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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 12138 scientific papers returned from the database with the search filters currently being used below.
There are 12138 scientific papers returned from the database with the search filters currently being used below.
Growth differentiation factor-9 signaling in the ovary
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Citation:
Mol Cell Endocrinol. 2003 Apr 28;202(1-2):31-6 Epub:
Not Epub Abstract:
Growth differentiation factor-9 (GDF-9) is an oocyte-derived growth factor and a member of the transforming growth factor-beta... Delivery Method:
not published Organism or Cell Type:
Mouse embryo Citation Extract: Mazerbourg S, Hsueh AJ. Growth differentiation factor-9 signaling in the ovary. Mol Cell Endocrinol. 2003 Apr 28;202(1-2):31-6. |
Hypokinesia and reduced dopamine levels in zebrafish lacking β- and γ1-synucleins
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Citation:
J Biol Chem. 2012 Jan 27;287(5):2971-83. doi: 10.1074/jbc.M111.308312. Epub 2011 Nov 29 Epub:
Not Epub Abstract:
α-Synuclein is strongly implicated in the pathogenesis of Parkinson disease. However, the normal functions of synucleins and... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Milanese C, Sager JJ, Bai Q, Farrell TC, Cannon JR, Greenamyre JT, Burton EA. Hypokinesia and reduced dopamine levels in zebrafish lacking β- and γ1-synucleins. J Biol Chem. 2012 Jan 27;287(5):2971-83. doi: 10.1074/jbc.M111.308312. Epub 2011 Nov 29. |
Identification of chaperonin CCTgamma subunit as a determinant of retinotectal development by whole-genome subtraction cloning from zebrafish no tectal neuron mutant
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Citation:
Development. 2004 May;131(9):1913-25. Epub:
Not Epub Abstract:
Zebrafish no tectal neuron (ntn) mutant obtained by trimethylpsoralen (TMP) mutagenesis showed defects in tectal neuropil... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Matsuda N, Mishina M. Identification of chaperonin CCTgamma subunit as a determinant of retinotectal development by whole-genome subtraction cloning from zebrafish no tectal neuron mutant. Development. 2004 May;131(9):1913-25.. |
Induced dystrophin exon skipping in human muscle explants
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Citation:
Neuromuscul Disord. 2006 Oct;16(9-10):583-90. Epub 2006 Aug 21 Epub:
Not Epub Abstract:
Antisense oligonucleotide (AO) manipulation of pre-mRNA splicing of the dystrophin gene is showing promise in overcoming... Delivery Method:
peptide-coupled Organism or Cell Type:
muscle explants, mouse and human Citation Extract: McClorey G, Fall AM, Moulton HM, Iversen PL, Rasko JE, Ryan M, Fletcher S, Wilton SD. Induced dystrophin exon skipping in human muscle explants. Neuromuscul Disord. 2006 Oct;16(9-10):583-90. Epub 2006 Aug 21. |
Integration of Hedgehog and BMP signalling by the engrailed2a gene in the zebrafish myotome
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Citation:
Development. 2011 Feb;138(4):755-65. doi: 10.1242/dev.062521. Erratum in: Development. 2012 May;139(10):1885 Epub:
Not Epub Abstract:
Different levels and timing of Hedgehog (Hh) signalling activity have been proposed to specify three distinct cell types in the... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Maurya AK, Tan H, Souren M, Wang X, Wittbrodt J, Ingham PW. Integration of Hedgehog and BMP signalling by the engrailed2a gene in the zebrafish myotome. Development. 2011 Feb;138(4):755-65. doi: 10.1242/dev.062521. Erratum in: Development. 2012 May;139(10):1885. |
Interaction with Notch determines endocytosis of specific Delta ligands in zebrafish neural tissue
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Citation:
Development. 2009 Jan;136(2):197-206. Epub 2008 Dec 4 Epub:
Not Epub Abstract:
Mind bomb1 (Mib1)-mediated endocytosis of the Notch ligand DeltaD is essential for activation of Notch in a neighboring cell.... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Matsuda M, Chitnis AB. Interaction with Notch determines endocytosis of specific Delta ligands in zebrafish neural tissue. Development. 2009 Jan;136(2):197-206. Epub 2008 Dec 4. |
JunB-CBF{beta} signaling is essential to maintain sarcomeric Z-disc structure and when defective leads to heart failure
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Citation:
J Cell Sci. 2010 Jul 6. [Epub ahead of print] Epub:
Not Epub Abstract:
In muscle cells, a complex network of Z-disc proteins allows proper reception, transduction and transmission of mechanical and... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Meder B, Just S, Vogel B, Rudloff J, Gärtner L, Dahme T, Huttner I, Zankl A, Katus HA, Rottbauer W. JunB-CBF{beta} signaling is essential to maintain sarcomeric Z-disc structure and when defective leads to heart failure. J Cell Sci. 2010 Jul 6. [Epub ahead of print]. |
Knockdown of duplicated zebrafish hoxb1 genes reveals distinct roles in hindbrain patterning and a novel mechanism of duplicate gene retention
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Citation:
Development. 2002 May 15;129(10):2339-2354 Epub:
Not Epub Abstract:
We have used a morpholino-based knockdown approach to investigate the functions of a pair of zebrafish Hox gene duplicates,... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: McClintock JM, Kheirbek MA, Prince VE. Knockdown of duplicated zebrafish hoxb1 genes reveals distinct roles in hindbrain patterning and a novel mechanism of duplicate gene retention. Development. 2002 May 15;129(10):2339-2354. |
Knockdown of the complete Hox paralogous group 1 leads to dramatic hindbrain and neural crest defects
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Citation:
Development. 2005 Jun;132(12):2861-71 Epub:
Not Epub Abstract:
The Hox paralogous group 1 (PG1) genes are the first and initially most anterior Hox genes expressed in the embryo. In Xenopus... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus Citation Extract: McNulty CL, Peres JN, Bardine N, van den Akker WM, Durston AJ. Knockdown of the complete Hox paralogous group 1 leads to dramatic hindbrain and neural crest defects. Development. 2005 Jun;132(12):2861-71. |
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
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Citation:
J Cell Biol. 2003 Sep 1;162(5):919-32 Epub:
Not Epub Abstract:
Spinal muscular atrophy (SMA) is an autosomal recessive disorder characterized by a loss of alpha motoneurons in the spinal... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: McWhorter ML, Monani UR, Burghes AH, Beattie CE. Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. J Cell Biol. 2003 Sep 1;162(5):919-32. |