Brox V - Search Results

1

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.

Nystad M, Fagerheim T, Brox V, Fortunato EA, Nilssen Ø. Nystad M, et al. Among authors: brox v. Mutat Res. 2008 Jan 1;637(1-2):56-65. doi: 10.1016/j.mrfmmm.2007.07.009. Epub 2007 Jul 25. Mutat Res. 2008. PMID: 17765268 Free PMC article.

2

Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.

Fagerheim T, Nilssen O, Raeymaekers P, Brox V, Moum T, Elverland HH, Teig E, Omland HH, Fostad GK, Tranebjaerg L. Fagerheim T, et al. Among authors: brox v. Hum Mol Genet. 1996 Aug;5(8):1187-91. doi: 10.1093/hmg/5.8.1187. Hum Mol Genet. 1996. PMID: 8842739

3

Spectrum of USH2A mutations in Scandinavian patients with Usher syndrome type II.

Dreyer B, Brox V, Tranebjaerg L, Rosenberg T, Sadeghi AM, Möller C, Nilssen O. Dreyer B, et al. Among authors: brox v. Hum Mutat. 2008 Mar;29(3):451. doi: 10.1002/humu.9524. Hum Mutat. 2008. PMID: 18273898

4

Alhamidi M, Kjeldsen Buvang E, Fagerheim T, Brox V, Lindal S, Van Ghelue M, Nilssen Ø. Alhamidi M, et al. Among authors: brox v. PLoS One. 2011;6(8):e22968. doi: 10.1371/journal.pone.0022968. Epub 2011 Aug 23. PLoS One. 2011. PMID: 21886772 Free PMC article.

5

Homozygosity mapping to the USH2A locus in two isolated populations.

Fagerheim T, Raeymaekers P, Merren J, Mani K, Jha GK, Baumbach L, Brox V, Breines E, Holdø BE, Holdø A, Tranebjaerg L. Fagerheim T, et al. Among authors: brox v. J Med Genet. 1999 Feb;36(2):144-7. J Med Genet. 1999. PMID: 10051015 Free PMC article.

6

Limb girdle muscular dystrophy type 2I: No correlation between clinical severity, histopathology and glycosylated α-dystroglycan levels in patients homozygous for common FKRP mutation.

Alhamidi M, Brox V, Stensland E, Liset M, Lindal S, Nilssen Ø. Alhamidi M, et al. Among authors: brox v. Neuromuscul Disord. 2017 Jul;27(7):619-626. doi: 10.1016/j.nmd.2017.02.015. Epub 2017 Mar 4. Neuromuscul Disord. 2017. PMID: 28479227

7

A common ancestral origin of the frequent and widespread 2299delG USH2A mutation.

Dreyer B, Tranebjaerg L, Brox V, Rosenberg T, Möller C, Beneyto M, Weston MD, Kimberling WJ, Cremers CW, Liu XZ, Nilssen O. Dreyer B, et al. Among authors: brox v. Am J Hum Genet. 2001 Jul;69(1):228-34. doi: 10.1086/321269. Epub 2001 Jun 8. Am J Hum Genet. 2001. PMID: 11402400 Free PMC article.

8

Usher syndrome in Denmark: mutation spectrum and some clinical observations.

Dad S, Rendtorff ND, Tranebjærg L, Grønskov K, Karstensen HG, Brox V, Nilssen Ø, Roux AF, Rosenberg T, Jensen H, Møller LB. Dad S, et al. Among authors: brox v. Mol Genet Genomic Med. 2016 Jun 28;4(5):527-539. doi: 10.1002/mgg3.228. eCollection 2016 Sep. Mol Genet Genomic Med. 2016. PMID: 27957503 Free PMC article.

9

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.

Van Belle W, Gerits N, Jakobsen K, Brox V, Van Ghelue M, Moens U. Van Belle W, et al. Among authors: brox v. Gene Regul Syst Bio. 2007 Jul 17;1:57-72. Gene Regul Syst Bio. 2007. PMID: 19936079 Free PMC article.

10

Genetic variability among isolates of Listeria monocytogenes from food products, clinical samples and processing environments, estimated by RAPD typing.

Martinez I, Rørvik LM, Brox V, Lassen J, Seppola M, Gram L, Fonnesbech-Vogel B. Martinez I, et al. Among authors: brox v. Int J Food Microbiol. 2003 Aug 1;84(3):285-97. doi: 10.1016/s0168-1605(02)00423-3. Int J Food Microbiol. 2003. PMID: 12810292

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