Impaired K+-binding to the glial EAAT1 in hemiplegic migraine

被引：0

作者：

Kovermann, P. ^{[1
]}

Hessel, M. ^{[1
,2
]}

Kortzak, D. ^{[1
]}

Koch, J. ^{[3
]}

Jen, J. C. ^{[4
]}

Freilinger, T. ^{[5
]}

Fahlke, C. ^{[1
]}

机构：

[1] Forschungszentrum Julich, Zellulare Biophys ICS 4, Julich, Germany

[2] Westfal Wilhelms Univ Munster, Neurophysiol, Munster, Germany

[3] Univ Klinikum Salzburg, Salzburg, Austria

[4] UCLA Sch Med, Los Angeles, CA USA

[5] Hertie Inst Clin Brain Res, Tubingen, Germany

来源：

ACTA PHYSIOLOGICA | 2017年 / 219卷

关键词：

D O I：

暂无

中图分类号：

Q4 [生理学];

学科分类号：

071003 ;

摘要：

OS09-1

引用

页码：50 / 50

页数：1

共 38 条

[21] Impaired plasma membrane targeting or protein stability by certain ATP1A2 mutation identified in sporadic or familial hemiplegic migraine
Tavraz, Neslihan N.
Durr, Katharina L.
Koenderink, Jan B.
Freilinger, Tobias
Bamberg, Ernst
Dichgans, Martin
Friedrich, Thomas
CHANNELS, 2009, 3 (02) : 82 - 87
[22] First case of compound heterozygosity in Na,K-ATPase gene ATP1A2 in familial hemiplegic migraine
Kaate R J Vanmolkot
Anine H Stam
Ashok Raman
Jan B Koenderink
Boukje de Vries
Eelke H van den Boogerd
Judith van Vark
Jeroen J M W van den Heuvel
Nin Bajaj
Gisela M Terwindt
Joost Haan
Rune R Frants
Michel D Ferrari
Arn M J M van den Maagdenberg
European Journal of Human Genetics, 2007, 15 : 884 - 888
[23] Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 in familial hemiplegic migraine
Vanmolkot, KRJ
Kors, EE
Hottenga, J
Terwindt, GM
Haan, J
Hoefnagels, WAJ
Black, DF
Sandkuijl, LA
CEPHALALGIA, 2003, 23 (07) : 576 - 576
[24] First case of compound heterozygosity in Na, K-ATPase gene ATP1A2 in familial hemiplegic migraine
Vanmolkot, Kaate R. J.
Stam, Anine H.
Raman, Ashok
Koenderink, Jan B.
de Vries, Boukje
van den Boogerd, Eelke H.
van Vark, Judith
van den Heuvel, Jeroen J. M. W.
Bajaj, Nin
Terwindt, Gisela M.
Haan, Joost
Frants, Rune R.
Ferrari, Michel D.
van den Maagdenberg, Arn M. J. M.
EUROPEAN JOURNAL OF HUMAN GENETICS, 2007, 15 (08) : 884 - 888
[25] Binding and transport of [3H] (2S,4R)4-methylglutamate, a new ligand for glutamate transporters, demonstrate labeling of EAAT1 in cultured murine astrocytes
Apricò, K
Beart, PM
Crawford, D
O'Shea, RD
JOURNAL OF NEUROSCIENCE RESEARCH, 2004, 75 (06) : 751 - 759
[26] Two de novo mutations in the Na, K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine
Vanmolkot, KR
Kors, EE
Turk, U
Turkdogan, D
Keyser, A
Broos, LA
Kia, SK
van den Heuvel, JJ
Black, DF
Haan, J
Frants, RR
Barone, V
Ferrari, MD
Casari, G
Koenderink, JB
van den Maagdenberg, AM
EUROPEAN JOURNAL OF HUMAN GENETICS, 2006, 14 (05) : 555 - 560
[27] Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine
Kaate R J Vanmolkot
Esther E Kors
Ulku Turk
Dylsad Turkdogan
Antoine Keyser
Ludo A M Broos
Sima Kheradmand Kia
Jeroen J M W van den Heuvel
David F Black
Joost Haan
Rune R Frants
Virginia Barone
Michel D Ferrari
Giorgio Casari
Jan B Koenderink
Arn M J M van den Maagdenberg
European Journal of Human Genetics, 2006, 14 : 555 - 560
[28] First case of compound heterozygosity in familial hemiplegic migraine: two mutations in Na,K-ATPase gene ATP1A2
Bajaj, N.
de Vries, B.
Ferrari, M. D.
Frants, R. R.
Haan, J.
Koenderink, J. B.
Raman, A.
Stam, A. H.
Terwindt, G. M.
van den Boogerd, E. H.
van den Heuvel, J. J. M. W.
van den Maagdenberg, A. M. J. M.
van Vark, J.
Vanmolkot, Kaate
Vanmolkot, K. R. J.
CEPHALALGIA, 2007, 27 (06) : 584 - 585
[29] Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
Maurizio De Fusco
Roberto Marconi
Laura Silvestri
Luigia Atorino
Luca Rampoldi
Letterio Morgante
Andrea Ballabio
Paolo Aridon
Giorgio Casari
Nature Genetics, 2003, 33 : 192 - 196
[30] Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump α2 subunit associated with familial hemiplegic migraine type 2
De Fusco, M
Marconi, R
Silvestri, L
Atorino, L
Rampoldi, L
Morgante, L
Ballabio, A
Aridon, P
Casari, G
NATURE GENETICS, 2003, 33 (02) : 192 - 196

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