Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Lida Stroomer"'
Acute Aerobic Exercise Leads to Increased Plasma Levels of R- and S-β-Aminoisobutyric Acid in Humans
Autor:
Jan Stautemas, André B. P. Van Kuilenburg, Lida Stroomer, Fred Vaz, Laura Blancquaert, Filip B. D. Lefevere, Inge Everaert, Wim Derave
Publikováno v:
Frontiers in Physiology, Vol 10 (2019)
Recently, it was suggested that β-aminoisobutyric acid (BAIBA) is a myokine involved in browning of fat. However, there is no evidence for an acute effect of exercise supporting this statement and the metabolic distinct enantiomers of BAIBA were not
Externí odkaz:
https://doaj.org/article/aa9c06565de8498089bf9f29e61ad10f
Autor:
Muhammad Wasim, Haq N. Khan, Hina Ayesha, Mazhar Iqbal, Abdul Tawab, Muhammad Irfan, Warsha Kanhai, Susanna M. I. Goorden, Lida Stroomer, Gajja Salomons, Frederic M. Vaz, Clara D. M. van Karnebeek, Fazli R. Awan
Publikováno v:
Journal of pediatric endocrinology & metabolism, 35(3), 325-332. Walter de Gruyter GmbH
Background Classical homocystinuria (HCU) is an autosomal recessive inborn error of metabolism, which is caused by the cystathionine-β-synthase (CBS: encoded by CBS) deficiency. Symptoms of untreated classical HCU patients include intellectual disab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ebd9ea5c2cc5c279f5a7be47f4b1aa0
https://pure.amc.nl/en/publications/identification-of-three-novel-pathogenic-mutations-in-cystathionine-betasynthase-gene-of-pakistani-intellectually-disabled-patients(7b1bd1e5-63da-482c-a0a5-b812b941cdc4).html
https://pure.amc.nl/en/publications/identification-of-three-novel-pathogenic-mutations-in-cystathionine-betasynthase-gene-of-pakistani-intellectually-disabled-patients(7b1bd1e5-63da-482c-a0a5-b812b941cdc4).html
Acute aerobic exercise leads to increased plasma levels of R- and S-β-aminoisobutyric acid in humans
Autor:
Lida Stroomer, Laura Blancquaert, Wim Derave, Fred M. Vaz, André B.P. van Kuilenburg, Filip Lefevere, Jan Stautemas, Inge Everaert
Publikováno v:
FRONTIERS IN PHYSIOLOGY
Frontiers in physiology, 10(SEP):1240. Frontiers Media S.A.
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology
Frontiers in physiology, 10(SEP):1240. Frontiers Media S.A.
Frontiers in Physiology, Vol 10 (2019)
Frontiers in Physiology
Recently, it was suggested that beta-aminoisobutyric acid (BAIBA) is a myokine involved in browning of fat. However, there is no evidence for an acute effect of exercise supporting this statement and the metabolic distinct enantiomers of BAIBA were n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d5ffed90e6b89efdae53325e888cb4a
https://hdl.handle.net/1854/LU-8637424
https://hdl.handle.net/1854/LU-8637424
Autor:
Jan Booij, Nico G.G.M. Abeling, Henk D. Bakker, Lida Stroomer, Beat Thöny, Marinus Duran, Nenad Blau, Bwee Tien Poll-The
Publikováno v:
Molecular genetics and metabolism, 89(1-2), 116-120. Academic Press Inc.
The diagnosis of a 14-year-old girl with a new homoallelic mutation in the sepiapterin reductase (SR) gene is reported. Initially she presented at the age of 2 with hypotonia and mild cognitive developmental delay, and was diagnosed as having mild me
Autor:
Alfried Kohlschütter, Simone Denis, Sacha Ferdinandusse, Yvette C de Hingh, Ronald J.A. Wanders, Barbara Finckh, Lida Stroomer
Publikováno v:
Molecular genetics and metabolism, 79(4), 281-287. Academic Press Inc.
Peroxisome biogenesis disorders (PBDs) and D-bifunctional protein (D-BP) deficiency are two types of inherited peroxisomal disorders. Patients with a PBD lack functional peroxisomes and patients with D-BP deficiency lack the enzyme, which is responsi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::167756746a16574a18fd33b7a375515c
https://pure.amc.nl/en/publications/evidence-for-increased-oxidative-stress-in-peroxisomal-dbifunctional-protein-deficiency(805cb89c-14c9-4d79-bc74-c0ddf89e01b3).html
https://pure.amc.nl/en/publications/evidence-for-increased-oxidative-stress-in-peroxisomal-dbifunctional-protein-deficiency(805cb89c-14c9-4d79-bc74-c0ddf89e01b3).html
Publikováno v:
Purine and Pyrimidine Metabolism in Man VIII ISBN: 9781461361053
In humans molybdenum-cofactor deficiency (MCF) leads to the combined deficient activities of sulphite oxidase (SO), aldehyde oxidase (AO) and xanthine dehydrogenase (XDH). Patients present from birth on with frequent severe seizures refractory to ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33f7a9e9b8149da45028ff66489e0efe
https://doi.org/10.1007/978-1-4615-2584-4_81
https://doi.org/10.1007/978-1-4615-2584-4_81
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781461577058
In man pyrimidines are degraded in four steps catalysed by dihydropyrimidine dehydrogenase (DHPD, EC 1. 3. 1. 2.), dihydropyrimidinase (DHP, EC 3. 5. 2. 2.), ureidopropionase (UP, EC 3. 5. 1. 6.) and a transaminase (Fig. 1). As yet only deficiencies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d045449a61767897fe3a0880e6fe5013
https://doi.org/10.1007/978-1-4615-7703-4_4
https://doi.org/10.1007/978-1-4615-7703-4_4