Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Kirsten Fenger"'
Autor:
Kirsten Fenger
Publikováno v:
Magasin fra Det Kongelige Bibliotek. 27:27-43
De eventyrlige, tyske brødre havde et stort netværk blandt samtidens europæiske forfattere og sprogforskere, og de korresponderede flittigt med både H.C. Andersen og videnskabsmændene Chr. Molbech, Rasmus Rask og C.C. Rafn – blandt mange andre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::769d7eec22452b679e1dd6186bfc5418
https://doi.org/10.7146/mag.v27i3.66147
https://doi.org/10.7146/mag.v27i3.66147
Publikováno v:
Clinical Genetics. 41:6-11
HLA-A and -B alleles in 74 Danish patients and 21 homozygous relatives with idiopathic haemochromatosis (IH) were compared with those in a sample of 1719 chromosomes from healthy Danish control subjects. The following alleles occurred with higher fre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f5b9cfd4fe251fcc076455388a223ff
https://doi.org/10.1111/j.1399-0004.1992.tb03619.x
https://doi.org/10.1111/j.1399-0004.1992.tb03619.x
Publikováno v:
Europe PubMed Central
An increasing number of diseases are being found to be due to elongation of specific trinucleotide repeat sequences. Inverse correlation between the age at onset and the length of the repeat has been found in most of these. The elongated CAG repeat c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eeab3d4b373a9dfb26172577717e2350
https://doi.org/10.1111/j.1399-0004.1995.tb03941.x
https://doi.org/10.1111/j.1399-0004.1995.tb03941.x
Autor:
Arne Schousboe, J. Gordon Lindsay, Helle S. Waagepetersen, Gary E. Gibson, Gert H. Hansen, Kirsten Fenger
Publikováno v:
Glia. 53:225-231
In brain cells, various metabolites and metabolic pathways, largely of mitochondrial origin, have been shown to be compartmentalized. Attention has therefore been focused on the possible existence of mitochondrial heterogeneity in the brain at the ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c6dc394056ae3f17b953c0eb1253414
https://doi.org/10.1002/glia.20276
https://doi.org/10.1002/glia.20276
Autor:
Nils Milman, Kirsten Fenger, Finn Cilius Nielsen, Pernille Koefoed, Torkil á Steig, Palle Pedersen
Publikováno v:
Annals of Hematology. 84:146-149
The aim of the study was to assess the frequencies of the hereditary hemochromatosis HFE mutations C282Y, H63D, and S65C in the population in the Faroe Islands. The series comprised 200 randomly selected blood donors of Faroese heritage. The frequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cabf5c0d364370f6ab65f8de70927828
https://doi.org/10.1007/s00277-004-0865-8
https://doi.org/10.1007/s00277-004-0865-8
Autor:
Sally Dabelsteen, Jesper T. Troelsen, Patricia Simon-Assmann, Jørgen Olsen, Lars-Inge Larsson, Lene T. Kirkeby, Kirsten Fenger, Marianne M Brorsson, Randi Bordoy
Publikováno v:
Biochemical Journal. 371:211-221
The trimeric extracellular matrix molecule laminin-5 and its constituent chains (alpha 3, beta 3, gamma 2) are normally not detectable intracellularly in intestinal epithelial cells but the laminin gamma 2 chain can be detected in cancer cells at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4372b65c6a7b9c5b15a80c2986678591
https://doi.org/10.1042/bj20021454
https://doi.org/10.1042/bj20021454
Autor:
Christine Nellemann, Anne Nørremølle, Kathrine Abell, Lis Hasholt, Kirsten Fenger, Sven Asger Sørensen
Publikováno v:
The Journal of Gene Medicine. 5:528-538
Background Huntington's disease (HD) is an inherited neurodegenerative disorder which is caused by an expansion of a CAG repeat sequence in the HD gene. The repeat encodes an expanded polyglutamine tract in the protein huntingtin. The still unknown p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab3151ecbb8017fbcaf8f73a1965f46d
https://doi.org/10.1002/jgm.378
https://doi.org/10.1002/jgm.378
Publikováno v:
Annals of Hematology. 80:737-744
The object was to analyze, in a nationwide survey, the incidence and course of hereditary hemochromatosis in relation to the degree of iron overload and the presence of organ damage. The study included 179 Danish Caucasian patients with clinically ov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a63f732751f11f0f12426d1dcf21e94c
https://doi.org/10.1007/s002770100371
https://doi.org/10.1007/s002770100371
Publikováno v:
European Journal of Neurology. 8:335-339
There are at least seven clinically indistinguishable but genetically different types of autosomal dominant pure spastic paraplegia (ADPSP). In this study we investigated electrophysiological characteristics in patients with ADPSP linked to chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa2282ec04c027b8f3c51bc2788f3353
https://doi.org/10.1046/j.1468-1331.2001.00249.x
https://doi.org/10.1046/j.1468-1331.2001.00249.x
Publikováno v:
Cancer. 86:1342-1346
BACKGROUND The authors of this study have previously observed that cancer is rarely reported on the death certificates of patients with Huntington disease. This study was undertaken to investigate whether this disorder is associated with a lower inci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d530bba68c2304ca2aa0ba5e203ada9
https://doi.org/10.1002/(sici)1097-0142(19991001)86:7<1342::aid-cncr33>3.0.co
https://doi.org/10.1002/(sici)1097-0142(19991001)86:7<1342::aid-cncr33>3.0.co