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Results of search for 'au:"Van Ghelue, M"'
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Authors
Akkermans, A D
Andréasson, S
Bendiksen, S
Bisseling, T
Degré, M
Elgjo, K
Eriksen, H L
Evseeva, I
Haga, H J
Holmgren, G
Jensen, P K
Johannessen, M
Johansen, B
Moens, U
Rekvig, O P
Sun, C
Torbergsen, T
Tranebjaerg, L
Van Ghelue, M
van Ghelue, M
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Your search returned 15 results.
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1.
Oncogenic potentials of the human polyomavirus regulatory proteins.
[electronic resource]
by
Moens, U
Van Ghelue, M
Johannessen, M
Producer:
20070829
In:
Cellular and molecular life sciences : CMLS
vol. 64
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2.
X-linked recessive deafness-dystonia syndrome (Mohr-Tranebjaerg syndrome).
[electronic resource]
by
Tranebjaerg, L
Jensen, P K
van Ghelue, M
Producer:
20001002
In:
Advances in oto-rhino-laryngology
vol. 56
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3.
Concerted expression of BK virus large T- and small t-antigens strongly enhances oestrogen receptor-mediated transcription.
[electronic resource]
by
Moens, U
Van Ghelue, M
Johansen, B
Seternes, O M
Producer:
19990415
In:
The Journal of general virology
vol. 80 ( Pt 3)
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4.
Spectrum of CLCN1 mutations in patients with myotonia congenita in Northern Scandinavia.
[electronic resource]
by
Sun, C
Tranebjaerg, L
Torbergsen, T
Holmgren, G
Van Ghelue, M
Producer:
20020507
In:
European journal of human genetics : EJHG
vol. 9
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5.
The multifunctional roles of the four-and-a-half-LIM only protein FHL2.
[electronic resource]
by
Johannessen, M
Møller, S
Hansen, T
Moens, U
Van Ghelue, M
Producer:
20060316
In:
Cellular and molecular life sciences : CMLS
vol. 63
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6.
The zebrafish homeobox gene hox[zf-114]: primary structure, expression pattern and evolutionary aspects.
[electronic resource]
by
Molven, A
Hordvik, I
Njølstad, P R
van Ghelue, M
Fjose, A
Producer:
19921022
In:
The International journal of developmental biology
vol. 36
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7.
Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
[electronic resource]
by
Sun, C
Van Ghelue, M
Tranebjærg, L
Thyssen, F
Nilssen, Ø
Torbergsen, T
Producer:
20120216
In:
Clinical genetics
vol. 80
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8.
Sucrose synthase and enolase expression in actinorhizal nodules of Alnus glutinosa: comparison with legume nodules.
[electronic resource]
by
van Ghelue, M
Ribeiro, A
Solheim, B
Akkermans, A D
Bisseling, T
Pawlowski, K
Producer:
19960509
In:
Molecular & general genetics : MGG
vol. 250
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9.
Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.
[electronic resource]
by
Larsen, L A
Vuust, J
Nystad, M
Evseeva, I
Van Ghelue, M
Tranebjaerg, L
Producer:
20011204
In:
European journal of human genetics : EJHG
vol. 9
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10.
A de novo missense mutation in a critical domain of the X-linked DDP gene causes the typical deafness-dystonia-optic atrophy syndrome.
[electronic resource]
by
Tranebjaerg, L
Hamel, B C
Gabreels, F J
Renier, W O
Van Ghelue, M
Producer:
20001016
In:
European journal of human genetics : EJHG
vol. 8
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11.
A longitudinal study of human cytomegalovirus serology and viruria fails to detect active viral infection in 20 systemic lupus erythematosus patients.
[electronic resource]
by
Bendiksen, S
Van Ghelue, M
Rekvig, O P
Gutteberg, T
Haga, H J
Moens, U
Producer:
20000608
In:
Lupus
vol. 9
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12.
Simian virus 40 large T-antigen, but not small T-antigen, trans-activates the human cytomegalovirus major immediate early promoter.
[electronic resource]
by
Moens, U
Van Ghelue, M
Kristoffersen, A K
Johansen, B
Rekvig, O P
Degré, M
Rollag, H
Producer:
20020418
In:
Virus genes
vol. 23
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13.
BK and JC viruses in patients with systemic lupus erythematosus: prevalent and persistent BK viruria, sequence stability of the viral regulatory regions, and nondetectable viremia.
[electronic resource]
by
Sundsfjord, A
Osei, A
Rosenqvist, H
Van Ghelue, M
Silsand, Y
Haga, H J
Rekvig, O P
Moens, U
Producer:
19990729
In:
The Journal of infectious diseases
vol. 180
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14.
Autosomal dominant cone-rod dystrophy due to a missense mutation (R838C) in the guanylate cyclase 2D gene (GUCY2D) with preserved rod function in one branch of the family.
[electronic resource]
by
Van Ghelue , M
Eriksen, H L
Ponjavic, V
Fagerheim, T
Andréasson, S
Forsman-Semb, K
Sandgren, O
Holmgren, G
Tranebjaerg, L
Producer:
20010208
In:
Ophthalmic genetics
vol. 21
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15.
Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a gene.
[electronic resource]
by
Tranebjaerg, L
Jensen, P K
Van Ghelue, M
Vnencak-Jones, C L
Sund, S
Elgjo, K
Jakobsen, J
Lindal, S
Warburg, M
Fuglsang-Frederiksen, A
Skullerud, K
Producer:
20020208
In:
Ophthalmic genetics
vol. 22
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