☰

Brian P. Delisle - Publications

Affiliations: 
Physiology University of Kentucky, Lexington, KY 
Area:
Physiology Biology, General Biophysics
Tree Info Similar researchers PubMed Report error

70 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
2023 Anees P, Saminathan A, Rozmus ER, Di A, Malik AB, Delisle BP, Krishnan Y. Detecting organelle-specific activity of potassium channels with a DNA nanodevice. Nature Biotechnology. PMID 37735264 DOI: 10.1038/s41587-023-01928-z  0.336
2023 Fang X, Immadisetty K, Ramon GS, Hartle CM, McCoy TP, Center RG, Mirshahi T, Delisle BP, Kekenes-Huskey PM. Prediction of Kv11.1 potassium channel PAS-domain variants trafficking via machine learning. Journal of Molecular and Cellular Cardiology. PMID 37187232 DOI: 10.1016/j.yjmcc.2023.05.002  0.315
2022 Anderson CL, Munawar S, Reilly L, Kamp TJ, January CT, Delisle BP, Eckhardt LL. How Functional Genomics Can Keep Pace With VUS Identification. Frontiers in Cardiovascular Medicine. 9: 900431. PMID 35859585 DOI: 10.3389/fcvm.2022.900431  0.524
2022 Kekenes-Huskey PM, Burgess DE, Sun B, Bartos DC, Rozmus ER, Anderson CL, January CT, Eckhardt LL, Delisle BP. Mutation-Specific Differences in Kv7.1 () and Kv11.1 () Channel Dysfunction and Long QT Syndrome Phenotypes. International Journal of Molecular Sciences. 23. PMID 35806392 DOI: 10.3390/ijms23137389  0.809
2021 Schroder EA, Wayland JL, Samuels KM, Shah SF, Burgess DE, Seward T, Elayi CS, Esser KA, Delisle BP. Cardiomyocyte Deletion of Exacerbates QT- and RR-Interval Prolongation in Mice. Frontiers in Physiology. 12: 681011. PMID 34248669 DOI: 10.3389/fphys.2021.681011  0.316
2020 Ono M, Burgess DE, Schroder EA, Elayi CS, Anderson CL, January CT, Sun B, Immadisetty K, Kekenes-Huskey PM, Delisle BP. Long QT Syndrome Type 2: Emerging Strategies for Correcting Class 2 () Mutations and Identifying New Patients. Biomolecules. 10. PMID 32759882 DOI: 10.3390/biom10081144  0.679
2020 Anderson CL, Routes TC, Eckhardt LL, Delisle BP, January CT, Kamp TJ. A rapid solubility assay of protein domain misfolding for pathogenicity assessment of rare DNA sequence variants. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32475984 DOI: 10.1038/S41436-020-0842-1  0.526
2020 Qile M, Ji Y, Golden TD, Houtman MJC, Romunde F, Fransen D, van Ham WB, IJzerman AP, January CT, Heitman LH, Stary-Weinzinger A, Delisle BP, van der Heyden MAG. LUF7244 plus dofetilide rescues aberrant Kv11.1 trafficking and produces functional IKv11.1. Molecular Pharmacology. PMID 32241959 DOI: 10.1124/mol.119.118190  0.629
2018 van der Heyden MAG, Delisle BP, Abriel H. Editorial: Ion Channel Trafficking and Cardiac Arrhythmias. Frontiers in Physiology. 9: 1254. PMID 30319434 DOI: 10.3389/Fphys.2018.01254  0.379
2018 Hall AR, Anderson CL, Smith JL, Mirshahi T, Elayi CS, January CT, Delisle BP. Visualizing Mutation-Specific Differences in the Trafficking-Deficient Phenotype of Kv11.1 Proteins Linked to Long QT Syndrome Type 2. Frontiers in Physiology. 9: 584. PMID 29875689 DOI: 10.3389/Fphys.2018.00584  0.679
2018 Smith JL, Tester DJ, Hall AR, Burgess DE, Hsu CC, Claude Elayi S, Anderson CL, January CT, Luo JZ, Hartzel DN, Mirshahi UL, Murray MF, Mirshahi T, Ackerman MJ, Delisle BP. Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the -Encoded Kv11.1 Channel. Circulation. Arrhythmia and Electrophysiology. 11: e005859. PMID 29752375 DOI: 10.1161/Circep.117.005859  0.607
2018 Delisle BP, January CT. Advancing precision medicine for the treatment of long-QT syndrome type 2: shedding light on lumacaftor. European Heart Journal. 39: 1456-1458. PMID 29040441 DOI: 10.1093/Eurheartj/Ehx561  0.557
2018 Burgess DE, Smith JL, Amin AS, Anderson CL, January CT, Delisle BP. Changes in IKR Amplitude (NOT Gating) is the Key Determinant for Ventricular Action Potential Prolongation Biophysical Journal. 114: 311a-312a. DOI: 10.1016/J.Bpj.2017.11.1760  0.57
2016 Grandi E, Sanguinetti MC, Bartos DC, Bers DM, Chen-Izu Y, Chiamvimonvat N, Colecraft HM, Delisle BP, Heijman J, Navedo MF, Noskov S, Proenza C, Vandenberg JI, Yarov-Yarovoy V. Potassium channels in the heart: structure, function and regulation. The Journal of Physiology. PMID 27861921 DOI: 10.1113/Jp272864  0.764
2016 Ackerman JP, Bartos DC, Kapplinger JD, Tester DJ, Delisle BP, Ackerman MJ. The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most. Mayo Clinic Proceedings. PMID 27810088 DOI: 10.1016/j.mayocp.2016.08.008  0.706
2016 Smith JL, Anderson CL, Burgess DE, Elayi CS, January CT, Delisle BP. Molecular pathogenesis of long QT syndrome type 2. Journal of Arrhythmia. 32: 373-380. PMID 27761161 DOI: 10.1016/J.Joa.2015.11.009  0.671
2016 Smith JL, Anderson CL, January CT, Delisle B. Trafficking Deficient KV11.1 (HERG) Mutations Linked to Long QT Syndrome Localize to Different Endoplasmic Reticulum Subcompartments Biophysical Journal. 110: 105a. DOI: 10.1016/J.Bpj.2015.11.622  0.433
2015 Schroder EA, Burgess DE, Zhang X, Lefta M, Smith JL, Patwardhan A, Bartos DC, Elayi CS, Esser KA, Delisle BP. The cardiomyocyte molecular clock regulates the circadian expression of Kcnh2 and contributes to ventricular repolarization. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 12: 1306-14. PMID 25701773 DOI: 10.1016/J.Hrthm.2015.02.019  0.71
2015 Smith JL, Anderson CL, Burgess DE, Elayi CS, January CT, Delisle BP. Molecular pathogenesis of long QT syndrome type 2 Journal of Arrhythmia. DOI: 10.1016/j.joa.2015.11.009  0.537
2014 Anderson CL, Kuzmicki CE, Childs RR, Hintz CJ, Delisle BP, January CT. Large-scale mutational analysis of Kv11.1 reveals molecular insights into type 2 long QT syndrome. Nature Communications. 5: 5535. PMID 25417810 DOI: 10.1038/Ncomms6535  0.699
2014 Schroder EA, Burgess DE, Manning CL, Zhao Y, Moss AJ, Patwardhan A, Elayi CS, Esser KA, Delisle BP. Light phase-restricted feeding slows basal heart rate to exaggerate the type-3 long QT syndrome phenotype in mice. American Journal of Physiology. Heart and Circulatory Physiology. 307: H1777-85. PMID 25343952 DOI: 10.1152/Ajpheart.00341.2014  0.336
2014 Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP. A KCNQ1 mutation contributes to the concealed type 1 long QT phenotype by limiting the Kv7.1 channel conformational changes associated with protein kinase A phosphorylation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 459-68. PMID 24269949 DOI: 10.1016/J.Hrthm.2013.11.021  0.799
2014 Wu J, Naiki N, Ding WG, Ohno S, Kato K, Zang WJ, Delisle BP, Matsuura H, Horie M. A molecular mechanism for adrenergic-induced long QT syndrome. Journal of the American College of Cardiology. 63: 819-27. PMID 24184248 DOI: 10.1016/J.Jacc.2013.08.1648  0.396
2014 Hasegawa K, Ohno S, Ashihara T, Itoh H, Ding WG, Toyoda F, Makiyama T, Aoki H, Nakamura Y, Delisle BP, Matsuura H, Horie M. A novel KCNQ1 missense mutation identified in a patient with juvenile-onset atrial fibrillation causes constitutively open IKs channels. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 11: 67-75. PMID 24096004 DOI: 10.1016/J.Hrthm.2013.09.073  0.429
2014 Smith J, Tester D, Reloj A, Burgess D, Hsu C, Ackerman M, Delisle B. KCNH2 MUTATIONS THAT ALTER KV11.1 CHANNEL GATING ARE LINKED TO SUDDEN INFANT DEATH SYNDROME Heart Rhythm. 11: 2132-2133. DOI: 10.1016/J.Hrthm.2014.09.022  0.463
2013 Smith JL, Reloj AR, Nataraj PS, Bartos DC, Schroder EA, Moss AJ, Ohno S, Horie M, Anderson CL, January CT, Delisle BP. Pharmacological correction of long QT-linked mutations in KCNH2 (hERG) increases the trafficking of Kv11.1 channels stored in the transitional endoplasmic reticulum. American Journal of Physiology. Cell Physiology. 305: C919-30. PMID 23864605 DOI: 10.1152/Ajpcell.00406.2012  0.823
2013 Crotti L, Tester DJ, White WM, Bartos DC, Insolia R, Besana A, Kunic JD, Will ML, Velasco EJ, Bair JJ, Ghidoni A, Cetin I, Van Dyke DL, Wick MJ, Brost B, ... Delisle BP, et al. Long QT syndrome-associated mutations in intrauterine fetal death. Jama. 309: 1473-82. PMID 23571586 DOI: 10.1001/Jama.2013.3219  0.723
2013 McBride CM, Smith AM, Smith JL, Reloj AR, Velasco EJ, Powell J, Elayi CS, Bartos DC, Burgess DE, Delisle BP. Mechanistic basis for type 2 long QT syndrome caused by KCNH2 mutations that disrupt conserved arginine residues in the voltage sensor. The Journal of Membrane Biology. 246: 355-64. PMID 23546015 DOI: 10.1007/S00232-013-9539-6  0.804
2013 Schroder EA, Lefta M, Zhang X, Bartos DC, Feng HZ, Zhao Y, Patwardhan A, Jin JP, Esser KA, Delisle BP. The cardiomyocyte molecular clock, regulation of Scn5a, and arrhythmia susceptibility. American Journal of Physiology. Cell Physiology. 304: C954-65. PMID 23364267 DOI: 10.1152/Ajpcell.00383.2012  0.742
2013 Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP. A KCNQ1 mutation causes a high penetrance for familial atrial fibrillation. Journal of Cardiovascular Electrophysiology. 24: 562-9. PMID 23350853 DOI: 10.1111/Jce.12068  0.727
2013 Burgess DE, Bartos DC, Reloj AR, Campbell KS, Johnson JN, Tester DJ, Ackerman MJ, Fressart V, Denjoy I, Guicheney P, Moss AJ, Ohno S, Horie M, Delisle B. Malignant Long QT Syndrome KCNQ1 Mutations in the Pore Disrupt the Molecular Basis for Rapid K+ Permeation Biophysical Journal. 104: 268a. DOI: 10.1016/J.Bpj.2012.11.1503  0.786
2013 Bartos DC, Burgess DE, Reloj AR, Giudicessi J, Tester DJ, Ackerman MJ, Delisle BP. A Mutation in the Voltage-Sensor of Kv7.1 Prevents PKA Activation of IKs to Elicit Concealed Type 1 Long QT Syndrome during Stress Biophysical Journal. 104: 267a-268a. DOI: 10.1016/J.Bpj.2012.11.1502  0.768
2013 Smith JL, Reloj AR, Nataraj PS, Bartos DC, January CT, Delisle BP. Cellular Mechanism for the Pharmacological Correction of hERG Mutations Linked to the Long QT Syndrome Biophysical Journal. 104: 266a. DOI: 10.1016/J.Bpj.2012.11.1496  0.826
2012 Balijepalli SY, Lim E, Concannon SP, Chew CL, Holzem KE, Tester DJ, Ackerman MJ, Delisle BP, Balijepalli RC, January CT. Mechanism of loss of Kv11.1 K+ current in mutant T421M-Kv11.1-expressing rat ventricular myocytes: Interaction of trafficking and gating Circulation. 126: 2809-2818. PMID 23136156 DOI: 10.1161/Circulationaha.112.118018  0.7
2012 Burgess DE, Bartos DC, Reloj AR, Campbell KS, Johnson JN, Tester DJ, Ackerman MJ, Fressart V, Denjoy I, Guicheney P, Moss AJ, Ohno S, Horie M, Delisle BP. High-risk long QT syndrome mutations in the Kv7.1 (KCNQ1) pore disrupt the molecular basis for rapid K(+) permeation. Biochemistry. 51: 9076-85. PMID 23092362 DOI: 10.1021/Bi3009449  0.79
2012 Bartos D, Giudicessi J, Tester D, Ackerman M, Delisle B. Protracted QTc Prolongation following Treadmill Testing Identifies a Type 1 Long QT Mutation that is Resistant to PKA Activation Heart Rhythm. 9: 1916. DOI: 10.1016/J.Hrthm.2012.09.109  0.769
2011 Smith JL, McBride CM, Nataraj PS, Bartos DC, January CT, Delisle BP. Trafficking-deficient hERG K⁺ channels linked to long QT syndrome are regulated by a microtubule-dependent quality control compartment in the ER. American Journal of Physiology. Cell Physiology. 301: C75-85. PMID 21490315 DOI: 10.1152/Ajpcell.00494.2010  0.823
2011 Best JM, Foell JD, Buss CR, Delisle BP, Balijepalli RC, January CT, Kamp TJ. Small GTPase Rab11b regulates degradation of surface membrane L-type Cav1.2 channels. American Journal of Physiology. Cell Physiology. 300: C1023-33. PMID 21248079 DOI: 10.1152/Ajpcell.00288.2010  0.616
2011 Bartos DC, Duchatelet S, Burgess DE, Klug D, Denjoy I, Peat R, Lupoglazoff JM, Fressart V, Berthet M, Ackerman MJ, January CT, Guicheney P, Delisle BP. R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation. Heart Rhythm : the Official Journal of the Heart Rhythm Society. 8: 48-55. PMID 20850564 DOI: 10.1016/J.Hrthm.2010.09.010  0.816
2011 Burgess D, Bartos D, Schmidt E, Johnson J, Tester D, Ohno S, Horie M, Ackerman M, Delisle B. Atomic-Scale Modeling Predicts a Mechanism for Long QT Type 1 Dysfunction Associated With Pore Mutations Heart Rhythm. 8: 1821-1822. DOI: 10.1016/J.Hrthm.2011.09.034  0.734
2011 Burgess DE, Bartos DC, Schmidt ES, Delisle B. A Computational Model for the Effect that a KCNQ1 Mutation Linked to Jervell and Lange-Nielson Syndrome has on Human Cardiac Action Potential Duration Biophysical Journal. 100: 436a-437a. DOI: 10.1016/J.Bpj.2010.12.2573  0.764
2011 Smith JL, Nataraj P, January CT, Delisle BP. The Trafficking of Mutant HERG K+ Channels Linked to Long QT Syndrome are Regulated by a Subdomain in the Endoplasmic Reticulum Biophysical Journal. 100: 427a. DOI: 10.1016/J.Bpj.2010.12.2526  0.654
2011 McBride CM, Powell J, Smith A, Delisle BP. Long QT-Linked HERG Mutations at R531 of the S4 Alter the Gating Properties of Wt-HERG Biophysical Journal. 100: 427a. DOI: 10.1016/J.Bpj.2010.12.2525  0.506
2011 Bartos DC, Schmidt ES, Burgess DE, Delisle BP. A Spectrum of Functional Phenotypes Associated with LQT1 Mutations Identified in Patients with Early-Onset Atrial Fibrillation Biophysical Journal. 100: 427a. DOI: 10.1016/J.Bpj.2010.12.2524  0.789
2010 Lin EC, Holzem KM, Anson BD, Moungey BM, Balijepalli SY, Tester DJ, Ackerman MJ, Delisle BP, Balijepalli RC, January CT. Properties of WT and mutant hERG K(+) channels expressed in neonatal mouse cardiomyocytes. American Journal of Physiology. Heart and Circulatory Physiology. 298: H1842-9. PMID 20363883 DOI: 10.1152/Ajpheart.01236.2009  0.731
2010 McBride CM, Smith JL, Delisle BP. Pharmacological-Induced Increase in the Functional Expression Of hERG Current Biophysical Journal. 98: 119a. DOI: 10.1016/J.Bpj.2009.12.649  0.445
2010 Smith JL, McBride CM, Bartos DC, January CT, Delisle B. Microtubule Dependent Mechanisms Regulate the Trafficking Deficient Phenotype of hERG Mutations Linked to Long QT Syndrome Biophysical Journal. 98: 118a-119a. DOI: 10.1016/J.Bpj.2009.12.647  0.825
2009 Delisle BP, Underkofler HA, Moungey BM, Slind JK, Kilby JA, Best JM, Foell JD, Balijepalli RC, Kamp TJ, January CT. Small GTPase determinants for the Golgi processing and plasmalemmal expression of human ether-a-go-go related (hERG) K+ channels. The Journal of Biological Chemistry. 284: 2844-53. PMID 19029296 DOI: 10.1074/Jbc.M807289200  0.704
2009 Smith JL, Bartos DC, January CT, Delisle BP. Trafficking-deficient LQT2 Mutations Disrupt Different Steps of hERG Channel Transport Biophysical Journal. 96: 190a. DOI: 10.1016/J.Bpj.2008.12.894  0.824
2009 Lin E, Moungey B, Delisle BP, January CT. LQT2 Linked Mutations E444d And P451l In The S1-S2 Linker Lead To Biophysical Abnormalities Of Herg Channels Biophysical Journal. 96: 189a. DOI: 10.1016/J.Bpj.2008.12.887  0.66
2009 Bartos DC, Smith JL, Kilby JA, January CT, Delisle BP. Wild-Type KCNQ1 Modulates the Gating of the LQT1 Mutation R231C Biophysical Journal. 96: 380a. DOI: 10.1016/J.Bpj.2008.12.2847  0.819
2008 Amin AS, Herfst LJ, Delisle BP, Klemens CA, Rook MB, Bezzina CR, Underkofler HAS, Holzem KM, Ruijter JM, Tan HL, January CT, Wilde AAM. Fever-induced QTc prolongation and ventricular arrhythmias in individuals with type 2 congenital long QT syndrome Journal of Clinical Investigation. 118: 2552-2561. PMID 18551196 DOI: 10.1172/Jci35337  0.691
2008 Takemasa H, Nagatomo T, Abe H, Kawakami K, Igarashi T, Tsurugi T, Kabashima N, Tamura M, Okazaki M, Delisle BP, January CT, Otsuji Y. Coexistence of hERG current block and disruption of protein trafficking in ketoconazole-induced long QT syndrome British Journal of Pharmacology. 153: 439-447. PMID 17965736 DOI: 10.1038/Sj.Bjp.0707537  0.691
2007 Balijepalli RC, Delisle BP, Balijepalli SY, Foell JD, Slind JK, Kamp TJ, January CT. Kv11.1 (ERG1) K+ channels localize in cholesterol and sphingolipid enriched membranes and are modulated by membrane cholesterol. Channels (Austin, Tex.). 1: 263-72. PMID 18708743 DOI: 10.4161/Chan.4946  0.622
2006 Rajamani S, Eckhardt LL, Valdivia CR, Klemens CA, Gillman BM, Anderson CL, Holzem KM, Delisle BP, Anson BD, Makielski JC, January CT. Drug-induced long QT syndrome: hERG K+ channel block and disruption of protein trafficking by fluoxetine and norfluoxetine. British Journal of Pharmacology. 149: 481-9. PMID 16967046 DOI: 10.1038/Sj.Bjp.0706892  0.679
2006 Anderson CL, Delisle BP, Anson BD, Kilby JA, Will ML, Tester DJ, Gong Q, Zhou Z, Ackerman MJ, January CT. Most LQT2 mutations reduce Kv11.1 (hERG) current by a class 2 (trafficking-deficient) mechanism. Circulation. 113: 365-73. PMID 16432067 DOI: 10.1161/Circulationaha.105.570200  0.704
2006 Kawakami K, Nagatomo T, Abe H, Kikuchi K, Takemasa H, Anson BD, Delisle BP, January CT, Nakashima Y. Comparison of HERG channel blocking effects of various beta-blockers-- implication for clinical strategy. British Journal of Pharmacology. 147: 642-52. PMID 16314852 DOI: 10.1038/Sj.Bjp.0706508  0.609
2006 Delisle BP, Underkofler HA, Anderson CL, January CT. AB1-4 Heart Rhythm. 3: S2. DOI: 10.1016/J.Hrthm.2006.02.025  0.5
2005 Delisle BP, Slind JK, Kilby JA, Anderson CL, Anson BD, Balijepalli RC, Tester DJ, Ackerman MJ, Kamp TJ, January CT. Intragenic suppression of trafficking-defective KCNH2 channels associated with long QT syndrome. Molecular Pharmacology. 68: 233-40. PMID 15851652 DOI: 10.1124/Mol.105.012914  0.694
2005 Delisle BP, Anderson CL, Anson BD, Kilby JA, Will ML, Tester DJ, Ackerman MJ, Gong Q, Zhou Z, January CT. Most LQT-linked KCNH2 mutations are trafficking-defective Heart Rhythm. 2: S175-S176. DOI: 10.1016/J.Hrthm.2005.02.547  0.632
2004 Delisle BP, Anson BD, Rajamani S, January CT. Biology of cardiac arrhythmias: ion channel protein trafficking. Circulation Research. 94: 1418-28. PMID 15192037 DOI: 10.1161/01.Res.0000128561.28701.Ea  0.645
2004 Anson BD, Ackerman MJ, Tester DJ, Will ML, Delisle BP, Anderson CL, January CT. Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channels. American Journal of Physiology. Heart and Circulatory Physiology. 286: H2434-41. PMID 14975928 DOI: 10.1152/Ajpheart.00891.2003  0.669
2004 Foell JD, Balijepalli RC, Delisle BP, Yunker AM, Robia SL, Walker JW, McEnery MW, January CT, Kamp TJ. Molecular heterogeneity of calcium channel beta-subunits in canine and human heart: evidence for differential subcellular localization. Physiological Genomics. 17: 183-200. PMID 14762176 DOI: 10.1152/Physiolgenomics.00207.2003  0.555
2003 Delisle BP, Satin J. Monovalent cations contribute to T-type calcium channel (Cav3.1 and Cav3.2) selectivity. The Journal of Membrane Biology. 193: 185-94. PMID 12962279 DOI: 10.1007/S00232-003-2017-9  0.661
2003 Delisle BP, Anderson CL, Balijepalli RC, Anson BD, Kamp TJ, January CT. Thapsigargin selectively rescues the trafficking defective LQT2 channels G601S and F805C. The Journal of Biological Chemistry. 278: 35749-54. PMID 12837749 DOI: 10.1074/Jbc.M305787200  0.703
2002 Mbai M, Rajamani S, Delisle BP, Anson BD, Anderson C, Makielski JC, January CT. Genetic basis for the origin of cardiac arrhythmias: implications for therapy. Current Cardiology Reports. 4: 411-7. PMID 12169238 DOI: 10.1007/S11886-002-0041-5  0.566
2002 Burgess DE, Crawford O, Delisle BP, Satin J. Mechanism of inactivation gating of human T-type (low-voltage activated) calcium channels. Biophysical Journal. 82: 1894-906. PMID 11916848 DOI: 10.1016/S0006-3495(02)75539-2  0.684
2002 Delisle B, Anderson C, January CT. 06 E4031 Rescue of HERG does not require the restoration of N-linked glycosyoltion Journal of Molecular and Cellular Cardiology. 34: A18. DOI: 10.1016/S0022-2828(02)90135-5  0.529
2001 Cribbs LL, Martin BL, Schroder EA, Keller BB, Delisle BP, Satin J. Identification of the t-type calcium channel (Ca(v)3.1d) in developing mouse heart. Circulation Research. 88: 403-7. PMID 11230107 DOI: 10.1161/01.Res.88.4.403  0.681
2000 Delisle BP, Satin J. pH modification of human T-type calcium channel gating. Biophysical Journal. 78: 1895-905. PMID 10733969 DOI: 10.1016/S0006-3495(00)76738-5  0.642
Show low-probability matches.