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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 10164 scientific papers returned from the database with the search filters currently being used below.

If you know of a publication that is not in this database and you feel it should be, please submit a new publication to the database and we'll get it in there.

Two Quantitative Assays for the Phosphorodiamidate Morpholino Oligomer (PMO) SRP-4045 in Mouse Plasma Using HPLC-MS/MS Coupled with Solid Phase Micro-Extraction

Authors:
Liu A, Zhang J, Zhao N, Burton S, Carver M, Liu S, Meng M, SReuschel S, Voelker T
Citation:
Presented at ASMS Conference on Mass Spectrometry and Allied Topics, San Antonio, Texas, June 5-9, 2016
Abstract:
Phosphorodiamidate morpholino oligomers (PMO) are among the most advanced antisense therapeutics and a promising strategy for...
Organism or Cell Type:
mice
Citation Extract:
Liu A, Zhang J, Zhao N, Burton S, Carver M, Liu S, Meng M, SReuschel S, Voelker T. Two Quantitative Assays for the Phosphorodiamidate Morpholino Oligomer (PMO) SRP-4045 in Mouse Plasma Using HPLC-MS/MS Coupled with Solid Phase Micro-Extraction. Presented at ASMS Conference on Mass Spectrometry and Allied Topics, San Antonio, Texas, June 5-9, 2016.

Downregulation of p16 decreases biliary damage and liver fibrosis in the Mdr2-/- mouse model of primary sclerosing cholangitis

Authors:
Kyritsi K, Francis H, Zhou T, Ceci L, Wu N, Yhang Z, Meng F, Chen L, Baiocchi L, Kundu D, Kennedy L, Liangpunsakul S, Wu C, Glaser S, Alpini G
Citation:
Gene Expr. 2020 May 11. doi: 10.3727/105221620X15889714507961. [Epub ahead of print]
Abstract:
Biliary senescence and hepatic fibrosis are hallmarks of cholangiopathies including primary sclerosing cholangitis (PSC)....
Delivery Method:
Vivo-Morpholino
Organism or Cell Type:
mice
Citation Extract:
Kyritsi K, Francis H, Zhou T, Ceci L, Wu N, Yhang Z, Meng F, Chen L, Baiocchi L, Kundu D, Kennedy L, Liangpunsakul S, Wu C, Glaser S, Alpini G. Downregulation of p16 decreases biliary damage and liver fibrosis in the Mdr2-/- mouse model of primary sclerosing cholangitis. Gene Expr. 2020 May 11. doi: 10.3727/105221620X15889714507961. [Epub ahead of print].

The micropeptide LEMP plays an evolutionarily conserved role in myogenesis

Authors:
Wang L, Fan J, Han L, Qi H, Wang Y, Wang H, Chen S, Du L, Li S, Zhang Y, Tang W, Ge G, Pan W, Hu P, Cheng H
Citation:
Cell Death Dis. 2020;11:357. doi:10.1038/s41419-020-2570-5
Abstract:
In recent years, micropeptides have been increasingly identified as important regulators in various biological processes....
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Wang L, Fan J, Han L, Qi H, Wang Y, Wang H, Chen S, Du L, Li S, Zhang Y, Tang W, Ge G, Pan W, Hu P, Cheng H. The micropeptide LEMP plays an evolutionarily conserved role in myogenesis. Cell Death Dis. 2020;11:357. doi:10.1038/s41419-020-2570-5.

Effective Pseudo-Exon Skipping of a COL6A1 Intronic Mutation in Cultured Muscle Interstitial Fibroblasts from a Novel Humanized Mouse Model

Authors:
Bolduc V, Guirguis F, Aguti S, Zhou H, Cheng J, Garrett L, Muntoni F, Bönnemann CG
Citation:
Molec Ther. 2020;28(4S1):401. abstract 925. doi:10.1016/j.ymthe.2020.04.019
Abstract:
Collagen VI-related dystrophies (COL6-RDs) are a group of frequently severe, congenital-onset muscular dystrophies for which...
Delivery Method:
Vivo-Morpholino
Organism or Cell Type:
mice
Citation Extract:
Bolduc V, Guirguis F, Aguti S, Zhou H, Cheng J, Garrett L, Muntoni F, Bönnemann CG. Effective Pseudo-Exon Skipping of a COL6A1 Intronic Mutation in Cultured Muscle Interstitial Fibroblasts from a Novel Humanized Mouse Model. Molec Ther. 2020;28(4S1):401. abstract 925. doi:10.1016/j.ymthe.2020.04.019.

A Reversible RNA On-Switch That Controls Expression of Aav-Delivered Transgenes In Vivo

Authors:
Zhong G, Wang H, Farzan M
Citation:
Molec Ther. 2020;28(4S1):224. abstract 510. doi:10.1016/j.ymthe.2020.04.019
Abstract:
Widespread use of gene therapy technologies is limited in part by the lack of small genetic switches with wide dynamic ranges...
Delivery Method:
Vivo-Morpholino
Organism or Cell Type:
mice
Citation Extract:
Zhong G, Wang H, Farzan M. A Reversible RNA On-Switch That Controls Expression of Aav-Delivered Transgenes In Vivo. Molec Ther. 2020;28(4S1):224. abstract 510. doi:10.1016/j.ymthe.2020.04.019.

Development of a Minimized Exons 45-55 Skipping Cocktail for the Treatment of Duchenne Muscular Dystrophy

Authors:
Lim KRQ, Huang Y, Maruyama R, Woo S, Dzierlega K, Moulton H, Yokota T
Citation:
Molec Ther. 2020;28(4S1):113 abstract 237. doi:10.1016/j.ymthe.2020.04.019
Abstract:
Duchenne muscular dystrophy (DMD) is a fatal X-linked recessive neuromuscular disorder characterized by...
Delivery Method:
peptide-linked
Organism or Cell Type:
mice
Citation Extract:
Lim KRQ, Huang Y, Maruyama R, Woo S, Dzierlega K, Moulton H, Yokota T. Development of a Minimized Exons 45-55 Skipping Cocktail for the Treatment of Duchenne Muscular Dystrophy. Molec Ther. 2020;28(4S1):113 abstract 237. doi:10.1016/j.ymthe.2020.04.019.

Restoration of Full-Length Dystrophin Expression in the Dup2 Mouse Induced by Systemic Delivery of a Peptide-Conjugated Morpholino Oligomer

Authors:
Gushchina LV, Grounds KM, Huang N, Frair E, Schnell FJ, Hanson GJ, Simmons T, Wein N, Flanigan KM
Citation:
Molec Ther. 2020;28(4S1):20 abstract 39. doi:10.1016/j.ymthe.2020.04.019
Abstract:
Duchenne muscular dystrophy (DMD) is an x-linked recessive genetic disorder caused by mutations that disrupt the...
Delivery Method:
peptide-linked
Organism or Cell Type:
mice
Citation Extract:
Gushchina LV, Grounds KM, Huang N, Frair E, Schnell FJ, Hanson GJ, Simmons T, Wein N, Flanigan KM. Restoration of Full-Length Dystrophin Expression in the Dup2 Mouse Induced by Systemic Delivery of a Peptide-Conjugated Morpholino Oligomer. Molec Ther. 2020;28(4S1):20 abstract 39. doi:10.1016/j.ymthe.2020.04.019.

Pharyngeal pouches provide a niche microenvironment for arch artery progenitor specification

Authors:
Mao A, Li L, Liu J, Mingming Z, Ning G, Cao Y, Wang Q
Citation:
bioRxiv. 2020;[preprint] doi:10.1101/2020.05.07.083493
Abstract:
The paired pharyngeal arch arteries (PAAs) are transient blood vessels connecting the heart with the dorsal aorta during...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Mao A, Li L, Liu J, Mingming Z, Ning G, Cao Y, Wang Q. Pharyngeal pouches provide a niche microenvironment for arch artery progenitor specification. bioRxiv. 2020;[preprint] doi:10.1101/2020.05.07.083493.

Furry is required for cell movements during gastrulation and functionally interacts with NDR1

Authors:
Cervino AS, Moretti B, Stuckenholz C, Grecco HE, Davidson LA, Cirio MC
Citation:
bioRxiv. 2020;[preprint] doi:10.1101/2020.05.08.083980
Abstract:
Gastrulation is a key event in animal embryogenesis during which the germ layers precursors are rearranged and the embryonic...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Cervino AS, Moretti B, Stuckenholz C, Grecco HE, Davidson LA, Cirio MC. Furry is required for cell movements during gastrulation and functionally interacts with NDR1. bioRxiv. 2020;[preprint] doi:10.1101/2020.05.08.083980.

Aryl hydrocarbon receptor mediates larval zebrafish fin duplication following exposure to benzofluoranthenes

Authors:
Garland MA, Geier MC, Bugel SM, Shankar P, Dunham CL, Brown JM, Tilton SC, Tanguay RL
Citation:
Toxicol Sci. 2020 May 8. pii: kfaa063. doi: 10.1093/toxsci/kfaa063. [Epub ahead of print]
Abstract:
The aryl hydrocarbon receptor (AHR) mediates developmental toxicity of several xenobiotic classes including polycyclic aromatic...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Garland MA, Geier MC, Bugel SM, Shankar P, Dunham CL, Brown JM, Tilton SC, Tanguay RL. Aryl hydrocarbon receptor mediates larval zebrafish fin duplication following exposure to benzofluoranthenes. Toxicol Sci. 2020 May 8. pii: kfaa063. doi: 10.1093/toxsci/kfaa063. [Epub ahead of print].

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