Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Per Hove Andreasen"'
Autor:
L. G. Jensen, Per Hove Andreasen, Henrik Jensen, Peter S. Hansen, Mogens Lytken Larsen, Henrik Uffe Holst, Ole Faergeman, Steen Kølvraa, Niels Gregersen, Lars Bolund
Publikováno v:
Clinical Genetics. 56:379-389
In the present study, we have characterized a unique splice donor G to A substitution in the moderately conserved + 5 position in intron 10 of the low-density lipoprotein (LDL) receptor gene. In two Danish families, carriers of the 1592 + 5G --> A mu
Publikováno v:
Larsen, L K, Andreasen, P H & Kristiansen, K 1999, ' Ribosome synthesis in T etrahymena : A quantitative analysis ', Cell Biology International, vol. 23, no. 11, pp. 729-738 . https://doi.org/10.1006/cbir.1999.0376
We have performed a detailed quantitative analysis of the transcription and accumulation of ribosomal RNA and ribosomal protein mRNA in the ciliated protozoan Tetrahymena thermophila during changes in growth conditions, and found that: (1) nutritiona
Autor:
Per Hove Andreasen, Søren Rittig, T G Jensen, Lars Bolund, Gary L. Robertson, Charlotte Siggaard, Niels Gregersen, Erling B. Pedersen, Brage S. Andresen, Thomas J. Corydon
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 84:2933-2941
The autosomal dominant form of familial neurohypophyseal diabetes insipidus (adFNDI) is a rare disease characterized by postnatal onset of polyuria and a deficient neurosecretion of the antidiuretic hormone, arginine vasopressin (AVP). Since 1991, ad
Autor:
Henrik Nielsen, Lisbeth Palm, Karsten Kristiansen, Leif K. Larsen, Hanne Dreisig, Per Hove Andreasen, Jan Engberg
Publikováno v:
Cell Biology International. 23:551-560
We have cloned and characterized the cDNA and the macronuclear genomic copy of the highly conserved ribosomal protein (r-protein) L3 of Tetrahymena thermophila. The r-protein L3 is encoded by a single copy gene interrupted by one intron. The organiza
Autor:
Stig Ravn, Niels Gregersen, Rene Hummel, Susanne Mandrup, Gurli Jensen, Per Hove Andreasen, Karsten Kristiansen, Jens Knudsen
Publikováno v:
Journal of Molecular Biology. 228:1011-1022
Acyl-CoA-binding protein (ACBP) is a 10 kDa protein isolated from bovine liver by virtue of its ability to bind and induce the synthesis of medium-chain acyl-CoA esters. Surprisingly, it turned out to be identical to a protein named diazepam-binding
Autor:
Peter Nørgaard, Karsten Skjødt, Søren Neve, Per Hove Andreasen, Rene Hummel, Ditte Tornehave, Karsten Kristiansen
Publikováno v:
Hummel, R, Nørgaard, P, Andreasen, P H, Neve, S, Skjødt, K, Tornehave, D & Kristiansen, K 1992, ' Tetrahymena gene encodes a protein that is homologous with the liver-specific F-antigen and associated with membranes of the Golgi apparatus and transport vesicles. ', Journal of Molecular Biology, vol. 228, no. 3, pp. 850-61 .
University of Southern Denmark
University of Southern Denmark
The F-antigen is a prominent liver protein which has been extensively used in studies on natural and induced immunological tolerance. However, its intracellular localization and biological function have remained elusive. It has generally been assumed
Autor:
Torben Hansen, Jan Engberg, Per Hove Andreasen, Hanne Dreisig, Karsten Kristiansen, Peter Højrup, Henrik Nielsen
Publikováno v:
Gene. 105:143-150
We have cloned and characterized a Tetrahymena thermophila macronuclear gene (L37) encoding the acidic ribosomal protein (A-protein) L37. The gene contains a single intron located in the 3'-part of the coding region. Two major and three minor transcr
Autor:
T G Jensen, Steen Kølvraa, Per Hove Andreasen, Frederik Dagnæs-Hansen, Malene Munk Jørgensen, Thomas J. Corydon, Henrik Uffe Holst, Lars Bolund
Publikováno v:
Holst, H U, Dagnaes-Hansen, F, Corydon, T J, Andreasen, P H, Jørgensen, M M, Kølvraa, S, Bolund, L & Jensen, T G 2001, ' LDL receptor-GFP fusion proteins : new tools for the characterisation of disease-causing mutations in the LDL receptor gene ', European Journal of Human Genetics, vol. 9, no. 11, pp. 815-22 . https://doi.org/10.1038/sj.ejhg.5200718
UC Viden
Holst, H U, Dagnaes-Hansen, F, Corydon, T J, Andreasen, P H, Jørgensen, M M, Kølvraa, S, Bolund, L & Jensen, T G 2001, ' LDL receptor-GFP fusion proteins: new tools for the characterisation of disease-causing mutations in the LDL receptor gene ', Eur J Hum Genet, vol. 9, no. 11, pp. 815-822 .
Aarhus University
UC Viden
Holst, H U, Dagnaes-Hansen, F, Corydon, T J, Andreasen, P H, Jørgensen, M M, Kølvraa, S, Bolund, L & Jensen, T G 2001, ' LDL receptor-GFP fusion proteins: new tools for the characterisation of disease-causing mutations in the LDL receptor gene ', Eur J Hum Genet, vol. 9, no. 11, pp. 815-822 .
Aarhus University
The function of a series of LDL receptor GFP fusion proteins with different, flexible, unstructured spacer regions was analysed. An optimised version of the fusion protein was used to analyse the effect of an LDL receptor mutation (W556S) found in FH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23617fc1df86351a9c5e6a3ff7db772c
https://pure.au.dk/portal/da/publications/ldl-receptorgfp-fusion-proteins(2f74ae4f-9500-43ea-ad80-5d22e1c04c36).html
https://pure.au.dk/portal/da/publications/ldl-receptorgfp-fusion-proteins(2f74ae4f-9500-43ea-ad80-5d22e1c04c36).html
Autor:
Morten J. Corydon, Nils Gregersen, Hans Eiberg, Brage S. Andresen, Per Hove Andreasen, Margrethe Kjeldsen, Steen Kølvraa, Peter Bross
Publikováno v:
ResearcherID
Short-chain acyl-CoA dehydrogenase (SCAD) is a homotetrameric mitochondrial flavoenzyme that catalyzes the initial reaction in short-chain fatty acid beta-oxidation. Defects in the SCAD enzyme are associated with failure to thrive, often with neuromu
Autor:
T G Jensen, L. G. Jensen, Ole Faergeman, Henrik Uffe Holst, Karsten Kristiansen, Niels Gregersen, Søren Neve, Brage S. Andresen, Lars Bolund, Peter Steen Hansen, Finn Heath, Malene Munk Jørgensen, Per Hove Andreasen, Henrik Jensen, Steen Kølvraa
Publikováno v:
Atherosclerosis. 131(1)
In a group of unrelated Danish patients with familial hypercholesterolemia (FH) we recently reported two common low-density lipoprotein (LDL) receptor mutations, W23X and W66G, accounting for 30% of the cases. In this study, we describe another commo