References of "Runte, Maren 50002144"
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See detailExclusion of the C/D box snoRNA gene cluster HBII-52 from a major role in Prader–Willi syndrome
Runte, Maren UL; Varon, R; Horn, D et al

in Human Genetics (2005), 116(3), 228-230

Detailed reference viewed: 103 (0 UL)
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See detailSNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndrome
Runte, Maren UL; Kroisel, PM; Gillessen-Kaesbach, G et al

in Human Genetics (2004), 114(6), 553-561

Detailed reference viewed: 97 (0 UL)
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See detailComprehensive methylation analysis in typical and atypical PWS and AS patients with normal biparental chromosomes 15
Runte, Maren UL; Faerber, Claudia; Lich, Christina et al

in European Journal of Human Genetics (2001), 9(7), 519-526

Detailed reference viewed: 97 (2 UL)
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See detailThe IC-SNURF–SNRPN transcript serves as a host for multiple small nucleolar RNA species and as an antisense RNA for UBE3A
Runte, Maren UL; Huettenhofer, A; Groß, S et al

in Human Molecular Genetics (2001), 10(23), 2687-2700

Detailed reference viewed: 111 (0 UL)
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See detailThe IL-10 gene is not involved in the predisposition to inflammatory bowel disease.
Klein, Wolfram; Tromm, Andreas; Griga, Thomas et al

in Electrophoresis (2000), 21(17), 3578-3582

Detailed reference viewed: 106 (1 UL)
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See detailEvaluation of RDS/Peripherin and ROM1 as candidate genes in generalised progressive retinal atrophy and exclusion of digenic inheritance
Runte, Maren UL; Dekomien, Gabriele; Epplen, Jörg T

in Animal Genetics (2000), 31(3), 223-227

Detailed reference viewed: 105 (1 UL)
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See detailGeneralized progressive retinal atrophy of Sloughi dogs is due to an 8-bp insertion in exon 21 of the PDE6B gene
Dekomien, Gabriele; Runte, Maren UL; Goedde, René et al

in CytoGenetics and Cell Genetics (2000), 90(3-4), 261-267

Detailed reference viewed: 170 (2 UL)