Výsledky vyhledávání

The Structural Requirements of Epitopes with Ige Binding Capacity Demonstrated by Three Major Allergens from Fish, Egg and Tree Pollen

Autor: J Apold, E Holen, Erik Florvaag, S. Elsayed, T Dybendal, H. Vik

Publikováno v: Scandinavian Journal of Clinical and Laboratory Investigation. 51:17-31

Three major allergens from cod fish, egg white and tree pollen, were characterized by studies on their allergenic and antigenic structures. The major allergen of cod fish, Allergen M "parvalbumins pI 4.75", is composed of 113 amino acid residues with

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::086aae14adffd3f980ceaa41048b88fb
https://doi.org/10.3109/00365519109104592

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Prediction of the outcome of genetic testing in HNPCC kindreds using the revised Amsterdam criteria and immunohistochemistry

Autor: A T, Stormorken, W, Müller, B, Lemkemeyer, J, Apold, J T, Wijnen, R, Fodde, G, Möslein, P, Møller

Publikováno v: Familial cancer. 1(3-4)

Hereditary non-polyposis colorectal cancer (HNPCC) may be caused by mutations in the mismatch repair (MMR) genes MLH1, MSH2 or MSH6. Family history (Amsterdam criteria) has traditionally been used to select patients for mutation testing. It has been

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4e81c1dae26df9d09358a4151c1936c6
https://pubmed.ncbi.nlm.nih.gov/14574174

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[Gene therapy for monogenic inherited diseases]

Autor: K H, Ørstavik, J, Apold

Publikováno v: Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 121(3)

Monogenic inherited disorders are caused by a mutation in one single gene. Each of these disorders is very rare, but as there are many thousand different monogenic disorders, they represent a significant health problem. Most monogenic disorders are s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bd5ceb0cf95949f79eacc7e0018a3dcd
https://pubmed.ncbi.nlm.nih.gov/11242881

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Efficacy of early diagnosis and treatment in women with a family history of breast cancer. European Familial Breast Cancer Collaborative Group

Autor: P, Møller, M M, Reis, G, Evans, H, Vasen, N, Haites, E, Anderson, C M, Steel, J, Apold, F, Lalloo, L, Maehle, P, Preece, H, Gregory, K, Heimdal

Publikováno v: Disease Markers

BACKGROUND: Surveillance programmes for women at increased genetic risk of breast cancer are being established worldwide but little is known of their efficacy in early detection of cancers and hence reduction in mortality. METHODS: Data were contribu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::16b0d3f91b4bb34eeac9529d680d9805
https://pubmed.ncbi.nlm.nih.gov/10595275

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PKU mutation G46S is associated with increased aggregation and degradation of the phenylalanine hydroxylase enzyme

Autor: H G, Eiken, P M, Knappskog, J, Apold, T, Flatmark

Publikováno v: Human mutation. 7(3)

The G46S mutation in the phenylalanine hydroxylase (PAH) gene was identified by fluorescence-based single-strand conformation polymorphism (F-SSCP) analysis on phenylketonuria (PKU) haplotype 5.9 alleles. DNA sequencing of PAH exon 2 revealed a G-to-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f5431f0b3129060b8016cc33c55da85b
https://pubmed.ncbi.nlm.nih.gov/8829656

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DGGE analysis as supplement to SSCP analysis of the phenylalanine hydroxylase gene: detection of eight (one de novo, seven inherited) of nine remaining Norwegian PKU mutations

Autor: H G, Eiken, P M, Knappskog, P, Guldberg, J, Apold

Publikováno v: Human mutation. 8(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::403653639f9ce8398c70c80e3604a2e1
https://pubmed.ncbi.nlm.nih.gov/8807331

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Expression of wild type and mutant forms of human phenylalanine hydroxylase in E. coli

Autor: M, Knappskog, H G, Eiken, A, Martinez, S, Olafsdotti, J, Haavik, T, Flatmark, J, Apold

Publikováno v: Advances in experimental medicine and biology. 338

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e1fcc226af36df6300772243eaf4418f
https://pubmed.ncbi.nlm.nih.gov/8304187

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The structural requirements of epitopes with IgE binding capacity demonstrated by three major allergens from fish, egg and tree pollen

Autor: S, Elsayed, J, Apold, E, Holen, H, Vik, E, Florvaag, T, Dybendal

Publikováno v: Scandinavian journal of clinical and laboratory investigation. Supplementum. 204

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c527fd46e9171a1ecfe7ab81946885c5
https://pubmed.ncbi.nlm.nih.gov/1710368

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Prophylactic bilateral salpingo-oophorectomy (PBSO) with or without prophylactic bilateral mastectomy (PBM) or no intervention in BRCA1 mutation carriers. A cost-effectiveness analysis

Autor: J. Norum, A.I. Hagen, L. Maehle, J. Apold, J. Burn, P. Moller

Publikováno v: European Journal of Cancer Supplements. 6:91

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::992bfc1398cc99721f210ef6a25565f3
https://doi.org/10.1016/s1359-6349(08)70463-4

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The zebrafish homeobox gene hox-2.2: transcription unit, potential regulatory regions and in situ localization of transcripts

Autor: Anders Molven, J. Apold, Pål R. Njølstad, Anders Fjose

Publikováno v: The EMBO journal. 9(2)

The data presented in this report strongly suggest that the genome of the zebrafish, Brachydanio rerio, has a homeobox cluster which is equivalent to the murine Hox-2 locus. In support of this conclusion, we have found two closely linked zebrafish ge

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddc2b492d1942b16f57f5f1873131417
https://pubmed.ncbi.nlm.nih.gov/1968004

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