van Ghelue M - Search Results

1

The zebrafish homeobox gene hox[zf-114]: primary structure, expression pattern and evolutionary aspects.

Molven A, Hordvik I, Njølstad PR, van Ghelue M, Fjose A. Molven A, et al. Among authors: van ghelue m. Int J Dev Biol. 1992 Jun;36(2):229-37. Int J Dev Biol. 1992. PMID: 1356006 Free article.

2

A heterozygous 21-bp deletion in CAPN3 causes dominantly inherited limb girdle muscular dystrophy.

Vissing J, Barresi R, Witting N, Van Ghelue M, Gammelgaard L, Bindoff LA, Straub V, Lochmüller H, Hudson J, Wahl CM, Arnardottir S, Dahlbom K, Jonsrud C, Duno M. Vissing J, et al. Among authors: van ghelue m. Brain. 2016 Aug;139(Pt 8):2154-63. doi: 10.1093/brain/aww133. Epub 2016 Jun 3. Brain. 2016. PMID: 27259757

3

Sucrose synthase and enolase expression in actinorhizal nodules of Alnus glutinosa: comparison with legume nodules.

van Ghelue M, Ribeiro A, Solheim B, Akkermans AD, Bisseling T, Pawlowski K. van Ghelue M, et al. Mol Gen Genet. 1996 Mar 7;250(4):437-46. doi: 10.1007/BF02174032. Mol Gen Genet. 1996. PMID: 8602161

4

Genome analysis of the new human polyomaviruses.

Van Ghelue M, Khan MT, Ehlers B, Moens U. Van Ghelue M, et al. Rev Med Virol. 2012 Nov;22(6):354-77. doi: 10.1002/rmv.1711. Epub 2012 Mar 28. Rev Med Virol. 2012. PMID: 22461085 Review.

5

The multifunctional roles of the four-and-a-half-LIM only protein FHL2.

Johannessen M, Møller S, Hansen T, Moens U, Van Ghelue M. Johannessen M, et al. Among authors: van ghelue m. Cell Mol Life Sci. 2006 Feb;63(3):268-84. doi: 10.1007/s00018-005-5438-z. Cell Mol Life Sci. 2006. PMID: 16389449 Free PMC article. Review.

6

Agrin mutations lead to a congenital myasthenic syndrome with distal muscle weakness and atrophy.

Nicole S, Chaouch A, Torbergsen T, Bauché S, de Bruyckere E, Fontenille MJ, Horn MA, van Ghelue M, Løseth S, Issop Y, Cox D, Müller JS, Evangelista T, Stålberg E, Ioos C, Barois A, Brochier G, Sternberg D, Fournier E, Hantaï D, Abicht A, Dusl M, Laval SH, Griffin H, Eymard B, Lochmüller H. Nicole S, et al. Among authors: van ghelue m. Brain. 2014 Sep;137(Pt 9):2429-43. doi: 10.1093/brain/awu160. Epub 2014 Jun 20. Brain. 2014. PMID: 24951643

7

Kennedy disease in two sisters with biallelic CAG expansions of the androgen receptor gene.

Müller KI, Nilssen Ø, Nebuchenykh M, Løseth S, Jonsrud C, Hoem G, Van Ghelue M, Arntzen KA. Müller KI, et al. Among authors: van ghelue m. Neuromuscul Disord. 2022 Jan;32(1):75-79. doi: 10.1016/j.nmd.2021.11.007. Epub 2021 Nov 19. Neuromuscul Disord. 2022. PMID: 34922802 Free article.

8

Novel mutations in the HADHB gene causing a mild phenotype of mitochondrial trifunctional protein (MTP) deficiency.

Ørstavik K, Arntzen KA, Mathisen P, Backe PH, Tangeraas T, Rasmussen M, Kristensen E, Van Ghelue M, Jonsrud C, Bliksrud YT. Ørstavik K, et al. Among authors: van ghelue m. JIMD Rep. 2022 Mar 1;63(3):193-198. doi: 10.1002/jmd2.12276. eCollection 2022 May. JIMD Rep. 2022. PMID: 35433169 Free PMC article.

9

Identifying sequence variants contributing to hereditary breast and ovarian cancer in BRCA1 and BRCA2 negative breast and ovarian cancer patients.

Jarhelle E, Riise Stensland HMF, Hansen GÅM, Skarsfjord S, Jonsrud C, Ingebrigtsen M, Strømsvik N, Van Ghelue M. Jarhelle E, et al. Among authors: van ghelue m. Sci Rep. 2019 Dec 27;9(1):19986. doi: 10.1038/s41598-019-55515-x. Sci Rep. 2019. PMID: 31882575 Free PMC article.

10

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

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