Distribution analysis of human two pore domain potassium channels in tissues of the central nervous system and periphery
Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions. The most recently described family of K+ channels, the ‘two pore-domain family’, contain four membrane spanning domains and two pore-forming do...
Saved in:
Published in | Brain research. Molecular brain research. Vol. 86; no. 1-2; pp. 101 - 114 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
31.01.2001
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0169-328X 1872-6941 |
DOI | 10.1016/S0169-328X(00)00263-1 |
Cover
Abstract | Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions. The most recently described family of K+ channels, the ‘two pore-domain family’, contain four membrane spanning domains and two pore-forming domains, suggesting that two channel subunits associate to form a functional K+ pore. Several sub-families of the two pore domain potassium channel family have been described, including the weakly inward rectifying K+ channel (TWIK), the acid-sensitive K+ channel (TASK), the TWIK-related K+ channel (TREK) and the TWIK-related arachidonic acid stimulated K+ channel (TRAAK). However, comparison of the mRNA expression of these channels has been difficult due to the differences in methods used and the species studied. In the present study, we used a single technique, TaqMan semi-quantitative reverse transcription polymerase chain reaction (RT-PCR), to investigate the mRNA distribution of all currently known two pore potassium channels in human central nervous system (CNS) and peripheral tissues. TWIK-1 and the TWIK-1-like channel KCNK7 were predominantly expressed in the CNS, in contrast to TWIK-2 which was preferentially expressed in peripheral tissues such as pancreas, stomach, spleen and uterus. TASK-1 was expressed in the CNS and some peripheral tissues, whereas TASK-2 was exclusively expressed in the periphery except for mRNA expression observed in dorsal root ganglion and spinal cord. In addition, mRNA expression of the recently identified TASK-3, was almost completely exclusive to cerebellum with little or no mRNA detected in any other tissues. TREK-1 and TRAAK mRNA expression was predominantly CNS specific in contrast to the closely related TREK-2, which was expressed in both CNS and peripheral tissues. Studying the mRNA expression profiles of known two pore domain K+ channels will aid in the understanding of the biological roles of these channels. Furthermore, identification of common areas of expression may help identify which channels, if any, associate to form heteromeric K+ channel complexes. |
---|---|
AbstractList | Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions. The most recently described family of K super(+) channels, the 'two pore-domain family', contain four membrane spanning domains and two pore-forming domains, suggesting that two channel subunits associate to form a functional K super(+) pore. Several sub-families of the two pore domain potassium channel family have been described, including the weakly inward rectifying K super(+) channel (TWIK), the acid-sensitive K super(+) channel (TASK), the TWIK-related K super(+) channel (TREK) and the TWIK-related arachidonic acid stimulated K super(+) channel (TRAAK). However, comparison of the mRNA expression of these channels has been difficult due to the differences in methods used and the species studied. In the present study, we used a single technique, TaqMan semi-quantitative reverse transcription polymerase chain reaction (RT-PCR), to investigate the mRNA distribution of all currently known two pore potassium channels in human central nervous system (CNS) and peripheral tissues. TWIK-1 and the TWIK-1-like channel KCNK7 were predominantly expressed in the CNS, in contrast to TWIK-2 which was preferentially expressed in peripheral tissues such as pancreas, stomach, spleen and uterus. TASK-1 was expressed in the CNS and some peripheral tissues, whereas TASK-2 was exclusively expressed in the periphery except for mRNA expression observed in dorsal root ganglion and spinal cord. In addition, mRNA expression of the recently identified TASK-3, was almost completely exclusive to cerebellum with little or no mRNA detected in any other tissues. TREK-1 and TRAAK mRNA expression was predominantly CNS specific in contrast to the closely related TREK-2, which was expressed in both CNS and peripheral tissues. Studying the mRNA expression profiles of known two pore domain K super(+) channels will aid in the understanding of the biological roles of these channels. Furthermore, identification of common areas of expression may help identify which channels, if any, associate to form heteromeric K super(+) channel complexes. Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions. The most recently described family of K+ channels, the ‘two pore-domain family’, contain four membrane spanning domains and two pore-forming domains, suggesting that two channel subunits associate to form a functional K+ pore. Several sub-families of the two pore domain potassium channel family have been described, including the weakly inward rectifying K+ channel (TWIK), the acid-sensitive K+ channel (TASK), the TWIK-related K+ channel (TREK) and the TWIK-related arachidonic acid stimulated K+ channel (TRAAK). However, comparison of the mRNA expression of these channels has been difficult due to the differences in methods used and the species studied. In the present study, we used a single technique, TaqMan semi-quantitative reverse transcription polymerase chain reaction (RT-PCR), to investigate the mRNA distribution of all currently known two pore potassium channels in human central nervous system (CNS) and peripheral tissues. TWIK-1 and the TWIK-1-like channel KCNK7 were predominantly expressed in the CNS, in contrast to TWIK-2 which was preferentially expressed in peripheral tissues such as pancreas, stomach, spleen and uterus. TASK-1 was expressed in the CNS and some peripheral tissues, whereas TASK-2 was exclusively expressed in the periphery except for mRNA expression observed in dorsal root ganglion and spinal cord. In addition, mRNA expression of the recently identified TASK-3, was almost completely exclusive to cerebellum with little or no mRNA detected in any other tissues. TREK-1 and TRAAK mRNA expression was predominantly CNS specific in contrast to the closely related TREK-2, which was expressed in both CNS and peripheral tissues. Studying the mRNA expression profiles of known two pore domain K+ channels will aid in the understanding of the biological roles of these channels. Furthermore, identification of common areas of expression may help identify which channels, if any, associate to form heteromeric K+ channel complexes. Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions. The most recently described family of K+ channels, the 'two pore-domain family', contain four membrane spanning domains and two pore-forming domains, suggesting that two channel subunits associate to form a functional K+ pore. Several sub-families of the two pore domain potassium channel family have been described, including the weakly inward rectifying K+ channel (TWIK), the acid-sensitive K+ channel (TASK), the TWIK-related K+ channel (TREK) and the TWIK-related arachidonic acid stimulated K+ channel (TRAAK). However, comparison of the mRNA expression of these channels has been difficult due to the differences in methods used and the species studied. In the present study, we used a single technique, TaqMan semi-quantitative reverse transcription polymerase chain reaction (RT-PCR), to investigate the mRNA distribution of all currently known two pore potassium channels in human central nervous system (CNS) and peripheral tissues. TWIK-1 and the TWIK-1-like channel KCNK7 were predominantly expressed in the CNS, in contrast to TWIK-2 which was preferentially expressed in peripheral tissues such as pancreas, stomach, spleen and uterus. TASK-1 was expressed in the CNS and some peripheral tissues, whereas TASK-2 was exclusively expressed in the periphery except for mRNA expression observed in dorsal root ganglion and spinal cord. In addition, mRNA expression of the recently identified TASK-3, was almost completely exclusive to cerebellum with little or no mRNA detected in any other tissues. TREK-1 and TRAAK mRNA expression was predominantly CNS specific in contrast to the closely related TREK-2, which was expressed in both CNS and peripheral tissues. Studying the mRNA expression profiles of known two pore domain K+ channels will aid in the understanding of the biological roles of these channels. Furthermore, identification of common areas of expression may help identify which channels, if any, associate to form heteromeric K+ channel complexes.Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions. The most recently described family of K+ channels, the 'two pore-domain family', contain four membrane spanning domains and two pore-forming domains, suggesting that two channel subunits associate to form a functional K+ pore. Several sub-families of the two pore domain potassium channel family have been described, including the weakly inward rectifying K+ channel (TWIK), the acid-sensitive K+ channel (TASK), the TWIK-related K+ channel (TREK) and the TWIK-related arachidonic acid stimulated K+ channel (TRAAK). However, comparison of the mRNA expression of these channels has been difficult due to the differences in methods used and the species studied. In the present study, we used a single technique, TaqMan semi-quantitative reverse transcription polymerase chain reaction (RT-PCR), to investigate the mRNA distribution of all currently known two pore potassium channels in human central nervous system (CNS) and peripheral tissues. TWIK-1 and the TWIK-1-like channel KCNK7 were predominantly expressed in the CNS, in contrast to TWIK-2 which was preferentially expressed in peripheral tissues such as pancreas, stomach, spleen and uterus. TASK-1 was expressed in the CNS and some peripheral tissues, whereas TASK-2 was exclusively expressed in the periphery except for mRNA expression observed in dorsal root ganglion and spinal cord. In addition, mRNA expression of the recently identified TASK-3, was almost completely exclusive to cerebellum with little or no mRNA detected in any other tissues. TREK-1 and TRAAK mRNA expression was predominantly CNS specific in contrast to the closely related TREK-2, which was expressed in both CNS and peripheral tissues. Studying the mRNA expression profiles of known two pore domain K+ channels will aid in the understanding of the biological roles of these channels. Furthermore, identification of common areas of expression may help identify which channels, if any, associate to form heteromeric K+ channel complexes. |
Author | Gloger, Israel I. Medhurst, Andrew D. Rennie, Gillian Pangalos, Menelas N. Chapman, Conrad G. Meadows, Helen Kelsell, Rosemary E. Duckworth, Malcolm D. |
Author_xml | – sequence: 1 givenname: Andrew D. surname: Medhurst fullname: Medhurst, Andrew D. organization: Neuroscience Research, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 2 givenname: Gillian surname: Rennie fullname: Rennie, Gillian organization: Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 3 givenname: Conrad G. surname: Chapman fullname: Chapman, Conrad G. organization: Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 4 givenname: Helen surname: Meadows fullname: Meadows, Helen organization: Neuroscience Research, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 5 givenname: Malcolm D. surname: Duckworth fullname: Duckworth, Malcolm D. organization: Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 6 givenname: Rosemary E. surname: Kelsell fullname: Kelsell, Rosemary E. organization: Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 7 givenname: Israel I. surname: Gloger fullname: Gloger, Israel I. organization: Biotechnology and Genetics, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK – sequence: 8 givenname: Menelas N. surname: Pangalos fullname: Pangalos, Menelas N. email: menelas_n_pangalos@sbphrd.com organization: Neuroscience Research, SmithKline Beecham Pharmaceuticals, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=870938$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/11165377$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkU2L1TAUhoOMOHdGf4ISEEQX1ZOmbXoRERk_YcCFCu5Cmpxyo23SSdLR_ntzPxxhNtdNEsLzPpzkPSMnzjsk5CGD5wxY8-JLXtYFL9vvTwGeAZQNL9gdsmKtKItmXbETsrpBTslZjD8AgLWM3SOnjLGm5kKsyO-3NqZguzlZ76hyaliijdT3dDOPytH0y9PJB6TGj8q6fE4qRjuPVG-UczhEmm-TjXHGXSxtkGp0KaiBOgzXfo40LjHhmO2GThjstMGw3Cd3ezVEfHDYz8m39---XnwsLj9_-HTx5rLQdQWpqBRTLfC6q_MqeFmX3Vp0Ak3XVetG8LYSCjowVa8q0wtViZIbaEEz1ZgKO35Onuy9U_BXecYkRxs1DoNymGeTAhoOoqyPgkyI7G7aDD46gHM3opFTsKMKi_z7qRl4fABU1Grog3LaxhuuFbDmW029p3TwMQbs_4lAbiuWu4rltj8JIHcVS5ZzL2_ltE1qW1_-czscTb_ep3NzeG0xyKgtOo3GBtRJGm-PGl7dMujBOpsf-hOX_8j_AUqH1PQ |
CitedBy_id | crossref_primary_10_1016_j_neubiorev_2023_105301 crossref_primary_10_1016_j_pharmthera_2018_10_003 crossref_primary_10_1213_01_ANE_0000062524_90936_1F crossref_primary_10_1371_journal_pone_0077998 crossref_primary_10_1155_2021_8643129 crossref_primary_10_1007_s00424_014_1634_8 crossref_primary_10_3390_ijms20102371 crossref_primary_10_1007_s00249_008_0326_8 crossref_primary_10_1038_nrn2993 crossref_primary_10_1530_rep_1_00442 crossref_primary_10_3390_ijms21155206 crossref_primary_10_1007_s00424_014_1585_0 crossref_primary_10_1016_j_bbrc_2005_09_007 crossref_primary_10_3390_oxygen4010004 crossref_primary_10_1016_j_ejphar_2014_05_056 crossref_primary_10_1152_ajpheart_00963_2001 crossref_primary_10_1007_s00232_005_7012_x crossref_primary_10_12677_HJBM_2023_132015 crossref_primary_10_3390_cells10112914 crossref_primary_10_1016_j_neuroscience_2007_05_054 crossref_primary_10_1073_pnas_0910059107 crossref_primary_10_1054_plef_2001_0342 crossref_primary_10_1016_j_neuroscience_2007_12_011 crossref_primary_10_1038_s41531_022_00293_z crossref_primary_10_1371_journal_pone_0174071 crossref_primary_10_1016_j_bbrc_2019_09_093 crossref_primary_10_1056_NEJMoa1211097 crossref_primary_10_1016_j_mcn_2008_12_004 crossref_primary_10_1111_j_1745_7254_2008_00853_x crossref_primary_10_1007_s00232_002_2001_9 crossref_primary_10_1161_01_RES_0000219677_12988_e9 crossref_primary_10_1016_j_bbr_2008_05_010 crossref_primary_10_1016_S0304_3940_02_00665_1 crossref_primary_10_1523_JNEUROSCI_23_36_11427_2003 crossref_primary_10_1111_cns_13450 crossref_primary_10_1371_journal_pone_0025602 crossref_primary_10_1016_j_molbrainres_2004_06_007 crossref_primary_10_1021_acs_jmedchem_6b01285 crossref_primary_10_3390_ijms22126635 crossref_primary_10_1016_j_bmcl_2019_04_048 crossref_primary_10_3389_fphar_2019_00379 crossref_primary_10_1111_j_1460_9568_2008_06400_x crossref_primary_10_1038_sj_emboj_7601116 crossref_primary_10_1111_jpi_12705 crossref_primary_10_1111_j_1460_9568_2006_05102_x crossref_primary_10_1124_mol_63_3_646 crossref_primary_10_1155_2017_5435831 crossref_primary_10_1152_jn_2002_87_5_2408 crossref_primary_10_1152_physrev_00020_2007 crossref_primary_10_5339_gcsp_2014_19 crossref_primary_10_1152_physrev_00029_2009 crossref_primary_10_1016_S0169_328X_01_00330_8 crossref_primary_10_1523_JNEUROSCI_4017_09_2010 crossref_primary_10_1152_ajpcell_00629_2005 crossref_primary_10_1016_j_conb_2009_07_008 crossref_primary_10_1016_j_neulet_2009_02_069 crossref_primary_10_1016_j_eplepsyres_2005_03_002 crossref_primary_10_1152_physrev_00051_2003 crossref_primary_10_5387_fms_2015_20 crossref_primary_10_1007_s11481_014_9530_8 crossref_primary_10_1002_hbm_20858 crossref_primary_10_1371_journal_pone_0128951 crossref_primary_10_1016_j_bbrc_2021_12_031 crossref_primary_10_1007_s00210_013_0952_2 crossref_primary_10_1007_s00424_005_1505_4 crossref_primary_10_1074_jbc_M110_190702 crossref_primary_10_1111_j_1523_1755_2004_00458_x crossref_primary_10_1002_jcp_20536 crossref_primary_10_1038_s41398_024_03069_6 crossref_primary_10_1007_s00232_021_00189_8 crossref_primary_10_1007_s00424_015_1779_0 crossref_primary_10_3389_fphys_2018_00760 crossref_primary_10_1016_j_molbrainres_2003_09_020 crossref_primary_10_1007_s12031_011_9598_z crossref_primary_10_3390_ijms22169062 crossref_primary_10_1007_s00424_014_1655_3 crossref_primary_10_1111_j_1582_4934_2012_01656_x crossref_primary_10_1074_jbc_M107138200 crossref_primary_10_1080_10799890600637522 crossref_primary_10_1002_dvdy_20558 crossref_primary_10_1016_j_bbamem_2011_09_015 crossref_primary_10_1113_JP275178 crossref_primary_10_1016_j_neulet_2008_09_038 crossref_primary_10_1213_01_ANE_0000056921_15974_EC crossref_primary_10_1007_s00428_005_1205_7 crossref_primary_10_1016_j_mce_2011_11_009 crossref_primary_10_1007_s10735_010_9276_4 crossref_primary_10_1016_j_brainres_2004_05_012 crossref_primary_10_1016_S0169_328X_01_00095_X crossref_primary_10_1016_j_brainres_2006_03_122 crossref_primary_10_1097_FJC_0000000000000099 crossref_primary_10_1038_ncomms4227 crossref_primary_10_1111_bph_15243 crossref_primary_10_1016_j_brainres_2014_10_021 crossref_primary_10_1161_CIRCRESAHA_115_305043 crossref_primary_10_1152_ajpgi_00417_2010 crossref_primary_10_1016_j_fertnstert_2006_06_051 crossref_primary_10_1113_jphysiol_2004_079020 crossref_primary_10_1016_j_molbrainres_2004_05_007 crossref_primary_10_1097_FJC_0b013e318280c5a9 crossref_primary_10_1111_jnc_13980 crossref_primary_10_1016_S0169_328X_02_00527_2 crossref_primary_10_1016_S0006_8993_02_02261_8 crossref_primary_10_3389_fnmol_2017_00351 crossref_primary_10_1016_j_neuron_2006_04_032 crossref_primary_10_1016_j_yjmcc_2015_01_017 crossref_primary_10_1111_j_1440_1681_2004_03964_x crossref_primary_10_1369_jhc_5A6755_2005 crossref_primary_10_1016_j_mcn_2014_04_007 crossref_primary_10_1016_S0028_3908_02_00339_8 crossref_primary_10_1038_nrn2117 crossref_primary_10_1161_HYPERTENSIONAHA_114_03406 crossref_primary_10_1007_s12031_012_9780_y crossref_primary_10_1371_journal_pone_0133136 crossref_primary_10_1007_s00232_014_9632_5 crossref_primary_10_1186_s12894_019_0475_3 crossref_primary_10_4161_chan_5_1_13905 crossref_primary_10_1101_gr_6584707 crossref_primary_10_1007_s11724_008_0108_1 crossref_primary_10_1007_s00249_008_0318_8 crossref_primary_10_1111_j_1582_4934_2004_tb00258_x crossref_primary_10_1002_dvdy_20636 crossref_primary_10_1113_jphysiol_2003_054387 crossref_primary_10_1371_journal_pone_0053266 crossref_primary_10_1007_s00424_003_1075_2 crossref_primary_10_1152_ajpcell_00334_2003 crossref_primary_10_1016_S0166_2236_00_01810_5 crossref_primary_10_1152_ajpregu_90321_2008 crossref_primary_10_1016_j_neuroscience_2006_04_019 crossref_primary_10_1016_j_bbamem_2014_12_008 crossref_primary_10_1006_mcne_2001_1045 crossref_primary_10_1016_j_cbpc_2022_109497 crossref_primary_10_1021_acschemneuro_5c00032 crossref_primary_10_1093_femsyr_foz044 crossref_primary_10_1523_JNEUROSCI_3153_05_2005 crossref_primary_10_1152_ajpheart_01377_2005 crossref_primary_10_1007_s12264_023_01118_6 crossref_primary_10_1016_j_neuroscience_2004_06_066 crossref_primary_10_1038_jcbfm_2010_223 crossref_primary_10_1016_j_bbrc_2004_05_023 crossref_primary_10_4161_chan_26100 crossref_primary_10_1016_j_lfs_2013_12_006 crossref_primary_10_1111_j_1442_9071_2005_00981_x crossref_primary_10_1371_journal_pone_0012372 crossref_primary_10_3390_molecules27238296 crossref_primary_10_1016_j_mcn_2012_01_002 crossref_primary_10_1152_ajpcell_00047_2006 crossref_primary_10_1002_glia_10051 crossref_primary_10_1016_j_neulet_2006_07_039 crossref_primary_10_1007_s11724_016_0482_z crossref_primary_10_1021_nn5020775 crossref_primary_10_1113_jphysiol_2002_032094 crossref_primary_10_1007_s00399_017_0541_z crossref_primary_10_1093_hmg_ddm216 crossref_primary_10_1113_jphysiol_2004_081059 crossref_primary_10_1016_j_mehy_2007_06_016 crossref_primary_10_1016_j_bbrc_2004_08_089 crossref_primary_10_1016_j_ejphar_2019_172631 crossref_primary_10_1007_s12031_012_9875_5 crossref_primary_10_1186_1744_8069_8_2 crossref_primary_10_4161_chan_22213 crossref_primary_10_1113_jphysiol_2007_145649 crossref_primary_10_1177_154405910608500716 crossref_primary_10_1016_j_lfs_2009_05_009 crossref_primary_10_3390_ijms21238997 crossref_primary_10_1016_j_tips_2003_10_008 crossref_primary_10_1111_bph_12596 crossref_primary_10_1111_cns_12384 crossref_primary_10_1016_j_gca_2019_07_038 crossref_primary_10_5607_en_2016_25_5_222 crossref_primary_10_1038_aps_2011_62 crossref_primary_10_1113_jphysiol_2014_271718 crossref_primary_10_1177_2472555220976126 crossref_primary_10_1074_jbc_M408246200 crossref_primary_10_4196_kjpp_2008_12_5_245 crossref_primary_10_1038_emboj_2009_57 crossref_primary_10_1016_j_msard_2022_103557 crossref_primary_10_3390_ijms232213776 crossref_primary_10_1002_jemt_22028 crossref_primary_10_1007_s00424_014_1651_7 crossref_primary_10_1016_j_jaci_2017_10_012 crossref_primary_10_1007_s12035_018_1288_1 crossref_primary_10_1016_j_bbrc_2004_01_137 crossref_primary_10_1113_jphysiol_2009_170746 crossref_primary_10_1038_s41583_021_00544_7 crossref_primary_10_1016_j_pain_2014_09_013 crossref_primary_10_1152_ajpcell_00030_2016 crossref_primary_10_3390_ijms24021311 crossref_primary_10_1007_s00424_014_1637_5 crossref_primary_10_1016_j_mehy_2007_06_030 crossref_primary_10_1038_s41598_018_33664_9 crossref_primary_10_1038_sj_embor_7400449 crossref_primary_10_1111_j_1460_9568_2004_03097_x crossref_primary_10_1177_1073858402239590 crossref_primary_10_1016_j_jsgi_2004_08_004 crossref_primary_10_1038_aps_2010_210 crossref_primary_10_1111_bph_12011 crossref_primary_10_1016_S0955_0674_00_00231_3 crossref_primary_10_5492_wjccm_v1_i3_80 crossref_primary_10_1007_s12013_007_0007_8 crossref_primary_10_1097_j_pain_0000000000000368 crossref_primary_10_3389_fncel_2021_744702 crossref_primary_10_4161_chan_5_5_16469 crossref_primary_10_1016_j_neuroscience_2017_03_033 crossref_primary_10_3181_0903_RM_110 crossref_primary_10_1152_ajpheart_00107_2017 crossref_primary_10_1007_s11626_011_9388_5 crossref_primary_10_1016_S0378_5955_03_00162_X crossref_primary_10_3390_ijms21249639 crossref_primary_10_1146_annurev_physiol_032420_035509 crossref_primary_10_1186_s12974_019_1485_5 crossref_primary_10_1016_j_bbrc_2005_04_042 crossref_primary_10_1093_chemse_bjz016 crossref_primary_10_1097_00115550_200505000_00009 crossref_primary_10_1016_j_bbrc_2022_05_051 crossref_primary_10_1364_BOE_444577 |
Cites_doi | 10.1093/emboj/16.17.5464 10.1016/S0014-5793(00)01388-0 10.1016/S0014-5793(96)01491-3 10.1152/physrev.1992.72.suppl_4.S69 10.1074/jbc.274.12.7887 10.1523/JNEUROSCI.18-03-00868.1998 10.1074/jbc.274.17.11751 10.1074/jbc.M000030200 10.1016/S1050-3862(98)00019-9 10.1016/0028-3908(96)00126-8 10.1007/s004240050997 10.1074/jbc.273.47.30863 10.1016/0896-6273(95)90327-5 10.1093/emboj/17.15.4283 10.1093/emboj/17.12.3297 10.1074/jbc.M000445200 10.1146/annurev.neuro.20.1.91 10.1074/jbc.M003755200 10.1126/science.282.5396.2028 10.1074/jbc.274.3.1381 10.1002/j.1460-2075.1996.tb00437.x 10.1016/0959-4388(95)80038-7 10.1093/emboj/19.11.2483 10.1016/S0958-1669(98)80082-7 10.1016/0896-6273(95)90021-7 10.1074/jbc.275.13.9340 10.1016/S0165-0270(00)00178-3 10.1161/01.RES.82.4.513 10.1016/S0896-6273(00)80903-4 10.1016/S0306-4522(99)00484-4 10.1002/j.1460-2075.1996.tb01077.x 10.1038/8084 10.1159/000154823 10.1073/pnas.97.7.3614 |
ContentType | Journal Article |
Copyright | 2001 Elsevier Science B.V. 2001 INIST-CNRS |
Copyright_xml | – notice: 2001 Elsevier Science B.V. – notice: 2001 INIST-CNRS |
DBID | AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM 7TK 7X8 |
DOI | 10.1016/S0169-328X(00)00263-1 |
DatabaseName | CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Neurosciences Abstracts MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Neurosciences Abstracts MEDLINE - Academic |
DatabaseTitleList | Neurosciences Abstracts MEDLINE MEDLINE - Academic |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Anatomy & Physiology Biology |
EISSN | 1872-6941 |
EndPage | 114 |
ExternalDocumentID | 11165377 870938 10_1016_S0169_328X_00_00263_1 S0169328X00002631 |
Genre | Journal Article |
GroupedDBID | --K --M -DZ -~X .55 .GJ .~1 0R~ 123 1B1 1RT 1~. 1~5 23N 3O- 4.4 4G. 53G 5RE 5VS 7-5 71M 8P~ AABNK AAEDT AAEDW AAIKJ AAKOC AALRI AAOAW AAQFI AAQXK AATTM AAXKI AAXUO AAYWO ABJNI ABMAC ABWVN ACDAQ ACGFS ACIUM ACNCT ACRLP ACRPL ACVFH ADBBV ADCNI ADEZE ADIYS ADMUD ADNMO AEIPS AEKER AEUPX AFFNX AFPUW AFTJW AFXIZ AGCQF AGHFR AGQPQ AGRDE AGUBO AGYEJ AHHHB AI. AIEXJ AIGII AIIUN AIKHN AITUG AKBMS AKRWK AKYEP ALMA_UNASSIGNED_HOLDINGS AMRAJ ANKPU ASPBG AVWKF AXJTR AZFZN BKOJK BLXMC CS3 EBS EFJIC EFKBS EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU FYGXN G-Q HVGLF HZ~ IHE KOM L7B M2V M41 MO0 MOBAO MVM O-L O9- OAUVE OZT P-9 PC. Q38 R2- ROL RPZ SDF SDG SNS SSN SSZ T5K VH1 X7M XPP ZGI AACTN AADPK ABYKQ AFKWA AHPSJ AJBFU AJOXV AMFUW RIG AAYXX ABXDB AEBSH AGRNS CITATION G-2 GBLVA HMQ SEW SSH WUQ XJT IQODW CGR CUY CVF ECM EIF NPM 7TK 7X8 |
ID | FETCH-LOGICAL-c540t-4a1a8035b580373252b97b7edbb49673847a0b0d4fa4df7a4723d080c1a6d4eb3 |
IEDL.DBID | .~1 |
ISSN | 0169-328X |
IngestDate | Fri Sep 05 03:26:45 EDT 2025 Fri Sep 05 06:42:59 EDT 2025 Wed Feb 19 02:33:02 EST 2025 Mon Jul 21 09:16:52 EDT 2025 Tue Jul 01 02:12:34 EDT 2025 Thu Apr 24 22:56:39 EDT 2025 Fri Feb 23 02:20:56 EST 2024 Tue Aug 26 16:34:30 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1-2 |
Keywords | 2P domain Polymerase chain reaction Expression Potassium channel Central nervous system Anaesthetics Human Tissue Distribution Ionic channel Potassium Aminoacid sequence |
Language | English |
License | https://www.elsevier.com/tdm/userlicense/1.0 CC BY 4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c540t-4a1a8035b580373252b97b7edbb49673847a0b0d4fa4df7a4723d080c1a6d4eb3 |
Notes | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Article-1 ObjectType-Feature-2 |
PMID | 11165377 |
PQID | 17772368 |
PQPubID | 23462 |
PageCount | 14 |
ParticipantIDs | proquest_miscellaneous_70630725 proquest_miscellaneous_17772368 pubmed_primary_11165377 pascalfrancis_primary_870938 crossref_primary_10_1016_S0169_328X_00_00263_1 crossref_citationtrail_10_1016_S0169_328X_00_00263_1 elsevier_sciencedirect_doi_10_1016_S0169_328X_00_00263_1 elsevier_clinicalkey_doi_10_1016_S0169_328X_00_00263_1 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2001-01-31 |
PublicationDateYYYYMMDD | 2001-01-31 |
PublicationDate_xml | – month: 01 year: 2001 text: 2001-01-31 day: 31 |
PublicationDecade | 2000 |
PublicationPlace | Amsterdam |
PublicationPlace_xml | – name: Amsterdam – name: Netherlands |
PublicationTitle | Brain research. Molecular brain research. |
PublicationTitleAlternate | Brain Res Mol Brain Res |
PublicationYear | 2001 |
Publisher | Elsevier B.V Elsevier |
Publisher_xml | – name: Elsevier B.V – name: Elsevier |
References | Salinas, Reyes, Lesage, Fosset, Heurteaux, Romey, Lazdunski (BIB35) 1999; 274 Hill (BIB10) 1992 Reyes, Duprat, Lesage, Fink, Salinas, Farman, Lazdunski (BIB34) 1998; 273 Bang, Kim, Kim (BIB1) 2000; 275 Doyle, Cabral, Pfuetzner, Kuo, Gulbis, Cohen, Chait, MacKinnon (BIB5) 1998; 280 Mackinnon (BIB22) 1995; 14 Livak (BIB21) 1999; 14 Jan, Jan (BIB11) 1997; 20 Fakler, Ruppensberg (BIB7) 1996; 6 Doupnik, Davidson, Lester (BIB4) 1995; 5 Wei, Jegla, Salkoff (BIB37) 1997; 35 Patel, Honore, Maingret, Lesage, Fink, Duprat, Lazdunski (BIB30) 1998; 17 Medhurst, Harrison, Read, Campbell, Robbins, Pangalos (BIB26) 2000; 98 Kim, Fujita, Horio, Kurachi (BIB12) 1998; 82 Kim, Bang, Kim (BIB14) 1999; 277 Maingret, Lauritzen, Patel, Heurteaux, Reyes, Lesage, Lazdunski, Honore (BIB24) 2000; 19 Fink, Lesage, Duprat, Heurteaux, Reyes, Fosset, Lazdunski (BIB9) 1998; 17 Maingret, Fosset, Lesage, Lazdunski, Honore (BIB23) 1999; 274 Patel, Honore, Lesage, Fink, Romey, Lazdunski (BIB28) 1999; 2 Bargmann (BIB2) 1998; 282 Leonoudakis, Gray, Winegar, Kindler, Harada, Taylor, Chavez, Forsayeth, Yost (BIB15) 1998; 18 Duprat, Lesage, Fink, Reyes, Heurteaux, Lazdunski (BIB6) 1997; 16 Fink, Duprat, Lesage, Reyes, Romey, Heurteaux, Lazdunski (BIB8) 1996; 15 Reyes, Lauritzen, Lesage, Ettaiche, Fosset, Lazdunski (BIB33) 2000; 95 Lesage, Lauritzen, Duprat, Reyes, Fink, Heurteaux, Lazdunski (BIB18) 1997; 402 Chavez, Gray, Zhao, Kindler, Mazurek, Mehta, Forsayeth, Yost (BIB3) 1999; 274 Lesage, Lazdunski (BIB16) 1999; Vol. 46 Lesage, Guillemare, Fink, Duprat, Lazdunski, Romey, Barhanin (BIB19) 1996; 15 Patel, Maingret, Magnone, Fosset, Lazdunski, Honore (BIB29) 2000; 275 Lesage, Maingret, Lazdunski (BIB17) 2000; 471 Millar, Barratt, Southan, Page, Fyffe, Robertson, Mathie (BIB27) 2000; 97 Lie, Petropoulos (BIB20) 1998; 9 Kim, Bang, Kim (BIB13) 2000; 275 Yang, Jan, Jan (BIB38) 1995; 15 Pongs (BIB31) 1992; 72 Rajan, Wischmeyer, Liu, Preisig-Muller, Daut, Karschin, Derst (BIB32) 2000; 275 Talley, Lei, Sirois, Bayliss (BIB36) 2000; 25 Meadows, Benham, Cairns, Gloger, Jennings, Medhurst, Murdock, Chapman (BIB25) 2000; 439 Doyle (10.1016/S0169-328X(00)00263-1_BIB5) 1998; 280 Mackinnon (10.1016/S0169-328X(00)00263-1_BIB22) 1995; 14 Meadows (10.1016/S0169-328X(00)00263-1_BIB25) 2000; 439 Jan (10.1016/S0169-328X(00)00263-1_BIB11) 1997; 20 Patel (10.1016/S0169-328X(00)00263-1_BIB30) 1998; 17 Duprat (10.1016/S0169-328X(00)00263-1_BIB6) 1997; 16 Maingret (10.1016/S0169-328X(00)00263-1_BIB23) 1999; 274 Fakler (10.1016/S0169-328X(00)00263-1_BIB7) 1996; 6 Leonoudakis (10.1016/S0169-328X(00)00263-1_BIB15) 1998; 18 Bargmann (10.1016/S0169-328X(00)00263-1_BIB2) 1998; 282 Reyes (10.1016/S0169-328X(00)00263-1_BIB33) 2000; 95 Hill (10.1016/S0169-328X(00)00263-1_BIB10) 1992 Medhurst (10.1016/S0169-328X(00)00263-1_BIB26) 2000; 98 Lesage (10.1016/S0169-328X(00)00263-1_BIB19) 1996; 15 Doupnik (10.1016/S0169-328X(00)00263-1_BIB4) 1995; 5 Lesage (10.1016/S0169-328X(00)00263-1_BIB18) 1997; 402 Pongs (10.1016/S0169-328X(00)00263-1_BIB31) 1992; 72 Rajan (10.1016/S0169-328X(00)00263-1_BIB32) 2000; 275 Kim (10.1016/S0169-328X(00)00263-1_BIB12) 1998; 82 Chavez (10.1016/S0169-328X(00)00263-1_BIB3) 1999; 274 Bang (10.1016/S0169-328X(00)00263-1_BIB1) 2000; 275 Kim (10.1016/S0169-328X(00)00263-1_BIB14) 1999; 277 Patel (10.1016/S0169-328X(00)00263-1_BIB28) 1999; 2 Patel (10.1016/S0169-328X(00)00263-1_BIB29) 2000; 275 Livak (10.1016/S0169-328X(00)00263-1_BIB21) 1999; 14 Wei (10.1016/S0169-328X(00)00263-1_BIB37) 1997; 35 Salinas (10.1016/S0169-328X(00)00263-1_BIB35) 1999; 274 Reyes (10.1016/S0169-328X(00)00263-1_BIB34) 1998; 273 Yang (10.1016/S0169-328X(00)00263-1_BIB38) 1995; 15 Maingret (10.1016/S0169-328X(00)00263-1_BIB24) 2000; 19 Fink (10.1016/S0169-328X(00)00263-1_BIB8) 1996; 15 Millar (10.1016/S0169-328X(00)00263-1_BIB27) 2000; 97 Lesage (10.1016/S0169-328X(00)00263-1_BIB17) 2000; 471 Lie (10.1016/S0169-328X(00)00263-1_BIB20) 1998; 9 Fink (10.1016/S0169-328X(00)00263-1_BIB9) 1998; 17 Lesage (10.1016/S0169-328X(00)00263-1_BIB16) 1999; Vol. 46 Kim (10.1016/S0169-328X(00)00263-1_BIB13) 2000; 275 Talley (10.1016/S0169-328X(00)00263-1_BIB36) 2000; 25 |
References_xml | – volume: 17 start-page: 4283 year: 1998 end-page: 4290 ident: BIB30 article-title: A mammalian two pore domain mechano-gated S-like K publication-title: EMBO J. – volume: 72 start-page: S69 year: 1992 end-page: 88 ident: BIB31 article-title: Molecular biology of voltage-dependent potassium channels publication-title: Physiol. Rev. – volume: 280 start-page: 69 year: 1998 end-page: 77 ident: BIB5 publication-title: The structure of the potassium channel: molecular basis of K – volume: 15 start-page: 1004 year: 1996 end-page: 1011 ident: BIB19 article-title: TWIK-1, a ubiquitous human weakly inward rectifying K publication-title: EMBO J. – volume: 277 start-page: H1669 year: 1999 end-page: H1678 ident: BIB14 article-title: TBAK-1 and TASK-1, two pore K publication-title: Am. J. Physiol. – volume: 16 start-page: 5464 year: 1997 end-page: 5471 ident: BIB6 article-title: TASK, a human background K publication-title: EMBO J. – volume: 274 start-page: 11751 year: 1999 end-page: 11760 ident: BIB35 article-title: Cloning of a new mouse two P-domain channel subunit and a human homologue with a unique pore structure publication-title: J. Biol. Chem. – volume: 19 start-page: 2483 year: 2000 end-page: 2491 ident: BIB24 article-title: TREK-1 is a heat-activated background K+ channel publication-title: EMBO J. – volume: 5 start-page: 268 year: 1995 end-page: 277 ident: BIB4 article-title: The inward rectifier potassium channel family publication-title: Curr. Opin. Neurobiol. – volume: 20 start-page: 91 year: 1997 end-page: 123 ident: BIB11 article-title: Cloned potassium channels from eukaryotes and prokaryotes publication-title: Ann. Rev. Neurosci. – volume: 273 start-page: 30863 year: 1998 end-page: 30869 ident: BIB34 article-title: Cloning and expression of a novel pH-sensitive two pore domain K publication-title: J. Biol. Chem. – volume: Vol. 46 start-page: 199 year: 1999 end-page: 222 ident: BIB16 article-title: Potassium channels with two P domains publication-title: Potassium Ion Channels – Molecular Structure, Function and Diseases – volume: 6 start-page: 195 year: 1996 end-page: 209 ident: BIB7 article-title: Functional and molecular diversity classifies the family of inward rectifier K publication-title: Cell. Physiol. Biochem. – volume: 275 start-page: 9340 year: 2000 end-page: 9347 ident: BIB13 article-title: TASK-3, a new member of the tandem pore K publication-title: J. Biol. Chem. – volume: 18 start-page: 868 year: 1998 end-page: 877 ident: BIB15 article-title: An open rectifier potassium channel with two pore domains in tandem cloned from rat cerebellum publication-title: J. Neurosci. – volume: 274 start-page: 1381 year: 1999 end-page: 1387 ident: BIB23 article-title: TRAAK is a mammalian neuronal mechano-gated K publication-title: J. Biol. Chem. – volume: 471 start-page: 137 year: 2000 end-page: 140 ident: BIB17 article-title: Cloning and expression of human TRAAK, a polyunsaturated fatty acids-activated and mechano-sensitive K publication-title: FEBS Lett. – volume: 282 start-page: 2028 year: 1998 end-page: 2033 ident: BIB2 article-title: Neurobiology of the publication-title: Science – volume: 275 start-page: 17412 year: 2000 end-page: 17419 ident: BIB1 article-title: TREK-2, a novel member of the mechanosensitive tandem pore K publication-title: J. Biol. Chem. – volume: 14 start-page: 889 year: 1995 end-page: 892 ident: BIB22 article-title: Pore loops: an emerging theme in ion channel structure publication-title: Neuron – volume: 82 start-page: 513 year: 1998 end-page: 518 ident: BIB12 article-title: Cloning and functional expression of a novel cardiac two pore background K publication-title: Circ. Res. – volume: 14 start-page: 143 year: 1999 end-page: 149 ident: BIB21 article-title: Allelic discrimination using fluorogenic probes and the 5′-nuclease assay publication-title: Gen. Anal. Biomol. Eng. – volume: 439 start-page: 714 year: 2000 end-page: 722 ident: BIB25 article-title: Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel publication-title: Pfluger’s Arch. – Eur. J. Physiol. – volume: 97 start-page: 3614 year: 2000 end-page: 3618 ident: BIB27 article-title: A functional role for the two-pore domain potassium channel TASK-1 in cerebellar granule neurons publication-title: Proc. Natl. Acad. Sci. – volume: 275 start-page: 16650 year: 2000 end-page: 16657 ident: BIB32 article-title: TASK-3, a novel tandem pore-domain acid-sensitive K publication-title: J. Biol. Chem. – volume: 95 start-page: 893 year: 2000 end-page: 901 ident: BIB33 article-title: Immunolocalisation of the arachidonic acid and mechanosensitive baseline TRAAK potassium channel in the nervous system publication-title: Neuroscience – volume: 35 start-page: 805 year: 1997 end-page: 829 ident: BIB37 article-title: Eight potassium channel families revealed by the publication-title: Neuropharmacology – volume: 274 start-page: 7887 year: 1999 end-page: 7892 ident: BIB3 article-title: TWIK-2, a new weak inward rectifying member of the tandem pore domain potassium channel family member publication-title: J. Biol. Chem. – start-page: 1 year: 1992 end-page: 607 ident: BIB10 article-title: Ionic channels in excitable membranes publication-title: Ionic Channels of Excitable Membranes – volume: 9 start-page: 43 year: 1998 end-page: 48 ident: BIB20 article-title: Advances in quantitative PCR technology: 5′ nuclease assays publication-title: Curr. Opin. Biotechnol. – volume: 402 start-page: 28 year: 1997 end-page: 32 ident: BIB18 article-title: The structure, function and distribution of the mouse TWIK-1 K publication-title: FEBS Lett. – volume: 275 start-page: 28722 year: 2000 end-page: 28730 ident: BIB29 article-title: TWIK-2, an inactivating 2P domain K+ channel publication-title: J. Biol. Chem. – volume: 15 start-page: 6854 year: 1996 end-page: 6862 ident: BIB8 article-title: Cloning, functional expression and brain localisation of a novel unconventional outward rectifier K publication-title: EMBO J. – volume: 15 start-page: 1441 year: 1995 end-page: 1447 ident: BIB38 article-title: Determination of the subunit stoichiometry of an inwardly rectifying potassium channel publication-title: Neuron – volume: 98 start-page: 9 year: 2000 end-page: 20 ident: BIB26 article-title: The use of TaqMan RT-PCR assays for semiquantitative analysis of gene expression in CNS tissues and disease models publication-title: J. Neurosci. Methods – volume: 17 start-page: 3297 year: 1998 end-page: 3308 ident: BIB9 article-title: A neuronal two P domain K publication-title: EMBO J. – volume: 25 start-page: 399 year: 2000 end-page: 410 ident: BIB36 article-title: TASK-1, a two-pore domain K+ channel, is modulated by multiple neurotransmitters in motorneurons publication-title: Neuron – volume: 2 start-page: 422 year: 1999 end-page: 426 ident: BIB28 article-title: Inhalation anesthetics activate two-pore domain background K publication-title: Nat. Neurosci. – volume: 16 start-page: 5464 year: 1997 ident: 10.1016/S0169-328X(00)00263-1_BIB6 article-title: TASK, a human background K+ channel to sense external pH variations near physiological pH publication-title: EMBO J. doi: 10.1093/emboj/16.17.5464 – volume: 471 start-page: 137 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB17 article-title: Cloning and expression of human TRAAK, a polyunsaturated fatty acids-activated and mechano-sensitive K+ channel publication-title: FEBS Lett. doi: 10.1016/S0014-5793(00)01388-0 – volume: 402 start-page: 28 year: 1997 ident: 10.1016/S0169-328X(00)00263-1_BIB18 article-title: The structure, function and distribution of the mouse TWIK-1 K+ channel publication-title: FEBS Lett. doi: 10.1016/S0014-5793(96)01491-3 – volume: 72 start-page: S69 year: 1992 ident: 10.1016/S0169-328X(00)00263-1_BIB31 article-title: Molecular biology of voltage-dependent potassium channels publication-title: Physiol. Rev. doi: 10.1152/physrev.1992.72.suppl_4.S69 – volume: 274 start-page: 7887 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB3 article-title: TWIK-2, a new weak inward rectifying member of the tandem pore domain potassium channel family member publication-title: J. Biol. Chem. doi: 10.1074/jbc.274.12.7887 – volume: 18 start-page: 868 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB15 article-title: An open rectifier potassium channel with two pore domains in tandem cloned from rat cerebellum publication-title: J. Neurosci. doi: 10.1523/JNEUROSCI.18-03-00868.1998 – volume: 274 start-page: 11751 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB35 article-title: Cloning of a new mouse two P-domain channel subunit and a human homologue with a unique pore structure publication-title: J. Biol. Chem. doi: 10.1074/jbc.274.17.11751 – volume: 275 start-page: 16650 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB32 article-title: TASK-3, a novel tandem pore-domain acid-sensitive K+ channel: an extracellular histidine as pH sensor publication-title: J. Biol. Chem. doi: 10.1074/jbc.M000030200 – volume: 14 start-page: 143 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB21 article-title: Allelic discrimination using fluorogenic probes and the 5′-nuclease assay publication-title: Gen. Anal. Biomol. Eng. doi: 10.1016/S1050-3862(98)00019-9 – start-page: 1 year: 1992 ident: 10.1016/S0169-328X(00)00263-1_BIB10 article-title: Ionic channels in excitable membranes – volume: 35 start-page: 805 year: 1997 ident: 10.1016/S0169-328X(00)00263-1_BIB37 article-title: Eight potassium channel families revealed by the C. elegans genome project publication-title: Neuropharmacology doi: 10.1016/0028-3908(96)00126-8 – volume: 439 start-page: 714 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB25 article-title: Cloning, localisation and functional expression of the human orthologue of the TREK-1 potassium channel publication-title: Pfluger’s Arch. – Eur. J. Physiol. doi: 10.1007/s004240050997 – volume: 273 start-page: 30863 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB34 article-title: Cloning and expression of a novel pH-sensitive two pore domain K+ channel from human kidney publication-title: J. Biol. Chem. doi: 10.1074/jbc.273.47.30863 – volume: 14 start-page: 889 year: 1995 ident: 10.1016/S0169-328X(00)00263-1_BIB22 article-title: Pore loops: an emerging theme in ion channel structure publication-title: Neuron doi: 10.1016/0896-6273(95)90327-5 – volume: 17 start-page: 4283 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB30 article-title: A mammalian two pore domain mechano-gated S-like K+ channel publication-title: EMBO J. doi: 10.1093/emboj/17.15.4283 – volume: 17 start-page: 3297 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB9 article-title: A neuronal two P domain K+ channel stimulated by arachidonic acid and polyunsaturated fatty acids publication-title: EMBO J. doi: 10.1093/emboj/17.12.3297 – volume: 275 start-page: 17412 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB1 article-title: TREK-2, a novel member of the mechanosensitive tandem pore K+ channel family publication-title: J. Biol. Chem. doi: 10.1074/jbc.M000445200 – volume: 20 start-page: 91 year: 1997 ident: 10.1016/S0169-328X(00)00263-1_BIB11 article-title: Cloned potassium channels from eukaryotes and prokaryotes publication-title: Ann. Rev. Neurosci. doi: 10.1146/annurev.neuro.20.1.91 – volume: 275 start-page: 28722 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB29 article-title: TWIK-2, an inactivating 2P domain K+ channel publication-title: J. Biol. Chem. doi: 10.1074/jbc.M003755200 – volume: 282 start-page: 2028 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB2 article-title: Neurobiology of the Caenorhabditis elegans genome publication-title: Science doi: 10.1126/science.282.5396.2028 – volume: 274 start-page: 1381 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB23 article-title: TRAAK is a mammalian neuronal mechano-gated K+ channel publication-title: J. Biol. Chem. doi: 10.1074/jbc.274.3.1381 – volume: 15 start-page: 1004 year: 1996 ident: 10.1016/S0169-328X(00)00263-1_BIB19 article-title: TWIK-1, a ubiquitous human weakly inward rectifying K+ channel with a novel structure publication-title: EMBO J. doi: 10.1002/j.1460-2075.1996.tb00437.x – volume: 5 start-page: 268 year: 1995 ident: 10.1016/S0169-328X(00)00263-1_BIB4 article-title: The inward rectifier potassium channel family publication-title: Curr. Opin. Neurobiol. doi: 10.1016/0959-4388(95)80038-7 – volume: 280 start-page: 69 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB5 publication-title: The structure of the potassium channel: molecular basis of K+ conductance and selectivity – volume: 19 start-page: 2483 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB24 article-title: TREK-1 is a heat-activated background K+ channel publication-title: EMBO J. doi: 10.1093/emboj/19.11.2483 – volume: 9 start-page: 43 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB20 article-title: Advances in quantitative PCR technology: 5′ nuclease assays publication-title: Curr. Opin. Biotechnol. doi: 10.1016/S0958-1669(98)80082-7 – volume: 15 start-page: 1441 year: 1995 ident: 10.1016/S0169-328X(00)00263-1_BIB38 article-title: Determination of the subunit stoichiometry of an inwardly rectifying potassium channel publication-title: Neuron doi: 10.1016/0896-6273(95)90021-7 – volume: 275 start-page: 9340 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB13 article-title: TASK-3, a new member of the tandem pore K+ channel family publication-title: J. Biol. Chem. doi: 10.1074/jbc.275.13.9340 – volume: 277 start-page: H1669 issue: Heart Circ. Physiol. 46 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB14 article-title: TBAK-1 and TASK-1, two pore K+ channel subunits: kinetic properties and expression in rat heart publication-title: Am. J. Physiol. – volume: 98 start-page: 9 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB26 article-title: The use of TaqMan RT-PCR assays for semiquantitative analysis of gene expression in CNS tissues and disease models publication-title: J. Neurosci. Methods doi: 10.1016/S0165-0270(00)00178-3 – volume: 82 start-page: 513 year: 1998 ident: 10.1016/S0169-328X(00)00263-1_BIB12 article-title: Cloning and functional expression of a novel cardiac two pore background K+ channel publication-title: Circ. Res. doi: 10.1161/01.RES.82.4.513 – volume: 25 start-page: 399 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB36 article-title: TASK-1, a two-pore domain K+ channel, is modulated by multiple neurotransmitters in motorneurons publication-title: Neuron doi: 10.1016/S0896-6273(00)80903-4 – volume: Vol. 46 start-page: 199 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB16 article-title: Potassium channels with two P domains – volume: 95 start-page: 893 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB33 article-title: Immunolocalisation of the arachidonic acid and mechanosensitive baseline TRAAK potassium channel in the nervous system publication-title: Neuroscience doi: 10.1016/S0306-4522(99)00484-4 – volume: 15 start-page: 6854 year: 1996 ident: 10.1016/S0169-328X(00)00263-1_BIB8 article-title: Cloning, functional expression and brain localisation of a novel unconventional outward rectifier K+ channel publication-title: EMBO J. doi: 10.1002/j.1460-2075.1996.tb01077.x – volume: 2 start-page: 422 issue: 5 year: 1999 ident: 10.1016/S0169-328X(00)00263-1_BIB28 article-title: Inhalation anesthetics activate two-pore domain background K+ channels publication-title: Nat. Neurosci. doi: 10.1038/8084 – volume: 6 start-page: 195 year: 1996 ident: 10.1016/S0169-328X(00)00263-1_BIB7 article-title: Functional and molecular diversity classifies the family of inward rectifier K+ channels publication-title: Cell. Physiol. Biochem. doi: 10.1159/000154823 – volume: 97 start-page: 3614 year: 2000 ident: 10.1016/S0169-328X(00)00263-1_BIB27 article-title: A functional role for the two-pore domain potassium channel TASK-1 in cerebellar granule neurons publication-title: Proc. Natl. Acad. Sci. doi: 10.1073/pnas.97.7.3614 |
SSID | ssj0001811 |
Score | 1.9312665 |
Snippet | Potassium channels are amongst the most heterogeneous class of ion channels known and are responsible for mediating a diverse range of biological functions.... |
SourceID | proquest pubmed pascalfrancis crossref elsevier |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 101 |
SubjectTerms | 2P domain Anaesthetics Anatomy Biological and medical sciences Central nervous system Central Nervous System - chemistry Central Nervous System - physiology Expression Fundamental and applied biological sciences. Psychology Ganglia, Spinal - chemistry Ganglia, Spinal - physiology Gene Expression - physiology Humans Molecular Sequence Data Nerve Tissue Proteins Polymerase Chain Reaction Potassium channel Potassium Channels - chemistry Potassium Channels - genetics Potassium Channels, Tandem Pore Domain Protein Structure, Tertiary RNA, Messenger - analysis Sequence Homology, Amino Acid Vertebrates: nervous system and sense organs |
Title | Distribution analysis of human two pore domain potassium channels in tissues of the central nervous system and periphery |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S0169328X00002631 https://dx.doi.org/10.1016/S0169-328X(00)00263-1 https://www.ncbi.nlm.nih.gov/pubmed/11165377 https://www.proquest.com/docview/17772368 https://www.proquest.com/docview/70630725 |
Volume | 86 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3db9MwELemISQkhGDjozCGHxCCB69x7MTJYzWYChV7ACb6FjmxLVWiScVSQV_427mznZY9jCFeksjKWZbvch_x3e8IeSmcdkYUOdOJqZl0qWNlUWfM2VSXjUWXHwPFj-f59EJ-mGfzPXI61MJgWmXU_UGne20dR8ZxN8erxWL82eOIpMUcVW6a-1pqKRXK-smvXZoHWLDQkzAvGb69q-IJM_jB10nyxk_C-HX26e5KX8KuudDu4np_1Nuls_vkXnQo6SSs-QHZs-0BOZy0EEwvN_QV9Sme_t_5AbkdOk9uDsnPtwiYG3tdUR2RSWjnqG_aR_sfHQXP3FLTLfWihecevOzFekmxUriFBVMY7T3XPBn4kTQmetIW9E-3vqQBJRpmNxTxlBHAYPOQXJy9-3I6ZbEJA2vAmeuZ1FwXicjqDK5KpFlal6pW1tS1LLFlqFQ6qRMjnZbGKS1VKgy4oQ3XuZEQqj8i-23X2ieEgrgIUfKiEXi2WECslTSJbXieyoy7Ro6IHLa-aiJCOTbK-Fb9kYqWlxVyrEoQ1hQ4VvEROdmSrQJEx00E-cDXaqg_BY1ZgRG5ibDYEl4R0n8hPboiQNuVgr4sRTEiLwZ5quD7xkMb3VpgVcUVxD8i_8sbCmHTVJqNyOMgiLtdQGwlodTT_1_3M3InZN1xsNZHZL__vrbPwQ3r62P_nR2TW5P3s-k53mefvs5-A8cXLdw |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELaqIgQSQtDyWCjUB4TgkG5iO3ZyrArVAm0vtNLeLDuJpZXYZNVmVfbCb2fGdnbpoRRxiSLLY1meyTzimW8IecedcTUvZGLS2ibCMZeUhc0T1zBTVg26_Bgonp7JyYX4Os2nW-RoqIXBtMqo-4NO99o6jozjaY4Xs9n4u8cRYcUUVS6TWEt9T-RcYV7fwa9NngeYsNCUUJYJTt-U8YQl_OCHNP3oV0my2wzUo4W5gmNzod_F7Q6pN0zHT8jj6FHSw7Dpp2SraXfI7mEL0fR8Rd9Tn-Ppf57vkPuh9eRql_z8hIi5sdkVNRGahHaO-q59tL_uKLjmDa27uZm18N6Dmz1bzimWCrewYQqjvWebJwNHksZMT9qCAuqWVzTARMPqNUVAZUQwWD0jF8efz48mSezCkFTgzfWJMJkpUp7bHJ6Ks5zZUlnV1NaKEnuGCmVSm9bCGVE7ZYRivAY_tMqMrAXE6s_Jdtu1zUtCQV44L7Oi4ni5WECwlVZpU2WSiTxzlRgRMRy9riJEOXbK-KH_yEWTpUaO6RRxTYFjOhuRgzXZImB03EUgB77qoQAVVKYGK3IXYbEmvCGl_0K6d0OA1jsFhVnyYkT2B3nS8IHjrY1pG2CVzhQEQFz-ZYZC3DTF8hF5EQRxcwoIrsSVevX_-94nDybnpyf65MvZt9fkYUjBy8B075Ht_nLZvAGfrLdv_Tf3GwqmLcw |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Distribution+analysis+of+human+two+pore+domain+potassium+channels+in+tissues+of+the+central+nervous+system+and+periphery&rft.jtitle=Brain+research.+Molecular+brain+research.&rft.au=Medhurst%2C+Andrew+D.&rft.au=Rennie%2C+Gillian&rft.au=Chapman%2C+Conrad+G.&rft.au=Meadows%2C+Helen&rft.date=2001-01-31&rft.pub=Elsevier+B.V&rft.issn=0169-328X&rft.volume=86&rft.issue=1-2&rft.spage=101&rft.epage=114&rft_id=info:doi/10.1016%2FS0169-328X%2800%2900263-1&rft.externalDocID=S0169328X00002631 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0169-328X&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0169-328X&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0169-328X&client=summon |