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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.
Jagged2a-notch signaling mediates cell fate choice in the zebrafish pronephric duct
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Citation:
PLoS Genet. 2007 Jan 26;3(1):e18 Epub:
Not Epub Abstract:
Pronephros, a developmental model for adult mammalian kidneys (metanephros) and a functional kidney in early teleosts, consists... Organism or Cell Type:
zebrafish Citation Extract: Ma M, Jiang YJ. Jagged2a-notch signaling mediates cell fate choice in the zebrafish pronephric duct. PLoS Genet. 2007 Jan 26;3(1):e18. |
KBP is essential for axonal structure, outgrowth and maintenance in zebrafish, providing insight into the cellular basis of Goldberg-Shprintzen syndrome
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Citation:
Development. 2008 Feb;135(3):599-608 Epub:
Not Epub Abstract:
Mutations in Kif1-binding protein/KIAA1279 (KBP) cause the devastating neurological disorder Goldberg-Shprintzen syndrome (GSS... Organism or Cell Type:
zebrafish Citation Extract: Lyons DA, Naylor SG, Mercurio S, Dominguez C, Talbot WS. KBP is essential for axonal structure, outgrowth and maintenance in zebrafish, providing insight into the cellular basis of Goldberg-Shprintzen syndrome. Development. 2008 Feb;135(3):599-608. |
Kif1b is essential for mRNA localization in oligodendrocytes and development of myelinated axons
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Citation:
Nat Genet. 2009 Jul;41(7):854-8. Epub 2009 Jun 7 Epub:
Not Epub Abstract:
The kinesin motor protein Kif1b has previously been implicated in the axonal transport of mitochondria and synaptic vesicles.... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Lyons DA, Naylor SG, Scholze A, Talbot WS. Kif1b is essential for mRNA localization in oligodendrocytes and development of myelinated axons. Nat Genet. 2009 Jul;41(7):854-8. Epub 2009 Jun 7. |
Killing the messenger: The role of CXCR7 in regulating primordial germ cell migration
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Citation:
Cell Adh Migr. 2008 Apr;2(2):69-70. Epub 2008 Apr 3 Epub:
Not Epub Abstract:
Primordial Germ Cell (PGC) migration in zebrafish is guided by SDF-1a. Binding of this chemokine to its receptor CXCR4b... Organism or Cell Type:
zebrafish Citation Extract: Mahabaleshwar H, Boldajipour B, Raz E. Killing the messenger: The role of CXCR7 in regulating primordial germ cell migration. Cell Adh Migr. 2008 Apr;2(2):69-70. Epub 2008 Apr 3. |
Laser-scanning velocimetry: A confocal microscopy method for quantitative measurement of cardiovascular performance in zebrafish embryos and larvae
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Citation:
BMC Biotechnol. 2007 Jul 10;7(1):40 [Epub ahead of print] Epub:
Not Epub Abstract:
ABSTRACT: BACKGROUND: The zebrafish Danio rerio is an important model system for drug discovery and to study cardiovascular... Organism or Cell Type:
zebrafish Citation Extract: Malone MH, Sciaky N, Stalheim L, Hahn KM, Linney E, Johnson GL. Laser-scanning velocimetry: A confocal microscopy method for quantitative measurement of cardiovascular performance in zebrafish embryos and larvae. BMC Biotechnol. 2007 Jul 10;7(1):40 [Epub ahead of print]. |
Long-term systemic administration of unconjugated morpholino oligomers for therapeutic expression of dystrophin by exon skipping in skeletal muscle: implications for cardiac muscle integrity
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Citation:
Nucleic Acid Ther. 2011 Aug;21(4):293-8 Epub:
Not Epub Abstract:
Duchenne muscular dystrophy (DMD) is a lethal X-linked inherited disease caused by mutations in the dystrophin gene and... Delivery Method:
Injection Organism or Cell Type:
mice, mdx Citation Extract: Malerba A, Boldrin L, Dickson G. Long-term systemic administration of unconjugated morpholino oligomers for therapeutic expression of dystrophin by exon skipping in skeletal muscle: implications for cardiac muscle integrity. Nucleic Acid Ther. 2011 Aug;21(4):293-8. |
Loss of p53 synthesis in zebrafish tumors with ribosomal protein gene mutations
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Citation:
Proc Natl Acad Sci U S A. 2008 Jul 29;105(30):10408-13. Epub 2008 Jul 18 Epub:
Not Epub Abstract:
Zebrafish carrying heterozygous mutations for 17 different ribosomal protein (rp) genes are prone to developing malignant... Organism or Cell Type:
zebrafish Citation Extract: MacInnes AW, Amsterdam A, Whittaker CA, Hopkins N, Lees JA. Loss of p53 synthesis in zebrafish tumors with ribosomal protein gene mutations. Proc Natl Acad Sci U S A. 2008 Jul 29;105(30):10408-13. Epub 2008 Jul 18. |
Lowe syndrome: Between primary cilia assembly and Rac1-mediated membrane remodeling
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Citation:
Commun Integr Biol. 2012 Nov 1;5(6):641-4. doi: 10.4161/cib.21952 Epub:
Not Epub Abstract:
Lowe syndrome (LS) is a lethal X-linked genetic disease caused by functional deficiencies of the phosphatidlyinositol 5-... Organism or Cell Type:
zebrafish Citation Extract: Madhivanan K, Mukherjee D, Aguilar RC. Lowe syndrome: Between primary cilia assembly and Rac1-mediated membrane remodeling. Commun Integr Biol. 2012 Nov 1;5(6):641-4. doi: 10.4161/cib.21952. |
Maternally-Recruited DCP1A and DCP2 Contribute to Messenger RNA Degradation During Oocyte Maturation and Genome Activation in Mouse
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Citation:
Biol Reprod. 2012 Nov 7. [Epub ahead of print] Epub:
Not Epub Abstract:
The oocyte-to-zygote transition entails transforming a highly differentiated oocyte into totipotent blastomeres and represents... Organism or Cell Type:
mouse oocytes Citation Extract: Ma J, Flemr M, Strnad H, Svoboda P, Schultz RM. Maternally-Recruited DCP1A and DCP2 Contribute to Messenger RNA Degradation During Oocyte Maturation and Genome Activation in Mouse. Biol Reprod. 2012 Nov 7. [Epub ahead of print]. |
Megalencephalic leukoencephalopathy with subcortical cysts type 1 (MLC1) due to a homozygous deep intronic splicing mutation (c.895-226T>G) abrogated in vitro using an antisense morpholino oligonucleotide
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Citation:
Neurogenetics. 2012 May 3. [Epub ahead of print] Epub:
Not Epub Abstract:
Megalencephalic leukoencephalopathy with subcortical cysts is an autosomal recessive disease characterized by early onset... Organism or Cell Type:
cell culture Citation Extract: Mancini C, Vaula G, Scalzitti L, Cavalieri S, Bertini E, Aiello C, Lucchini C, Gatti RA, Brussino A, Brusco A. Megalencephalic leukoencephalopathy with subcortical cysts type 1 (MLC1) due to a homozygous deep intronic splicing mutation (c.895-226T>G) abrogated in vitro using an antisense morpholino oligonucleotide. Neurogenetics. 2012 May 3. [Epub ahead of print]. |