Search Results - "Arreguín, Andrea"

Retinoic Acid Increases Fatty Acid Oxidation and Irisin Expression in Skeletal Muscle Cells and Impacts Irisin In Vivo by Amengual, Jaume, García-Carrizo, Francisco J., Arreguín, Andrea, Mušinović, Hana, Granados, Nuria, Palou, Andreu, Bonet, M. Luisa, Ribot, Joan

“…Background/Aims: All-trans retinoic acid (ATRA) has protective effects against obesity and metabolic syndrome. We here aimed to gain further insight into the…”
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Novel Markers of the Metabolic Impact of Exogenous Retinoic Acid with A Focus on Acylcarnitines and Amino Acids by Ribot, Joan, Arreguín, Andrea, Kuda, Ondrej, Kopecky, Jan, Palou, Andreu, Bonet, Maria Luisa

“…Treatment with all-trans retinoic acid (ATRA), the carboxylic form of vitamin A, lowers body weight in rodents by promoting oxidative metabolism in multiple…”
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Spent coffee (Coffea arabica L.) grounds promote satiety and attenuate energy intake: A pilot study by Campos‐Vega, Rocio, Arreguín‐Campos, Andrea, Cruz‐Medrano, Miguel A., Castillo Bilbao, María Dolores

“…We evaluated the effects of acute intake of biscuits (B) containing either spent coffee grounds (SCG), (added with fructooligosaccharides; SC‐FOS) or SCG…”
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Construcción y validación de cuestionarios para evaluar el riesgo de los antibióticos veterinarios en el consumo de huevo e impacto en la seguridad alimentaria by Tejeda Rodríguez, Eriberto Joel, Arreguín, Andrea

“…La producción avícola es uno de los sectores agropecuarios de mayor importancia a nivel mundial por sus grandes aportes nutricionales en productos como la…”
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Dmd mdx mice have defective oligodendrogenesis, delayed myelin compaction and persistent hypomyelination by Arreguin, Andrea J, Shao, Zijian, Colognato, Holly

“…Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, resulting in the loss of dystrophin, a large cytosolic protein that links the…”
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Rewiring of Glutamine Metabolism Is a Bioenergetic Adaptation of Human Cells with Mitochondrial DNA Mutations by Chen, Qiuying, Kirk, Kathryne, Shurubor, Yevgeniya I., Zhao, Dazhi, Arreguin, Andrea J., Shahi, Ifrah, Valsecchi, Federica, Primiano, Guido, Calder, Elizabeth L., Carelli, Valerio, Denton, Travis T., Beal, M. Flint, Gross, Steven S., Manfredi, Giovanni, D'Aurelio, Marilena

“…Using molecular, biochemical, and untargeted stable isotope tracing approaches, we identify a previously unappreciated glutamine-derived α-ketoglutarate (αKG)…”
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Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models by Arreguin, Andrea J, Colognato, Holly

“…Laminin α2 gene (LAMA2)-related Congenital Muscular Dystrophy (CMD) was distinguished by a defining central nervous system (CNS) abnormality-aberrant white…”
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Parkin is a disease modifier in the mutant SOD1 mouse model of ALS by Palomo, Gloria M, Granatiero, Veronica, Kawamata, Hibiki, Konrad, Csaba, Kim, Michelle, Arreguin, Andrea J, Zhao, Dazhi, Milner, Teresa A, Manfredi, Giovanni

“…Mutant Cu/Zn superoxide dismutase (SOD1) causes mitochondrial alterations that contribute to motor neuron demise in amyotrophic lateral sclerosis (ALS). When…”
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All-trans retinoic acid induces oxidative phosphorylation and mitochondria biogenesis in adipocytes by Tourniaire, Franck, Musinovic, Hana, Gouranton, Erwan, Astier, Julien, Marcotorchino, Julie, Arreguin, Andrea, Bernot, Denis, Palou, Andreu, Bonet, M.Luisa, Ribot, Joan, Landrier, Jean-François

“…A positive effect of all-trans retinoic acid (ATRA) on white adipose tissue (WAT) oxidative and thermogenic capacity has been described and linked to an in…”
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Innate immunity receptor CD36 promotes cerebral amyloid angiopathy by Park, Laibaik, Zhou, Joan, Zhou, Ping, Pistick, Rose, Jamal, Sleiman El, Younkin, Linda, Pierce, Joseph, Arreguin, Andrea, Anrather, Josef, Younkin, Steven G., Carlson, George A., McEwen, Bruce S., ladecola, Costantino

“…Deposition of amyloid-β (Aβ) in cerebral arteries, known as cerebral amyloid angiopathy (CAA), occurs both in the setting of Alzheimer's disease and…”
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Fibroblast bioenergetics to classify amyotrophic lateral sclerosis patients by Konrad, Csaba, Kawamata, Hibiki, Bredvik, Kirsten G, Arreguin, Andrea J, Cajamarca, Steven A, Hupf, Jonathan C, Ravits, John M, Miller, Timothy M, Maragakis, Nicholas J, Hales, Chadwick M, Glass, Jonathan D, Gross, Steven, Mitsumoto, Hiroshi, Manfredi, Giovanni

“…The objective of this study was to investigate cellular bioenergetics in primary skin fibroblasts derived from patients with amyotrophic lateral sclerosis…”
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Acute sleep deprivation enhances susceptibility to the migraine substrate cortical spreading depolarization by Negro, Andrea, Seidel, Jessica L., Houben, Thijs, Yu, Esther S., Rosen, Ike, Arreguin, Andrea J., Yalcin, Nilufer, Shorser-Gentile, Lea, Pearlman, Lea, Sadhegian, Homa, Vetrivelan, Ramalingam, Chamberlin, Nancy L., Ayata, Cenk, Martelletti, Paolo, Moskowitz, Michael A., Eikermann-Haerter, Katharina

“…Background Migraine is a common headache disorder, with cortical spreading depolarization (CSD) considered as the underlying electrophysiological event. CSD is…”
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Dmdmdx mice have defective oligodendrogenesis, delayed myelin compaction and persistent hypomyelination by Arreguin, Andrea J., Shao, Zijian, Colognato, Holly

“…Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene, resulting in the loss of dystrophin, a large cytosolic protein that links the…”
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Abnormal synaptic Ca2+ homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant mice by Eikermann-Haerter, Katharina, Arbel-Ornath, Michal, Yalcin, Nilufer, Yu, Esther S., Kuchibhotla, Kishore V., Yuzawa, Izumi, Hudry, Eloise, Willard, Carli R., Climov, Mihail, Keles, Fatmagul, Belcher, Arianna M., Sengul, Buse, Negro, Andrea, Rosen, Isaac A., Arreguin, Andrea, Ferrari, Michel D., van den Maagdenberg, Arn M. J. M., Bacskai, Brian J., Ayata, Cenk

“…Objective Migraine is among the most common and debilitating neurological conditions. Familial hemiplegic migraine type 1 (FHM1), a monogenic migraine subtype,…”
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Understanding the Role of the DMD Protein Dystrophin in the Subventricular Zone (4587) by Arreguin, Andrea, Colognato, Holly

“…Abstract only…”
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Miranda Pacheco, S. (2021). La caída de Tenochtitlan y la posconquista ambiental de la cuenca y ciudad de México by Arreguín Rodríguez, Andrea Lizette

“…México: Dirección General de Publicaciones y Fomento Editorial, Instituto de Investigaciones Históricas, Universidad Nacional Autónoma de México (Colección…”
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Sex specific activation of the ERα axis of the mitochondrial UPR (UPRmt) in the G93A-SOD1 mouse model of familial ALS by Riar, Amanjot K, Burstein, Suzanne R, Palomo, Gloria M, Arreguin, Andrea, Manfredi, Giovanni, Germain, Doris

“…The mitochondrial unfolded protein response (UPRmt) is a transcriptional program aimed at restoring proteostasis in mitochondria. Upregulation of mitochondrial…”
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Abnormal Oligodendrogenesis and Myelination in Mouse Models of Duchenne Muscular Dystrophy by Arreguin, Andrea Jasmine

“…Duchenne Muscular Dystrophy (DMD) is caused by mutations in the DMD gene, resulting in the loss of the protein dystrophin. The DMD gene is one of the largest…”
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Calcium sensing receptor effects in adipocytes and liver cells: Implications for an adipose-hepatic crosstalk by Villarroel, Pia, Mattar, Pamela, D'Espessailles, Amanda, Arrese, Marco, Arreguin, Andrea, Fuentes, Cecilia, Reyes, Marcela, Cifuentes, Mariana

“…The calcium sensing receptor (CaSR) is expressed in human adipose cells, and its activation may associate with adipose tissue (AT) dysfunction. We evaluated…”
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Abnormal synaptic Ca(2+) homeostasis and morphology in cortical neurons of familial hemiplegic migraine type 1 mutant mice by Eikermann-Haerter, Katharina, Arbel-Ornath, Michal, Yalcin, Nilufer, Yu, Esther S, Kuchibhotla, Kishore V, Yuzawa, Izumi, Hudry, Eloise, Willard, Carli R, Climov, Mihail, Keles, Fatmagul, Belcher, Arianna M, Sengul, Buse, Negro, Andrea, Rosen, Isaac A, Arreguin, Andrea, Ferrari, Michel D, van den Maagdenberg, Arn M J M, Bacskai, Brian J, Ayata, Cenk

“…Migraine is among the most common and debilitating neurological conditions. Familial hemiplegic migraine type 1 (FHM1), a monogenic migraine subtype, is caused…”
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