Bé Wieringa
Affiliations: | Cell Biology | Radboud University Nijmegen, Nijmegen, Gelderland, Netherlands |
Area:
Energy & Redox MetabolismWebsite:
http://ncmls.nl/people/wieringa/Google:
"Bé Wieringa"Bio:
https://www.radboudumc.nl/OverhetRadboudumc/Hoogleraren/Pages/BerendWieringa.aspx
http://www.systembiology.net/sbnl/NLgroups/Wieringagroup.htm
http://alba.ub.rug.nl/promotorum/?page=showPerson&promovendus_id=2657
Mean distance: 12.21 | S | N | B | C | P |
Cross-listing: Cell Biology Tree
Children
Sign in to add traineeFrans P.M. Cremers | grad student | 1991 | Radboud University Nijmegen (Cell Biology Tree) |
Han G. Brunner | grad student | 1993 | Radboud University Nijmegen (Cell Biology Tree) |
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Publications
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André LM, van Cruchten RTP, Willemse M, et al. (2019) Recovery in the Myogenic Program of Congenital Myotonic Dystrophy Myoblasts after Excision of the Expanded (CTG) Repeat. International Journal of Molecular Sciences. 20 |
van Cruchten RTP, Wieringa B, Wansink DG. (2019) Expanded CUG repeats in transcripts adopt diverse hairpin conformations without influencing the structure of the flanking sequences. Rna (New York, N.Y.). 25: 481-495 |
André LM, Ausems CRM, Wansink DG, et al. (2018) Abnormalities in Skeletal Muscle Myogenesis, Growth, and Regeneration in Myotonic Dystrophy. Frontiers in Neurology. 9: 368 |
Gudde AEEG, van Kessel IDG, André LM, et al. (2017) Trinucleotide-repeat expanded and normal DMPK transcripts contain unusually long poly(A) tails despite differential nuclear residence. Biochimica Et Biophysica Acta |
van Agtmaal EL, André LM, Willemse M, et al. (2017) CRISPR/Cas9-Induced (CTG⋅CAG)n Repeat Instability in the Myotonic Dystrophy Type 1 Locus: Implications for Therapeutic Genome Editing. Molecular Therapy : the Journal of the American Society of Gene Therapy. 25: 24-43 |
Gudde AE, van Heeringen SJ, de Oude AI, et al. (2017) Antisense transcription of the myotonic dystrophy locus yields low-abundant RNAs with and without (CAG)n repeat. Rna Biology. 0 |
Gudde AE, González-Barriga A, van den Broek WJ, et al. (2016) A low absolute number of expanded transcripts is involved in myotonic dystrophy type 1 manifestation in muscle. Human Molecular Genetics |
González-Barriga A, Kranzen J, Croes HJ, et al. (2015) Cell membrane integrity in myotonic dystrophy type 1: implications for therapy. Plos One. 10: e0121556 |
González-Barriga A, Kranzen J, Croes HJE, et al. (2014) G.P.131: Cell membrane integrity in myotonic dystrophy type 1: Implications for therapy Neuromuscular Disorders. 24: 840 |
González-Barriga A, Mulders SA, van de Giessen J, et al. (2013) Design and analysis of effects of triplet repeat oligonucleotides in cell models for myotonic dystrophy. Molecular Therapy. Nucleic Acids. 2: e81 |