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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 12376 scientific papers returned from the database with the search filters currently being used below.
There are 12376 scientific papers returned from the database with the search filters currently being used below.
A combinatorial code of maternal GATA, Ets and beta-catenin-TCF transcription factors specifies and patterns the early ascidian ectoderm
Citation:
Development. 2007 Nov;134(22):4023-32 Epub:
Not Epub Abstract:
Our understanding of the maternal factors that initiate early chordate development, and of their direct zygotic targets, is... Organism or Cell Type:
Ciona intestinalis Citation Extract: Rothbächer U, Bertrand V, Lamy C, Lemaire P. A combinatorial code of maternal GATA, Ets and beta-catenin-TCF transcription factors specifies and patterns the early ascidian ectoderm. Development. 2007 Nov;134(22):4023-32. |
A Framework for the Establishment of a Cnidarian Gene Regulatory Network for “Endomesoderm” Specification: The Inputs of ß-Catenin/TCF Signaling
Citation:
PLoS Genet. 2012;8(12):e1003164. doi:10.1371/journal.pgen.1003164 Epub:
Not Epub Abstract:
Understanding the functional relationship between intracellular factors and extracellular signals is required for... Delivery Method:
Microinjection Organism or Cell Type:
Nematostella vectensis (cnidarian) Citation Extract: Röttinger E, Dahlin P, Martindale MQ. A Framework for the Establishment of a Cnidarian Gene Regulatory Network for “Endomesoderm” Specification: The Inputs of ß-Catenin/TCF Signaling. PLoS Genet. 2012;8(12):e1003164. doi:10.1371/journal.pgen.1003164. |
A genetic screen in zebrafish identifies the mutants vps18, nf2 and foie gras as models of liver disease.
Citation:
Development. 2005 Aug;132(15):3561-72. Epub 2005 Jul 6. Epub:
Not Epub Abstract:
Hepatomegaly is a sign of many liver disorders. To identify zebrafish mutants to serve as models for hepatic pathologies, we... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Sadler KC, Amsterdam A, Soroka C, Boyer J, Hopkins N.. A genetic screen in zebrafish identifies the mutants vps18, nf2 and foie gras as models of liver disease.. Development. 2005 Aug;132(15):3561-72. Epub 2005 Jul 6.. |
A Key Role for Poly(ADP-Ribose) Polymerase 3 in Ectodermal Specification and Neural Crest Development
Citation:
PLoS ONE. 2011;6(1):e15834. doi:10.1371/journal.pone.0015834 Epub:
Not Epub Abstract:
Background The PARP family member poly(ADP-ribose) polymerase 3 (PARP3) is structurally related to the well characterized PARP1... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Rouleau M, Saxena V, Rodrigue A, Paquet ER, Gagnon A, Hendzel MJ, Masson J-Y, Ekker M, Poirier GG. A Key Role for Poly(ADP-Ribose) Polymerase 3 in Ectodermal Specification and Neural Crest Development. PLoS ONE. 2011;6(1):e15834. doi:10.1371/journal.pone.0015834. |
A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development
Citation:
Development. 2008 Jun;135(11):1903-11 Epub:
Not Epub Abstract:
Myc-deficient mice fail to develop normal vascular networks and Myc-deficient embryonic stem cells fail to provoke a tumor... Organism or Cell Type:
Xenopus laevis Citation Extract: Rodrigues CO, Nerlick ST, White EL, Cleveland JL, King ML. A Myc-Slug (Snail2)/Twist regulatory circuit directs vascular development. Development. 2008 Jun;135(11):1903-11. |
A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system
Citation:
Dev Biol. 2004 Sep 15;273(2):210-25. Epub:
Not Epub Abstract:
The product of the Drosophila gene tribbles inhibits cell division in the ventral furrow of the embryo and thereby allows the... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus Citation Extract: Saka Y, Smith JC. A Xenopus tribbles orthologue is required for the progression of mitosis and for development of the nervous system. Dev Biol. 2004 Sep 15;273(2):210-25.. |
An early Fgf signal required for gene expression in the zebrafish hindbrain primordium
Citation:
Brain Res Dev Brain Res. 2004 Jan 31;148(1):27-42 Epub:
Not Epub Abstract:
We have explored the role of fibroblast growth factor (Fgf) signaling in regulating gene expression in the early zebrafish... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Roy NM, Sagerstrom CG. An early Fgf signal required for gene expression in the zebrafish hindbrain primordium. Brain Res Dev Brain Res. 2004 Jan 31;148(1):27-42. |
Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development
Citation:
PNAS. 2013;[Epub ahead of print] doi:10.1073/pnas.1300805110 Epub:
Not Epub Abstract:
The mechanisms by which arterial fate is established and maintained are not clearly understood. Although a number of signaling... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Sacilotto N, Monteiro R, Fritzsche M, Becker PW, Sanchez-del-Campo L, Liu K, Pinheiro P, Ratnayaka I, Davies B, Goding CR, Patient R, Bou-Gharios G, De Val S. Analysis of Dll4 regulation reveals a combinatorial role for Sox and Notch in arterial development. PNAS. 2013;[Epub ahead of print] doi:10.1073/pnas.1300805110 . |
Antisense oligonucleotide treatment for a pseudoexon-generating mutation in the NPC1 gene causing Niemann-Pick type C disease
Citation:
Hum Mutat. 2009 Aug 30. [Epub ahead of print] Epub:
Not Epub Abstract:
Niemann-Pick type C disease is an autosomal recessive disorder caused by mutations in either the NPC1 or NPC2 gene. While most... Delivery Method:
Endo-Porter Organism or Cell Type:
cell culture: human fibroblasts Citation Extract: Rodríguez-Pascau L, Coll MJ, Vilageliu L, Grinberg D. Antisense oligonucleotide treatment for a pseudoexon-generating mutation in the NPC1 gene causing Niemann-Pick type C disease. Hum Mutat. 2009 Aug 30. [Epub ahead of print]. |
Antisense PMO Found in Dystrophic Dog Model Was Effective in Cells from Exon 7-Deleted DMD Patient
Citation:
PLoS ONE. 2010 Aug;5(8):e12239. doi:10.1371/journal.pone.0012239 Epub:
Not Epub Abstract:
Background Antisense oligonucleotide-induced exon skipping is a promising approach for treatment of Duchenne muscular dystrophy... Delivery Method:
Endo-Porter Organism or Cell Type:
cell culture: dog and human Citation Extract: Saito T, Nakamura A, Aoki Y, Yokota T, Okada T, Osawa M, Takeda S. Antisense PMO Found in Dystrophic Dog Model Was Effective in Cells from Exon 7-Deleted DMD Patient. PLoS ONE. 2010 Aug;5(8):e12239. doi:10.1371/journal.pone.0012239. |