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Items: 1 to 20 of 43

1.
The role of SK3 in progesterone-induced inhibition of human fallopian tubal contraction
Duo Zhang, Qian Zhu, Wei Xia, Chenfeng Zhu, Xiaoya Zhao, Yiqin Zhang, Chuqing He, Sifan Ji, Xiaocui Li, Jian Zhang
Reprod Biol Endocrinol. 2022; 20: 73. Published online 2022 Apr 29. doi: 10.1186/s12958-022-00932-3
PMCID:
PMC9052544
AbstractArticlePDF–5.0M
2.
Low expression of KCNN3 may affect drug resistance in ovarian cancer
Xia Liu, Luwei Wei, Bingbing Zhao, Xiangxue Cai, Caihua Dong, Fuqiang Yin
Mol Med Rep. 2018 Aug; 18(2): 1377–1386. Published online 2018 May 31. doi: 10.3892/mmr.2018.9107
PMCID:
PMC6072180
AbstractArticlePDF–1.8M
3.
The impact of down-regulated SK3 expressions on Hirschsprung disease
Gunadi, Mukhamad Sunardi, Nova Yuli Prasetyo Budi, Alvin Santoso Kalim, Kristy Iskandar, Andi Dwihantoro
BMC Med Genet. 2018; 19: 24. Published online 2018 Feb 13. doi: 10.1186/s12881-018-0539-3
PMCID:
PMC5811966
AbstractArticlePDF–454K
4.
Immunolocalization and expression of small-conductance calcium-activated potassium channels in human myometrium
Sofia T Rosenbaum, Julie Svalø, Karsten Nielsen, Torben Larsen, Jørgen C Jørgensen, Pierre Bouchelouche
J Cell Mol Med. 2012 Dec; 16(12): 3001–3008. Published online 2012 Dec 13. doi: 10.1111/j.1582-4934.2012.01627.x
PMCID:
PMC4393728
AbstractArticlePDF–725K
5.
Intermediate Conductance Ca2+-Activated K+ Channels Modulate Human Placental Trophoblast Syncytialization
Paula Díaz, Amber M. Wood, Colin P. Sibley, Susan L. Greenwood
PLoS One. 2014; 9(3): e90961. Published online 2014 Mar 3. doi: 10.1371/journal.pone.0090961
PMCID:
PMC3940956
AbstractArticlePDF–8.7M
6.
Disruption of Dopamine Neuron Activity Pattern Regulation through Selective Expression of a Human KCNN3 Mutation
Marta E. Soden, Graham L. Jones, Christina A. Sanford, Amanda S. Chung, Ali D. Güler, Charles Chavkin, Rafael Luján, Larry S. Zweifel
Neuron. Author manuscript; available in PMC 2014 Nov 20.
Published in final edited form as: Neuron. 2013 Nov 20; 80(4): 10.1016/j.neuron.2013.07.044. Published online 2013 Oct 24. doi: 10.1016/j.neuron.2013.07.044
PMCID:
PMC3840077
AbstractArticlePDF–2.0M
7.
Two Conserved Arginine Residues from the SK3 Potassium Channel Outer Vestibule Control Selectivity of Recognition by Scorpion Toxins
Jing Feng, Youtian Hu, Hong Yi, Shijin Yin, Song Han, Jun Hu, Zongyun Chen, Weishan Yang, Zhijian Cao, Michel De Waard, Jean-Marc Sabatier, Wenxin Li, Yingliang Wu
J Biol Chem. 2013 May 3; 288(18): 12544–12553. Published online 2013 Mar 19. doi: 10.1074/jbc.M112.433888
PMCID:
PMC3642302
AbstractArticlePDF–3.5M
8.
A CAG repeat polymorphism of KCNN3 predicts SK3 channel function and cognitive performance in schizophrenia
Sabrina Grube, Martin F Gerchen, Bartosz Adamcio, Luis A Pardo, Sabine Martin, Dörthe Malzahn, Sergi Papiol, Martin Begemann, Katja Ribbe, Heidi Friedrichs, Konstantin A Radyushkin, Michael Müller, Fritz Benseler, Joachim Riggert, Peter Falkai, Heike Bickeböller, Klaus-Armin Nave, Nils Brose, Walter Stühmer, Hannelore Ehrenreich
EMBO Mol Med. 2011 Jun; 3(6): 309–319. doi: 10.1002/emmm.201100135
PMCID:
PMC3377084
AbstractArticlePDF–612K
9.
Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate
Hannah C. Cox, Rod A. Lea, Claire Bellis, Melanie Carless, Tom Dyer, John Blangero, Lyn R. Griffiths
J Headache Pain. 2011 Dec; 12(6): 603–608. Published online 2011 Oct 22. doi: 10.1007/s10194-011-0392-7
PMCID:
PMC3208049
AbstractArticlePDF–217K
10.
Single-Nucleotide Polymorphisms in the KCNN3 Gene Associate With Preterm Birth
Lori J. Day, Kendra L. Schaa, Kelli K. Ryckman, Meg Cooper, John M. Dagle, Chin-To Fong, Hyagriv N. Simhan, David C. Merrill, Mary L. Marazita, Jeffrey C. Murray, Sarah K. England
Reprod Sci. 2011 Mar; 18(3): 286–295. doi: 10.1177/1933719110391277
PMCID:
PMC3053422
AbstractArticlePDF–453K
11.
Analysis of Single Nucleotide Polymorphisms (SNPs) of the small-conductance calcium activated potassium channel (SK3) gene as genetic modifier of the cardiac phenotype in myotonic dystrophy type 1 patients
F Rinaldi, A Botta, L Vallo, G Contino, A Morgante, R Iraci, C Catalli, G Silvestri, VM Ventriglia, L Politano, G Novelli
Acta Myol. 2008 Dec; 27(3): 82–89.
PMCID:
PMC2858941
AbstractArticlePDF–475K
12.
Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility
Robert Curtain, James Sundholm, Rod Lea, Mick Ovcaric, John MacMillan, Lyn Griffiths
BMC Med Genet. 2005; 6: 32. Published online 2005 Sep 14. doi: 10.1186/1471-2350-6-32
PMCID:
PMC1236929
AbstractArticlePDF–294K
13.
Preferential formation of human heteromeric SK2:SK3 channels limits homomeric SK channel assembly and function
Andrew S. Butler, Jules C. Hancox, Neil V. Marrion
J Biol Chem. 2023 Jan; 299(1): 102783. Published online 2022 Dec 9. doi: 10.1016/j.jbc.2022.102783
PMCID:
PMC9841042
AbstractArticlePDF–1.9M
14.
Hypoxia Promotes Prostate Cancer Aggressiveness by Upregulating EMT-Activator Zeb1 and SK3 Channel Expression
Fanny Bery, Sandy Figiel, Sana Kouba, Delphine Fontaine, Maxime Guéguinou, Marie Potier-Cartereau, Christophe Vandier, Roseline Guibon, Franck Bruyère, Gaëlle Fromont, Karine Mahéo
Int J Mol Sci. 2020 Jul; 21(13): 4786. Published online 2020 Jul 6. doi: 10.3390/ijms21134786
PMCID:
PMC7369999
AbstractArticlePDF–1.1M
15.
Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome
Christiane K. Bauer, Pauline E. Schneeberger, Fanny Kortüm, Janine Altmüller, Fernando Santos-Simarro, Laura Baker, Jennifer Keller-Ramey, Susan M. White, Philippe M. Campeau, Karen W. Gripp, Kerstin Kutsche
Am J Hum Genet. 2019 Jun 6; 104(6): 1139–1157. Published online 2019 May 30. doi: 10.1016/j.ajhg.2019.04.012
PMCID:
PMC6562147
AbstractArticlePDF–2.5M
16.
SK3 channel and mitochondrial ROS mediate NADPH oxidase-independent NETosis induced by calcium influx
David Nobuhiro Douda, Meraj A. Khan, Hartmut Grasemann, Nades Palaniyar
Proc Natl Acad Sci U S A. 2015 Mar 3; 112(9): 2817–2822. Published online 2015 Feb 17. doi: 10.1073/pnas.1414055112
PMCID:
PMC4352781
AbstractArticlePDF–1.2M
17.
Genetic Influences on Preterm Birth in Argentina
Paul C. Mann, Margaret E. Cooper, Kelli K. Ryckman, Belén Comas, Juan Gili, Suzanne Crumley, Elise N.A. Bream, Heather M. Byers, Travis Piester, Amanda Schaefer, Paul J. Christine, Amy Lawrence, Kendra L. Schaa, Keegan J.P. Kelsey, Susan K. Berends, Enrique Gadow, Viviana Cosentino, Eduardo E. Castilla, Jorge López Camelo, Cesar Saleme, Lori J. Day, Sarah K. England, Mary L. Marazita, John M. Dagle, Jeffrey C. Murray
J Perinatol. Author manuscript; available in PMC 2013 Nov 1.
Published in final edited form as: J Perinatol. 2013 May; 33(5): 336–340. Published online 2012 Sep 27. doi: 10.1038/jp.2012.118
PMCID:
PMC3719965
AbstractArticlePDF–399K
18.
Regulation of the SK3 channel by MicroRNA-499 - potential role in atrial fibrillation
Tian-You Ling, Xiao-Li Wang, Qiang Chai, Tin-Wah Lau, Celeste M. Koestler, Soon J. Park, Richard C. Daly, Kevin L. Greason, Jin Jen, Li-Qun Wu, Wei-Feng Shen, Win-Kuang Shen, Yong-Mei Cha, Hon-Chi Lee
Heart Rhythm. Author manuscript; available in PMC 2014 Jul 1.
Published in final edited form as: Heart Rhythm. 2013 Jul; 10(7): 1001–1009. Published online 2013 Mar 14. doi: 10.1016/j.hrthm.2013.03.005
PMCID:
PMC3710704
AbstractArticlePDF–1.9M
19.
Recycling of the Ca2+-activated K+ Channel, KCa2.3, Is Dependent upon RME-1, Rab35/EPI64C, and an N-terminal Domain
Yajuan Gao, Corina M. Balut, Mark A. Bailey, Genaro Patino-Lopez, Stephen Shaw, Daniel C. Devor
J Biol Chem. 2010 Jun 4; 285(23): 17938–17953. Published online 2010 Apr 1. doi: 10.1074/jbc.M109.086553
PMCID:
PMC2878556
AbstractArticlePDF–3.3M
20.
Common Variants in KCNN3 are Associated with Lone Atrial Fibrillation
Patrick T. Ellinor, Kathryn L. Lunetta, Nicole L. Glazer, Arne Pfeufer, Alvaro Alonso, Mina K. Chung, Moritz F. Sinner, Paul I. W. de Bakker, Martina Mueller, Steven A. Lubitz, Ervin Fox, Dawood Darbar, Nicholas L. Smith, Jonathan D. Smith, Renate B. Schnabel, Elsayed Z. Soliman, Kenneth M. Rice, David R. Van Wagoner, Britt-M. Beckmann, Charlotte van Noord, Ke Wang, Georg B. Ehret, Jerome I. Rotter, Stanley L. Hazen, Gerhard Steinbeck, Albert V. Smith, Lenore J. Launer, Tamara B. Harris, Seiko Makino, Mari Nelis, David J. Milan, Siegfried Perz, Tõnu Esko, Anna Köttgen, Susanne Moebus, Christopher Newton-Cheh, Man Li, Stefan Möhlenkamp, Thomas J. Wang, W.H. Linda Kao, Ramachandran S. Vasan, Markus M. Nöthen, Calum A. MacRae, Bruno H. Ch. Stricker, Albert Hofman, André G. Uitterlinden, Daniel Levy, Eric Boerwinkle, Andres Metspalu, Eric J. Topol, Aravinda Chakravarti, Vilmundur Gudnason, Bruce M. Psaty, Dan M. Roden, Thomas Meitinger, H.-Erich Wichmann, Jacqueline C.M. Witteman, John Barnard, Dan E. Arking, Emelia J. Benjamin, Susan R. Heckbert, Stefan Kääb
Nat Genet. Author manuscript; available in PMC 2010 Sep 1.
Published in final edited form as: Nat Genet. 2010 Mar; 42(3): 240–244. Published online 2010 Feb 21. doi: 10.1038/ng.537
PMCID:
PMC2871387
AbstractArticlePDF–355K

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