Cargando…

Corticosterone enhances CSD susceptibility via glucocorticoid receptor activation in familial hemiplegic migraine 1 Cacna1a knock-in mice

Detalles Bibliográficos
Autores principales:	Shyti, R, Eikermann-Haerter, K, Meijer, OC, van Heiningen, SH, De Groote, L, Ferrari, MD, Ayata, C, van den Maagdenberg, AMJ, Tolner, EA
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer 2013
Materias:	Poster Presentation
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3620500/ http://dx.doi.org/10.1186/1129-2377-14-S1-P85

Ejemplares similares

Monitoring cortical neuronal activity and spreading depression in freely behaving familial hemiplegic migraine Cacna1a R192Q knockin mice
por: Houben, T, et al.
Publicado: (2013)

EHMTI-0262. Dysregulation of inflammatory pathways in a familial hemiplegic migraine 1 mouse model after the induction of cortical spreading depression
por: de Vries, B, et al.
Publicado: (2014)

Optogenetic cortical spreading depolarization induces headache-related behaviour and neuroinflammatory responses some prolonged in familial hemiplegic migraine type 1 mice
por: Dehghani, Anisa, et al.
Publicado: (2023)

Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes
por: Maksemous, Neven, et al.
Publicado: (2023)

Current understanding of cortical structure and function in migraine
por: Tolner, Else A, et al.
Publicado: (2019)

Trigeminovascular calcitonin gene-related peptide function in Cacna1a R192Q-mutated knock-in mice
por: Chan, Kayi Y, et al.
Publicado: (2017)

Sporadic Hemiplegic Migraine with CACNA1A Mutation Masquerading as Acute Meningoencephalitis
por: Gajam, Siddhartha, et al.
Publicado: (2022)

Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine
por: Maksemous, Neven, et al.
Publicado: (2022)

Mass spectrometry imaging of amino neurotransmitters: a comparison of derivatization methods and application in mouse brain tissue
por: Esteve, Clara, et al.
Publicado: (2016)

Changes in Plasma Lipid Levels Following Cortical Spreading Depolarization in a Transgenic Mouse Model of Familial Hemiplegic Migraine
por: Loonen, Inge C. M., et al.
Publicado: (2022)

Responsivity to light in familial hemiplegic migraine type 1 mutant mice reveals frequency‐dependent enhancement of visual network excitability
por: Perenboom, Matthijs J. L., et al.
Publicado: (2020)

Large-Scale Mass Spectrometry Imaging Investigation of Consequences of Cortical Spreading Depression in a Transgenic Mouse Model of Migraine
por: Carreira, Ricardo J., et al.
Publicado: (2015)

Cerebellar Atrophy and Changes in Cytokines Associated with the CACNA1A R583Q Mutation in a Russian Familial Hemiplegic Migraine Type 1 Family
por: Khaiboullina, Svetlana F., et al.
Publicado: (2017)

CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report
por: Scoppola, Chiara, et al.
Publicado: (2021)

Novel SCN1A mutation in the IFMT motif of the α1 subunit of the voltage-gated NaV1.1 channel causing familial hemiplegic migraine
por: De Vries, B, et al.
Publicado: (2013)

Mutated Ca(V)2.1 channels dysregulate CASK/P2X3 signaling in mouse trigeminal sensory neurons of R192Q Cacna1a knock-in mice
por: Gnanasekaran, Aswini, et al.
Publicado: (2013)

The Ataxic Cacna1a-Mutant Mouse Rolling Nagoya: An Overview of Neuromorphological and Electrophysiological Findings
por: Plomp, Jaap J., et al.
Publicado: (2009)

Screening of cacna1a and ATP1A2 genes in hemiplegic migraine: clinical, genetic and functional studies
por: Sintas, C, et al.
Publicado: (2013)

Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine: clinical, genetic, and functional studies
por: Carreño, Oriel, et al.
Publicado: (2013)

CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report
por: Romozzi, Marina, et al.
Publicado: (2021)

CSD Communications of the Cambridge Structural Database
por: Ferrence, Gregory M., et al.
Publicado: (2023)

Familial Hemiplegic Migraine with Prolonged Coma and Cerebellar Atrophy: CACNA1A T666M Mutation in a Korean Family
por: Choi, Kyung-Ho, et al.
Publicado: (2012)

P016. Congenital ataxia, hemiplegic migraine due to a novel mutation of CACNA1A: a case report
por: Frusciante, Roberto, et al.
Publicado: (2015)

Thermal expansion properties of organic crystals: a CSD study
por: van der Lee, Arie, et al.
Publicado: (2021)

Aura and Stroke: relationship and what we have learnt from preclinical models
por: Yemisci, Muge, et al.
Publicado: (2019)

Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant
por: Nardello, Rosaria, et al.
Publicado: (2020)

Structural Basis of the Heterodimer Formation between Cell Shape-Determining Proteins Csd1 and Csd2 from Helicobacter pylori
por: An, Doo Ri, et al.
Publicado: (2016)

WebCSD: the online portal to the Cambridge Structural Database
por: Thomas, Ian R., et al.
Publicado: (2010)

Differential regulation of cell functions by CSD peptide subdomains
por: Reese, Charles, et al.
Publicado: (2013)

A mathematical model for persistent post-CSD vasoconstriction
por: Xu, Shixin, et al.
Publicado: (2020)

Identifying a Hidden Conglomerate Chiral Pool in the CSD
por: Walsh, Mark P., et al.
Publicado: (2022)

Recognition of polymorphic Csd proteins determines sex in the honeybee
por: Otte, Marianne, et al.
Publicado: (2023)

R1352Q CACNA1A Variant in a Patient with Sporadic Hemiplegic Migraine, Ataxia, Seizures and Cerebral Oedema: A Case Report
por: Stubberud, Anker, et al.
Publicado: (2021)

Advanced brain MRI may help understand the link between migraine and multiple sclerosis
por: Huang, Susie Y., et al.
Publicado: (2023)

Deciphering in silico the Role of Mutated Na(V)1.1 Sodium Channels in Enhancing Trigeminal Nociception in Familial Hemiplegic Migraine Type 3
por: Suleimanova, Alina, et al.
Publicado: (2021)

Migraine-relevant sex-dependent activation of mouse meningeal afferents by TRPM3 agonists
por: Krivoshein, G., et al.
Publicado: (2022)

The Cambridge Structural Database (CSD): Current Activities and Future Plans
por: Watson, David G.
Publicado: (1996)

csdR, an R package for differential co-expression analysis
por: Pettersen, Jakob P., et al.
Publicado: (2022)

An altered GABA-A receptor function in spinocerebellar ataxia type 6 and familial hemiplegic migraine type 1 associated with the CACNA1A gene mutation
por: Kono, Satoshi, et al.
Publicado: (2014)

Familial Hemiplegic Migraine With Progressive Cerebellar Ataxia Caused by a p.Thr666Met CACNA1A Gene Mutation in a Chinese Family
por: Li, Mengmeng, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_lqk5ii6evvhg79hpra2dd4nqae