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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 12371 scientific papers returned from the database with the search filters currently being used below.
There are 12371 scientific papers returned from the database with the search filters currently being used below.
Zebrafish assays of ciliopathies
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Citation:
Methods Cell Biol. 2011;105:257-72. doi: 10.1016/B978-0-12-381320-6.00011-4 Epub:
Not Epub Abstract:
In light of the growing list of human disorders associated with their dysfunction, primary cilia have recently come to... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Zaghloul NA, Katsanis N. Zebrafish assays of ciliopathies. Methods Cell Biol. 2011;105:257-72. doi: 10.1016/B978-0-12-381320-6.00011-4. |
Zebrafish dax1 is required for development of the interrenal organ, the adrenal cortex equivalent
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Citation:
Mol. Endocrinol., Nov 2006; 20: 2630 - 2640. Epub:
Not Epub Abstract:
Mutations in the human nuclear receptor, DAX1, cause X-linked adrenal hypoplasia congenita (AHC). We report the isolation and... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Zhao Y, Yang Z, Phelan JK, Wheeler DA, Lin S, McCabe ER. Zebrafish dax1 is required for development of the interrenal organ, the adrenal cortex equivalent. Mol. Endocrinol., Nov 2006; 20: 2630 - 2640.. |
Zebrafish Dpr2 inhibits mesoderm induction by promoting degradation of nodal receptors
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Citation:
Science. 2004 Oct 1;306(5693):114-7 Epub:
Not Epub Abstract:
Nodal proteins, members of the transforming growth factor-beta (TGFbeta) superfamily, have been identified as key endogenous... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Zhang L, Zhou H, Su Y, Sun Z, Zhang H, Zhang L, Zhang Y, Ning Y, Chen YG, Meng A. Zebrafish Dpr2 inhibits mesoderm induction by promoting degradation of nodal receptors. Science. 2004 Oct 1;306(5693):114-7. |
Zebrafish Models for Dyskeratosis Congenita Reveal Critical Roles of p53 Activation Contributing to Hematopoietic Defects through RNA Processing
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Citation:
PLoS ONE. 2012;7(1):e30188. doi:10.1371/journal.pone.0030188 Epub:
Not Epub Abstract:
Dyskeratosis congenita (DC) is a rare bone marrow failure syndrome in which hematopoietic defects are the main cause of... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Zhang Y, Morimoto K, Danilova N, Zhang B, Lin S. Zebrafish Models for Dyskeratosis Congenita Reveal Critical Roles of p53 Activation Contributing to Hematopoietic Defects through RNA Processing. PLoS ONE. 2012;7(1):e30188. doi:10.1371/journal.pone.0030188. |
ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6
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Citation:
Am J Hum Genet. 2013 Jul 24. doi:pii: S0002-9297(13)00276-0. 10.1016/j.ajhg.2013.06.007. [Epub ahead of print] Epub:
Not Epub Abstract:
Defects of motile cilia cause primary ciliary dyskinesia (PCD), characterized by recurrent respiratory infections and male... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, Diaz KA, Olbrich H, Wolf WE, Sheridan E, Batten TF, Halbritter J, Porath JD, Kohl S, Lovric S, Hwang DY, Pittman JE, Burns KA, Ferkol TW, Sagel SD, Olivier KN, Morgan LC, Werner C, Raidt J, Pennekamp P, Sun Z, Zhou W, Airik R, Natarajan S, Allen SJ, Amirav I, Wieczorek D, Landwehr K, Nielsen K, Schwerk N, Sertic J, Köhler G, Washburn J, Levy S, Fan S, Koerner-Rettberg C, Amselem S, Williams DS, Mitchell BJ, Drummond IA, Otto EA, Omran H, Knowles MR, Hildebrandt F. . ZMYND10 Is Mutated in Primary Ciliary Dyskinesia and Interacts with LRRC6. Am J Hum Genet. 2013 Jul 24. doi:pii: S0002-9297(13)00276-0. 10.1016/j.ajhg.2013.06.007. [Epub ahead of print]. |
[Knockdown and overexpression of miR-219 lead to embryonic defects in zebrafish development]
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Citation:
Fen Zi Xi Bao Sheng Wu Xue Bao. 2008 Oct;41(5):341-8. Chinese. Epub:
Not Epub Abstract:
MicroRNAs (miRNAs) are important post-transcriptional modulators of gene expression, which have been implicated in many... Organism or Cell Type:
zebrafish Citation Extract: Zhang MC, Lv Y, Qi YT, Zhang Z, Fu XN, Yuan CG, Lai LH. [Knockdown and overexpression of miR-219 lead to embryonic defects in zebrafish development]. Fen Zi Xi Bao Sheng Wu Xue Bao. 2008 Oct;41(5):341-8. Chinese. . |
β-Catenin 1 and β-catenin 2 play similar and distinct roles in left-right asymmetric development of zebrafish embryos
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Citation:
Development. 2012 Apr 25. [Epub ahead of print] Epub:
Not Epub Abstract:
β-Catenin-mediated canonical Wnt signaling has been found to be required for left-right (LR) asymmetric development. However,... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Zhang M, Zhang J, Lin SC, Meng A. β-Catenin 1 and β-catenin 2 play similar and distinct roles in left-right asymmetric development of zebrafish embryos. Development. 2012 Apr 25. [Epub ahead of print]. |
14-3-3 proteins regulate retinal axon growth by modulating ADF/cofilin activity
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Citation:
Dev Neurobiol. 2012 Apr;72(4):600-14. doi: 10.1002/dneu.20955. Epub:
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Precise navigation of axons to their targets is critical for establishing proper neuronal networks during development. Axon... Organism or Cell Type:
Xenopus laevis Citation Extract: Yoon BC, Zivraj KH, Strochlic L, Holt CE. 14-3-3 proteins regulate retinal axon growth by modulating ADF/cofilin activity. Dev Neurobiol. 2012 Apr;72(4):600-14. doi: 10.1002/dneu.20955.. |
A fusion peptide directs enhanced systemic dystrophin exon skipping and functional restoration in dystrophin-deficient mdx mice
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Citation:
Hum Mol Genet. 2009 Aug 18. [Epub ahead of print] Epub:
Not Epub Abstract:
Duchenne muscular dystrophy (DMD) is caused by mutations in the DMD gene that abolish the synthesis of dystrophin protein.... Delivery Method:
peptide-coupled Organism or Cell Type:
mice, mdx Citation Extract: Yin H, Moulton HM, Betts C, Seow Y, Boutilier J, Iverson PL, Wood MJ. A fusion peptide directs enhanced systemic dystrophin exon skipping and functional restoration in dystrophin-deficient mdx mice. Hum Mol Genet. 2009 Aug 18. [Epub ahead of print]. |
A novel role for a nodal-related protein; Xnr3 regulates convergent extension movements via the FGF receptor
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Citation:
Development. 2003 May;130(10):2199-212. Erratum in: Development. 2004 Aug;13(15):3821 Epub:
Not Epub Abstract:
Convergent extension behaviour is critical for the formation of the vertebrate body axis. In Xenopus, components of the Wnt... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Yokota C, Kofron M, Zuck M, Houston DW, Isaacs H, Asashima M, Wylie CC, Heasman J. A novel role for a nodal-related protein; Xnr3 regulates convergent extension movements via the FGF receptor. Development. 2003 May;130(10):2199-212. Erratum in: Development. 2004 Aug;13(15):3821. |