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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.
Coordinated genomic control of ciliogenesis and cell movement by RFX2
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Citation:
eLife. 2014; 3: e01439. Published online 2014 January 14. doi: 10.7554/eLife.01439 Epub:
Not Epub Abstract:
The mechanisms linking systems-level programs of gene expression to discrete cell biological processes in vivo remain poorly... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Chung M-I, Kwon T, Tu F, Brooks ER, Gupta R, Meyer M, Baker JC, Marcotte EM, Wallingford JB. Coordinated genomic control of ciliogenesis and cell movement by RFX2. eLife. 2014; 3: e01439. Published online 2014 January 14. doi: 10.7554/eLife.01439. |
Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome
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Citation:
Front Endocrinol (Lausanne). 2013;4:203. doi:10.3389/fendo.2013.00203 Epub:
Not Epub Abstract:
During embryonic development, immature neurons in the olfactory epithelium (OE) extend axons through the nasal mesenchyme, to... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Garaffo G, Provero P, Molineris I, Pinciroli P, Peano C, Battaglia C, Tomaiuolo D, Etzion T, Gothilf Y, Santoro M, Merlo GR. Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome. Front Endocrinol (Lausanne). 2013;4:203. doi:10.3389/fendo.2013.00203. |
PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa
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Citation:
Hum Mol Genet. 2014 Jan 12. [Epub ahead of print] Epub:
Yes Abstract:
Retinitis pigmentosa (RP), a disease characterized by progressive loss of photoreceptors, exhibits significant genetic... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C. PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa. Hum Mol Genet. 2014 Jan 12. [Epub ahead of print]. |
Zebrafish Stem/Progenitor Factor msi2b Exhibits Two Phases of Activity Mediated by Different Splice Variants
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Citation:
Stem Cells. 2014 Feb;32(2):558-71. doi: 10.1002/stem.1583 Epub:
Not Epub Abstract:
The Musashi (Msi) family of RNA-binding proteins is important in stem and differentiating cells in many species. Here, we... Organism or Cell Type:
zebrafish Citation Extract: Hochgreb-Hägele T, Koo DE, Das NM, Bronner ME. Zebrafish Stem/Progenitor Factor msi2b Exhibits Two Phases of Activity Mediated by Different Splice Variants. Stem Cells. 2014 Feb;32(2):558-71. doi: 10.1002/stem.1583. |
Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish
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Citation:
Int J Biochem Cell Biol. 2014 Jan 10. pii: S1357-2725(14)00015-6. doi: 10.1016/j.biocel.2014.01.006. [Epub ahead of print] Epub:
Yes Abstract:
Diamond-Blackfan anemia is an inherited genetic disease caused by mutations in ribosomal protein genes. The disease is... Organism or Cell Type:
zebrafish Citation Extract: Yadav GV, Chakraborty A, Uechi T, Kenmochi N. Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish. Int J Biochem Cell Biol. 2014 Jan 10. pii: S1357-2725(14)00015-6. doi: 10.1016/j.biocel.2014.01.006. [Epub ahead of print]. |
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
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Citation:
Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13 Epub:
Not Epub Abstract:
Deletion 1p36 syndrome is recognized as the most common terminal deletion syndrome. Here, we describe the loss of a gene within... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13. |
Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy
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Citation:
Am J Hum Genet. 2013 Jul 11;93(1):6-18. doi: 10.1016/j.ajhg.2013.05.004. Epub 2013 Jun 6 Epub:
Not Epub Abstract:
Nemaline myopathy (NEM) is a common congenital myopathy. At the very severe end of the NEM clinical spectrum are genetically... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Ravenscroft G, Miyatake S, Lehtokari VL, Todd EJ, Vornanen P, Yau KS, Hayashi YK, Miyake N, Tsurusaki Y, Doi H, Saitsu H, Osaka H, Yamashita S, Ohya T, Sakamoto Y, Koshimizu E, Imamura S, Yamashita M, Ogata K, Shiina M, Bryson-Richardson RJ, Vaz R, Ceyhan O, Brownstein CA, Swanson LC, Monnot S, Romero NB, Amthor H, Kresoje N, Sivadorai P, Kiraly-Borri C, Haliloglu G, Talim B, Orhan D, Kale G, Charles AK, Fabian VA, Davis MR, Lammens M, Sewry CA, Manzur A, Muntoni F, Clarke NF, North KN, Bertini E, Nevo Y, Willichowski E, Silberg IE, Topaloglu H, Beggs AH, Allcock RJ, Nishino I, Wallgren-Pettersson C, Matsumoto N, Laing NG. Mutations in KLHL40 are a frequent cause of severe autosomal-recessive nemaline myopathy. Am J Hum Genet. 2013 Jul 11;93(1):6-18. doi: 10.1016/j.ajhg.2013.05.004. Epub 2013 Jun 6. |
Mirror-symmetric microtubule assembly and cell interactions drive lumen formation in the zebrafish neural rod
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Citation:
EMBO J. 2013 Jan 9;32(1):30-44. doi: 10.1038/emboj.2012.305. Epub 2012 Nov 30 Epub:
Not Epub Abstract:
By analysing the cellular and subcellular events that occur in the centre of the developing zebrafish neural rod, we have... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Buckley CE, Ren X, Ward LC, Girdler GC, Araya C, Green MJ, Clark BS, Link BA, Clarke JD. Mirror-symmetric microtubule assembly and cell interactions drive lumen formation in the zebrafish neural rod. EMBO J. 2013 Jan 9;32(1):30-44. doi: 10.1038/emboj.2012.305. Epub 2012 Nov 30. |
An injury-responsive gata4 program shapes the zebrafish cardiac ventricle
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Citation:
Curr Biol. 2013 Jul 8;23(13):1221-7. doi: 10.1016/j.cub.2013.05.028. Epub 2013 Jun 20 Epub:
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A common principle of tissue regeneration is the reactivation of previously employed developmental programs. During zebrafish... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Gupta V, Gemberling M, Karra R, Rosenfeld GE, Evans T, Poss KD. An injury-responsive gata4 program shapes the zebrafish cardiac ventricle. Curr Biol. 2013 Jul 8;23(13):1221-7. doi: 10.1016/j.cub.2013.05.028. Epub 2013 Jun 20. |
Dysregulated phosphatidylinositol signaling promotes endoplasmic-reticulum-stress-mediated intestinal mucosal injury and inflammation in zebrafish
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Citation:
Dis Model Mech. 2014 Jan-Feb;7(1):93-106. doi: 10.1242/dmm.012864. Epub 2013 Oct 17 Epub:
Not Epub Abstract:
Dysregulated phosphatidylinositol (PI) signaling has been implicated in human gastrointestinal (GI) malignancies and... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Thakur PC, Davison JM, Stuckenholz C, Lu L, Bahary N. Dysregulated phosphatidylinositol signaling promotes endoplasmic-reticulum-stress-mediated intestinal mucosal injury and inflammation in zebrafish. Dis Model Mech. 2014 Jan-Feb;7(1):93-106. doi: 10.1242/dmm.012864. Epub 2013 Oct 17. |