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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 12132 scientific papers returned from the database with the search filters currently being used below.

A 50 kdyne contusion spinal cord injury with or without the drug SS‐31 was not associated with major changes in muscle mass or gene expression 14 d after injury in young male mice

Authors:
Graham ZA, DeBerry JJ, Cardozo CP, Bamman MM
Citation:
Physiol Rep. 2021;9(4)e14751 doi:/10.14814/phy2.14751
Epub:
Not Epub
Abstract:
Spinal cord injury (SCI) leads to rapid muscle atrophy due to paralysis/paresis and subsequent disuse. SS‐31 is a mitochondrial...
Organism or Cell Type:
cell culture: C2C12
Citation Extract:
Graham ZA, DeBerry JJ, Cardozo CP, Bamman MM. A 50 kdyne contusion spinal cord injury with or without the drug SS‐31 was not associated with major changes in muscle mass or gene expression 14 d after injury in young male mice. Physiol Rep. 2021;9(4)e14751 doi:/10.14814/phy2.14751.

Visualization of Transcriptional Activity in Early Zebrafish Primordial Germ Cells

Authors:
D'Orazio FM, Jasiulewicz A, Hadzhiev Y, Müller F
Citation:
Methods Mol Biol. 2021;2218:185-194. doi: 10.1007/978-1-0716-0970-5_15
Epub:
Not Epub
Abstract:
Here, we describe a fast and straightforward methodology to in vivo detect transcriptional activity in the early zebrafish germ...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
D'Orazio FM, Jasiulewicz A, Hadzhiev Y, Müller F. Visualization of Transcriptional Activity in Early Zebrafish Primordial Germ Cells. Methods Mol Biol. 2021;2218:185-194. doi: 10.1007/978-1-0716-0970-5_15.

In Vitro Induction of Teleost PGCs

Authors:
Robles V, Valcarce DG, Riesco MF
Citation:
Methods Mol Biol. 2021;2218:75-83. doi:10.1007/978-1-0716-0970-5_7
Epub:
Not Epub
Abstract:
Primordial germ cells (PGCs) are unique cells in an embryo. These cells contain all genetic information and therefore represent...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Robles V, Valcarce DG, Riesco MF. In Vitro Induction of Teleost PGCs. Methods Mol Biol. 2021;2218:75-83. doi:10.1007/978-1-0716-0970-5_7.

Antisense Oligonucleotide Treatment in a Humanized Mouse Model of Duchenne Muscular Dystrophy and Highly Sensitive Detection of Dystrophin Using Western Blotting

Authors:
Maruyama R, Yokota T
Citation:
Methods Mol Biol. 2021;2224:203-214. doi: 10.1007/978-1-0716-1008-4_15
Epub:
Not Epub
Abstract:
Duchenne muscular dystrophy (DMD) is a devastating X-linked muscle disorder affecting many children. The disease is caused by...
Delivery Method:
injection
Organism or Cell Type:
mice
Citation Extract:
Maruyama R, Yokota T. Antisense Oligonucleotide Treatment in a Humanized Mouse Model of Duchenne Muscular Dystrophy and Highly Sensitive Detection of Dystrophin Using Western Blotting. Methods Mol Biol. 2021;2224:203-214. doi: 10.1007/978-1-0716-1008-4_15.

Heterochromatin protein 1 beta (HP1β) regulates neural and neural crest development by repressing pluripotency-associated gene pou5f3.2/oct25 in Xenopus

Authors:
Tien CL, Mohammadparast S, Chang C
Citation:
Dev Dyn. 2021 Feb 17. doi: 10.1002/dvdy.319. Online ahead of print
Epub:
Yes
Abstract:
Background: Heterochromatin protein 1 (HP1) is associated with and plays a role in compact chromatin conformation, but the...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Tien CL, Mohammadparast S, Chang C. Heterochromatin protein 1 beta (HP1β) regulates neural and neural crest development by repressing pluripotency-associated gene pou5f3.2/oct25 in Xenopus. Dev Dyn. 2021 Feb 17. doi: 10.1002/dvdy.319. Online ahead of print.

Using linkage logic theory to control dynamics of a gene regulatory network of a chordate embryo

Authors:
Kobayashi K, Maeda K, Tokuoka M, Mochizuki A, Satou Y
Citation:
Sci Rep. 2021;11(1):4001. doi:10.1038/s41598-021-83045-y
Epub:
Not Epub
Abstract:
Linkage logic theory provides a mathematical criterion to control network dynamics by manipulating activities of a subset of...
Delivery Method:
microinjection
Organism or Cell Type:
Ciona intestinalis (ascidian)
Citation Extract:
Kobayashi K, Maeda K, Tokuoka M, Mochizuki A, Satou Y. Using linkage logic theory to control dynamics of a gene regulatory network of a chordate embryo. Sci Rep. 2021;11(1):4001. doi:10.1038/s41598-021-83045-y.

A Zebrafish Forward Genetic Screen Identifies an Indispensible Threonine Residue in the Kinase Domain of PRKD2

Authors:
Giardoglou P, Bournele D, Park M, Kanoni S, Dedoussis GV, Steinberg SF, Deloukas P, Beis D
Citation:
Bio Open. 2021;bio.058542 doi:10.1242/bio.058542
Epub:
Not Epub
Abstract:
Protein Kinase D2 belongs to a family of evolutionarily conserved enzymes regulating several biological processes. In a forward...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Giardoglou P, Bournele D, Park M, Kanoni S, Dedoussis GV, Steinberg SF, Deloukas P, Beis D. A Zebrafish Forward Genetic Screen Identifies an Indispensible Threonine Residue in the Kinase Domain of PRKD2. Bio Open. 2021;bio.058542 doi:10.1242/bio.058542.

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome

Authors:
Mann N, Mzoughi S, Schneider R, Kühl SJ, Schanze D, Klämbt V, Lovric S, Mao Y, Shi S, Tan W, Kühl M, Onuchic-Whitford AC, Treimer E, Kitzler TM, Kause F, Schumann S, Nakayama M, Buerger F, Shril S, van der Ven AT, Majmundar AJ, Holton KM, Kolb A, Braun DA, Rao J, Jobst-Schwan T, Mildenberger E, Lennert T, Kuechler A, Wieczorek D, Gross O, Ermisch-Omran B, Werberger A, Skalej M, Janecke AR, Soliman NA, Mane SM, Lifton RP, Kadlec J, Guccione E, Schmeisser MJ, Zenker M, Hildebrandt F
Citation:
J Am Soc Nephrol. 2021 Mar;32(3):580-596. doi: 10.1681/ASN.2020040490
Epub:
Not Epub
Abstract:
Background: Galloway-Mowat syndrome (GAMOS) is characterized by neurodevelopmental defects and a progressive nephropathy, which...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus
Citation Extract:
Mann N, Mzoughi S, Schneider R, Kühl SJ, Schanze D, Klämbt V, Lovric S, Mao Y, Shi S, Tan W, Kühl M, Onuchic-Whitford AC, Treimer E, Kitzler TM, Kause F, Schumann S, Nakayama M, Buerger F, Shril S, van der Ven AT, Majmundar AJ, Holton KM, Kolb A, Braun DA, Rao J, Jobst-Schwan T, Mildenberger E, Lennert T, Kuechler A, Wieczorek D, Gross O, Ermisch-Omran B, Werberger A, Skalej M, Janecke AR, Soliman NA, Mane SM, Lifton RP, Kadlec J, Guccione E, Schmeisser MJ, Zenker M, Hildebrandt F. Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome. J Am Soc Nephrol. 2021 Mar;32(3):580-596. doi: 10.1681/ASN.2020040490.

Functional identification of an opsin kinase underlying inactivation of the pineal bistable opsin parapinopsin in zebrafish

Authors:
Shen B, Wada S, Nishioka H, Nagata T, Kawano-Yamashita E, Koyanagi M, Terakita A
Citation:
Zoological Lett. 2021;7(1),1. doi:10.1186/s40851-021-00171-1
Epub:
Not Epub
Abstract:
In the pineal organ of zebrafish larvae, the bistable opsin parapinopsin alone generates color opponency between UV and visible...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Shen B, Wada S, Nishioka H, Nagata T, Kawano-Yamashita E, Koyanagi M, Terakita A. Functional identification of an opsin kinase underlying inactivation of the pineal bistable opsin parapinopsin in zebrafish. Zoological Lett. 2021;7(1),1. doi:10.1186/s40851-021-00171-1.

Highly sensitive screening of antisense sequences for different types of DMD mutations in patients' urine-derived cells

Authors:
Takizawa H, Takeshita E, Sato M, Shimizu-Motohashi Y, Ishiyama A, Mori-Yoshimura M, Takahashi Y, Komaki H, Aoki Y
Citation:
J Neurol Sci. 2021;[Epub ahead of print] doi:10.1016/j.jns.2021.117337
Epub:
Not Epub
Abstract:
Exon skipping using short antisense oligonucleotides (AONs) is a promising treatment for Duchenne muscular dystrophy (DMD)....
Delivery Method:
Endo-Porter, electroporation
Organism or Cell Type:
cell culture: UDC-myotubes, rhabdomyosarcoma cells, human skeletal myoblasts
Citation Extract:
Takizawa H, Takeshita E, Sato M, Shimizu-Motohashi Y, Ishiyama A, Mori-Yoshimura M, Takahashi Y, Komaki H, Aoki Y. Highly sensitive screening of antisense sequences for different types of DMD mutations in patients' urine-derived cells. J Neurol Sci. 2021;[Epub ahead of print] doi:10.1016/j.jns.2021.117337.

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