| Year |
Citation |
Score |
| 2021 |
Mathiharan YK, Glaaser IW, Zhao Y, Robertson MJ, Skiniotis G, Slesinger PA. Structural insights into GIRK2 channel modulation by cholesterol and PIP. Cell Reports. 36: 109619. PMID 34433062 DOI: 10.1016/j.celrep.2021.109619 |
0.41 |
|
| 2021 |
Zhao Y, Gameiro-Ros I, Glaaser IW, Slesinger PA. Advances in Targeting GIRK Channels in Disease. Trends in Pharmacological Sciences. 42: 203-215. PMID 33468322 DOI: 10.1016/j.tips.2020.12.002 |
0.367 |
|
| 2020 |
Zhao Y, Ung PM, Zahoránszky-Kőhalmi G, Zakharov AV, Martinez NJ, Simeonov A, Glaaser IW, Rai G, Schlessinger A, Marugan JJ, Slesinger PA. Identification of a G-Protein-Independent Activator of GIRK Channels. Cell Reports. 31: 107770. PMID 32553165 DOI: 10.1016/J.Celrep.2020.107770 |
0.46 |
|
| 2020 |
Glaaser IW, Mathiharan YK, Zhao Y, Skiniotis G, Slesinger PA. CRYO-EM Structures of the GIRK2 Channel Reveal Mechanisms for Lipid Modulation Biophysical Journal. 118: 497a-498a. DOI: 10.1016/J.Bpj.2019.11.2749 |
0.523 |
|
| 2017 |
Lacin E, Aryal P, Glaaser IW, Bodhinathan K, Tsai E, Marsh N, Tucker SJ, Sansom MSP, Slesinger PA. Dynamic role of the tether helix in PIP2-dependent gating of a G protein-gated potassium channel. The Journal of General Physiology. PMID 28720589 DOI: 10.1085/Jgp.201711801 |
0.515 |
|
| 2017 |
Glaaser IW, Slesinger PA. Dual activation of neuronal G protein-gated inwardly rectifying potassium (GIRK) channels by cholesterol and alcohol. Scientific Reports. 7: 4592. PMID 28676630 DOI: 10.1038/S41598-017-04681-X |
0.4 |
|
| 2017 |
Glaaser IW, Slesinger PA. Small Molecule Modulation of Brain GIRK Channels Biophysical Journal. 112: 182a-183a. DOI: 10.1016/J.Bpj.2016.11.1012 |
0.45 |
|
| 2015 |
Glaaser IW, Slesinger PA. Structural Insights into GIRK Channel Function. International Review of Neurobiology. 123: 117-60. PMID 26422984 DOI: 10.1016/Bs.Irn.2015.05.014 |
0.524 |
|
| 2015 |
Glaaser IW, Marsh NO, Choe S, Slesinger PA. Alcohol Inhibition of a Chemically-Activated GIRK2 Channel Biophysical Journal. 108: 367a. DOI: 10.1016/J.Bpj.2014.11.2013 |
0.352 |
|
| 2012 |
Glaaser IW, Osteen JD, Puckerin A, Sampson KJ, Jin X, Kass RS. Perturbation of sodium channel structure by an inherited Long QT Syndrome mutation. Nature Communications. 3: 706. PMID 22426227 DOI: 10.1038/Ncomms1717 |
0.746 |
|
| 2011 |
Glaaser IW, Osteen JD, Puckerin A, Kass RS. Mapping the Structure of the Cardiac Voltage-Gated Sodium Channel (Nav1.5) C-Terminus: Implications of An Lqt3 Mutant Biophysical Journal. 100: 15a. DOI: 10.1016/J.Bpj.2010.12.293 |
0.717 |
|
| 2008 |
Holland KD, Kearney JA, Glauser TA, Buck G, Keddache M, Blankston JR, Glaaser IW, Kass RS, Meisler MH. Mutation of sodium channel SCN3A in a patient with cryptogenic pediatric partial epilepsy. Neuroscience Letters. 433: 65-70. PMID 18242854 DOI: 10.1016/J.Neulet.2007.12.064 |
0.668 |
|
| 2007 |
Bankston JR, Sampson KJ, Kateriya S, Glaaser IW, Malito DL, Chung WK, Kass RS. A novel LQT-3 mutation disrupts an inactivation gate complex with distinct rate-dependent phenotypic consequences. Channels (Austin, Tex.). 1: 273-80. PMID 18708744 DOI: 10.4161/Chan.4956 |
0.748 |
|
| 2007 |
Kass RS, Cormier JW, Glaaser IW. The Cardiac Sodium-Channel Carboxy Terminus: Predicted and Detected Structure Provide a Novel Target For Antiarrhythmic Drugs Development New Arrhythmia Technologies. 36-47. DOI: 10.1002/9780470988725.ch4 |
0.717 |
|
| 2006 |
Glaaser IW, Bankston JR, Liu H, Tateyama M, Kass RS. A carboxyl-terminal hydrophobic interface is critical to sodium channel function. Relevance to inherited disorders. The Journal of Biological Chemistry. 281: 24015-23. PMID 16798729 DOI: 10.1074/Jbc.M605473200 |
0.764 |
|
| 2006 |
Glaaser IW, Clancy CE. Cardiac Na+ channels as therapeutic targets for antiarrhythmic agents. Handbook of Experimental Pharmacology. 99-121. PMID 16610342 DOI: 10.1007/3-540-29715-4_4 |
0.604 |
|
| 2005 |
Lam AD, Chikina MD, McNulty MM, Glaaser IW, Hanck DA. Role of Domain IV/S4 outermost arginines in gating of T-type calcium channels. Pflã¼Gers Archiv : European Journal of Physiology. 451: 349-61. PMID 16133267 DOI: 10.1007/S00424-005-1407-5 |
0.474 |
|
| 2004 |
Sunami A, Tracey A, Glaaser IW, Lipkind GM, Hanck DA, Fozzard HA. Accessibility of mid-segment domain IV S6 residues of the voltage-gated Na+ channel to methanethiosulfonate reagents. The Journal of Physiology. 561: 403-13. PMID 15579536 DOI: 10.1113/jphysiol.2004.067579 |
0.518 |
|
| 2004 |
Sandtner W, Szendroedi J, Zarrabi T, Zebedin E, Hilber K, Glaaser I, Fozzard HA, Dudley SC, Todt H. Lidocaine: A foot in the door of the inner vestibule prevents ultra-slow inactivation of a voltage-gated sodium channel Molecular Pharmacology. 66: 648-657. PMID 15322257 DOI: 10.1124/Mol.66.3 |
0.541 |
|
| 2004 |
Motoike HK, Liu H, Glaaser IW, Yang AS, Tateyama M, Kass RS. The Na+ channel inactivation gate is a molecular complex: a novel role of the COOH-terminal domain. The Journal of General Physiology. 123: 155-65. PMID 14744988 DOI: 10.1085/Jgp.200308929 |
0.731 |
|
| 2003 |
Glaaser IW, Kass RS, Clancy CE. Mechanisms of genetic arrhythmias: from DNA to ECG. Progress in Cardiovascular Diseases. 46: 259-70. PMID 14685943 DOI: 10.1016/S0033-0620(03)00073-2 |
0.591 |
|
| 2003 |
Bai CX, Glaaser IW, Sawanobori T, Sunami A. Involvement of local anesthetic binding sites on IVS6 of sodium channels in fast and slow inactivation. Neuroscience Letters. 337: 41-5. PMID 12524167 DOI: 10.1016/S0304-3940(02)01288-0 |
0.424 |
|
| 2002 |
Hilber K, Sandtner W, Kudlacek O, Schreiner B, Glaaser I, Schütz W, Fozzard HA, Dudley SC, Todt H. Interaction between fast and ultra-slow inactivation in the voltage-gated sodium channel. Does the inactivation gate stabilize the channel structure? Journal of Biological Chemistry. 277: 37105-37115. PMID 12138168 DOI: 10.1074/jbc.M205661200 |
0.534 |
|
| 2001 |
Hilber K, Sandtner W, Kudlacek O, Glaaser IW, Weisz E, Kyle JW, French RJ, Fozzard HA, Dudley SC, Todt H. The selectivity filter of the voltage-gated sodium channel is involved in channel activation. The Journal of Biological Chemistry. 276: 27831-9. PMID 11382756 DOI: 10.1074/jbc.M101933200 |
0.504 |
|
| 2001 |
Sunami A, Glaaser IW, Fozzard HA. Structural and gating changes of the sodium channel induced by mutation of a residue in the upper third of IVS6, creating an external access path for local anesthetics. Molecular Pharmacology. 59: 684-91. PMID 11259611 |
0.401 |
|
| 2000 |
Sunami A, Glaaser IW, Fozzard HA. A critical residue for isoform difference in tetrodotoxin affinity is a molecular determinant of the external access path for local anesthetics in the cardiac sodium channel. Proceedings of the National Academy of Sciences of the United States of America. 97: 2326-31. PMID 10681444 DOI: 10.1073/pnas.030438797 |
0.521 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2019 |
Zuo H, Glaaser I, Zhao Y, Kurinov I, Mosyak L, Wang H, Liu J, Park J, Frangaj A, Sturchler E, Zhou M, McDonald P, Geng Y, Slesinger PA, Fan QR. Structural basis for auxiliary subunit KCTD16 regulation of the GABA receptor. Proceedings of the National Academy of Sciences of the United States of America. PMID 30971491 DOI: 10.1073/Pnas.1903024116 |
0.292 |
|
| Hide low-probability matches. |