Search Results - "HOVE, K"

Digital technologies, Fourth Industrial Revolution (4IR) & Global Value Chains (GVCs) nexus with emerging economies' future industrial innovation dynamics by Nyagadza, Brighton, Pashapa, R, Chare, A, Mazuruse, G, Hove, P. K

“…The advent of the Fourth Industrial Revolution (4IR) has the potential to transform emerging economies to another developmental echelon by increasing…”
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Feeding of palm oil fatty acids or rapeseed oil throughout lactation: Effects on mammary gene expression and milk production in Norwegian dairy goats by Bernard, L., Chilliard, Y., Hove, K., Volden, H., Inglingstad, R.A., Eknæs, M.

“…Lipid added as rapeseed or palm oil to the diet of dairy goats over 8 mo of one lactation alters fat secretion and milk fatty acid (FA) and protein…”
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Effects of 12 weeks of treatment with fermented milk on blood pressure, glucose metabolism and markers of cardiovascular risk in patients with type 2 diabetes: a randomised double-blind placebo-controlled study by Hove, K D, Brøns, C, Færch, K, Lund, S S, Rossing, P, Vaag, A

“…ObjectiveStudies have indicated a blood pressure (BP)-lowering effect of milk-derived peptides in non-diabetic individuals, but the cardiometabolic effects of…”
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Mitochondrial calcium uniporter stabilization preserves energetic homeostasis during Complex I impairment by Balderas, Enrique, Eberhardt, David R., Lee, Sandra, Pleinis, John M., Sommakia, Salah, Balynas, Anthony M., Yin, Xue, Parker, Mitchell C., Maguire, Colin T., Cho, Scott, Szulik, Marta W., Bakhtina, Anna, Bia, Ryan D., Friederich, Marisa W., Locke, Timothy M., Van Hove, Johan L. K., Drakos, Stavros G., Sancak, Yasemin, Tristani-Firouzi, Martin, Franklin, Sarah, Rodan, Aylin R., Chaudhuri, Dipayan

“…Calcium entering mitochondria potently stimulates ATP synthesis. Increases in calcium preserve energy synthesis in cardiomyopathies caused by mitochondrial…”
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The behavioral phenotype of children and adolescents with attenuated non-ketotic hyperglycinemia, intermediate to good subtype by Van Hirtum, Liesbet D F M, Van Damme, Tine, Van Hove, Johan L K, Steyaert, Jean G

“…We aim to describe the behavioral phenotype of children and adolescents with the good to intermediate attenuated form of non-ketotic hyperglycinemia (NKH) and…”
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Pathogenic variants in SQOR encoding sulfide:quinone oxidoreductase are a potentially treatable cause of Leigh disease by Friederich, Marisa W., Elias, Abdallah F., Kuster, Alice, Laugwitz, Lucia, Larson, Austin A., Landry, Aaron P., Ellwood‐Digel, Logan, Mirsky, David M., Dimmock, David, Haven, Jaclyn, Jiang, Hua, MacLean, Kenneth N., Styren, Katie, Schoof, Jonathan, Goujon, Louise, Lefrancois, Thomas, Friederich, Maike, Coughlin, Curtis R., Banerjee, Ruma, Haack, Tobias B., Van Hove, Johan L. K.

“…Hydrogen sulfide, a signaling molecule formed mainly from cysteine, is catabolized by sulfide:quinone oxidoreductase (gene SQOR). Toxic hydrogen sulfide…”
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Identification of a novel biomarker for pyridoxine‐dependent epilepsy: Implications for newborn screening by Wempe, Michael F., Kumar, Amit, Kumar, Vijay, Choi, Yu J., Swanson, Michael A., Friederich, Marisa W., Hyland, Keith, Yue, Wyatt W., Van Hove, Johan L. K., Coughlin, Curtis R.

“…Pyridoxine‐dependent epilepsy (PDE) is often characterized as an early onset epileptic encephalopathy with dramatic clinical improvement following pyridoxine…”
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Prediction of long-term outcome in glycine encephalopathy: a clinical survey by Hennermann, Julia B., Berger, Jeanne-Marie, Grieben, Ulrike, Scharer, Gunter, Van Hove, Johan L. K.

“…Objective Glycine encephalopathy (GE) is a rare autosomal recessive inborn error of glycine degradation resulting in severe encephalopathy with ensuing poor…”
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Feeding of palm oil fatty acids or rapeseed oil throughout lactation: Effects on energy status, body composition, and milk production in Norwegian dairy goats by Eknæs, M, Chilliard, Y, Hove, K, Inglingstad, R A, Bernard, L, Volden, H

“…The objective of this experiment was to examine how supplements of rapeseed oil or palm oil fatty acids would affect milk production and composition, body…”
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Interplay of Impaired Cellular Bioenergetics and Autophagy in PMM2-CDG by Ligezka, Anna N, Budhraja, Rohit, Nishiyama, Yurika, Fiesel, Fabienne C, Preston, Graeme, Edmondson, Andrew, Ranatunga, Wasantha, Van Hove, Johan L K, Watzlawik, Jens O, Springer, Wolfdieter, Pandey, Akhilesh, Morava, Eva, Kozicz, Tamas

“…Congenital disorders of glycosylation (CDG) and mitochondrial disorders are multisystem disorders with overlapping symptomatology. Pathogenic variants in the…”
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Effects of 12 weeks’ treatment with a proton pump inhibitor on insulin secretion, glucose metabolism and markers of cardiovascular risk in patients with type 2 diabetes: a randomised double-blind prospective placebo-controlled study by Hove, K. D., Brøns, C., Færch, K., Lund, S. S., Petersen, J. S., Karlsen, A. E., Rossing, P., Rehfeld, J. F., Vaag, A.

“…Aims/hypothesis Recent studies suggest that proton pump inhibitor treatment may increase insulin secretion and improve glucose metabolism in type 2 diabetes…”
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Author Correction: Mitochondrial calcium uniporter stabilization preserves energetic homeostasis during Complex I impairment by Balderas, Enrique, Eberhardt, David R., Lee, Sandra, Pleinis, John M., Sommakia, Salah, Balynas, Anthony M., Yin, Xue, Parker, Mitchell C., Maguire, Colin T., Cho, Scott, Szulik, Marta W., Bakhtina, Anna, Bia, Ryan D., Friederich, Marisa W., Locke, Timothy M., Van Hove, Johan L. K., Drakos, Stavros G., Sancak, Yasemin, Tristani-Firouzi, Martin, Franklin, Sarah, Rodan, Aylin R., Chaudhuri, Dipayan

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Ketogenic diet as a glycine lowering therapy in nonketotic hyperglycinemia and impact on brain glycine levels by Shelkowitz, Emily, Saneto, Russell P, Al-Hertani, Walla, Lubout, Charlotte M A, Stence, Nicholas V, Brown, Mark S, Long, Patrick, Walleigh, Diana, Nelson, Julie A, Perez, Francisco E, Shaw, Dennis W W, Michl, Emma J, Van Hove, Johan L K

“…Nonketotic hyperglycinemia (NKH) is a severe neurometabolic disorder characterized by increased glycine levels. Current glycine reduction therapy uses high…”
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Correction: Ketogenic diet as a glycine lowering therapy in nonketotic hyperglycinemia and impact on brain glycine levels by Shelkowitz, Emily, Saneto, Russell P, Al-Hertani, Walla, Lubout, Charlotte M A, Stence, Nicholas V, Brown, Mark S, Long, Patrick, Walleigh, Diana, Nelson, Julie A, Perez, Francisco E, Shaw, Dennis W W, Michl, Emma J, Van Hove, Johan L K

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Treatment with a proton pump inhibitor improves glycaemic control in Psammomys obesus, a model of type 2 diabetes by Bödvarsdóttir, T. B, Hove, K. D, Gotfredsen, C. F, Pridal, L, Vaag, A, Karlsen, A. E, Petersen, J. S

“…Aims/hypothesis Gastrin has been implicated in islet growth/neogenesis, and proton pump inhibitors (PPIs) have been shown to increase endogenous gastrin levels…”
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genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy due to mutations in ALDH7A1 by Scharer, Gunter, Brocker, Chad, Vasiliou, Vasilis, Creadon-Swindell, Geralyn, Gallagher, Renata C, Spector, Elaine, Van Hove, Johan L. K

“…Pyridoxine-dependent epilepsy is a disorder associated with severe seizures that may be caused by deficient activity of α-aminoadipic semialdehyde…”
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Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor by Wortmann, Saskia B., Van Hove, Johan L.K., Derks, Terry G.J., Chevalier, Nathalie, Knight, Vijaya, Koller, Andreas, Oussoren, Esmee, Mayr, Johannes A., van Spronsen, Francjan J., Lagler, Florian B., Gaughan, Sommer, Van Schaftingen, Emile, Veiga-da-Cunha, Maria

“…Neutropenia and neutrophil dysfunction cause serious infections and inflammatory bowel disease in glycogen storage disease type Ib (GSD-Ib). Our discovery that…”
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Effects of sensor location during in situ measurements on pH in caecal digesta of the horse, and post-observational treatment of sensor data by Næsset, J. A., Hove, K., Jensen, R. B.

“…Measurements of caecal pH are useful when studying the effect of a ration on the hindgut environment in horses. Frequent in situ measurements of caecal pH have…”
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Evaluation of the Child With Suspected Mitochondrial Liver Disease by Molleston, Jean P., Sokol, Ronald J., Karnsakul, Wikrom, Miethke, Alexander, Horslen, Simon, Magee, John C., Romero, René, Squires, Robert H., Van Hove, Johan L.K.

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Cerebrospinal fluid amino acids glycine, serine, and threonine in nonketotic hyperglycinemia by Swanson, Michael A., Miller, Kristen, Young, Sarah P., Tong, Suhong, Ghaloul‐Gonzalez, Lina, Neira‐Fresneda, Juanita, Schlichting, Lisa, Peck, Cheryl, Gabel, Linda, Friederich, Marisa W., Van Hove, Johan L. K.

“…Nonketotic hyperglycinemia (NKH) is caused by deficient glycine cleavage enzyme activity and characterized by elevated brain glycine. Metabolism of glycine is…”
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