Publications by authors named "Vigdis Brox"

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Limb girdle muscular dystrophy type 2I: No correlation between clinical severity, histopathology and glycosylated α-dystroglycan levels in patients homozygous for common FKRP mutation.
Maisoon Alhamidi, Vigdis Brox, Eva Stensland, Merete Liset, Sigurd Lindal

Neuromuscul Disord· July 2017

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Usher syndrome in Denmark: mutation spectrum and some clinical observations.
Shzeena Dad, Nanna Dahl Rendtorff, Lisbeth Tranebjærg, Karen Grønskov, Helena Gásdal Karstensen, Vigdis Brox

Mol Genet Genomic Med· September 2016

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Fukutin-related protein resides in the Golgi cisternae of skeletal muscle fibres and forms disulfide-linked homodimers via an N-terminal interaction.
Maisoon Alhamidi, Elisabeth Kjeldsen Buvang, Toril Fagerheim, Vigdis Brox, Sigurd Lindal

PLoS One· January 2012

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Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II.
Bo Dreyer, Vigdis Brox, Lisbeth Tranebjaerg, Thomas Rosenberg, Andrè M Sadeghi

Hum Mutat· March 2008

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Human cytomegalovirus (HCMV) and hearing impairment: infection of fibroblast cells with HCMV induces chromosome breaks at 1q23.3, between loci DFNA7 and DFNA49 -- both involved in dominantly inherited, sensorineural, hearing impairment.
Mona Nystad, Toril Fagerheim, Vigdis Brox, Elizabeth A Fortunato, Øivind Nilssen

Mutat Res· January 2008

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Intensity dependent confidence intervals on microarray measurements of differentially expressed genes: a case study of the effect of MK5, FKRP and TAF4 on the transcriptome.
Werner Van Belle, Nancy Gerits, Kirsti Jakobsen, Vigdis Brox, Marijke Van Ghelue

Gene Regul Syst Bio· July 2007

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Genetic variability among isolates of Listeria monocytogenes from food products, clinical samples and processing environments, estimated by RAPD typing.
Iciar Martinez, Liv Marit Rørvik, Vigdis Brox, Jørgen Lassen, Marit Seppola

Int J Food Microbiol· August 2003

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