E, Eberl DF, Kernan MJ. An IFT-A protein is required to delimit functionally distinct zones in mechanosensory cilia. Current Biology : Cb. 18: 1899-906. PMID 19097904 DOI: 10.1016/j.cub.2008.11.020 |
0.675 |
|
| 2007 |
Kernan MJ. Mechanotransduction and auditory transduction in Drosophila. PflüGers Archiv : European Journal of Physiology. 454: 703-20. PMID 17436012 DOI: 10.1007/s00424-007-0263-x |
0.4 |
|
| 2005 |
Elliott SL, Cullen CF, Wrobel N, Kernan MJ, Ohkura H. EB1 is essential during Drosophila development and plays a crucial role in the integrity of chordotonal mechanosensory organs. Molecular Biology of the Cell. 16: 891-901. PMID 15591130 DOI: 10.1091/Mbc.E04-07-0633 |
0.4 |
|
| 2004 |
Gong Z, Son W, Chung YD, Kim J, Shin DW, McClung CA, Lee Y, Lee HW, Chang DJ, Kaang BK, Cho H, Oh U, Hirsh J, Kernan MJ, Kim C. Two interdependent TRPV channel subunits, inactive and Nanchung, mediate hearing in Drosophila. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 24: 9059-66. PMID 15483124 DOI: 10.1523/Jneurosci.1645-04.2004 |
0.387 |
|
| 2004 |
Baker JD, Adhikarakunnathu S, Kernan MJ. Mechanosensory-defective, male-sterile unc mutants identify a novel basal body protein required for ciliogenesis in Drosophila. Development (Cambridge, England). 131: 3411-22. PMID 15226257 DOI: 10.1242/dev.01229 |
0.416 |
|
| 2004 |
Martinez-Campos M, Basto R, Baker J, Kernan M, Raff JW. The Drosophila pericentrin-like protein is essential for cilia/flagella function, but appears to be dispensable for mitosis. The Journal of Cell Biology. 165: 673-83. PMID 15184400 DOI: 10.1083/Jcb.200402130 |
0.47 |
|
| 2003 |
Watnick TJ, Jin Y, Matunis E, Kernan MJ, Montell C. A flagellar polycystin-2 homolog required for male fertility in Drosophila. Current Biology : Cb. 13: 2179-84. PMID 14680634 DOI: 10.1016/J.Cub.2003.12.002 |
0.386 |
|
| 2003 |
Han YG, Kwok BH, Kernan MJ. Intraflagellar transport is required in Drosophila to differentiate sensory cilia but not sperm. Current Biology : Cb. 13: 1679-86. PMID 14521833 DOI: 10.1016/j.cub.2003.08.034 |
0.667 |
|
| 2003 |
Kim J, Chung YD, Park DY, Choi S, Shin DW, Soh H, Lee HW, Son W, Yim J, Park CS, Kernan MJ, Kim C. A TRPV family ion channel required for hearing in Drosophila. Nature. 424: 81-4. PMID 12819662 DOI: 10.1038/Nature01733 |
0.323 |
|
| 2002 |
Dubruille R, Laurençon A, Vandaele C, Shishido E, Coulon-Bublex M, Swoboda P, Couble P, Kernan M, Durand B. Drosophila regulatory factor X is necessary for ciliated sensory neuron differentiation. Development (Cambridge, England). 129: 5487-98. PMID 12403718 DOI: 10.1242/dev.00148 |
0.473 |
|
| 2001 |
Chung YD, Zhu J, Han Y, Kernan MJ. nompA encodes a PNS-specific, ZP domain protein required to connect mechanosensory dendrites to sensory structures. Neuron. 29: 415-28. PMID 11239432 DOI: 10.1016/S0896-6273(01)00215-X |
0.641 |
|
| 2000 |
Eberl DF, Hardy RW, Kernan MJ. Genetically similar transduction mechanisms for touch and hearing in Drosophila. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: 5981-8. PMID 10934246 DOI: 10.1523/Jneurosci.20-16-05981.2000 |
0.707 |
|
| 1995 |
Kernan M, Zuker C. Genetic approaches to mechanosensory transduction. Current Opinion in Neurobiology. 5: 443-8. PMID 7488844 DOI: 10.1016/0959-4388(95)80003-4 |
0.606 |
|
| 1994 |
Kernan M, Cowan D, Zuker C. Genetic dissection of mechanosensory transduction: mechanoreception-defective mutations of Drosophila. Neuron. 12: 1195-206. PMID 8011334 DOI: 10.1016/0896-6273(94)90437-5 |
0.635 |
|
| 1991 |
Kernan MJ, Kuroda MI, Kreber R, Baker BS, Ganetzky B. napts, a mutation affecting sodium channel activity in Drosophila, is an allele of mle, a regulator of X chromosome transcription. Cell. 66: 949-59. PMID 1653649 DOI: 10.1016/0092-8674(91)90440-A |
0.581 |
|
| 1991 |
Kuroda MI, Kernan MJ, Kreber R, Ganetzky B, Baker BS. The maleless protein associates with the X chromosome to regulate dosage compensation in Drosophila. Cell. 66: 935-47. PMID 1653648 DOI: 10.1016/0092-8674(91)90439-6 |
0.515 |
|
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