Výsledky vyhledávání - "E van Berkel"

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Fusagene vectors: a novel strategy for the expression of multiple genes from a single cistron

Autor: Kenn C. Daniel, Jie Jiang, Marcel Kuiper, Farzin Farzaneh, Stephen J. Russell, Mahvash Tavassoli, E van Berkel, Kevin G. Ford, Joop Gaken, M Kemeny, David Darling, Joanna Galea-Lauri, Christopher S. Hughes

Transduction of cells with multiple genes, allowing their stable and co-ordinated expression, is difficult with the available methodologies. A method has been developed for expression of multiple gene products, as fusion proteins, from a single cistr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98cc2689525a819d908e3ad0da2a0856
https://ora.ox.ac.uk/objects/uuid:317383e2-2ea2-40aa-b6dc-a984c424fd3a

Zobrazit plný text záznamu

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Akademický článek

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Non-Uniform Inflow Effects on Propeller Performance

Autor: Marios Kotsonis, Llm Veldhuis, E van Berkel, Georg Eitelberg

Publikováno v: 31st AIAA Applied Aerodynamics Conference.

In this paper we address the effects of a non-uniform flow field on the performance characteristics of a single rotation propeller. After the recent installation of a new propeller test rig, a first test campaign was launched to check its capabilitie

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::865131c5810743b1232fab40243dfedf
https://doi.org/10.2514/6.2013-2801

Zobrazit plný text záznamu

D-Hydroxyacyl-CoA Dehydrogenase Deficiency

Autor: Petra A.W. Mooijer, R. J. A. Wanders, Simone Denis, E. G. van Grunsven, E. van Berkel

Publikováno v: Current Views of Fatty Acid Oxidation and Ketogenesis ISBN: 9780306462009

The second and third steps of peroxisomal β-oxidation are catalysed by two multifunctional enzymes: D-bifunctional protein and L-bifunctional protein. Here we show that fibroblasts of a patient described as being deficient in the 3-hydroxyacyl-CoA d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::63db69ceea8d9ff2a3cfc0b72f0bb67a
https://doi.org/10.1007/0-306-46818-2_42

Zobrazit plný text záznamu

D-hydroxyacyl-CoA dehydrogenase deficiency. Identification of a new peroxisomal disorder with implications for other disorders of beta-oxidation

Autor: E G, van Grunsven, E, van Berkel, S, Denis, P A, Mooijer, R J, Wanders

Publikováno v: Advances in experimental medicine and biology. 466

The second and third steps of peroxisomal beta-oxidation are catalysed by two multifunctional enzymes: D-bifunctional protein and L-bifunctional protein. Here we show that fibroblasts of a patient described as being deficient in the 3-hydroxyacyl-CoA

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4ed2fd53882b9a77b21a5a8f27e42ba1
https://pubmed.ncbi.nlm.nih.gov/10709664

Zobrazit plný text záznamu

Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis

Autor: E. G. van Grunsven, Takashi Hashimoto, Hugo W. Moser, Petra A.W. Mooijer, Jerzy Adamski, Ronald J.A. Wanders, Gerald Hoefler, Paul A. Watkins, E. van Berkel, L.L. Jiang, Yasuyuki Suzuki

Publikováno v: American journal of human genetics, 64(1), 99-107. Cell Press
American Journal of Human Genetics, 64, 99-107. Cell Press

SummaryIn the past few years, many patients have been described who have a defect of unknown origin in the peroxisomal β-oxidation pathway. Complementation analysis has been done by various groups to establish the extent of the genetic heterogeneity

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d7628250334a8b85b93e7c014848669
https://pure.amc.nl/en/publications/peroxisomal-bifunctional-protein-deficiency-revisited-resolution-of-its-true-enzymatic-and-molecular-basis(521371bc-582b-4332-90fa-88286f874192).html

Zobrazit plný text záznamu

Peroxisomal D-hydroxyacyl-CoA dehydrogenase deficiency: resolution of the enzyme defect and its molecular basis in bifunctional protein deficiency

Autor: R. J. A. Wanders, E. G. van Grunsven, E. van Berkel, Jerzy Adamski, Peter E. Clayton, J. B. C. De Klerk, Lodewijk IJlst, Dean Cuebas, Hugh Lemonde, Peter Vreken

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 95(5), 2128-2133. National Academy of Sciences

Peroxisomes play an essential role in a number of different metabolic pathways, including the β-oxidation of a distinct set of fatty acids and fatty acid derivatives. The importance of the peroxisomal β-oxidation system in humans is made apparent b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f43b1011f00edcb79c87745ceed0792
https://pure.amc.nl/en/publications/peroxisomal-dhydroxyacylcoa-dehydrogenase-deficiency-resolution-of-the-enzyme-defect-and-its-molecular-basis-in-bifunctional-protein-deficiency(94622cfd-b8ec-4946-baaa-23f76894de42).html

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání