Helge Klungland
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Explore the profile of Helge Klungland including associated specialties, affiliations and a list of published articles.
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10
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93
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Recent Articles
1.
Lund B, Najmi L, Wesolowska-Andersen A, Landsem V, Rasmussen K, Borst L, et al.
Appl Immunohistochem Mol Morphol
. 2015 Jan;
23(1):71-7.
PMID: 25621358
AB Archival samples represent a significant potential for genetic studies, particularly in severe diseases with risk of lethal outcome, such as in cancer. In this pilot study, we aimed to...
2.
Lund B, Wesolowska-Andersen A, Lausen B, Borst L, Rasmussen K, Muller K, et al.
Eur J Haematol
. 2013 Dec;
92(4):321-30.
PMID: 24330153
Objectives: To investigate association of host genomic variation and risk of infections during treatment for childhood acute lymphoblastic leukaemia (ALL). Methods: We explored association of 34,000 single-nucleotide polymorphisms (SNPs) related...
3.
Nusier M, Brodtkorb H, Rein S, Odeh A, Radaideh A, Klungland H
Ital J Pediatr
. 2010 Feb;
36:16.
PMID: 20181131
Background: Celiac disease (CD) emerged as a public health problem, and the disease prevalence varies among different races. The present study was designed to investigate the prevalence of CD using...
4.
Myhre R, Steinkjer S, Stormyr A, Nilsen G, Abu Zayyad H, Horany K, et al.
BMC Neurol
. 2008 Dec;
8:47.
PMID: 19087301
Background: Parkinson's disease is a progressive neurodegenerative disorder, where most cases are sporadic with a late onset. In rare incidences familial forms of early-onset parkinsonism occur, and when recessively inherited,...
5.
Iversen A, Nguyen O, Tommerdal L, Eide I, Landsem V, Acar N, et al.
J Reprod Immunol
. 2008 Apr;
78(2):158-65.
PMID: 18423887
Trophoblast expression of the non-classical MHC, HLA-G, is considered essential for feto-maternal immune tolerance and successful placentation in pregnancy. The HLA-G 14bp polymorphism in the 3'-untranslated region (UTR) of the...
6.
Myhre R, Klungland H, Farrer M, Aasly J
BMC Med Genet
. 2008 Mar;
9:19.
PMID: 18366718
Background: Post-mortem Lewy body and Lewy neuritic inclusions are a defining feature of Parkinson's disease (PD) and dementia with Lewy bodies (DLB). With the discovery of missense and multiplication mutations...
7.
Svaasand E, Aasly J, Landsem V, Klungland H
Muscle Nerve
. 2007 Jul;
36(5):679-84.
PMID: 17661373
The X-linked recessive disease phosphoglycerate kinase (PGK) deficiency is caused by altered expression of the PGK1 enzyme, which causes muscle stiffness, hemolytic anemia, and mental retardation. In this study we...
8.
Vage D, Fuglei E, Snipstad K, Beheim J, Landsem V, Klungland H
Peptides
. 2005 Jun;
26(10):1814-7.
PMID: 15982782
We have characterized two mutations in the MC1R gene of the blue variant of the arctic fox (Alopex lagopus) that both incorporate a novel cysteine residue into the receptor. A...
9.
Vage D, Fleet M, Ponz R, Olsen R, Monteagudo L, Tejedor M, et al.
Pigment Cell Res
. 2003 Nov;
16(6):693-7.
PMID: 14629728
Dominant black pigment synthesis in sheep is caused by alterations of the melanocortin-1 receptor (MC1-R) coding sequence. Using five bovine microsatellite markers we have mapped the sheep MC1-R gene to...
10.
Gomez-Raya L, Olsen H, Lingaas F, Klungland H, Vage D, Olsaker I, et al.
Genetics
. 2002 Nov;
162(3):1381-8.
PMID: 12454081
A method to measure genomic response to natural and artificial selection by means of genetic markers in livestock is proposed. Genomic response through several levels of selection was measured using...