Current status and influential factors for family health management during quarantine: A latent category analysis. oleh Guangming Li, Mengying Li, Shuzhen Peng, Ying Wang, Li Ran, Xuyu Chen, Ling Zhang, Sirong Zhu, Qi Chen, Wenjing Wang, Yang Xu, Yubin Zhang, Xiaodong Tan

"…<h4>Conclusions</h4>We found that multiple factors, including gender, household income, and body mass index, were correlated with latent FHM during home quarantine. We conclude that FHM can meaningfully improve individuals' health. …"
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Synaptic alterations in visual cortex reshape contrast-dependent gamma oscillations and inhibition-excitation ratio in a genetic mouse model of migraine oleh Nicolò Meneghetti, Chiara Cerri, Eleonora Vannini, Elena Tantillo, Angelita Tottene, Daniela Pietrobon, Matteo Caleo, Alberto Mazzoni

"…Additionally, we reproduced in silico the obtained experimental results with a novel spiking neurons network model of mouse V1, by implementing in the model both the synaptic alterations characterizing the FHM1 genetic mouse model adopted. Results FHM1 mice displayed similar amplitude but slower temporal evolution of visual evoked potentials. …"
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Optogenetic cortical spreading depolarization induces headache-related behaviour and neuroinflammatory responses some prolonged in familial hemiplegic migraine type 1 mice oleh Anisa Dehghani, Maarten Schenke, Sandra H. van Heiningen, Hulya Karatas, Else A. Tolner, Arn M. J. M. van den Maagdenberg

"…Nuclear HMGB1 release in the cortex of FHM1 mutant mice, at 30 min after CSD, was increased bilaterally in both WT and FHM1 mutant mice, albeit that contralateral release was more pronounced in the mutant mice. …"
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Specific activation of GluN1-N2B NMDA receptors underlies facilitation of cortical spreading depression in a genetic mouse model of migraine with reduced astrocytic glutamate clear... oleh Giovanna Crivellaro, Angelita Tottene, Marina Vitale, Marcello Melone, Giorgio Casari, Fiorenzo Conti, Mirko Santello, Daniela Pietrobon

"…In FHM type 2 (FHM2) knock-in mice with reduced expression of astrocytic Na+, K+-ATPases, the reduced rate of glutamate uptake into astrocytes can account for the facilitation of CSD initiation. …"
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CACNA1A-p.Thr501Met mutation associated with familial hemiplegic migraine: a family report oleh Marina Romozzi, Guido Primiano, Eleonora Rollo, Lorena Travaglini, Paolo Calabresi, Serenella Servidei, Catello Vollono

"…Familial hemiplegic migraine (FHM) is an autosomal dominant disorder, classified into 3 subtypes, based on the gene involved (CACNA1A in FHM1, ATP1A2 in FHM2 and SCN1A in FHM3). …"
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Functional polyaspartic acid fibers hydrogel membrane with enhanced mechanical performance prepared by coaxial electrospinning oleh Sijie Li, Caidan Zhang, Qiaozhen Yu, Lin Jia

"…In this work, polyaspartic acid (PASP) fibers hydrogel membrane (FHM) was enhanced by thermoplastic polyurethane (TPU) via coaxial electrospinning. …"
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Chemical composition and fatty acid profile in meat from grazing lamb diets supplemented with ryegrass hay, fishmeal and soya bean meal as PUFA sources oleh Jose Romero-Bernal, Ernesto Morales Almaraz, Octavio Alonso Castelán Ortega, Nazario Pescador Salas, Manuel González-Ronquillo

"…Total PUFA content was higher for RGH, followed by FHM and with the lowest content for SBM (P=0.001). …"
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Gain of Function for the SCN1A/hNav1.1-L1670W Mutation Responsible for Familial Hemiplegic Migraine oleh Sandra Dhifallah, Eric Lancaster, Shana Merrill, Nathalie Leroudier, Massimo Mantegazza, Sandrine Cestèle

"…Here, we report the characterization of the L1670W SCN1A mutation that has been previously identified in a Chinese family with pure FHM-3, and that we have identified also in a Caucasian American family with pure FHM-3. …"
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Modeling NaV1.1/SCN1A sodium channel mutations in a microcircuit with realistic ion concentration dynamics suggests differential GABAergic mechanisms leading to hyperexcitability i... oleh Louisiane Lemaire, Mathieu Desroches, Martin Krupa, Lara Pizzamiglio, Paolo Scalmani, Massimo Mantegazza

"…Therefore, we studied both FHM-3 and epileptogenic mutations within the same framework, modifying only two parameters. …"
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Linking a genetic defect in migraine to spreading depression in a computational model oleh Markus A. Dahlem, Julia Schumacher, Niklas Hübel

"…Familial hemiplegic migraine (FHM) is a rare subtype of migraine with aura. A mutation causing FHM type 3 (FHM3) has been identified in SCN1A encoding the Nav1.1 Na+ channel. …"
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Water Permeability of Pervious Concrete Is Dependent on the Applied Pressure and Testing Methods oleh Yinghong Qin, Haifeng Yang, Zhiheng Deng, Jiang He

"…Falling head method (FHM) and constant head method (CHM) are, respectively, used to test the water permeability of permeable concrete, using different water heads on the testing samples. …"
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Direct Probing of the Mott Crossover in the SU(N) Fermi-Hubbard Model oleh Christian Hofrichter, Luis Riegger, Francesco Scazza, Moritz Höfer, Diogo Rio Fernandes, Immanuel Bloch, Simon Fölling

"…In its more common spin-1/2 form, the FHM is a central model of condensed-matter physics. …"
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Familial hemiplegic migraine type 2: a case report of an adolescent with ATP1A2 mutation oleh Hui Zhang, Hui Zhang, Li Jiang, Li Jiang, Yuqi Xian, Yuqi Xian, Sen Yang, Sen Yang

"…This study presents a case report of a male adolescent diagnosed with familial hemiplegic migraine type 2 (FHM2), an autosomal dominant inheritance disorder caused by ATP1A2 mutation. …"
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Deciphering in silico the Role of Mutated NaV1.1 Sodium Channels in Enhancing Trigeminal Nociception in Familial Hemiplegic Migraine Type 3 oleh Alina Suleimanova, Max Talanov, Arn M. J. M. van den Maagdenberg, Arn M. J. M. van den Maagdenberg, Rashid Giniatullin, Rashid Giniatullin

"…Familial hemiplegic migraine type 3 (FHM3) is caused by gain-of-function mutations in the SCN1A gene that encodes the α1 subunit of voltage-gated NaV1.1 sodium channels. …"
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New relations between spin and charge dynamics of the Fermi Hubbard model oleh Hui Zhai, Ning Sun, Jinlong Yu, Pengfei Zhang

"…Utilizing the Fermi gas microscope, recently the MIT group has measured the spin transport of the Fermi Hubbard model (FHM) starting from a spin-density-wave state, and the Princeton group has measured the charge transport of the FHM starting from a charge-density-wave state. …"
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Risk of hematological malignancies in the families of patients treated for nodular lymphocyte-predominant Hodgkin lymphoma oleh Saad Akhtar, M. Shahzad Rauf, Amani Al-Kofide, Mahmoud A. Elshenawy, Ali Hassan Mushtaq, Irfan Maghfoor

"…Abstract Background Familial clustering of lymphoid and/or hematological malignancies (FHM) provides an opportunity to study the responsible genes. …"
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Widespread brain parenchymal HMGB1 and NF-κB neuroinflammatory responses upon cortical spreading depolarization in familial hemiplegic migraine type 1 mice oleh Anisa Dehghani, Thas Phisonkunkasem, Sinem Yilmaz Ozcan, Turgay Dalkara, Arn M.J.M. van den Maagdenberg, Else A. Tolner, Hulya Karatas

"…We therefore investigated in familial hemiplegic migraine type 1 (FHM1) knock-in mice, which express an intrinsic hyperexcitability phenotype, the extent of neuroinflammation without and after CSD. …"
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Chronic pregabalin treatment protects against spreading depolarization and alters hippocampal synaptic characteristics in a model of familial hemiplegic migraine-type 1 oleh Stuart M. Cain, Sascha R. A. Alles, Ray Gopaul, Louis-Philippe Bernier, Andrew C. Yung, Andrew Bauman, Yi Yang, Glen B. Baker, Piotr Kozlowski, Brian A. MacVicar, Terrance P. Snutch

"…Abstract Familial hemiplegic migraine type-1 (FHM-1) is a form of migraine with aura caused by mutations in the P/Q-type (Cav2.1) voltage-gated calcium channel. …"
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Potential use of () as a protein source fodder to improve nutrients digestibility, ruminal fermentation efficiency in beef cattle oleh Burarat Phesatcha, Bounnaxay Viennasay, Metha Wanapat

"…Four levels of Flemingia hay meal (FHM) were used to replace soybean meal (SBM) in the concentrate mixtures in four dietary treatments replacing levels at 0%, 30%, 60%, and 100% of SBM. …"
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Association analysis of chromosome 1 migraine candidate genes oleh MacMillan John, Colson Natalie J, Ovcaric Micky, Curtain Robert P, Fernandez Francesca, Griffiths Lyn R

"…Migraine with aura (MA) also encompasses a rare severe subtype Familial Hemiplegic Migraine (FHM) with several known genetic loci. The type 2 FHM (FHM-2) susceptibility locus maps to chromosome 1q23 and mutations in the ATP1A2 gene at this site have recently been implicated. …"
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