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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 12176 scientific papers returned from the database with the search filters currently being used below.

Zinc transporter Slc30a1 regulates melanocyte development by interacting with mt2 in zebrafish

Authors:
Xia Z, Yang X, Bi X, Tong X, Min J, Wang F
Citation:
Eur J Cell Biol. 2022;101(4):151272. doi:10.1016/j.ejcb.2022.151272
Epub:
Not Epub
Abstract:
The essential trace element zinc is involved in multiple biological processes including development and metabolism, while its...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Xia Z, Yang X, Bi X, Tong X, Min J, Wang F. Zinc transporter Slc30a1 regulates melanocyte development by interacting with mt2 in zebrafish. Eur J Cell Biol. 2022;101(4):151272. doi:10.1016/j.ejcb.2022.151272.

Evaluation of phages and liposomes as combination therapy to counteract Pseudomonas aeruginosa infection in wild-type and CFTR-null models

Authors:
Cafora M, Poerio N, Forti F, Loberto N, Pin D, Bassi R, Aureli M, Briani F, Pistocchi A, Fraziano M
Citation:
Front Microbiol. 2022;13:979610. doi:10.3389/fmicb.2022.979610
Epub:
Not Epub
Abstract:
Multi drug resistant (MDR) bacteria are insensitive to the most common antibiotics currently in use. The spread of antibiotic-...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Cafora M, Poerio N, Forti F, Loberto N, Pin D, Bassi R, Aureli M, Briani F, Pistocchi A, Fraziano M. Evaluation of phages and liposomes as combination therapy to counteract Pseudomonas aeruginosa infection in wild-type and CFTR-null models. Front Microbiol. 2022;13:979610. doi:10.3389/fmicb.2022.979610.

A self-generated Toddler gradient guides mesodermal cell migration

Authors:
Stock J, Kazmar T, Schlumm F, Hannezo E, Pauli A
Citation:
Sci Adv. 2022 Sep 16;8(37):eadd2488. doi: 10.1126/sciadv.add2488. Epub 2022 Sep 14
Epub:
Not Epub
Abstract:
The sculpting of germ layers during gastrulation relies on the coordinated migration of progenitor cells, yet the cues...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Stock J, Kazmar T, Schlumm F, Hannezo E, Pauli A. A self-generated Toddler gradient guides mesodermal cell migration. Sci Adv. 2022 Sep 16;8(37):eadd2488. doi: 10.1126/sciadv.add2488. Epub 2022 Sep 14.

Effects of pharmacological and genetic manipulation of glucocorticoids during early development of the zebrafish embryo

Authors:
Wilson K, Matrone G, Tucker C, Hadoke P, Kenyon C, Mullins J, Denvir M
Citation:
Endocrine Abstracts. 2013;32:P336 doi:10.1530/endoabs.32.P336
Epub:
Not Epub
Abstract:
Background: The effects of glucocorticoids (GC) on the developing zebrafish embryo (Zfe) are poorly characterised. We have...
Organism or Cell Type:
zebrafish
Citation Extract:
Wilson K, Matrone G, Tucker C, Hadoke P, Kenyon C, Mullins J, Denvir M. Effects of pharmacological and genetic manipulation of glucocorticoids during early development of the zebrafish embryo. Endocrine Abstracts. 2013;32:P336 doi:10.1530/endoabs.32.P336.

Selenoprotein deficiency disorder predisposes to aortic aneurysm formation

Authors:
Schoenmakers E, Marelli F, Jørgensen H, Visser WE, Moran C, Groeneweg S, Avalos C, Figg N, Finigan A, Wali N, Agostini M, Wardle-Jones H, Lyons G, Rusk R, Gopalan D, Visser JJ, Goddard M, Nashef S, Heijmen R, Clift P, Sinha S, Busch-Nentwich E, Ramirez-Solis R, Persani L, Bennett M, Chatterjee K
Citation:
Endocrine Abstracts. 2022;84;OP01-04 doi:10.1530/endoabs.84.OP-01-04
Epub:
Not Epub
Abstract:
Objectives: Mutations in SECISBP2 cause deficiency of selenoproteins, resulting in a multisystem disorder with abnormal...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Schoenmakers E, Marelli F, Jørgensen H, Visser WE, Moran C, Groeneweg S, Avalos C, Figg N, Finigan A, Wali N, Agostini M, Wardle-Jones H, Lyons G, Rusk R, Gopalan D, Visser JJ, Goddard M, Nashef S, Heijmen R, Clift P, Sinha S, Busch-Nentwich E, Ramirez-Solis R, Persani L, Bennett M, Chatterjee K. Selenoprotein deficiency disorder predisposes to aortic aneurysm formation. Endocrine Abstracts. 2022;84;OP01-04 doi:10.1530/endoabs.84.OP-01-04.

Programming of pluripotency and the germ line co-evolved from a Nanog ancestor

Authors:
Crowley D, Simpson L, Chatfield J, Forey T, Allegrucci C, Sang F, Holmes N, Genikhovich G, Technau U, Cunningham D, Silva E, Mullin N, Dixon JE, Loose M, Alberio R, Johnson AD.
Citation:
Cell Rep. 2025 Mar 25;44(3):115396. doi: 10.1016/j.celrep.2025.115396. Epub 2025 Mar 8. PMID: 40057954
Epub:
Not Epub
Abstract:
Francois Jacob proposed that evolutionary novelty arises through incremental tinkering with pre-existing genetic mechanisms....
Delivery Method:
microinjection
Organism or Cell Type:
Ambystoma mexicanum (axolotl)
Citation Extract:
Crowley D, Simpson L, Chatfield J, Forey T, Allegrucci C, Sang F, Holmes N, Genikhovich G, Technau U, Cunningham D, Silva E, Mullin N, Dixon JE, Loose M, Alberio R, Johnson AD. . Programming of pluripotency and the germ line co-evolved from a Nanog ancestor. Cell Rep. 2025 Mar 25;44(3):115396. doi: 10.1016/j.celrep.2025.115396. Epub 2025 Mar 8. PMID: 40057954.

RBFOX1 and working memory: from genome to transcriptome revealed post-transcriptional mechanism separate from ADHD

Authors:
Zhong Y, Zhang N, Zhao F, Chang S, Chen W, Cao Q, Sun L, Wang Y, Gong Z, Lu L, Liu D, Yang L
Citation:
Biol Psychiatry. 2022;[Epub ahead of print] doi:10.1016/j.bpsgos.2022.08.006
Epub:
Not Epub
Abstract:
BACKGROUND: Many psychiatric disorders share working memory (WM) impairment phenotype, yet the genetic causes remain unclear....
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Zhong Y, Zhang N, Zhao F, Chang S, Chen W, Cao Q, Sun L, Wang Y, Gong Z, Lu L, Liu D, Yang L. RBFOX1 and working memory: from genome to transcriptome revealed post-transcriptional mechanism separate from ADHD. Biol Psychiatry. 2022;[Epub ahead of print] doi:10.1016/j.bpsgos.2022.08.006.

A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly

Authors:
Bartoszewski S, Dawidziuk M, Kasica N, Durak R, Jurek M, Podwysocka A, Guilbride DL, Podlasz P, Winata CL, Gawlinski P
Citation:
Cells. 2022 Sep 1;11(17):2727. doi: 10.3390/cells11172727
Epub:
Not Epub
Abstract:
Microcephaly presents in neurodevelopmental disorders with multiple aetiologies, including bi-allelic mutation in TUBGCP2, a...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Bartoszewski S, Dawidziuk M, Kasica N, Durak R, Jurek M, Podwysocka A, Guilbride DL, Podlasz P, Winata CL, Gawlinski P. A Zebrafish/Drosophila Dual System Model for Investigating Human Microcephaly. Cells. 2022 Sep 1;11(17):2727. doi: 10.3390/cells11172727.

eif4ebp3l-A New Affector of Zebrafish Angiogenesis and Heart Regeneration?

Authors:
Born LI, Andree T, Frank S, Hübner J, Link S, Langheine M, Charlet A, Esser JS, Brehm R, Moser M
Citation:
Int J Mol Sci. 2022 Sep 3;23(17):10075. doi: 10.3390/ijms231710075
Epub:
Not Epub
Abstract:
The eukaryotic initiation factor 4E binding protein (4E-BP) family is involved in translational control of cell proliferation...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Born LI, Andree T, Frank S, Hübner J, Link S, Langheine M, Charlet A, Esser JS, Brehm R, Moser M. eif4ebp3l-A New Affector of Zebrafish Angiogenesis and Heart Regeneration?. Int J Mol Sci. 2022 Sep 3;23(17):10075. doi: 10.3390/ijms231710075.

Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia

Authors:
Guernsey DL, Jiang H, Campagna DR, Evans SC, Ferguson M, Kellogg MD, Lachance M, Matsuoka M, Nightingale M, Rideout A, Saint-Amant L, Schmidt PJ, Orr A, Bottomley SS, Fleming MD, Ludman M, Dyack S, Fernandez CV, Samuels ME
Citation:
Nat Genet. 2009 Jun;41(6):651-3. doi: 10.1038/ng.359. Epub 2009 May 3
Epub:
Not Epub
Abstract:
The sideroblastic anemias are a heterogeneous group of congenital and acquired hematological disorders whose morphological...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Guernsey DL, Jiang H, Campagna DR, Evans SC, Ferguson M, Kellogg MD, Lachance M, Matsuoka M, Nightingale M, Rideout A, Saint-Amant L, Schmidt PJ, Orr A, Bottomley SS, Fleming MD, Ludman M, Dyack S, Fernandez CV, Samuels ME. Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemia. Nat Genet. 2009 Jun;41(6):651-3. doi: 10.1038/ng.359. Epub 2009 May 3.

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