You are here
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 12245 scientific papers returned from the database with the search filters currently being used below.
There are 12245 scientific papers returned from the database with the search filters currently being used below.
xDnmt1 regulates transcriptional silencing in pre-MBT Xenopus embryos independently of its catalytic function
Citation:
Development. 2008 Apr;135(7):1295-302. Epub 2008 Feb 27. Epub:
Not Epub Abstract:
We previously reported that the maintenance cytosine methyltransferase xDnmt1 is essential for gene silencing in early Xenopus... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Dunican DS, Ruzov A, Hackett JA, Meehan RR. xDnmt1 regulates transcriptional silencing in pre-MBT Xenopus embryos independently of its catalytic function. Development. 2008 Apr;135(7):1295-302. Epub 2008 Feb 27.. |
Zebrafish cilia
Citation:
Methods Enzymol. 2013;525:219-44. doi: 10.1016/B978-0-12-397944-5.00011-0 Epub:
Not Epub Abstract:
Zebrafish are ideally suited for analysis of genes required for ciliogenesis and cilia function. Combining genetic manipulation... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Drummond I, Austin-Tse C. Zebrafish cilia. Methods Enzymol. 2013;525:219-44. doi: 10.1016/B978-0-12-397944-5.00011-0. |
Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates
Citation:
Development. 2001 Nov;128(21):4113-25 Epub:
Not Epub Abstract:
Waardenburg-Shah syndrome combines the reduced enteric nervous system characteristic of Hirschsprung's disease with... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Dutton KA, Pauliny A, Lopes SS, Elworthy S, Carney TJ, Rauch J, Geisler R, Haffter P, Kelsh RN. Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates. Development. 2001 Nov;128(21):4113-25. |
Zebrafish fgf24 functions with fgf8 to promote posterior mesodermal development
Citation:
Development. 2003 Oct;130(19):4639-54 Epub:
Not Epub Abstract:
Fibroblast growth factor (Fgf) signaling plays an important role during development of posterior mesoderm in vertebrate embryos... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Draper BW, Stock DW, Kimmel CB. Zebrafish fgf24 functions with fgf8 to promote posterior mesodermal development. Development. 2003 Oct;130(19):4639-54. |
Zebrafish MTMR14 is required for excitation-contraction coupling, developmental motor function, and the regulation of autophagy
Citation:
Hum Mol Genet. 2010 Apr 16. [Epub ahead of print] Epub:
Not Epub Abstract:
Myotubularins are a family of dual-specificity phosphatases that act to modify phosphoinositides and regulate membrane traffic... Organism or Cell Type:
zebrafish Citation Extract: Dowling JJ, Low SE, Busta AS, Feldman EL. Zebrafish MTMR14 is required for excitation-contraction coupling, developmental motor function, and the regulation of autophagy. Hum Mol Genet. 2010 Apr 16. [Epub ahead of print]. |
Zebrafish neurolin-a and -b, orthologs of ALCAM, are involved in retinal ganglion cell differentiation and retinal axon pathfinding
Citation:
J Comp Neurol. 2008 Dec 23;513(1):38-50. [Epub ahead of print] Epub:
Not Epub Abstract:
Neurolin-a and Neurolin-b (also called alcam and nlcam, respectively) are zebrafish orthologs of human ALCAM, an adhesion... Organism or Cell Type:
zebrafish Citation Extract: Diekmann H, Stuermer CA. Zebrafish neurolin-a and -b, orthologs of ALCAM, are involved in retinal ganglion cell differentiation and retinal axon pathfinding. J Comp Neurol. 2008 Dec 23;513(1):38-50. [Epub ahead of print]. |
Zebrafish scl functions independently in hematopoietic and endothelial development
Citation:
Dev Biol. 2005 Jan 15;277(2):522-36 Epub:
Not Epub Abstract:
The SCL transcription factor is critically important for vertebrate hematopoiesis and angiogenesis, and has been postulated to... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Dooley KA, Davidson AJ, Zon LI. Zebrafish scl functions independently in hematopoietic and endothelial development. Dev Biol. 2005 Jan 15;277(2):522-36. |
Prostate cancer: status of current treatments and emerging antisense-based therapies
Citation:
Curr Opin Mol Ther. 2002 Apr;4(2):138-48. Review. Epub:
Not Epub Abstract:
Prostate cancer, like most other solid tumors, represents a heterogeneous entity consisting of a mixture of androgen-dependent... Citation Extract: Devi GR. Prostate cancer: status of current treatments and emerging antisense-based therapies. Curr Opin Mol Ther. 2002 Apr;4(2):138-48. Review.. |
5-HT2B-mediated serotonin signaling is required for eye morphogenesis in Xenopus
Citation:
Mol Cell Neurosci. 2005 Jun;29(2):299-312 Epub:
Not Epub Abstract:
In this paper, we show that serotonin, via 5-HT2B receptor, is involved in Xenopus retinal histogenesis and eye morphogenesis... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus Citation Extract: De Lucchini S, Ori M, Cremisi F, Nardini M, Nardi I. 5-HT2B-mediated serotonin signaling is required for eye morphogenesis in Xenopus. Mol Cell Neurosci. 2005 Jun;29(2):299-312. |
A deep intronic mutation in FGB creates a consensus exonic splicing enhancer motif that results in afibrinogenemia caused by aberrant mRNA splicing, which can be corrected in vitro with antisense oligonucleotide treatment
Citation:
Hum Mutat. 2008 Oct 13. [Epub ahead of print] Epub:
Not Epub Abstract:
We previously described a novel homozygous point mutation (FGB c.115-600A>G) located deep within intron 1 of the fibrinogen... Delivery Method:
Endo-Porter Organism or Cell Type:
Cell culture: COS-7 cells (monkey kidney) Citation Extract: Davis RL, Homer VM, George PM, Brennan SO. A deep intronic mutation in FGB creates a consensus exonic splicing enhancer motif that results in afibrinogenemia caused by aberrant mRNA splicing, which can be corrected in vitro with antisense oligonucleotide treatment. Hum Mutat. 2008 Oct 13. [Epub ahead of print]. |