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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 12378 scientific papers returned from the database with the search filters currently being used below.
There are 12378 scientific papers returned from the database with the search filters currently being used below.
Molecular analysis and characterization of zebrafish keratocan (zKera) gene
Citation:
J Biol Chem. 2008 Jan 4;283(1):506-17. Epub 2007 Oct 26 Epub:
Not Epub Abstract:
Corneal small leucine-rich proteoglycans (SLRPs) play a pivotal role in maintaining corneal transparency and function. In this... Organism or Cell Type:
zebrafish Citation Extract: Yeh LK, Liu CY, Chien CL, Converse RL, Kao WW, Chen MS, Hsieh FJ, Wang IJ. Molecular analysis and characterization of zebrafish keratocan (zKera) gene. J Biol Chem. 2008 Jan 4;283(1):506-17. Epub 2007 Oct 26. |
Molecular cloning and functional analysis of zebrafish neutral ceramidase
Citation:
J Biol Chem. 2004 Oct 15;279(42):44012-22. Epub 2004 Jul 22. Epub:
Not Epub Abstract:
Almost all observations on the functions of neutral ceramidase have been carried out at cellular levels but not an individual... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Yoshimura Y, Tani M, Okino N, Iida H, Ito M. Molecular cloning and functional analysis of zebrafish neutral ceramidase. J Biol Chem. 2004 Oct 15;279(42):44012-22. Epub 2004 Jul 22.. |
Molecular components underlying nongenomic thyroid hormone signaling in embryonic zebrafish neurons
Citation:
Neural Dev. 2009 Jun 8;4(1):20. [Epub ahead of print] Epub:
Not Epub Abstract:
ABSTRACT: BACKGROUND: Neurodevelopment requires thyroid hormone, yet the mechanisms and targets of thyroid hormone action... Organism or Cell Type:
zebrafish Citation Extract: Yonkers MA, Ribera AB. Molecular components underlying nongenomic thyroid hormone signaling in embryonic zebrafish neurons. Neural Dev. 2009 Jun 8;4(1):20. [Epub ahead of print]. |
Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand-receptor relationships
Citation:
Dev Biol. 2006 Dec 23; [Epub ahead of print] Epub:
Not Epub Abstract:
Medaka (Oryzias latipes) is a small freshwater teleost that provides an excellent developmental genetic model complementary to... Organism or Cell Type:
Medaka embryos and zebrafish embryos Citation Extract: Yokoi H, Shimada A, Carl M, Takashima S, Kobayashi D, Narita T, Jindo T, Kimura T, Kitagawa T, Kage T, Sawada A, Naruse K, Asakawa S, Shimizu N, Mitani H, Shima A, Tsutsumi M, Hori H, Wittbrodt J, Saga Y, Ishikawa Y, Araki K, Takeda H. Mutant analyses reveal different functions of fgfr1 in medaka and zebrafish despite conserved ligand-receptor relationships. Dev Biol. 2006 Dec 23; [Epub ahead of print]. |
Mutant Prpf31 causes pre-mRNA splicing defects and rod photoreceptor cell degeneration in a zebrafish model for Retinitis pigmentosa
Citation:
Mol Neurodegener. 2011 Jul 30;6(1):56. [Epub ahead of print] Epub:
Not Epub Abstract:
BACKGROUND: Retinitis pigmentosa (RP) is an inherited eye disease characterized by the progressive degeneration of rod... Organism or Cell Type:
zebrafish Citation Extract: Yin J, Brocher J, Fischer U, Winkler C. Mutant Prpf31 causes pre-mRNA splicing defects and rod photoreceptor cell degeneration in a zebrafish model for Retinitis pigmentosa. Mol Neurodegener. 2011 Jul 30;6(1):56. [Epub ahead of print]. |
Mutation of RNA Pol III subunit rpc2/polr3b Leads to Deficiency of Subunit Rpc11 and disrupts zebrafish digestive development
Citation:
PLoS Biol. 2007 Nov;5(11):e312 Epub:
Not Epub Abstract:
The role of RNA polymerase III (Pol III) in developing vertebrates has not been examined. Here, we identify a causative... Organism or Cell Type:
zebrafish Citation Extract: Yee NS, Gong W, Huang Y, Lorent K, Dolan AC, Maraia RJ, Pack M. Mutation of RNA Pol III subunit rpc2/polr3b Leads to Deficiency of Subunit Rpc11 and disrupts zebrafish digestive development. PLoS Biol. 2007 Nov;5(11):e312. |
Mutation of the Bone Morphogenetic Protein GDF3 causes ocular and skeletal anomalies
Citation:
Hum Mol Genet. 2009 Oct 28. [Epub ahead of print] Epub:
Not Epub Abstract:
Ocular mal-development results in heterogeneous and frequently visually disabling phenotypes that include coloboma and... Organism or Cell Type:
zebrafish Citation Extract: Ye M, Berry-Wynne KM, Asai-Coakwell M, Sundaresan P, Footz T, French CR, Abitbol M, Fleisch VC, Corbett N, Allison WT, Drummond G, Walter MA, Underhill TM, Waskiewicz AJ, Lehmann OJ. Mutation of the Bone Morphogenetic Protein GDF3 causes ocular and skeletal anomalies. Hum Mol Genet. 2009 Oct 28. [Epub ahead of print]. |
Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss
Citation:
Am J Hum Genet. 2012 Nov 2;91(5):872-82. doi: 10.1016/j.ajhg.2012.09.011 Epub:
Not Epub Abstract:
Hereditary hearing loss is characterized by a high degree of genetic heterogeneity. Here we present OTOGL mutations, a... Organism or Cell Type:
zebrafish Citation Extract: Yariz KO, Duman D, Seco CZ, Dallman J, Huang M, Peters TA, Sirmaci A, Lu N, Schraders M, Skromne I, Oostrik J, Diaz-Horta O, Young JI, Tokgoz-Yilmaz S, Konukseven O, Shahin H, Hetterschijt L, Kanaan M, Oonk AM, Edwards YJ, Li H, Atalay S, Blanton S, Desmidt AA, Liu XZ, Pennings RJ, Lu Z, Chen ZY, Kremer H, Tekin M . Mutations in OTOGL, Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss. Am J Hum Genet. 2012 Nov 2;91(5):872-82. doi: 10.1016/j.ajhg.2012.09.011. |
New regulators of vertebrate appendage regeneration
Citation:
Curr Opin Genet Dev. 2008 Aug;18(4):381-6. Epub 2008 Aug 11 Epub:
Not Epub Abstract:
Appendage regeneration is a complex and fascinating biological process exhibited in vertebrates by urodele amphibians and... Organism or Cell Type:
zebrafish Citation Extract: Yin VP, Poss KD. New regulators of vertebrate appendage regeneration. Curr Opin Genet Dev. 2008 Aug;18(4):381-6. Epub 2008 Aug 11. |
Optimizing exon skipping therapies for DMD
Citation:
Acta Myol. 2007 Dec;26(3):179-84 Epub:
Not Epub Abstract:
Exon skipping is one of the more promising therapeutic options for Duchenne Muscular Dystrophy (DMD). The idea is to use... Citation Extract: Yokota T, Duddy W, Partridge T. Optimizing exon skipping therapies for DMD. Acta Myol. 2007 Dec;26(3):179-84. |