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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 12376 scientific papers returned from the database with the search filters currently being used below.
There are 12376 scientific papers returned from the database with the search filters currently being used below.
[Morpholino oligonucleotide-based screen of novel genes with developmental function]
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Citation:
Seikagaku. 2003 Jul;75(7):617-20 Epub:
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[Article in Japanese] Delivery Method:
Microinjection Organism or Cell Type:
Ciona savignyi Citation Extract: Wada S, Yamada L, Kobayashi K, Shoguchi E, Satoh N. [Morpholino oligonucleotide-based screen of novel genes with developmental function]. Seikagaku. 2003 Jul;75(7):617-20. |
A complex extracellular sphingomyelinase of Pseudomonas aeruginosa inhibits angiogenesis by selective cytotoxicity to endothelial cells
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Citation:
PLoS Pathog. 2009 May;5(5):e1000420. Epub 2009 May 8 Epub:
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The hemolytic phospholipase C (PlcHR) expressed by Pseudomonas aeruginosa is the original member of a Phosphoesterase... Organism or Cell Type:
zebrafish Citation Extract: Vasil ML, Stonehouse MJ, Vasil AI, Wadsworth SJ, Goldfine H, Bolcome RE 3rd, Chan J. A complex extracellular sphingomyelinase of Pseudomonas aeruginosa inhibits angiogenesis by selective cytotoxicity to endothelial cells. PLoS Pathog. 2009 May;5(5):e1000420. Epub 2009 May 8. |
A Congenital Neutrophil Defect Syndrome Associated with Mutations in VPS45
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Citation:
N Engl J Med. 2013;[Epub ahead of print]doi:10.1056/NEJMoa1301296 Epub:
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Background Neutrophils are the predominant phagocytes that provide protection against bacterial and fungal infections.... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Vilboux T, Lev A, Malicdan MCV, Simon AJ, Järvinen P, Racek T, Puchalka J, Sood R, Carrington B, Bishop K, Mullikin J, Huizing M, Garty BZ, Eyal E, Wolach B, Gavrieli R, Toren A, Soudack M, Atawneh OM, Babushkin T, Schiby G, Cullinane A, Avivi C, Polak-Charcon S, Barshack I, Amariglio N, Rechavi G, van der Werff ten Bosch J, Anikster Y, Klein C, Gahl WA, Somech R. . A Congenital Neutrophil Defect Syndrome Associated with Mutations in VPS45. N Engl J Med. 2013;[Epub ahead of print]doi:10.1056/NEJMoa1301296. |
A critical role for myoglobin in zebrafish development
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Citation:
Int J Dev Biol. 2009 Apr 2. [Epub ahead of print] Epub:
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The globin family, including hemoglobin, myoglobin, neuroglobin and cytoglobin, plays an important role in oxygen storage and... Organism or Cell Type:
zebrafish Citation Extract: Vlecken DH, Testerink J, Ott EB, Sakalis PA, Jaspers RT, Bagowski CP. A critical role for myoglobin in zebrafish development. Int J Dev Biol. 2009 Apr 2. [Epub ahead of print]. |
A mutation in the RNF170 gene causes autosomal dominant sensory ataxia
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Citation:
Brain. 2011 Feb;134(Pt 2):602-7. Epub 2010 Nov 28 Epub:
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Autosomal dominant sensory ataxia is a rare genetic condition that results in a progressive ataxia that is caused by... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Valdmanis PN, Dupré N, Lachance M, Stochmanski SJ, Belzil VV, Dion PA, Thiffault I, Brais B, Weston L, Saint-Amant L, Samuels ME, Rouleau GA. A mutation in the RNF170 gene causes autosomal dominant sensory ataxia. Brain. 2011 Feb;134(Pt 2):602-7. Epub 2010 Nov 28. |
A novel complex, RUNX1-MYEF2, represses hematopoietic genes in erythroid cells
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Citation:
Mol Cell Biol. 2012 Oct;32(19):3814-22. doi: 10.1128/MCB.05938-11. Epub 2012 Jul 16 Epub:
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RUNX1 is known to be an essential transcription factor for generating hematopoietic stem cells (HSC), but much less is known... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: van Riel B, Pakozdi T, Brouwer R, Monteiro R, Tuladhar K, Franke V, Bryne JC, Jorna R, Rijkers EJ, van Ijcken W, Andrieu-Soler C, Demmers J, Patient R, Soler E, Lenhard B, Grosveld F. A novel complex, RUNX1-MYEF2, represses hematopoietic genes in erythroid cells. Mol Cell Biol. 2012 Oct;32(19):3814-22. doi: 10.1128/MCB.05938-11. Epub 2012 Jul 16. |
A novel mechanism for the transcriptional regulation of Wnt signaling in development
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Citation:
Genes Dev. 2011 Sep 1;25(17):1783-95. Epub 2011 Aug 19. Epub:
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Axial patterning of the embryonic brain requires a precise balance between canonical Wnt signaling, which dorsalizes the... Delivery Method:
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Xenopus Citation Extract: Vacik T, Stubbs JL, Lemke G. A novel mechanism for the transcriptional regulation of Wnt signaling in development. Genes Dev. 2011 Sep 1;25(17):1783-95. Epub 2011 Aug 19.. |
A Spatial and Temporal Gradient of Fgf Differentially Regulates Distinct Stages of Neural Development in the Zebrafish Inner Ear
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Citation:
PLoS Genet. 2012;8(11):e1003068. doi:10.1371/journal.pgen.1003068 Epub:
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Neuroblasts of the statoacoustic ganglion (SAG) initially form in the floor of the otic vesicle during a relatively brief... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Vemaraju S, Kantarci H, Padanad MS, Riley BB. A Spatial and Temporal Gradient of Fgf Differentially Regulates Distinct Stages of Neural Development in the Zebrafish Inner Ear. PLoS Genet. 2012;8(11):e1003068. doi:10.1371/journal.pgen.1003068. |
A Zebrafish Model For The Shwachman-Diamond Syndrome (SDS)
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Pediatr Res. 2008 Apr;63(4):348-52. Epub:
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The Shwachman-Diamond Syndrome (SDS) is characterized by exocrine pancreatic insufficiency, neutrophil defect and skeletal... Organism or Cell Type:
zebrafish Citation Extract: Venkatasubramani N, Mayer AN. A Zebrafish Model For The Shwachman-Diamond Syndrome (SDS). Pediatr Res. 2008 Apr;63(4):348-52.. |
Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotides
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Citation:
Hum Mutat. 2006 May;27(5):420-6 Epub:
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An intronic point mutation was identified in the ocular albinism type 1 (OA1) gene (HUGO symbol, GPR143) in a family with the X... Delivery Method:
Special Delivery Organism or Cell Type:
Melanocyte from BA393 and BA399 patients Citation Extract: Vetrini F, Tammaro R, Bondanza S, Surace EM, Auricchio A, De Luca M, Ballabio A, Marigo V. Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotides. Hum Mutat. 2006 May;27(5):420-6. |