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Items: 1 to 20 of 112

1.

Synaptic gain-of-function effects of mutant Cav2.1 channels in a mouse model of familial hemiplegic migraine are due to increased basal [Ca2+]i.

Di Guilmi MN, Wang T, Inchauspe CG, Forsythe ID, Ferrari MD, van den Maagdenberg AM, Borst JG, Uchitel OD.

J Neurosci. 2014 May 21;34(21):7047-58. doi: 10.1523/JNEUROSCI.2526-13.2014.

2.

Mechanism underlying unaltered cortical inhibitory synaptic transmission in contrast with enhanced excitatory transmission in CaV2.1 knockin migraine mice.

Vecchia D, Tottene A, van den Maagdenberg AM, Pietrobon D.

Neurobiol Dis. 2014 Sep;69:225-34. doi: 10.1016/j.nbd.2014.05.035. Epub 2014 Jun 5.

3.

Gain of function in FHM-1 Cav2.1 knock-in mice is related to the shape of the action potential.

Inchauspe CG, Urbano FJ, Di Guilmi MN, Forsythe ID, Ferrari MD, van den Maagdenberg AM, Uchitel OD.

J Neurophysiol. 2010 Jul;104(1):291-9. doi: 10.1152/jn.00034.2010. Epub 2010 May 19.

4.

CaV2.1 voltage activated calcium channels and synaptic transmission in familial hemiplegic migraine pathogenesis.

Uchitel OD, Inchauspe CG, Urbano FJ, Di Guilmi MN.

J Physiol Paris. 2012 Jan;106(1-2):12-22. doi: 10.1016/j.jphysparis.2011.10.004. Epub 2011 Nov 2. Review.

PMID:
22074995
5.

Abnormal synaptic Ca(2+) homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant mice.

Eikermann-Haerter K, Arbel-Ornath M, Yalcin N, Yu ES, Kuchibhotla KV, Yuzawa I, Hudry E, Willard CR, Climov M, Keles F, Belcher AM, Sengul B, Negro A, Rosen IA, Arreguin A, Ferrari MD, van den Maagdenberg AM, Bacskai BJ, Ayata C.

Ann Neurol. 2015 Aug;78(2):193-210. doi: 10.1002/ana.24449. Epub 2015 Jul 6.

6.

Presynaptic CaV2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held.

Inchauspe CG, Urbano FJ, Di Guilmi MN, Ferrari MD, van den Maagdenberg AM, Forsythe ID, Uchitel OD.

J Neurophysiol. 2012 Dec;108(11):2967-76. doi: 10.1152/jn.01183.2011. Epub 2012 Sep 5.

7.

Severe and progressive neurotransmitter release aberrations in familial hemiplegic migraine type 1 Cacna1a S218L knock-in mice.

Kaja S, Van de Ven RC, Broos LA, Frants RR, Ferrari MD, Van den Maagdenberg AM, Plomp JJ.

J Neurophysiol. 2010 Sep;104(3):1445-55. doi: 10.1152/jn.00012.2010. Epub 2010 Jul 14.

8.

Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice.

Inchauspe CG, Pilati N, Di Guilmi MN, Urbano FJ, Ferrari MD, van den Maagdenberg AM, Forsythe ID, Uchitel OD.

Hear Res. 2015 Jan;319:56-68. doi: 10.1016/j.heares.2014.11.006. Epub 2014 Dec 4.

PMID:
25481823
9.

Insights into migraine mechanisms and CaV2.1 calcium channel function from mouse models of familial hemiplegic migraine.

Pietrobon D.

J Physiol. 2010 Jun 1;588(Pt 11):1871-8. doi: 10.1113/jphysiol.2010.188003. Epub 2010 Mar 1. Review.

10.

Abnormal cortical synaptic transmission in CaV2.1 knockin mice with the S218L missense mutation which causes a severe familial hemiplegic migraine syndrome in humans.

Vecchia D, Tottene A, van den Maagdenberg AM, Pietrobon D.

Front Cell Neurosci. 2015 Feb 17;9:8. doi: 10.3389/fncel.2015.00008. eCollection 2015.

11.

Enhanced excitatory transmission at cortical synapses as the basis for facilitated spreading depression in Ca(v)2.1 knockin migraine mice.

Tottene A, Conti R, Fabbro A, Vecchia D, Shapovalova M, Santello M, van den Maagdenberg AM, Ferrari MD, Pietrobon D.

Neuron. 2009 Mar 12;61(5):762-73. doi: 10.1016/j.neuron.2009.01.027.

12.

Calcium channels and synaptic transmission in familial hemiplegic migraine type 1 animal models.

Uchitel OD, González Inchauspe C, Di Guilmi MN.

Biophys Rev. 2014 Mar;6(1):15-26. doi: 10.1007/s12551-013-0126-y. Epub 2013 Dec 3. Review.

13.

RNA expression profiling in brains of familial hemiplegic migraine type 1 knock-in mice.

de Vries B, Eising E, Broos LA, Koelewijn SC, Todorov B, Frants RR, Boer JM, Ferrari MD, Hoen PA, van den Maagdenberg AM.

Cephalalgia. 2014 Mar;34(3):174-82. doi: 10.1177/0333102413502736. Epub 2013 Aug 28.

PMID:
23985897
14.

Genetic and hormonal factors modulate spreading depression and transient hemiparesis in mouse models of familial hemiplegic migraine type 1.

Eikermann-Haerter K, Dileköz E, Kudo C, Savitz SI, Waeber C, Baum MJ, Ferrari MD, van den Maagdenberg AM, Moskowitz MA, Ayata C.

J Clin Invest. 2009 Jan;119(1):99-109. doi: 10.1172/JCI36059. Epub 2008 Dec 22.

15.

Specific kinetic alterations of human CaV2.1 calcium channels produced by mutation S218L causing familial hemiplegic migraine and delayed cerebral edema and coma after minor head trauma.

Tottene A, Pivotto F, Fellin T, Cesetti T, van den Maagdenberg AM, Pietrobon D.

J Biol Chem. 2005 May 6;280(18):17678-86. Epub 2005 Mar 2.

16.

In vivo imaging reveals that pregabalin inhibits cortical spreading depression and propagation to subcortical brain structures.

Cain SM, Bohnet B, LeDue J, Yung AC, Garcia E, Tyson JR, Alles SR, Han H, van den Maagdenberg AM, Kozlowski P, MacVicar BA, Snutch TP.

Proc Natl Acad Sci U S A. 2017 Feb 28;114(9):2401-2406. doi: 10.1073/pnas.1614447114. Epub 2017 Feb 21.

17.

A Cacna1a knockin migraine mouse model with increased susceptibility to cortical spreading depression.

van den Maagdenberg AM, Pietrobon D, Pizzorusso T, Kaja S, Broos LA, Cesetti T, van de Ven RC, Tottene A, van der Kaa J, Plomp JJ, Frants RR, Ferrari MD.

Neuron. 2004 Mar 4;41(5):701-10.

18.

Contribution of calcium-dependent facilitation to synaptic plasticity revealed by migraine mutations in the P/Q-type calcium channel.

Adams PJ, Rungta RL, Garcia E, van den Maagdenberg AM, MacVicar BA, Snutch TP.

Proc Natl Acad Sci U S A. 2010 Oct 26;107(43):18694-9. doi: 10.1073/pnas.1009500107. Epub 2010 Oct 11.

19.

The S218L familial hemiplegic migraine mutation promotes deinhibition of Ca(v)2.1 calcium channels during direct G-protein regulation.

Weiss N, Sandoval A, Felix R, Van den Maagdenberg A, De Waard M.

Pflugers Arch. 2008 Nov;457(2):315-26. doi: 10.1007/s00424-008-0541-2. Epub 2008 Jun 26.

20.

Familial hemiplegic migraine type 1 mutations K1336E, W1684R, and V1696I alter Cav2.1 Ca2+ channel gating: evidence for beta-subunit isoform-specific effects.

Müllner C, Broos LA, van den Maagdenberg AM, Striessnig J.

J Biol Chem. 2004 Dec 10;279(50):51844-50. Epub 2004 Sep 23.

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