Zobrazeno 1 - 10
of 241
pro vyhledávání: '"Henrik Galbo"'
Publikováno v:
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-19 (2017)
Abstract Background The pathophysiology, including the impact of gene expression, of polymyalgia rheumatica (PMR) remains elusive. We profiled the gene expression in muscle tissue in PMR patients before and after glucocorticoid treatment. Methods Gen
Externí odkaz:
https://doaj.org/article/08e9abbfdf634b1a8833db8224a4372b
Autor:
Nicolai Preisler, Pascal Laforêt, Karen Lindhardt Madsen, Edith Husu, Christoffer Rasmus Vissing, Gitte Hedermann, Henrik Galbo, Christopher Lindberg, John Vissing
Publikováno v:
Endocrine Connections, Vol 6, Iss 6, Pp 384-394 (2017)
Objective: Pompe disease (glycogenosis type II) is caused by lysosomal alpha-glucosidase deficiency, which leads to a block in intra-lysosomal glycogen breakdown. In spite of enzyme replacement therapy, Pompe disease continues to be a progressive met
Externí odkaz:
https://doaj.org/article/d032e737ef6c480e9276334936f6913f
Autor:
Clara Prats, Morten Donsmark, Klaus Qvortrup, Constantine Londos, Carole Sztalryd, Cecilia Holm, Henrik Galbo, Thorkil Ploug
Publikováno v:
Journal of Lipid Research, Vol 47, Iss 11, Pp 2392-2399 (2006)
A better understanding of skeletal muscle lipid metabolism is needed to identify the molecular mechanisms relating intramuscular triglyceride (IMTG) to muscle metabolism and insulin sensitivity. An increasing number of proteins have been reported to
Externí odkaz:
https://doaj.org/article/6fdffc1e15fa4915a7bb19d68b1ed797
Autor:
Ola Hansson, Morten Donsmark, Charlotte Ling, Pernilla Nevsten, Mikael Danfelter, Jesper L. Andersen, Henrik Galbo, Cecilia Holm
Publikováno v:
Journal of Lipid Research, Vol 46, Iss 12, Pp 2614-2623 (2005)
Hormone-sensitive lipase (HSL), a key enzyme in fatty acid mobilization in adipocytes, has been demonstrated also in skeletal muscle. To gain further insight into the role and importance of HSL in skeletal muscle, a transcriptome analysis of soleus m
Externí odkaz:
https://doaj.org/article/2b5a161e406844019352f0faac777ada
Publikováno v:
Journal of Personalized Medicine; Volume 12; Issue 5; Pages: 837
Han, X X, Holst, J J & Galbo, H 2022, ' Studies in Rats of Combined Muscle and Liver Perfusion and of Muscle Extract Indicate That Contractions Release a Muscle Hormone Directly Enhancing Hepatic Glycogenolysis ', Journal of Personalized Medicine, vol. 12, no. 5, 837 . https://doi.org/10.3390/jpm12050837
Han, X X, Holst, J J & Galbo, H 2022, ' Studies in Rats of Combined Muscle and Liver Perfusion and of Muscle Extract Indicate That Contractions Release a Muscle Hormone Directly Enhancing Hepatic Glycogenolysis ', Journal of Personalized Medicine, vol. 12, no. 5, 837 . https://doi.org/10.3390/jpm12050837
Background: Established neuroendocrine signals do not sufficiently account for the exercise-induced increase in glucose production. Using an innovative, yet classical cross-circulation procedure, we studied whether contracting muscle produces a facto
Autor:
Gitte Hedermann, Kira Philipsen Prahm, Pascal Laforêt, Christoffer Rasmus Vissing, John Vissing, Nicolai Preisler, Henrik Galbo, Karen Lindhardt Madsen
Publikováno v:
Neurology. 84:1767-1771
Objective: Glycogen storage disease type IIIa (GSDIIIa) is classically regarded as a glycogenosis with fixed weakness, but we hypothesized that exercise intolerance in GSDIIIa is related to muscle energy failure and that oral fructose ingestion could
Publikováno v:
Kreiner, F F, Borup, R, Nielsen, F C, Schjerling, P & Galbo, H 2017, ' Gene expression profiling in patients with polymyalgia rheumatica before and after symptom-abolishing glucocorticoid treatment ', BMC Musculoskeletal Disorders, vol. 18, 341 . https://doi.org/10.1186/s12891-017-1705-z
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-19 (2017)
BMC Musculoskeletal Disorders
BMC Musculoskeletal Disorders, Vol 18, Iss 1, Pp 1-19 (2017)
BMC Musculoskeletal Disorders
BACKGROUND: The pathophysiology, including the impact of gene expression, of polymyalgia rheumatica (PMR) remains elusive. We profiled the gene expression in muscle tissue in PMR patients before and after glucocorticoid treatment.METHODS: Gene expres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f48e4b6d349e2f38604efc016b9a26b5
https://curis.ku.dk/ws/files/185238239/s12891_017_1705_z.pdf
https://curis.ku.dk/ws/files/185238239/s12891_017_1705_z.pdf
Autor:
Pedro Mancias, Nadine Romain, Jonathan C. Cohen, Lydia Sharp, Christoffer Rasmus Vissing, Nicolai Preisler, Lauren Phillips, Sun Young Park, Henrik Galbo, Ronald G. Haller, Karen Lindhardt Madsen, Phil Wyrick, John Vissing, Katja Heinicke, Marta Newby
Publikováno v:
Molecular genetics and metabolism. 122(3)
Objective We investigated metabolism and physiological responses to exercise in an 18-year-old woman with multiple congenital abnormalities and exertional muscle fatigue, tightness, and rhabdomyolysis. Methods We studied biochemistry in muscle and fi
Autor:
Pascal Laforêt, Christopher Lindberg, Henrik Galbo, Christoffer Rasmus Vissing, Edith Husu, John Vissing, Nicolai Preisler, Gitte Hedermann, Karen Lindhardt Madsen
Publikováno v:
Endocrine Connections
Endocrine Connections, BioScientifica Ltd., 2017, 6 (6), pp.384-394. ⟨10.1530/EC-17-0042⟩
Endocrine Connections, 2017, 6 (6), pp.384-394. ⟨10.1530/EC-17-0042⟩
Endocrine Connections, Vol 6, Iss 6, Pp 384-394 (2017)
Preisler, N, Laforêt, P, Madsen, K L, Husu, E, Vissing, C R, Hedermann, G, Galbo, H, Lindberg, C & Vissing, J 2017, ' Skeletal muscle metabolism during prolonged exercise in Pompe disease ', Endocrine Connections, vol. 6, no. 6, pp. 384-394 . https://doi.org/10.1530/EC-17-0042
Endocrine Connections, BioScientifica Ltd., 2017, 6 (6), pp.384-394. ⟨10.1530/EC-17-0042⟩
Endocrine Connections, 2017, 6 (6), pp.384-394. ⟨10.1530/EC-17-0042⟩
Endocrine Connections, Vol 6, Iss 6, Pp 384-394 (2017)
Preisler, N, Laforêt, P, Madsen, K L, Husu, E, Vissing, C R, Hedermann, G, Galbo, H, Lindberg, C & Vissing, J 2017, ' Skeletal muscle metabolism during prolonged exercise in Pompe disease ', Endocrine Connections, vol. 6, no. 6, pp. 384-394 . https://doi.org/10.1530/EC-17-0042
Objective Pompe disease (glycogenosis type II) is caused by lysosomal alpha-glucosidase deficiency, which leads to a block in intra-lysosomal glycogen breakdown. In spite of enzyme replacement therapy, Pompe disease continues to be a progressive meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb98b41908666dcd26a8f2ae74d7445a
https://hal.sorbonne-universite.fr/hal-01617884
https://hal.sorbonne-universite.fr/hal-01617884
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 99:3757-3765
Mitochondrial dysfunction has been proposed to cause insulin resistance and that might stimulate cytokine production.The objective of the study was to elucidate the association between mitochondrial myopathy, insulin sensitivity, and cytokine levels