Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Femke S. Stet"'
Autor:
Ruzica Jurakic Toncic, Ivone Jakasa, Suzana Ljubojevic Hadzavdic, Susan MI Goorden, Karen JM Ghauharali-van der Vlugt, Femke S Stet, Anamaria Balic, Mikela Petkovic, Borna Pavicic, Kristina Zuzul, Branka Marinovic, Sanja Kezic
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 6, p 1958 (2020)
Dysfunctional skin barrier plays a key role in the pathophysiology of atopic dermatitis (AD), a common inflammatory skin disease. Altered composition of ceramides is regarded as a major cause of skin barrier dysfunction, however it is not clear wheth
Externí odkaz:
https://doaj.org/article/b23c357165af49faa9b8e69f17a75acd
Autor:
Femke S. Stet, Frédéric M. Vaz, Johanne H. Klinkspoor, Susan M. I. Goorden, Riekelt H. Houtkooper, Martin A. T. Vervaart, Hilary J. Vernon, Ronald J.A. Wanders, Henk van Lenthe, Willem Kulik
Publikováno v:
Journal of inherited metabolic disease, 45(1), 29-37. Springer Netherlands
Barth syndrome is an X-linked disorder characterized by cardiomyopathy, skeletal myopathy and neutropenia, caused by deleterious variants in TAFAZZIN. This gene encodes a phospholipid-lysophospholipid transacylase that is required for the remodeling
Autor:
Maria Rasmussen Rinnov, Anne‐Sofie Halling, Trine Gerner, Nina Haarup Ravn, Mette Hjorslev Knudgaard, Simon Trautner, Susan M. I. Goorden, Karen J. M. Ghauharali‐van der Vlugt, Femke S. Stet, Lone Skov, Simon Francis Thomsen, Alexander Egeberg, Aske L. L. Rosted, Troels Petersen, Ivone Jakasa, Christoph Riethmüller, Sanja Kezic, Jacob P. Thyssen
Publikováno v:
Allergy: European Journal of Allergy and Clinical Immunology. Wiley-Blackwell
Rinnov, M R, Halling, A-S, Gerner, T, Ravn, N H, Knudgaard, M H, Trautner, S, Goorden, S M, Ghauharali-van der Vlugt, K J M, Stet, F S, Skov, L, Thomsen, S F, Egeberg, A, Rosted, A L L, Petersen, T, Jakasa, I, Riethmuller, C, Kezic, S & Thyssen, J P 2023, ' Skin biomarkers predict development of atopic dermatitis in infancy ', Allergy, vol. 78, no. 3, pp. 791-802 . https://doi.org/10.1111/all.15518
Rinnov, M R, Halling, A-S, Gerner, T, Ravn, N H, Knudgaard, M H, Trautner, S, Goorden, S M, Ghauharali-van der Vlugt, K J M, Stet, F S, Skov, L, Thomsen, S F, Egeberg, A, Rosted, A L L, Petersen, T, Jakasa, I, Riethmuller, C, Kezic, S & Thyssen, J P 2023, ' Skin biomarkers predict development of atopic dermatitis in infancy ', Allergy, vol. 78, no. 3, pp. 791-802 . https://doi.org/10.1111/all.15518
Background There is currently no insight into biomarkers that can predict the onset of pediatric atopic dermatitis (AD). Methods Nested in a prospective birth cohort study that examined the occurrence of physician-diagnosed AD in 300 children, 44 ran
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7970d1aa9a1cdba52fc3d268f772fa17
https://pure.amc.nl/en/publications/skin-biomarkers-predict-development-of-atopic-dermatitis-in-infancy(0fe3234c-b88f-4435-bf94-ce435ed39a40).html
https://pure.amc.nl/en/publications/skin-biomarkers-predict-development-of-atopic-dermatitis-in-infancy(0fe3234c-b88f-4435-bf94-ce435ed39a40).html
Autor:
B. Pavicic, Branka Marinović, Susan M. I. Goorden, Karen J. M. Ghauharali-van der Vlugt, Anamaria Balić, Ivone Jakasa, Ruzica Jurakic Toncic, Sanja Kezic, Kristina Zuzul, Mikela Petkovic, Suzana Ljubojevic Hadzavdic, Femke S. Stet
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 6
International journal of molecular sciences, 21(6):1958. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences, Vol 21, Iss 6, p 1958 (2020)
Volume 21
Issue 6
International journal of molecular sciences, 21(6):1958. Multidisciplinary Digital Publishing Institute (MDPI)
International Journal of Molecular Sciences, Vol 21, Iss 6, p 1958 (2020)
Dysfunctional skin barrier plays a key role in the pathophysiology of atopic dermatitis (AD), a common inflammatory skin disease. Altered composition of ceramides is regarded as a major cause of skin barrier dysfunction, however it is not clear wheth
Autor:
Carina Prip-Buus, Isabel Tavares de Almeida, Lodewijk IJlst, Margarida F. B. Silva, C. C. P. Aires, Marinus Duran, Femke S. Stet, Ronald J.A. Wanders
Publikováno v:
Biochemical Pharmacology
Biochemical Pharmacology, Elsevier, 2010, 79 (5), pp.792-799. ⟨10.1016/j.bcp.2009.10.011⟩
Biochemical pharmacology, 79(5), 792-799. Elsevier Inc.
Biochemical Pharmacology, Elsevier, 2010, 79 (5), pp.792-799. ⟨10.1016/j.bcp.2009.10.011⟩
Biochemical pharmacology, 79(5), 792-799. Elsevier Inc.
Background/Aims: Carnitine Palmitoyl-transferase I (CPT I) catalyses the synthesis of long-chain (LC)-acylcarnitines from LC-acyl-CoA esters. It is the rate-limiting enzyme of mitochondrial fatty acid, beta-oxidation (FAO) pathway and its activity is
Autor:
Ornella Ahouansou, Patrick Aubourg, Abdellatif Benraiss, Femke S. Stet, Eloise Hudry, André Delacourte, Pierre Bougnères, Debby Van Dam, Wim Kulik, Nathalie Cartier, Peter Paul De Deyn
Publikováno v:
Molecular therapy
Molecular therapy, 18(1), 44-53. Nature Publishing Group
Molecular therapy, 18(1), 44-53. Nature Publishing Group
The development of Alzheimer's disease (AD) is closely connected with cholesterol metabolism. Cholesterol increases the production and deposition of amyloid-beta (Abeta) peptides that result in the formation of amyloid plaques, a hallmark of the path
Autor:
Frédéric M. Vaz, Henk van Lenthe, Janet E. Stone, Femke S. Stet, Colin G. Steward, Willem Kulik, Ronald J.A. Wanders, Helena Kemp, Riekelt H. Houtkooper
Publikováno v:
Clinical chemistry, 54(2), 371-378. American Association for Clinical Chemistry Inc.
Background: Barth syndrome (BTHS) is a serious X-linked, metabolic, multisystem disorder characterized by cardiomyopathy, neutropenia, myopathy, and growth delay. Because early diagnosis and appropriate treatment are of key importance for the surviva
Autor:
Richard J. Rodenburg, Riekelt H. Houtkooper, Frédéric M. Vaz, Bwee Tien Poll-The, Ronald J.A. Wanders, Femke S. Stet, Janet E. Stone, Willem Kulik, Henk van Lenthe, Jan A.M. Smeitink, Colin G. Steward, Charlotte Thiels
Publikováno v:
Analytical biochemistry, 387(2), 230-237. Academic Press Inc.
Analytical Biochemistry, 387, 2, pp. 230-7
Analytical Biochemistry, 387, 230-7
Analytical Biochemistry, 387, 2, pp. 230-7
Analytical Biochemistry, 387, 230-7
Contains fulltext : 80267.pdf (Publisher’s version ) (Closed access) Barth syndrome (BTHS) is an X-linked recessive disorder caused by mutations in the tafazzin (or TAZ) gene and is clinically characterized by (cardio)myopathy, neutropenia, and gro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e08fd5ba860849364969524bb126137
https://pure.amc.nl/en/publications/cardiolipin-and-monolysocardiolipin-analysis-in-fibroblasts-lymphocytes-and-tissues-using-highperformance-liquid-chromatographymass-spectrometry-as-a-diagnostic-test-for-barth-syndrome(328592fc-3b2a-4f01-9947-018ba84d77f4).html
https://pure.amc.nl/en/publications/cardiolipin-and-monolysocardiolipin-analysis-in-fibroblasts-lymphocytes-and-tissues-using-highperformance-liquid-chromatographymass-spectrometry-as-a-diagnostic-test-for-barth-syndrome(328592fc-3b2a-4f01-9947-018ba84d77f4).html