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 12095 scientific papers returned from the database with the search filters currently being used below.
There are 12095 scientific papers returned from the database with the search filters currently being used below.
Ischemia Is Not Required for Arteriogenesis in Zebrafish Embryos
|
Citation:
Arterioscler Thromb Vasc Biol, Oct 2007; 27: 2135 - 2141 Epub:
Not Epub Abstract:
Objective— The role of ischemia in collateral vessel development (arteriogenesis) is a contentious issue that cannot be... Organism or Cell Type:
zebrafish Citation Extract: Gray C, Packham IM, Wurmser F, Eastley NC, Hellewell PG, Ingham PW, Crossman DC, Chico TJA. Ischemia Is Not Required for Arteriogenesis in Zebrafish Embryos. Arterioscler Thromb Vasc Biol, Oct 2007; 27: 2135 - 2141. |
Loss of Catalytically Inactive Lipid Phosphatase Myotubularin-related Protein 12 Impairs Myotubularin Stability and Promotes Centronuclear Myopathy in Zebrafish
|
Citation:
PLoS Genet. 2013;9(6):e1003583. doi:10.1371/journal.pgen.1003583 Epub:
Not Epub Abstract:
X-linked myotubular myopathy (XLMTM) is a congenital disorder caused by mutations of the myotubularin gene, MTM1. Myotubularin... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Gupta VA, Hnia K, Smith LL, Gundry SR, McIntire JE, Shimazu J, Bass JR, Talbot EA, Amoasii L, Goldman NE, Laporte J, Beggs AH. Loss of Catalytically Inactive Lipid Phosphatase Myotubularin-related Protein 12 Impairs Myotubularin Stability and Promotes Centronuclear Myopathy in Zebrafish. PLoS Genet. 2013;9(6):e1003583. doi:10.1371/journal.pgen.1003583. |
Loss of Function of Parathyroid Hormone Receptor 1 Induces Notch-Dependent Aortic Defects During Zebrafish Vascular Development
|
Citation:
Arterioscler Thromb Vasc Biol. 2013 Apr 4. [Epub ahead of print] Epub:
Not Epub Abstract:
OBJECTIVE: Coarctation of the aorta is rarely associated with known gene defects. Blomstrand chondrodysplasia, caused by... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Gray C, Bratt D, Lees J, Dacosta M, Plant K, Solaymani-Kohal S, Tazzyman S, Serbanovic-Canic J, Crossman DC, Keavney BD, Haase A, McMahon K, Gering M, Roehl H, Evans PC, Chico TJ. Loss of Function of Parathyroid Hormone Receptor 1 Induces Notch-Dependent Aortic Defects During Zebrafish Vascular Development. Arterioscler Thromb Vasc Biol. 2013 Apr 4. [Epub ahead of print]. |
Loss of Redox Factor 1 Decreases NF-kappaB Activity and Increases Susceptibility of Endothelial Cells to Apoptosis
|
Citation:
Arterioscler Thromb Vasc Biol. 2005 Jan;25(1):96-101. Epub 2004 Nov 11. Epub:
Not Epub Abstract:
OBJECTIVE: The aim of this project was to test the hypothesis that redox factor 1 (Ref-1) was a critical upstream determinant... Delivery Method:
Special Delivery Organism or Cell Type:
cell culture: Bovine pulmonary endothelial cells Citation Extract: Guan Z, Basi D, Li Q, Mariash A, Xia YF, Geng J, Kao E, Hall JL. Loss of Redox Factor 1 Decreases NF-kappaB Activity and Increases Susceptibility of Endothelial Cells to Apoptosis. Arterioscler Thromb Vasc Biol. 2005 Jan;25(1):96-101. Epub 2004 Nov 11.. |
Met and Hgf signaling controls hypaxial muscle and lateral line development in the zebrafish
|
Citation:
Development. 2004 Oct;131(19):4857-69. Epub 2004 Sep 1 Epub:
Not Epub Abstract:
Somites give rise to a number of different embryonic cell types, including the precursors of skeletal muscle populations. The... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Haines L, Neyt C, Gautier P, Keenan DG, Bryson-Richardson RJ, Hollway GE, Cole NJ, Currie PD. Met and Hgf signaling controls hypaxial muscle and lateral line development in the zebrafish. Development. 2004 Oct;131(19):4857-69. Epub 2004 Sep 1. |
Morpholino Mediated Knockdown of ERα, ERβa and ERβb mRNAs in Zebrafish (Danio rerio) Embryos Reveals Differential Regulation of Estrogen-Inducible Genes
|
Citation:
Endocrinology. 2013;[Epub ahead of print]. doi:10.1210/en.2013-1446 Epub:
Not Epub Abstract:
Genetically distinct estrogen receptor subtypes (ERα and ERβ) play a major role in mediating estrogen actions in vertebrates,... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Griffin LB, January KE, Ho KW, Cotter KA, Callard GV. Morpholino Mediated Knockdown of ERα, ERβa and ERβb mRNAs in Zebrafish (Danio rerio) Embryos Reveals Differential Regulation of Estrogen-Inducible Genes. Endocrinology. 2013;[Epub ahead of print]. doi:10.1210/en.2013-1446 . |
Movement and function of the pectoral fins of the larval zebrafish (Danio rerio) during slow swimming
|
Citation:
J Exp Biol. 2011 Sep 15;214(Pt 18):3111-23 Epub:
Not Epub Abstract:
Pectoral fins are known to play important roles in swimming for many adult fish; however, their functions in fish larvae are... Organism or Cell Type:
zebrafish Citation Extract: Green MH, Ho RK, Hale ME. Movement and function of the pectoral fins of the larval zebrafish (Danio rerio) during slow swimming. J Exp Biol. 2011 Sep 15;214(Pt 18):3111-23. |
Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene
|
Citation:
Neurobiol Aging. 2010 Jan 7. [Epub ahead of print] Epub:
Not Epub Abstract:
The Grb10-Interacting GYF Protein-2 (GIGYF2) gene has been proposed as the Parkinson-disease (PD) gene underlying the PARK11... Organism or Cell Type:
zebrafish Citation Extract: Guella I, Pistocchi A, Asselta R, Rimoldi V, Ghilardi A, Sironi F, Trotta L, Primignani P, Zini M, Zecchinelli A, Coviello D, Pezzoli G, Del Giacco L, Duga S, Goldwurm S. Mutational screening and zebrafish functional analysis of GIGYF2 as a Parkinson-disease gene. Neurobiol Aging. 2010 Jan 7. [Epub ahead of print]. |
Mutations in C10orf11, Encoding a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism
|
Citation:
Am J Hum Genet. 2013 Feb 5. doi:pii: S0002-9297(13)00037-2. 10.1016/j.ajhg.2013.01.006. [Epub ahead of print] Epub:
Not Epub Abstract:
Autosomal-recessive albinism is a hypopigmentation disorder with a broad phenotypic range. A substantial fraction of... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Grønskov K, Dooley CM, Ostergaard E, Kelsh RN, Hansen L, Levesque MP, Vilhelmsen K, Møllgård K, Stemple DL, Rosenberg T. Mutations in C10orf11, Encoding a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism. Am J Hum Genet. 2013 Feb 5. doi:pii: S0002-9297(13)00037-2. 10.1016/j.ajhg.2013.01.006. [Epub ahead of print]. |
MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis
|
Citation:
Hum Mol Genet. 2013 Dec 15;22(24):4967-77. doi: 10.1093/hmg/ddt344. Epub 2013 Jul 19. Epub:
Not Epub Abstract:
Myosin binding protein C1 (MYBPC1) is an abundant skeletal muscle protein that is expressed predominantly in slow twitch muscle... Organism or Cell Type:
zebrafish Citation Extract: Ha K, Buchan JG, Alvarado DM, McCall K, Vydyanath A, Luther PK, Goldsmith MI, Dobbs MB, Gurnett CA. MYBPC1 mutations impair skeletal muscle function in zebrafish models of arthrogryposis. Hum Mol Genet. 2013 Dec 15;22(24):4967-77. doi: 10.1093/hmg/ddt344. Epub 2013 Jul 19.. |