Year |
Citation |
Score |
2024 |
Miller JM, Carlson AE. Locking the hERG channel into place: Using a photoreactive unnatural amino acid to study voltage-gated channel movement. Biophysical Journal. PMID 39033327 DOI: 10.1016/j.bpj.2024.07.021 |
0.346 |
|
2024 |
Nguyen NH, Sheng S, Banerjee A, Guerriero CJ, Chen J, Wang X, Mackie TD, Welling PA, Kleyman TR, Bahar I, Carlson AE, Brodsky JL. Characterization of hyperactive mutations in the renal potassium channel ROMK uncovers unique effects on channel biogenesis and ion conductance. Molecular Biology of the Cell. mbcE23120494. PMID 39024255 DOI: 10.1091/mbc.E23-12-0494 |
0.314 |
|
2024 |
Nishio S, Emori C, Wiseman B, Fahrenkamp D, Dioguardi E, Zamora-Caballero S, Bokhove M, Han L, Stsiapanava A, Algarra B, Lu Y, Kodani M, Bainbridge RE, Komondor KM, Carlson AE, et al. ZP2 cleavage blocks polyspermy by modulating the architecture of the egg coat. Cell. 187: 1440-1459.e24. PMID 38490181 DOI: 10.1016/j.cell.2024.02.013 |
0.763 |
|
2023 |
Komondor KM, Bainbridge RE, Sharp KG, Iyer AR, Rosenbaum JC, Carlson AE. TMEM16A activation for the fast block to polyspermy in the African clawed frog does not require conventional activation of egg PLCs. The Journal of General Physiology. 155. PMID 37561060 DOI: 10.1085/jgp.202213258 |
0.81 |
|
2023 |
Bainbridge RE, Rosenbaum JC, Sau P, Carlson AE. lack the critical sperm factor PLCζ. Biorxiv : the Preprint Server For Biology. PMID 36778253 DOI: 10.1101/2023.02.02.526858 |
0.802 |
|
2022 |
Tembo M, Bainbridge RE, Lara-Santos C, Komondor KM, Daskivich GJ, Durrant JD, Rosenbaum JC, Carlson AE. Phosphate position is key in mediating transmembrane ion channel TMEM16A-phosphatidylinositol 4,5-bisphosphate interaction. The Journal of Biological Chemistry. 102264. PMID 35843309 DOI: 10.1016/j.jbc.2022.102264 |
0.736 |
|
2021 |
Tembo M, Sauer ML, Wisner BW, Beleny DO, Napolitano MA, Carlson AE. Actin polymerization is not required for the fast block to polyspermy in the African clawed frog, . Micropublication Biology. 2021. PMID 33598639 DOI: 10.17912/micropub.biology.000365 |
0.804 |
|
2020 |
Komondor KM, Carlson AE. The secrets of success. Elife. 9. PMID 33263540 DOI: 10.7554/eLife.64379 |
0.765 |
|
2020 |
Wozniak KL, Bainbridge RE, Summerville DW, Tembo M, Phelps WA, Sauer ML, Wisner BW, Czekalski ME, Pasumarthy S, Hanson ML, Linderman MB, Luu CH, Boehm ME, Sanders SM, Buckley KM, ... ... Carlson AE, et al. Zinc protection of fertilized eggs is an ancient feature of sexual reproduction in animals. Plos Biology. 18: e3000811. PMID 32735558 DOI: 10.1371/Journal.Pbio.3000811 |
0.774 |
|
2020 |
Bainbridge RE, Wozniak K, Phelps WA, Sanders SM, Nicotra ML, Lee MT, Carlson AE. Zinc Protection of Fertilized Eggs is Conserved in Non-Mammalian Species Biophysical Journal. 118: 563a. DOI: 10.1016/J.Bpj.2019.11.3072 |
0.765 |
|
2020 |
Tembo M, Carlson AE. Phosphate Position on Phosphoinositides is Key in Mediating TMEM16A Currents in Xenopus laevis Oocytes Biophysical Journal. 118: 554a. DOI: 10.1016/J.Bpj.2019.11.3029 |
0.799 |
|
2019 |
Carlson AE. Mechanical stimulation activates eggs via Trpm channels. Proceedings of the National Academy of Sciences of the United States of America. PMID 31455728 DOI: 10.1073/Pnas.1913150116 |
0.519 |
|
2019 |
Bainbridge RE, Carlson AE. Tiny Dancer: EFCAB9 Triggers Sperm Hyperactivation via CatSper. Trends in Biochemical Sciences. PMID 31447243 DOI: 10.1016/J.Tibs.2019.08.001 |
0.85 |
|
2019 |
Tembo M, Wozniak KL, Bainbridge RE, Carlson AE. Phosphatidylinositol 4,5-bisphosphate (PIP) and Ca are both required to open the Cl channel TMEM16A. The Journal of Biological Chemistry. PMID 31266809 DOI: 10.1074/Jbc.Ra118.007128 |
0.823 |
|
2019 |
Wozniak KL, Carlson AE. Ion channels and signaling pathways used in the fast polyspermy block. Molecular Reproduction and Development. PMID 31087507 DOI: 10.1002/Mrd.23168 |
0.805 |
|
2019 |
Tembo M, Carlson AE. Under pressure: Ano1 mediates pressure sensing in the lymphatic system. The Journal of General Physiology. PMID 30886053 DOI: 10.1085/Jgp.201912320 |
0.832 |
|
2019 |
Wozniak KL, Phelps WA, Lee MT, Carlson AE. Extracellular zinc Contributes to the Slow Polyspermy Block Biophysical Journal. 116: 525a. DOI: 10.1016/J.Bpj.2018.11.2829 |
0.333 |
|
2019 |
Tembo M, Bainbridge RE, Carlson AE. Pip2 Potentiates the Ca2+-Activated Cl− Channel TMEM16A in Xenopus laevis Oocytes Biophysical Journal. 116: 222a. DOI: 10.1016/J.Bpj.2018.11.1224 |
0.838 |
|
2018 |
Wozniak KL, Phelps WA, Tembo M, Lee MT, Carlson AE. The TMEM16A channel mediates the fast polyspermy block in . The Journal of General Physiology. PMID 30012842 DOI: 10.1085/Jgp.201812071 |
0.858 |
|
2018 |
Wozniak KL, Tembo M, Phelps WA, Lee MT, Carlson AE. PLC and IP-evoked Ca release initiate the fast block to polyspermy in eggs. The Journal of General Physiology. PMID 30012841 DOI: 10.1085/Jgp.201812069 |
0.84 |
|
2018 |
Tembo M, Carlson AE. PIP2 and CA2+ are Both Required to Open TMEM16a Channels in Xenopus Laevis Oocytes Biophysical Journal. 114: 610a. DOI: 10.1016/J.Bpj.2017.11.3336 |
0.857 |
|
2017 |
Wozniak KL, Mayfield BL, Duray AM, Tembo M, Beleny DO, Napolitano MA, Sauer ML, Wisner BW, Carlson AE. Extracellular Ca2+ Is Required for Fertilization in the African Clawed Frog, Xenopus laevis. Plos One. 12: e0170405. PMID 28114360 DOI: 10.1371/Journal.Pone.0170405 |
0.812 |
|
2017 |
Wozniak KL, Mayfield BL, Carlson AE. TMEM16A Mediates the Fast Block to Polyspermy in Xenopus Laevis Eggs Biophysical Journal. 112: 552a. DOI: 10.1016/J.Bpj.2016.11.2978 |
0.603 |
|
2016 |
Wozniak KL, Carlson AE. Calcium Signaling Required for the Fast Polyspermy Block in Xenopus Laevis Biophysical Journal. 110: 359a. DOI: 10.1016/J.Bpj.2015.11.1936 |
0.555 |
|
2014 |
Haitin Y, Carlson AE, Zagotta WN. The Molecular Basis of KCNH Channel Regulation by the EAG Domain Biophysical Journal. 106: 737a. DOI: 10.1016/J.Bpj.2013.11.4063 |
0.648 |
|
2013 |
Carlson AE, Rosenbaum JC, Brelidze TI, Klevit RE, Zagotta WN. Flavonoid regulation of HCN2 channels. The Journal of Biological Chemistry. 288: 33136-45. PMID 24085296 DOI: 10.1074/Jbc.M113.501759 |
0.812 |
|
2013 |
Haitin Y, Carlson AE, Zagotta WN. The structural mechanism of KCNH-channel regulation by the eag domain. Nature. 501: 444-8. PMID 23975098 DOI: 10.1038/Nature12487 |
0.656 |
|
2013 |
Carlson AE, Brelidze TI, Zagotta WN. Flavonoid regulation of EAG1 channels. The Journal of General Physiology. 141: 347-58. PMID 23440277 DOI: 10.1085/Jgp.201210900 |
0.812 |
|
2012 |
Brelidze TI, Carlson AE, Sankaran B, Zagotta WN. Structure of the carboxy-terminal region of a KCNH channel. Nature. 481: 530-3. PMID 22230959 DOI: 10.1038/Nature10735 |
0.805 |
|
2012 |
Brelidze TI, Carlson AE, Sankaran B, Zagotta WN. Structure of the C-Terminal Region of a KCNH Channel Biophysical Journal. 102: 37a. DOI: 10.1016/J.Bpj.2011.11.230 |
0.809 |
|
2012 |
Carlson AE, Brelidze TI, Zagotta WN. Fisetin Regulation of HCN2 and Eag1 Channels Reveals Conserved Gating Mechanisms Biophysical Journal. 102: 330a. DOI: 10.1016/J.Bpj.2011.11.1810 |
0.813 |
|
2011 |
Carlson AE, Drum BM, Zagotta WN. Deletion of the Amino-Terminus Uncovers an Inactivated State in Eag1 Channels Biophysical Journal. 100: 30a. DOI: 10.1016/J.Bpj.2010.12.367 |
0.694 |
|
2010 |
Brelidze TI, Carlson AE, Davies DR, Stewart LJ, Zagotta WN. Identifying regulators for EAG1 channels with a novel electrophysiology and tryptophan fluorescence based screen. Plos One. 5. PMID 20824064 DOI: 10.1371/Journal.Pone.0012523 |
0.797 |
|
2010 |
Carlson AE, Brelidze TI, Davies DR, Zagotta W. Flavonoids Regulate Eag1 Channels Biophysical Journal. 98: 1a. DOI: 10.1016/J.Bpj.2009.11.037 |
0.803 |
|
2009 |
Carlson AE, Burnett LA, del Camino D, Quill TA, Hille B, Chong JA, Moran MM, Babcock DF. Pharmacological targeting of native CatSper channels reveals a required role in maintenance of sperm hyperactivation. Plos One. 4: e6844. PMID 19718436 DOI: 10.1371/Journal.Pone.0006844 |
0.845 |
|
2009 |
Brelidze TI, Carlson AE, Zagotta WN. Absence of direct cyclic nucleotide modulation of mEAG1 and hERG1 channels revealed with fluorescence and electrophysiological methods. The Journal of Biological Chemistry. 284: 27989-97. PMID 19671703 DOI: 10.1074/Jbc.M109.016337 |
0.802 |
|
2009 |
Carlson AE, Davies D, Zagotta WN. A Regulator for Eag Family Channels Biophysical Journal. 96: 562a. DOI: 10.1016/J.Bpj.2008.12.3684 |
0.677 |
|
2007 |
Carlson AE, Hille B, Babcock DF. External Ca2+ acts upstream of adenylyl cyclase SACY in the bicarbonate signaled activation of sperm motility. Developmental Biology. 312: 183-92. PMID 17950270 DOI: 10.1016/J.Ydbio.2007.09.017 |
0.786 |
|
2006 |
Xie F, Garcia MA, Carlson AE, Schuh SM, Babcock DF, Jaiswal BS, Gossen JA, Esposito G, van Duin M, Conti M. Soluble adenylyl cyclase (sAC) is indispensable for sperm function and fertilization. Developmental Biology. 296: 353-62. PMID 16842770 DOI: 10.1016/J.Ydbio.2006.05.038 |
0.814 |
|
2006 |
Schuh SM, Carlson AE, McKnight GS, Conti M, Hille B, Babcock DF. Signaling pathways for modulation of mouse sperm motility by adenosine and catecholamine agonists. Biology of Reproduction. 74: 492-500. PMID 16291925 DOI: 10.1095/Biolreprod.105.047837 |
0.816 |
|
2005 |
Carlson AE, Quill TA, Westenbroek RE, Schuh SM, Hille B, Babcock DF. Identical phenotypes of CatSper1 and CatSper2 null sperm. The Journal of Biological Chemistry. 280: 32238-44. PMID 16036917 DOI: 10.1074/Jbc.M501430200 |
0.837 |
|
2003 |
Carlson AE, Westenbroek RE, Quill T, Ren D, Clapham DE, Hille B, Garbers DL, Babcock DF. CatSper1 required for evoked Ca2+ entry and control of flagellar function in sperm. Proceedings of the National Academy of Sciences of the United States of America. 100: 14864-8. PMID 14657352 DOI: 10.1073/Pnas.2536658100 |
0.832 |
|
2003 |
Wennemuth G, Carlson AE, Harper AJ, Babcock DF. Bicarbonate actions on flagellar and Ca2+ -channel responses: initial events in sperm activation. Development (Cambridge, England). 130: 1317-26. PMID 12588848 DOI: 10.1242/Dev.00353 |
0.77 |
|
2003 |
Rosenbaum T, Islas LD, Carlson AE, Gordon SE. Dequalinium: a novel, high-affinity blocker of CNGA1 channels. The Journal of General Physiology. 121: 37-47. PMID 12508052 DOI: 10.1085/Jgp.20028716 |
0.794 |
|
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