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Morpholino Publication Database
This database contains citations and abstracts for research using Morpholino oligos, as well as some review articles incorporating Morpholino data. You can search the content using the filter boxes below.
There are 12351 scientific papers returned from the database with the search filters currently being used below.
There are 12351 scientific papers returned from the database with the search filters currently being used below.
Deletion of miR-146a enhances therapeutic protein restoration in model of dystrophin exon skipping
Citation:
Mol Ther Nucleic Acids. 2024 May 24;35(3):102228. doi: 10.1016/j.omtn.2024.102228. eCollection 2024 Sep 10. PMID: 38975000 Epub:
Not Epub Abstract:
Duchenne muscular dystrophy (DMD) is a progressive muscle disease caused by the absence of dystrophin protein. One current DMD... Delivery Method:
intramuscular (i.m.) injection Organism or Cell Type:
mice Citation Extract: McCormack NM, Calabrese KA, Sun CM, Tully CB, Heier CR, Fiorillo AA. Deletion of miR-146a enhances therapeutic protein restoration in model of dystrophin exon skipping. Mol Ther Nucleic Acids. 2024 May 24;35(3):102228. doi: 10.1016/j.omtn.2024.102228. eCollection 2024 Sep 10. PMID: 38975000. |
Neuronal migration prevents spatial competition in retinal morphogenesis
Citation:
Nature. 2023:[Epub ahead of print]. doi:10.1038/s41586-023-06392-y Epub:
Yes Abstract:
The concomitant occurrence of tissue growth and organization is a hallmark of organismal development. This often means that... Organism or Cell Type:
zebrafish Citation Extract: Rocha-Martins M, Nerli E, Kretzschmar J, Weigert M, Icha J, Myers EW, Norden C. Neuronal migration prevents spatial competition in retinal morphogenesis. Nature. 2023:[Epub ahead of print]. doi:10.1038/s41586-023-06392-y. |
Unreprogrammed H3K9me3 prevents minor zygotic genome activation and lineage commitment in SCNT embryos
Citation:
Nat Commun. 2023;14:4807. doi:10.1038/s41467-023-40496-3 Epub:
Not Epub Abstract:
Somatic cell nuclear transfer (SCNT) can be used to reprogram differentiated somatic cells to a totipotent state but has poor... Delivery Method:
microinjection Organism or Cell Type:
mouse zygote Citation Extract: Xu R, Zhu Q, Zhao Y, Chen M, Yang L, Shen S, Yang G, Shi Z, Zhang X, Shi Q, Kou X, Zhao Y, Wang H, Jiang C, Li C, Gao S, Liu X. Unreprogrammed H3K9me3 prevents minor zygotic genome activation and lineage commitment in SCNT embryos. Nat Commun. 2023;14:4807. doi:10.1038/s41467-023-40496-3. |
An integeative GWAS followed by functional investigation reveals possible involvement of CNTNAP5 in glaucomatous neurodegeneration
Citation:
J Neurochem. Poster Sessions A. 2023;166: 30-88. Poster 3A. doi:10.1111/jnc.15896 Epub:
Not Epub Abstract:
Primary angle closure glaucoma (PACG) is one of the major leading causes of blindness. In India, ~30% of people show a narrow... Organism or Cell Type:
zebrafish Citation Extract: Chakraborty S, Roy SS, Sarma J, Das S, Saha S, Bhattacharjee S, Acharya M. An integeative GWAS followed by functional investigation reveals possible involvement of CNTNAP5 in glaucomatous neurodegeneration. J Neurochem. Poster Sessions A. 2023;166: 30-88. Poster 3A. doi:10.1111/jnc.15896. |
Ribo-On and Ribo-Off tools using a self-cleaving ribozyme allow manipulation of endogenous gene expression in C. elegans
Citation:
Commun Biol. 2023;6:816. doi:10.1038/s42003-023-05184-4 Epub:
Not Epub Abstract:
Investigating gene function relies on the efficient manipulation of endogenous gene expression. Currently, a limited number of... Delivery Method:
Vivo-Morpholino Organism or Cell Type:
Caenorhabditis elegans (roundworm) Citation Extract: Fang J, Wang J, Wang Y, Liu X, Chen B, Zou W. Ribo-On and Ribo-Off tools using a self-cleaving ribozyme allow manipulation of endogenous gene expression in C. elegans. Commun Biol. 2023;6:816. doi:10.1038/s42003-023-05184-4. |
The endosomal escape vehicle platform enhances delivery of oligonucleotides in preclinical models of neuromuscular disorders
Citation:
Mol Ther Nucleic Acids. 2023 Jun 29;33:273-285. doi: 10.1016/j.omtn.2023.06.022. eCollection 2023 Sep 12 Epub:
Not Epub Abstract:
Biological therapeutic agents are highly targeted and potent but limited in their ability to reach intracellular targets. These... Delivery Method:
peptide-linked Organism or Cell Type:
mice Citation Extract: Li X, Kheirabadi M, Dougherty PG, Kamer KJ, Shen X, Estrella NL, Peddigari S, Pathak A, Blake SL, Sizensky E, Genio CD, Gaur AB, Dhanabal M, Girgenrath M, Sethuraman N, Qian Z. The endosomal escape vehicle platform enhances delivery of oligonucleotides in preclinical models of neuromuscular disorders. Mol Ther Nucleic Acids. 2023 Jun 29;33:273-285. doi: 10.1016/j.omtn.2023.06.022. eCollection 2023 Sep 12. |
Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach
Citation:
Sci Rep. 2023;13:12576. doi:10.1038/s41598-023-38698-2 Epub:
Not Epub Abstract:
Phosphorodiamidate morpholino oligonucleotides (PMOs) are a promising type of antisense oligonucleotides, but their challenging... Citation Extract: Tsurusaki T, Sato K, Imai H, Hirai K, Takahashi D, Wada T. Convergent synthesis of phosphorodiamidate morpholino oligonucleotides (PMOs) by the H-phosphonate approach. Sci Rep. 2023;13:12576. doi:10.1038/s41598-023-38698-2. |
Alternative splicing of CEACAM1 by hypoxia-inducible factor-1α enhances tolerance to hepatic ischemia in mice and humans
Citation:
Sci Transl Med. 2023 Aug 2;15(707):eadf2059. doi: 10.1126/scitranslmed.adf2059. Epub 2023 Aug 2. PMID: 37531413 Epub:
Not Epub Abstract:
Although alternative splicing (AS) drives transcriptional responses and cellular adaptation to environmental stresses, its... Delivery Method:
Vivo-Morpholino Organism or Cell Type:
mice Citation Extract: Dery KJ, Kojima H, Kageyama S, Kadono K, Hirao H, Cheng B, Zhai Y, Farmer DG, Kaldas FM, Yuan X, Eltzschig HK, Kupiec-Weglinski JW. Alternative splicing of CEACAM1 by hypoxia-inducible factor-1α enhances tolerance to hepatic ischemia in mice and humans. Sci Transl Med. 2023 Aug 2;15(707):eadf2059. doi: 10.1126/scitranslmed.adf2059. Epub 2023 Aug 2. PMID: 37531413. |
Aicardi Syndrome Is a Genetically Heterogeneous Disorder
Citation:
Genes. 2023;14(8):1565. doi:10.3390/genes14081565 Epub:
Not Epub Abstract:
Aicardi Syndrome (AIC) is a rare neurodevelopmental disorder recognized by the classical triad of agenesis of the corpus... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Ha TT, Burgess R, Newman M, Moey C, Mandelstam SA, Gardner AE, Ivancevic AM, Pham D, Kumar R, Smith N, Patel C, Malone S, Ryan MM, Calvert S, van Eyk CL, Lardelli M, Berkovic SF, Leventer RJ, Richards LJ, Scheffer IE, Gecz J, Corbett MA. Aicardi Syndrome Is a Genetically Heterogeneous Disorder. Genes. 2023;14(8):1565. doi:10.3390/genes14081565. |
Recognition of H2AK119ub plays an important role in RSF1-regulated early Xenopus development
Citation:
Front Cell Dev Biol. 2023 Jul 17;11:1168643. doi: 10.3389/fcell.2023.1168643. eCollection 2023 Epub:
Not Epub Abstract:
Polycomb group (PcG) proteins are key regulators of gene expression and developmental programs via covalent modification of... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Parast SM, Yu D, Chen C, Dickinson AJ, Chang C, Wang H. Recognition of H2AK119ub plays an important role in RSF1-regulated early Xenopus development. Front Cell Dev Biol. 2023 Jul 17;11:1168643. doi: 10.3389/fcell.2023.1168643. eCollection 2023. |