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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 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.
Ewing sarcoma protein ewsr1 maintains mitotic integrity and proneural cell survival in the zebrafish embryo
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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?
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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] . |
Expression of LINE-1 retroposons is essential for murine preimplantation development
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Citation:
Mol Reprod Dev. 2006 Mar;73(3):279-87 Epub:
Not Epub Abstract:
In higher eukaryotes, reverse transcriptase (RT) activities are encoded by a variety of endogenous retroviruses and... Delivery Method:
Microinjection Organism or Cell Type:
mouse embryos,preimplantation Citation Extract: Beraldi R, Pittoggi C, Sciamanna I, Mattei E, Spadafora C. Expression of LINE-1 retroposons is essential for murine preimplantation development. Mol Reprod Dev. 2006 Mar;73(3):279-87. |
Extra-embryonic syndecan 2 regulates organ primordia migration and fibrillogenesis throughout the zebrafish embryo
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Citation:
Development. 2009 Sep;136(18):3143-52 Epub:
Not Epub Abstract:
One of the first steps in zebrafish heart and gut organogenesis is the migration of bilateral primordia to the midline to form... Organism or Cell Type:
zebrafish Citation Extract: Arrington CB, Yost HJ. Extra-embryonic syndecan 2 regulates organ primordia migration and fibrillogenesis throughout the zebrafish embryo. Development. 2009 Sep;136(18):3143-52. |
Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy
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Citation:
J Child Neurol. 2007 Aug;22(8):995-1003. Review Epub:
Not Epub Abstract:
Motoneuron diseases cause paralysis and death due to loss of motoneurons that innervate skeletal muscle. Spinal muscular... Organism or Cell Type:
zebrafish Citation Extract: Beattie CE, Carrel TL, McWhorter ML. Fishing for a mechanism: using zebrafish to understand spinal muscular atrophy. J Child Neurol. 2007 Aug;22(8):995-1003. Review. |
FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A
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Citation:
Hum Mol Genet. 2008 Feb 15;17(4):490-505. Epub 2007 Nov 9. Epub:
Not Epub Abstract:
Mutations in the human FOXC1 transcription factor gene underlie Axenfeld-Rieger (AR) syndrome, a disorder characterized by... Organism or Cell Type:
zebrafish Citation Extract: Berry FB, Skarie JM, Mirzayans F, Fortin Y, Hudson TJ, Raymond V, Link BA, Walter MA. FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A. Hum Mol Genet. 2008 Feb 15;17(4):490-505. Epub 2007 Nov 9.. |
FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish
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Citation:
Mol Syndromol 2010;1:255-261 DOI: 10.1159/000327707 Epub:
Not Epub Abstract:
Branchio-oculo-facial syndrome (BOFS) is a rare disorder characterized by maldevelopment of the first and second branchial... Organism or Cell Type:
zebrafish Citation Extract: Balikova I, Devriendt K, Fryns JP, Vermeesch JR. FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in Zebrafish. Mol Syndromol 2010;1:255-261 DOI: 10.1159/000327707. |
FoxF is essential for FGF-induced migration of heart progenitor cells in the ascidian Ciona intestinalis
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Citation:
Development. 2007 Sep;134(18):3297-305 Epub:
Not Epub Abstract:
Heart development requires precise coordination of morphogenetic movements with progressive cell fate specification and... Organism or Cell Type:
Ciona intestinalis Citation Extract: Beh J, Shi W, Levine M, Davidson B, Christiaen L. FoxF is essential for FGF-induced migration of heart progenitor cells in the ascidian Ciona intestinalis. Development. 2007 Sep;134(18):3297-305. |
Gata2 provides an early anterior bias and uncovers a global positioning system for polarity in the amniote embryo
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Citation:
Development. 2012 Nov;139(22):4232-8. doi: 10.1242/dev.081901 Epub:
Not Epub Abstract:
The first axis to be specified during vertebrate development is that between the site where gastrulation will begin and the... Delivery Method:
Injection then electroporation in vivo Organism or Cell Type:
chick embryo Citation Extract: Bertocchini F, Stern CD. Gata2 provides an early anterior bias and uncovers a global positioning system for polarity in the amniote embryo. Development. 2012 Nov;139(22):4232-8. doi: 10.1242/dev.081901. |
GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies
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Citation:
Am J Hum Genet. 2007 Feb;80(2):306-15. Epub 2006 Dec 29 Epub:
Not Epub Abstract:
Colobomata represent visually impairing ocular closure defects that are associated with a diverse range of developmental... Citation Extract: Asai-Coakwell M, French CR, Berry KM, Ye M, Koss R, Somerville M, Mueller R, van Heyningen V, Waskiewicz AJ, Lehmann OJ. GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies. Am J Hum Genet. 2007 Feb;80(2):306-15. Epub 2006 Dec 29. |