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Hasil Pencarian - "FHM"
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181
Overexpressed NaV1.7 Channels Confer Hyperexcitability to in vitro Trigeminal Sensory Neurons of CaV2.1 Mutant Hemiplegic Migraine Mice
Diterbitkan 2021-05-01"…Trigeminal sensory neurons of transgenic knock-in (KI) mice expressing the R192Q missense mutation in the α1A subunit of neuronal voltage-gated CaV2.1 Ca2+ channels, which leads to familial hemiplegic migraine type 1 (FHM1) in patients, exhibit a hyperexcitability phenotype. …"
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182
Protective Effects of Curcumin on Kidney Tissue in Ischemia-Reperfusion Injury in Rats
Diterbitkan 2023-03-01Dapatkan teks lengkap
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Largemouth Bass Virus Infection Induced Non-Apoptotic Cell Death in MsF Cells
Diterbitkan 2022-07-01"…In addition, the disruption of the mitochondrial membrane potential (ΔΨm) and reactive oxygen species (ROS) generation were detected in both LMBV-infected MsF cells and fathead minnow (FHM) cells. Combined with our previous study, we propose that cell death induced by LMBV infection was cell type dependent. …"
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186
Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant
Diterbitkan 2020-04-01"…Mutations in the CACNA1A gene were identified as responsible for at least three autosomal dominant disorders: FHM1 (Familial Hemiplegic Migraine), EA2 (Episodic Ataxia type 2), and SCA6 (Spinocerebellar Ataxia type 6). …"
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187
Comparison of Plant Health Aspect In Green Open Spaces of Alun-Alun Kebumen and Alun-Alun Karanganyar, Kebumen, Central Java
Diterbitkan 2024-01-01"…This plant damage research have been conducted using the FHM (Forest Health Monitoring) method and the USDA Forest Service damage index. …"
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188
New CACNA1A deletions are associated to migraine phenotypes
Diterbitkan 2018-08-01"…Abstract Background Familial hemiplegic migraine type 1 (FHM1) is a form of migraine with aura caused by heterozygous mutations in 4 genes: CACNA1A, ATP1A2, SNC1A and PRRT2, but further heterogeneity is expected. …"
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189
Effects of Single Compared to Dual Task Practice on Learning a Dynamic Balance Task in Young Adults
Diterbitkan 2018-03-01Dapatkan teks lengkap
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190
Herpes zoster in Germany: Quantifying the burden of disease
Diterbitkan 2011-06-01"…For the same time period annual number of HZ-inpatients and HZ-associated deaths were identified by using the Federal Health Monitoring System (FHM). PHN-incidence and loss of quality-adjusted life years (QALYs) caused by HZ were calculated by multiplying number of identified HZ-patients with upper and lower limit estimates for proportion of HZ-cases developing PHN and HZ-related QALY, respectively.…"
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De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Diterbitkan 2017-06-01"…Mutations in three different genes, two ion-channel genes and one encoding an ATP exchanger, CACNA1A, ATP1A2 and SCN1A are all responsible for the FHM phenotype, thus indicating a genetic heterogeneity for this disorder. …"
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193
Genetic and Pathogenic Characterization of an Iridovirus from the Cultured Largemouth Bass <i>Micropterus salmoides</i>
Diterbitkan 2024-08-01"…In the present study, a virus strain named LMBV-GDSD was isolated from cultured largemouth bass and was successfully proliferated in FHM and EPC cells, with numerous viral particles observed in the infected cells under transmission electron microscopy analysis. …"
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194
A comprehensive exploration of astrocytes in migraine: a bibliometric and visual analysis
Diterbitkan 2024-06-01"…Conclusions Future investigators may continue to focus on migraines with aura, familial hemiplegic migraine (FHM), and the crucial calcitonin gene-related peptide (CGRP) system. …"
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195
A novel heterozygous ATP1A2 pathogenic variant in a Chinese child with MELAS‐like alternating hemiplegia
Diterbitkan 2023-05-01"…Abstract Background Pathogenic variants of ATP1A2 (OMIM ID: 182340) are usually associated with familial hemiplegic migraine type 2 (FHM‐2), alternating hemiplegia of childhood (AHC), early infantile epileptic encephalopathy (EIEE), transient cytotoxic edema, and so on. …"
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196
Transferrin Mediated NCC Killing Activity through NCCRP-1 in Nile Tilapia (<i>Oreochromis niloticus</i>)
Diterbitkan 2022-09-01"…In vitro experiments showed that rOn-TF could up-regulate the expression of killing effector molecule of NCC by On-NCCRP-1, and rOn-TF-activated NCCs showed a significantly improved ability to kill FHM cells, indicating that rOn-TF could regulate the NCC signaling pathway through NCC receptor molecule On-NCCRP-1. …"
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197
Hypercontractile Cardiac Phenotype in Mice with Migraine-Associated Mutation in the Na<sup>+</sup>,K<sup>+</sup>-ATPase α<sub>2</sub>-Isoform
Diterbitkan 2023-04-01"…Mice heterozygous for the familial hemiplegic migraine type 2 (FHM2) associated mutation in the α<sub>2</sub>-isoform (G301R; α<sub>2</sub><sup>+/G301R</sup> mice) have decreased expression of cardiac α<sub>2</sub>-isoform but elevated expression of the α<sub>1</sub>-isoform. …"
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