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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 12353 scientific papers returned from the database with the search filters currently being used below.
There are 12353 scientific papers returned from the database with the search filters currently being used below.
Duplicate VegfA genes and orthologues of the KDR receptor tyrosine kinase family mediate vascular development in the zebrafish
Citation:
Blood. 2007 Nov 15;110(10):3627-36. Epub 2007 Aug 14 Epub:
Not Epub Abstract:
Vascular endothelial growth factor A (VEGFA) and the type III receptor tyrosine kinase receptors (RTKs), are both required for... Organism or Cell Type:
zebrafish Citation Extract: Bahary N, Goishi K, Stuckenholz C, Weber G, Leblanc J, Schafer CA, Berman SS, Klagsbrun M, Zon LI. Duplicate VegfA genes and orthologues of the KDR receptor tyrosine kinase family mediate vascular development in the zebrafish. Blood. 2007 Nov 15;110(10):3627-36. Epub 2007 Aug 14. |
E-cadherin regulates cell movements and tissue formation in early zebrafish embryos
Citation:
Dev Dyn. 2004 Jun;230(2):263-77 Epub:
Not Epub Abstract:
E-cadherin is maternally expressed in most vertebrate species, but its function during early development of the vertebrate... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Babb SG, Marrs JA. E-cadherin regulates cell movements and tissue formation in early zebrafish embryos. Dev Dyn. 2004 Jun;230(2):263-77. |
Early developmental pathology due to cytochrome c oxidase deficiency is revealed by a new zebrafish model
Citation:
J Biol Chem. 2007 Nov 30;282(48):34839-49. Epub 2007 Aug 30. Epub:
Not Epub Abstract:
Deficiency of cytochrome c oxidase (COX) is associated with significant pathology in humans. However, the consequences for... Organism or Cell Type:
zebrafish Citation Extract: Baden KN, Murray J, Capaldi RA, Guillemin K. Early developmental pathology due to cytochrome c oxidase deficiency is revealed by a new zebrafish model. J Biol Chem. 2007 Nov 30;282(48):34839-49. Epub 2007 Aug 30.. |
Early myocardial function affects endocardial cushion development in zebrafish
Citation:
PLoS Biol. 2004 May;2(5):E129. Epub 2004 May 11 Epub:
Not Epub Abstract:
Function of the heart begins long before its formation is complete. Analyses in mouse and zebrafish have shown that myocardial... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Bartman T, Walsh EC, Wen KK, McKane M, Ren J, Alexander J, Rubenstein PA, Stainier DY. Early myocardial function affects endocardial cushion development in zebrafish. PLoS Biol. 2004 May;2(5):E129. Epub 2004 May 11. |
Essential and opposing roles of zebrafish beta-catenins in the formation of dorsal axial structures and neurectoderm
Citation:
Development. 2006 Apr;133(7):1299-309. Epub 2006 Mar 1 Epub:
Not Epub Abstract:
In Xenopus, Wnt signals and their transcriptional effector beta-catenin are required for the development of dorsal axial... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Bellipanni G, Varga M, Maegawa S, Imai Y, Kelly C, Myers AP, Chu F, Talbot WS, Weinberg ES. Essential and opposing roles of zebrafish beta-catenins in the formation of dorsal axial structures and neurectoderm. Development. 2006 Apr;133(7):1299-309. Epub 2006 Mar 1. |
Evaluation of Exon-Skipping Strategies for Duchenne Muscular Dystrophy Utilizing Dystrophin-deficient Zebrafish
Citation:
J Cell Mol Med. 2011 Jan 20. doi: 10.1111/j.1582-4934.2011.01260.x. [Epub ahead of print] Epub:
Not Epub Abstract:
Duchenne Muscular Dystrophy is a severe muscle wasting disease caused by mutations in the dystrophin gene. By utilising... Organism or Cell Type:
zebrafish Citation Extract: Berger J, Berger S, Jacoby AS, Wilton SD, Currie PD. Evaluation of Exon-Skipping Strategies for Duchenne Muscular Dystrophy Utilizing Dystrophin-deficient Zebrafish. J Cell Mol Med. 2011 Jan 20. doi: 10.1111/j.1582-4934.2011.01260.x. [Epub ahead of print]. |
Evidence for a molecular mechanism of teratogenicity of SB-236057, a 5-HT1B receptor inverse agonist that alters axial formation
Citation:
Birth Defects Res A Clin Mol Teratol. 2004 Oct;70(10):789-807 Epub:
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BACKGROUND: SB-236057 is a potent skeletal teratogen in rodents and rabbits, producing axial and posterior somite malformations... Delivery Method:
Special Delivery Organism or Cell Type:
Rat embryo, cultured Citation Extract: Augustine-Rauch KA, Zhang QJ, Leonard JL, Chadderton A, Welsh MJ, Rami HK, Thompson M, Gaster L, Wier PJ. Evidence for a molecular mechanism of teratogenicity of SB-236057, a 5-HT1B receptor inverse agonist that alters axial formation. Birth Defects Res A Clin Mol Teratol. 2004 Oct;70(10):789-807. |
Evolutionarily conserved role of nucleostemin: controlling proliferation of stem/progenitor cells during early vertebrate development
Citation:
Mol Cell Biol. 2006 Dec;26(24):9291-301. Epub 2006 Sep 25 Epub:
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Nucleostemin (NS) is a putative GTPase expressed preferentially in the nucleoli of neuronal and embryonic stem cells and... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Beekman C, Nichane M, De Clercq S, Maetens M, Floss T, Wurst W, Bellefroid E, Marine JC. Evolutionarily conserved role of nucleostemin: controlling proliferation of stem/progenitor cells during early vertebrate development. Mol Cell Biol. 2006 Dec;26(24):9291-301. Epub 2006 Sep 25. |
Ewing sarcoma protein ewsr1 maintains mitotic integrity and proneural cell survival in the zebrafish embryo
Citation:
PLoS ONE. 2007 Oct 3;2(10):e979 Epub:
Not Epub Abstract:
BACKGROUND: The Ewing sarcoma breakpoint region 1 gene (EWSR1), also known as EWS, is fused to a number of different partner... Organism or Cell Type:
zebrafish Citation Extract: Azuma M, Embree LJ, Sabaawy H, Hickstein DD. Ewing sarcoma protein ewsr1 maintains mitotic integrity and proneural cell survival in the zebrafish embryo. PLoS ONE. 2007 Oct 3;2(10):e979. |
Exon skipping with morpholino oligomers: new treatment option for cardiomyopathy in Duchenne muscular dystrophy?
Citation:
Cardiovasc Res. 2010. [Epub ahead of print] Epub:
Not Epub Abstract:
No abstract available Citation Extract: Bauer R, Katus HA, Müller OJ. Exon skipping with morpholino oligomers: new treatment option for cardiomyopathy in Duchenne muscular dystrophy?. Cardiovasc Res. 2010. [Epub ahead of print] . |