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Bruce Tempel - Publications

Affiliations: 
University of Washington, Seattle, Seattle, WA 
Area:
Genetics of disease
Website:
http://depts.washington.edu/tempelab/index.html

44 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 Ison JR, Allen PD, Tempel BL, Brew HM. Sound Localization in Preweanling Mice Was More Severely Affected by Deleting the Kcna1 Gene Compared to Deleting Kcna2, and a Curious Inverted-U Course of Development That Appeared to Exceed Adult Performance Was Observed in All Groups. Journal of the Association For Research in Otolaryngology : Jaro. PMID 31410614 DOI: 10.1007/s10162-019-00731-5  0.795
2016 Weatherstone JH, Kopp-Scheinpflug C, Pilati N, Wang Y, Forsythe ID, Rubel EW, Tempel BL. Maintenance of neuronal size gradient in MNTB requires sound-evoked activit. Journal of Neurophysiology. jn.00528.2016. PMID 27881722 DOI: 10.1152/Jn.00528.2016  0.692
2015 Kopp-Scheinpflug C, Tempel BL. Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder. Hearing Research. PMID 26119177 DOI: 10.1016/J.Heares.2015.06.014  0.694
2015 Peguero B, Tempel BL. A Chromosome 17 Locus Engenders Frequency-Specific Non-Progressive Hearing Loss that Contributes to Age-Related Hearing Loss in Mice. Journal of the Association For Research in Otolaryngology : Jaro. 16: 459-71. PMID 25940139 DOI: 10.1007/S10162-015-0519-7  0.78
2015 Peguero B, Tempel BL. A Chromosome 17 Locus Engenders Frequency-Specific Non-Progressive Hearing Loss that Contributes to Age-Related Hearing Loss in Mice Jaro - Journal of the Association For Research in Otolaryngology. 16: 459-471. DOI: 10.1007/s10162-015-0519-7  0.772
2014 Watson CJ, Lies SM, Minich RR, Tempel BL. Changes in cochlear PMCA2 expression correlate with the maturation of auditory sensitivity. Journal of the Association For Research in Otolaryngology : Jaro. 15: 543-54. PMID 24799196 DOI: 10.1007/S10162-014-0454-Z  0.631
2014 Kopp-Scheinpflug C, Tempel BL. Decreased temporal precision of neuronal signaling as a candidate mechanism of auditory processing disorder Hearing Research. DOI: 10.1016/j.heares.2015.06.014  0.685
2013 Wang W, Kim HJ, Lv P, Tempel B, Yamoah EN. Association of the Kv1 family of K+ channels and their functional blueprint in the properties of auditory neurons as revealed by genetic and functional analyses. Journal of Neurophysiology. 110: 1751-64. PMID 23864368 DOI: 10.1152/jn.00290.2013  0.485
2013 Watson CJ, Tempel BL. A new Atp2b2 deafwaddler allele, dfw(i5), interacts strongly with Cdh23 and other auditory modifiers. Hearing Research. 304: 41-8. PMID 23792079 DOI: 10.1016/J.Heares.2013.06.003  0.62
2012 Robbins CA, Tempel BL. Kv1.1 and Kv1.2: similar channels, different seizure models. Epilepsia. 53: 134-41. PMID 22612818 DOI: 10.1111/j.1528-1167.2012.03484.x  0.336
2011 Kopp-Scheinpflug C, Tozer AJ, Robinson SW, Tempel BL, Hennig MH, Forsythe ID. The sound of silence: ionic mechanisms encoding sound termination. Neuron. 71: 911-25. PMID 21903083 DOI: 10.1016/J.Neuron.2011.06.028  0.76
2011 Karcz A, Hennig MH, Robbins CA, Tempel BL, Rübsamen R, Kopp-Scheinpflug C. Low-voltage activated Kv1.1 subunits are crucial for the processing of sound source location in the lateral superior olive in mice. The Journal of Physiology. 589: 1143-57. PMID 21224222 DOI: 10.1113/Jphysiol.2010.203331  0.807
2007 Brew HM, Gittelman JX, Silverstein RS, Hanks TD, Demas VP, Robinson LC, Robbins CA, McKee-Johnson J, Chiu SY, Messing A, Tempel BL. Seizures and reduced life span in mice lacking the potassium channel subunit Kv1.2, but hypoexcitability and enlarged Kv1 currents in auditory neurons. Journal of Neurophysiology. 98: 1501-25. PMID 17634333 DOI: 10.1152/Jn.00640.2006  0.746
2007 McCullough BJ, Adams JC, Shilling DJ, Feeney MP, Sie KC, Tempel BL. 3p-- syndrome defines a hearing loss locus in 3p25.3. Hearing Research. 224: 51-60. PMID 17208398 DOI: 10.1016/J.Heares.2006.11.006  0.718
2006 Duncan JL, Yang H, Doan T, Silverstein RS, Murphy GJ, Nune G, Liu X, Copenhagen D, Tempel BL, Rieke F, Krizaj D. Scotopic visual signaling in the mouse retina is modulated by high-affinity plasma membrane calcium extrusion. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 26: 7201-11. PMID 16822977 DOI: 10.1523/Jneurosci.5230-05.2006  0.771
2006 Silverstein RS, Tempel BL. Atp2b2, encoding plasma membrane Ca2+-ATPase type 2, (PMCA2) exhibits tissue-specific first exon usage in hair cells, neurons, and mammary glands of mice. Neuroscience. 141: 245-57. PMID 16675132 DOI: 10.1016/j.neuroscience.2006.03.036  0.776
2006 Gittelman JX, Tempel BL. Kv1.1-containing channels are critical for temporal precision during spike initiation. Journal of Neurophysiology. 96: 1203-14. PMID 16672305 DOI: 10.1152/Jn.00092.2005  0.776
2004 McCullough BJ, Tempel BL. Haplo-insufficiency revealed in deafwaddler mice when tested for hearing loss and ataxia. Hearing Research. 195: 90-102. PMID 15350283 DOI: 10.1016/J.Heares.2004.05.003  0.763
2004 Lu Y, Monsivais P, Tempel BL, Rubel EW. Activity-dependent regulation of the potassium channel subunits Kv1.1 and Kv3.1. The Journal of Comparative Neurology. 470: 93-106. PMID 14755528 DOI: 10.1002/Cne.11037  0.419
2003 Lopantsev V, Tempel BL, Schwartzkroin PA. Hyperexcitability of CA3 pyramidal cells in mice lacking the potassium channel subunit Kv1.1. Epilepsia. 44: 1506-12. PMID 14636320 DOI: 10.1111/J.0013-9580.2003.44602.X  0.343
2003 Kopp-Scheinpflug C, Fuchs K, Lippe WR, Tempel BL, Rübsamen R. Decreased temporal precision of auditory signaling in Kcna1-null mice: an electrophysiological study in vivo. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 23: 9199-207. PMID 14534254  0.821
2003 Jiang X, Zhang YH, Clark JD, Tempel BL, Nicol GD. Prostaglandin E2 inhibits the potassium current in sensory neurons from hyperalgesic Kv1.1 knockout mice. Neuroscience. 119: 65-72. PMID 12763069 DOI: 10.1016/S0306-4522(03)00073-3  0.407
2003 Brew HM, Hallows JL, Tempel BL. Hyperexcitability and reduced low threshold potassium currents in auditory neurons of mice lacking the channel subunit Kv1.1. The Journal of Physiology. 548: 1-20. PMID 12611922 DOI: 10.1113/jphysiol.2002.035568  0.8
2001 Parkinson NJ, Olsson CL, Hallows JL, McKee-Johnson J, Keogh BP, Noben-Trauth K, Kujawa SG, Tempel BL. Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice. Nature Genetics. 29: 61-5. PMID 11528393 DOI: 10.1038/Ng710  0.373
2001 Zaritsky JJ, Redell JB, Tempel BL, Schwarz TL. The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes. The Journal of Physiology. 533: 697-710. PMID 11410627 DOI: 10.1111/J.1469-7793.2001.T01-1-00697.X  0.417
2001 van Brederode JF, Rho JM, Cerne R, Tempel BL, Spain WJ. Evidence of altered inhibition in layer V pyramidal neurons from neocortex of Kcna1-null mice. Neuroscience. 103: 921-9. PMID 11301201 DOI: 10.1016/S0306-4522(01)00041-0  0.381
2001 Konrad-Martin D, Norton SJ, Mascher KE, Tempel BL. Effects of PMCA2 mutation on DPOAE amplitudes and latencies in deafwaddler mice. Hearing Research. 151: 205-220. PMID 11124466 DOI: 10.1016/S0378-5955(00)00228-8  0.333
2000 Grigg JJ, Brew HM, Tempel BL. Differential expression of voltage-gated potassium channel genes in auditory nuclei of the mouse brainstem. Hearing Research. 140: 77-90. PMID 10675636 DOI: 10.1016/S0378-5955(99)00187-2  0.78
1999 Rho JM, Szot P, Tempel BL, Schwartzkroin PA. Developmental seizure susceptibility of kv1.1 potassium channel knockout mice. Developmental Neuroscience. 21: 320-7. PMID 10575255 DOI: 10.1159/000017381  0.307
1998 Clark JD, Tempel BL. Hyperalgesia in mice lacking the Kv1.1 potassium channel gene. Neuroscience Letters. 251: 121-4. PMID 9718989 DOI: 10.1016/S0304-3940(98)00516-3  0.317
1998 Street VA, McKee-Johnson JW, Fonseca RC, Tempel BL, Noben-Trauth K. Mutations in a plasma membrane Ca2+-ATPase gene cause deafness in deafwaddler mice. Nature Genetics. 19: 390-4. PMID 9697703 DOI: 10.1038/1284  0.314
1998 Hallows JL, Tempel BL. Expression of Kv1.1, a Shaker-like potassium channel, is temporally regulated in embryonic neurons and glia. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 18: 5682-91. PMID 9671659  0.348
1997 Smart SL, Bosma MM, Tempel BL. Identification of the delayed rectifier potassium channel, Kv1.6, in cultured astrocytes. Glia. 20: 127-34. PMID 9179597 DOI: 10.1002/(SICI)1098-1136(199706)20:2<127::AID-GLIA4>3.0.CO;2-6  0.576
1997 Street VA, Bosma MM, Demas VP, Regan MR, Lin DD, Robinson LC, Agnew WS, Tempel BL. The type 1 inositol 1,4,5-trisphosphate receptor gene is altered in the opisthotonos mouse. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 17: 635-45. PMID 8987786  0.552
1994 Hopkins WF, Allen ML, Houamed KM, Tempel BL. Properties of voltage-gated K+ currents expressed in Xenopus oocytes by mKv1.1, mKv1.2 and their heteromultimers as revealed by mutagenesis of the dendrotoxin-binding site in mKv1.1. PflüGers Archiv : European Journal of Physiology. 428: 382-90. PMID 7816560 DOI: 10.1007/BF00724522  0.323
1993 Bosma MM, Allen ML, Martin TM, Tempel BL. PKA-dependent regulation of mKv1.1, a mouse Shaker-like potassium channel gene, when stably expressed in CHO cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 13: 5242-50. PMID 8254371  0.562
1990 Chandy KG, Williams CB, Spencer RH, Aguilar BA, Ghanshani S, Tempel BL, Gutman GA. A family of three mouse potassium channel genes with intronless coding regions. Science (New York, N.Y.). 247: 973-5. PMID 2305265 DOI: 10.1126/Science.2305265  0.381
1988 Papazian DM, Schwarz TL, Tempel BL, Timpe LC, Jan LY. Ion channels in Drosophila. Annual Review of Physiology. 50: 379-94. PMID 2454072 DOI: 10.1146/annurev.ph.50.030188.002115  0.588
1988 Tempel BL, Jan YN, Jan LY. Cloning of a probable potassium channel gene from mouse brain. Nature. 332: 837-9. PMID 2451788 DOI: 10.1038/332837a0  0.503
1988 Timpe LC, Schwarz TL, Tempel BL, Papazian DM, Jan YN, Jan LY. Expression of functional potassium channels from Shaker cDNA in Xenopus oocytes. Nature. 331: 143-5. PMID 2448636 DOI: 10.1038/331143a0  0.578
1988 Schwarz TL, Tempel BL, Papazian DM, Jan YN, Jan LY. Multiple potassium-channel components are produced by alternative splicing at the Shaker locus in Drosophila. Nature. 331: 137-42. PMID 2448635 DOI: 10.1038/331137a0  0.576
1988 Schwarz TL, Tempel BL, Papazian DM, Jan YN, Jan LY. Multiple potassium-channel components are produced by alternative splicing at the shaker locus in Drosophila Nature. 332: 740-740. DOI: 10.1038/332740a0  0.447
1987 Tempel BL, Papazian DM, Schwarz TL, Jan YN, Jan LY. Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila. Science (New York, N.Y.). 237: 770-5. PMID 2441471 DOI: 10.1126/Science.2441471  0.596
1987 Papazian DM, Schwarz TL, Tempel BL, Jan YN, Jan LY. Cloning of genomic and complementary DNA from Shaker, a putative potassium channel gene from Drosophila. Science (New York, N.Y.). 237: 749-53. PMID 2441470 DOI: 10.1126/Science.2441470  0.577
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