These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

292 related articles for article (PubMed ID: 28223480)

  • 21. 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; 41(5):701-10. PubMed ID: 15003170
    [TBL] [Abstract][Full Text] [Related]  

  • 22. The familial hemiplegic migraine type 1 mutation K1336E affects direct G protein-mediated regulation of neuronal P/Q-type Ca2+ channels.
    Garza-López E; González-Ramírez R; Gandini MA; Sandoval A; Felix R
    Cephalalgia; 2013 Apr; 33(6):398-407. PubMed ID: 23430985
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 61(5):762-73. PubMed ID: 19285472
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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; 280(18):17678-86. PubMed ID: 15743764
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Differential cerebellar GABAA receptor expression in mice with mutations in CaV2.1 (P/Q-type) calcium channels.
    Kaja S; Payne AJ; Nielsen EØ; Thompson CL; van den Maagdenberg AM; Koulen P; Snutch TP
    Neuroscience; 2015 Sep; 304():198-208. PubMed ID: 26208839
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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; 9():8. PubMed ID: 25741235
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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. PubMed ID: 18581134
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Role of different voltage-gated Ca2+ channels in cortical spreading depression: specific requirement of P/Q-type Ca2+ channels.
    Tottene A; Urbani A; Pietrobon D
    Channels (Austin); 2011; 5(2):110-4. PubMed ID: 21150292
    [TBL] [Abstract][Full Text] [Related]  

  • 29. CaV2.1 channelopathies.
    Pietrobon D
    Pflugers Arch; 2010 Jul; 460(2):375-93. PubMed ID: 20204399
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Migraine mutations impair hippocampal learning despite enhanced long-term potentiation.
    Dilekoz E; Houben T; Eikermann-Haerter K; Balkaya M; Lenselink AM; Whalen MJ; Spijker S; Ferrari MD; van den Maagdenberg AM; Ayata C
    J Neurosci; 2015 Feb; 35(8):3397-402. PubMed ID: 25716839
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Drosophila CaV2 channels harboring human migraine mutations cause synapse hyperexcitability that can be suppressed by inhibition of a Ca2+ store release pathway.
    Brusich DJ; Spring AM; James TD; Yeates CJ; Helms TH; Frank CA
    PLoS Genet; 2018 Aug; 14(8):e1007577. PubMed ID: 30080864
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A hyperexcitability phenotype in mouse trigeminal sensory neurons expressing the R192Q Cacna1a missense mutation of familial hemiplegic migraine type-1.
    Hullugundi SK; Ansuini A; Ferrari MD; van den Maagdenberg AM; Nistri A
    Neuroscience; 2014 Apr; 266():244-54. PubMed ID: 24583041
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The familial hemiplegic migraine mutation R192Q reduces G-protein-mediated inhibition of P/Q-type (Ca(V)2.1) calcium channels expressed in human embryonic kidney cells.
    Melliti K; Grabner M; Seabrook GR
    J Physiol; 2003 Jan; 546(Pt 2):337-47. PubMed ID: 12527722
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Enhanced circadian phase resetting in R192Q Cav2.1 calcium channel migraine mice.
    van Oosterhout F; Michel S; Deboer T; Houben T; van de Ven RC; Albus H; Westerhout J; Vansteensel MJ; Ferrari MD; van den Maagdenberg AM; Meijer JH
    Ann Neurol; 2008 Sep; 64(3):315-24. PubMed ID: 18825664
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Migraine: Calcium Channels and Glia.
    Kowalska M; Prendecki M; Piekut T; Kozubski W; Dorszewska J
    Int J Mol Sci; 2021 Mar; 22(5):. PubMed ID: 33799975
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Increased presynaptic excitability in a migraine with aura mutation.
    Suryavanshi P; Sawant-Pokam P; Clair S; Brennan KC
    Brain; 2024 Feb; 147(2):680-697. PubMed ID: 37831655
    [TBL] [Abstract][Full Text] [Related]  

  • 37. The E1015K variant in the synprint region of the CaV2.1 channel alters channel function and is associated with different migraine phenotypes.
    Condliffe SB; Fratangeli A; Munasinghe NR; Saba E; Passafaro M; Montrasio C; Ferrari M; Rosa P; Carrera P
    J Biol Chem; 2013 Nov; 288(47):33873-33883. PubMed ID: 24108129
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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. PubMed ID: 28509957
    [TBL] [Abstract][Full Text] [Related]  

  • 39. The mechanism of functional up-regulation of P2X3 receptors of trigeminal sensory neurons in a genetic mouse model of familial hemiplegic migraine type 1 (FHM-1).
    Hullugundi SK; Ferrari MD; van den Maagdenberg AM; Nistri A
    PLoS One; 2013; 8(4):e60677. PubMed ID: 23577145
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Characteristics of cortical spreading depression and c-Fos expression in transgenic mice having a mutation associated with familial hemiplegic migraine 2.
    Tang C; Unekawa M; Shibata M; Tomita Y; Izawa Y; Sugimoto H; Ikeda K; Kawakami K; Suzuki N; Nakahara J
    Cephalalgia; 2020 Oct; 40(11):1177-1190. PubMed ID: 32484063
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 15.