Results 91 to 100 of about 3,294 (160)

Screening of CACNA1A and ATP1A2 genes in hemiplegic migraine : clinical, genetic, and functional studies

Hemiplegic migraine (HM) is a rare and severe subtype of autosomal dominant migraine, characterized by a complex aura including some degree of motor weakness.
Sobrido, María-Jesús, Gené, Gemma G, Pons, Roser, Corominas, Roser, Macaya Ruiz, Alfons, Fernández-Castillo, Noèlia, Grinberg, Daniel, Valverde, Miguel Ángel, Fernández-Fernández, José Manuel, Llaneza, Miguel, Toma, Claudio, Serra, Selma Angèlica, Universitat Autònoma de Barcelona, Vila-Pueyo, Marta, Carreño, Oriel, Sintas, Cèlia, Cormand, Bru   +16 more
core   +2 more sources

Exploring variances in meat quality between Qingyuan partridge chicken and Cobb broiler: Insights from combined multi-omics analysis

Poultry Science
Previously, animal breeding prioritized enhancing key economic traits to improve production efficiency, leading to a gradual difference in meat quality. However, the genetic factors influencing meat quality remain unclear.
Xin Yang, Bolin Cai, Zhaofeng Zhang, Yu Mo, Zhen Zhou, Ruiquan Wu, Shaofen Kong, Danfeng Cai, Ruitong Zhang, Zhenhui Li, Qinghua Nie   +10 more
doaj   +1 more source

Sodium pump alpha-2 subunit (ATP1A2) alleviates cardiomyocyte anoxia–reoxygenation injury via inhibition of endoplasmic reticulum stress-related apoptosis

, 2018
Previous studies have found decreased functional capacity of the sodium pump (Na+-K+-ATPase) alpha and beta subunits and recovery of Na+-K+-ATPase activity significantly decreased myocyte apoptosis in myocardial ischemia–reperfusion (I/R) injury ...
Zheng Wang, Mingchao Zhang, Hegui Wang, Yulong Hu, Nannan Ge, Ting Huang   +5 more
core   +1 more source

Case Report Sporadic Hemiplegic Migraine with ATP1A2 and Prothrombin Gene Mutations [PDF]

, 2020
Background. Hemiplegic migraine is a rare type of migraine that may present in children and adolescents. Both familial and sporadic hemiplegic migraines have similar prevalence and clinical characteristics. Patient.
Batool F Kirmani, Diana Mungall, Jose Aceves   +2 more
core  

The genetic relationship between epilepsy and hemiplegic migraine

Neuropsychiatric Disease and Treatment, 2017
Yiqing Huang,1 Hai Xiao,1 Xingyue Qin,1 Yuan Nong,1 Donghua Zou,2 Yuan Wu3 1Department of Neurology, Guigang City People’s Hospital and the Eighth Affiliated Hospital of Guangxi Medical University, Guigang, People’s Republic of China ...
Huang Y, Xiao H, Qin X, Nong Y, Zou D, Wu Y   +5 more
doaj  

Novel missense mutation in the ATP1A2 gene associated with atypical sporapedic hemiplegic migraine

, 2019
Hemiplegic migraine (HM) is a rare subtype of migraine with aura in which attacks include transient motor weakness or hemiparesis that can last several days.
Rispoli M. G., De Angelis M. V., Di Stefano V., Mantuano E.   +3 more
core   +1 more source

Migrainous vertigo: mutation analysis of the candidate genes CACNA1A, ATP1A2, SCN1A, and CACNB4

, 2006
BACKGROUND: Migrainous vertigo (MV) is increasingly recognized as a common cause of episodic vertigo. MV displays several clinical similarities with familial hemiplegic migraine (FHM) and episodic ataxia type 2 (EA-2), which have been linked to mutations
Ta, N., Siegel, A., Shankar, A., Wiste, A., Radtke, A., Sander, T., von Brevern, M., Escayg, A.   +7 more
core   +1 more source

Apparent efficacy of NMDAR antagonist use as a targeted therapy for status epilepticus in an infant with ATP1A2-related developmental epileptic encephalopathy

Background: N-methyl-D-aspartate receptor (NMDAR) blockers are important to control seizures in patients with refractory status epilepticus. ATP1A2 gene plays a role in protecting neurons from glutamate and NMDAR-related excitotoxicity.
GÖK, ANIL, CIRDI, GÖKÇE, Akkoyunlu, DENİZ, Orgun, LEMAN, Deniz, Adnan, KARA, BÜLENT, Güneş, AYFER   +6 more
core   +1 more source

Hemiplegic migraine: genetics and pathophysiology. [PDF]

J Clin Invest
Pietrobon D.
europepmc   +1 more source

A Migraine-Associated Na/K-ATPase Mutation Disrupts Hepatic Glucose Uptake and Peripheral Metabolism in Mice. [PDF]

Acta Physiol (Oxf)
Pessoa MT, Sidarala V, Pierre SV.
europepmc   +1 more source