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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 12245 scientific papers returned from the database with the search filters currently being used below.
There are 12245 scientific papers returned from the database with the search filters currently being used below.
Zebrafish as a model for myelopoiesis during embryogenesis
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Citation:
Exp Hematol. 2005 Sep;33(9):997-1006 Epub:
Not Epub Abstract:
Zebrafish produce nearly identical hematopoeitic cell lineages to those found in mammals and other higher vertebrates. As in... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Berman JN, Kanki JP, Look AT. Zebrafish as a model for myelopoiesis during embryogenesis. Exp Hematol. 2005 Sep;33(9):997-1006. |
Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
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Citation:
Am Journal Hum Genet. 2013;93(4):672-686 Epub:
Not Epub Abstract:
Primary ciliary dyskinesia (PCD) is caused when defects of motile cilia lead to chronic airway infections, male infertility,... Organism or Cell Type:
zebrafish Citation Extract: Austin-Tse C, Halbritter J, Zariwala MA, Gilberti RM, Gee HY, Hellman N, Pathak N, Liu Y, Panizzi JR, Patel-King RS, Tritschler D Bower R, O'Toole E, Porath JD, Hurd TW, Chaki M, Diaz KA, Kohl S, Lovric S, Hwang D-Y, Braun DA, Schueler M, Airik R, Otto EA, Leigh MW, Noone PG, Carson JL, Davis SD, Pittman JE, Ferkol TW, Atkinson JJ, Olivier KN, Sagel SD, Dell SD, Rosenfeld M, Milla CE, Loges NT, Omran H, Porter ME, King SM, Knowles MR, Drummond IA, Hildebrandt F.. Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia. Am Journal Hum Genet. 2013;93(4):672-686. |
Zebrafish collagen XIV is transiently expressed in epithelia and is required for proper function of certain basement membranes
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Citation:
J. Biol. Chem. 2013;[Epub ahead of print] doi:10.1074/jbc.M112.430637 Epub:
Not Epub Abstract:
We found that zebrafish has two differentially expressed col14a1 paralogs. col14a1a expression peaked between 18-somite stage... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Bader HL, Lambert E, Guiraud A, Malbouyres M, Driever W, Koch M, Ruggiero F. Zebrafish collagen XIV is transiently expressed in epithelia and is required for proper function of certain basement membranes. J. Biol. Chem. 2013;[Epub ahead of print] doi:10.1074/jbc.M112.430637. |
Zebrafish DeltaNp63 is a direct target of Bmp signaling and encodes a transcriptional repressor blocking neural specification in the ventral ectoderm
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Citation:
Dev Cell. 2002 May;2(5):617-27 Epub:
Not Epub Abstract:
Bone morphogenetic proteins (Bmps) promote ventral specification in both the mesoderm and the ectoderm of vertebrate embryos.... Delivery Method:
zebrafish Citation Extract: Bakkers J, Hild M, Kramer C, Furutani-Seiki M, Hammerschmidt M. Zebrafish DeltaNp63 is a direct target of Bmp signaling and encodes a transcriptional repressor blocking neural specification in the ventral ectoderm. Dev Cell. 2002 May;2(5):617-27. |
Zebrafish R-cadherin (Cdh4) controls visual system development and differentiation
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Citation:
Dev Dyn. 2005 Jul;233(3):930-45 Epub:
Not Epub Abstract:
In zebrafish, R-cadherin (cadherin-4 or Cdh4) is expressed in the retina and in retinorecipient brain regions, suggesting that... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Babb SG, Kotradi SM, Shah B, Chiappini-Williamson C, Bell LN, Schmeiser G, Chen E, Liu Q, Marrs JA. Zebrafish R-cadherin (Cdh4) controls visual system development and differentiation. Dev Dyn. 2005 Jul;233(3):930-45. |
A Complex Regulatory Network of Transcription Factors Critical for Ocular Development and Disease
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Citation:
Hum Mol Genet. 2011 Jan 31. [Epub ahead of print] Epub:
Not Epub Abstract:
The PITX2 \"homeobox\" and FOXC1 and FOXC2 \"forkhead box\" transcription factors are critical for eye... Organism or Cell Type:
zebrafish Citation Extract: Acharya M, Huang L, Fleisch VC, Allison WT, Walter MA. A Complex Regulatory Network of Transcription Factors Critical for Ocular Development and Disease. Hum Mol Genet. 2011 Jan 31. [Epub ahead of print]. |
A dual requirement for Iroquois genes during Xenopus kidney development
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Citation:
Development. 2008 Aug 20. [Epub ahead of print] Epub:
Not Epub Abstract:
The Iroquois (Irx) genes encode evolutionary conserved homeoproteins. We report that Xenopus genes Irx1 and Irx3 are expressed... Organism or Cell Type:
Xenopus Citation Extract: Alarcón P, Rodríguez-Seguel E, Fernández-González A, Rubio R, Gómez-Skarmeta JL. A dual requirement for Iroquois genes during Xenopus kidney development. Development. 2008 Aug 20. [Epub ahead of print]. |
A meckelin-filamin A interaction mediates ciliogenesis
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Citation:
Hum. Mol. Genet. first published online November 25, 2011 doi:10.1093/hmg/ddr557 Epub:
Not Epub Abstract:
MKS3, encoding the transmembrane receptor meckelin, is mutated in Meckel-Gruber syndrome (MKS), an autosomal recessive... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Adams M, Simms RJ, Abdelhamed Z, Dawe HR, Szymanska K, Logan CV, Wheway G, Pitt E, Gull K, Knowles MA, Blair E, Cross SH, Sayer JA, Johnson CA. A meckelin-filamin A interaction mediates ciliogenesis. Hum. Mol. Genet. first published online November 25, 2011 doi:10.1093/hmg/ddr557. |
A transmembrane protein EIG121L is required for epidermal differentiation during early embryonic development
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Citation:
J Biol Chem. 2010 Dec 21. [Epub ahead of print] Epub:
Not Epub Abstract:
Epidermal differentiation in the ventral ectoderm of Xenopus embryos is regulated by the bone morphogenetic protein (BMP)... Organism or Cell Type:
Xenopus Citation Extract: Araki T, Kusakabe M, Nishida E. A transmembrane protein EIG121L is required for epidermal differentiation during early embryonic development. J Biol Chem. 2010 Dec 21. [Epub ahead of print]. |
Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6
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Citation:
Dev Biol. 2009 Dec 1;336(1):20-9. Epub 2009 Sep 19 Epub:
Not Epub Abstract:
Mechanisms coupling heart function and cardiac morphogenesis can be accessed in lower vertebrate embryos that can survive to... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Abu-Daya A, Sater AK, Wells DE, Mohun TJ, Zimmerman LB. Absence of heartbeat in the Xenopus tropicalis mutation muzak is caused by a nonsense mutation in cardiac myosin myh6. Dev Biol. 2009 Dec 1;336(1):20-9. Epub 2009 Sep 19. |