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Advanced Drug Delivery Reviews, ISSN 0169-409X, 06/2015, Volume 87, pp. 90 - 103
Journal Article
Journal Article
Genes, ISSN 2073-4425, 05/2019, Volume 10, Issue 5, p. 363
The recurrent missense variant in Nuclear Receptor Subfamily 2 Group E Member 3 (NR2E3), c.166G>A, p.(Gly56Arg) or G56R, underlies 1%-2% of cases with... 
putative dominant negative effect | retinitis pigmentosa | G56R | allele-specific knockdown | autosomal dominant | NR2E3 | gapmer antisense oligonucleotides
Journal Article
Current Opinion in Ophthalmology, ISSN 1040-8738, 2017, Volume 28, Issue 3, pp. 260 - 266
Journal Article
Molecular Therapy - Nucleic Acids, ISSN 2162-2531, 09/2017, Volume 8, pp. 416 - 427
Dominant-negative mutations in the genes that encode the three major α chains of collagen type VI, , , and , account for more than 50% of Ullrich congenital... 
collagen VI | congenital muscular dystrophy | antisense oligonucleotide therapy | allele-specific silencing | gapmer | dominant mutations | RNASE H1 | MEDICINE, RESEARCH & EXPERIMENTAL | DOSE-ESCALATION | VI-RELATED MYOPATHIES | NEUROMUSCULAR DISEASE | GENE-EXPRESSION | COLLAGEN-VI | OPEN-LABEL | DOMINANT | NATURAL-HISTORY | FIBROBLASTS
Journal Article
ANALYTICA CHIMICA ACTA, ISSN 0003-2670, 11/2007, Volume 603, Issue 1, pp. 82 - 86
A general approach that allows reliable detection of a single base-pair mismatch is presented. Specifically, how important a careful design of the... 
CHEMISTRY, ANALYTICAL | SEQUENCES | DNA | mismatch | enzyme label | ELECTRODES | SNPS | HYBRIDIZATION | electrochemical genosensor | allele-specific oligonucleotide | hybridisation stringency
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 07/2001, Volume 285, Issue 2, pp. 188 - 194
Journal Article
Journal Article
Journal Article