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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.
MicroRNA-mediated control of developmental lymphangiogenesis
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Citation:
bioRxiv. 2019;[preprint] doi:10.1101/555664 Epub:
Not Epub Abstract:
The post-transcriptional mechanisms contributing to molecular regulation of developmental lymphangiogenesis and lymphatic... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Jung HM, Hu C, Fister AM, Davis AE, Castranova D, Pham VN, Price LM, Weinstein BM. MicroRNA-mediated control of developmental lymphangiogenesis. bioRxiv. 2019;[preprint] doi:10.1101/555664. |
An alternatively spliced zebrafish jnk1a transcript has an essential and non-redundant role in development of the first heart field derived proximal ventricular chamber
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Citation:
bioRxiv. 2019;[preprint] doi:10.1101/546184 Epub:
Not Epub Abstract:
Alternative splicing is a ubiquitous mechanism for producing different mRNA species from a single gene, resulting in proteomic... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Santos-Ledo A, Washer SJ, Dhanaseelan T, Chrystal P, Papoutsi T, Henderson D, Chaudhry B. An alternatively spliced zebrafish jnk1a transcript has an essential and non-redundant role in development of the first heart field derived proximal ventricular chamber. bioRxiv. 2019;[preprint] doi:10.1101/546184. |
Dysregulated wild-type cell division at the interface between host and oncogenic epithelium
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Citation:
bioRxiv. 2019;[preprint] doi:10.1101/578146 Epub:
Not Epub Abstract:
Carcinomas dysregulate their microenvironment and this helps aid disease progression, in part by altering the behaviour of host... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Moruzzi M, Nestor-Bergmann A, Brennan K, Woolner S. Dysregulated wild-type cell division at the interface between host and oncogenic epithelium. bioRxiv. 2019;[preprint] doi:10.1101/578146. |
A Smart Imaging Workflow for Organ-Specific Screening in a Cystic Kidney Zebrafish Disease Model
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Citation:
Int J Med Sci. 2019;20(6):1290. doi:10.3390/ijms20061290 Epub:
Not Epub Abstract:
The zebrafish is being increasingly used in biomedical research and drug discovery to conduct large-scale compound screening.... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Pandey G, Westhoff JH, Schaefer F, Gehrig L. A Smart Imaging Workflow for Organ-Specific Screening in a Cystic Kidney Zebrafish Disease Model. Int J Med Sci. 2019;20(6):1290. doi:10.3390/ijms20061290. |
FoxN3 is necessary for the development of the interatrial septum, the ventricular trabeculae and the muscles at the head/trunk interface in the African clawed frog, Xenopus laevis (Lissamphibia: Anura: Pipidae)
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Citation:
Dev Dyn. 2019 Mar 11. doi: 10.1002/dvdy.25. [Epub ahead of print] Epub:
Yes Abstract:
BACKGROUND: Fox genes are a large family of transcription factors that play diverse roles in the immune system, metabolism,... Organism or Cell Type:
Xenopus laevis Citation Extract: Naumann B, Schmidt J, Olsson L. FoxN3 is necessary for the development of the interatrial septum, the ventricular trabeculae and the muscles at the head/trunk interface in the African clawed frog, Xenopus laevis (Lissamphibia: Anura: Pipidae). Dev Dyn. 2019 Mar 11. doi: 10.1002/dvdy.25. [Epub ahead of print]. |
The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1
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Citation:
Front Physiol. 2019 Feb 25;10:134. doi: 10.3389/fphys.2019.00134. eCollection 2019 Epub:
Not Epub Abstract:
Joubert syndrome (JS) is a congenital autosomal-recessive or-in rare cases-X-linked inherited disease. The diagnostic hallmark... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Ott T, Kaufmann L, Granzow M, Hinderhofer K, Bartram CR, Theiß S, Seitz A, Paramasivam N, Schulz A, Moog U, Blum M, Evers CM. The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1. Front Physiol. 2019 Feb 25;10:134. doi: 10.3389/fphys.2019.00134. eCollection 2019. |
Ultrasensitive detection of microRNA using an array of Au nanowires deposited within the channels of a porous anodized alumina membrane
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Citation:
Elecrochem Comm. 2019;[Epub ahead of print] doi:10.1016/j.elecom.2019.03.008 Epub:
Yes Abstract:
A new nanopore array/Au electrode was fabricated and applied to the detection of microRNA. The electrode was prepared via... Citation Extract: Li C, He L, Jiang S, Mo R, Yan X, Qian Z-J, Zhou C, Sun S, Hong P, Huang Y. Ultrasensitive detection of microRNA using an array of Au nanowires deposited within the channels of a porous anodized alumina membrane. Elecrochem Comm. 2019;[Epub ahead of print] doi:10.1016/j.elecom.2019.03.008. |
Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly
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Citation:
Nat Comm. 2019;10:1180. doi:10.1038/s41467-019-08547-w Epub:
Not Epub Abstract:
A failure in optic fissure fusion during development can lead to blinding malformations of the eye. Here, we report a syndrome... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Lahrouchi N, George A, Ratbi I, Schneider R, Elalaoui SC, Moosa S, Bharti S, Sharma R, Abu-Asab M, Onojafe F, Adadi N, Lodder EM, Laarabi F-Z, Lamsyah Y, Elorch H, Chebbar I, Postma AV, Lougaris V, Plebani A, Altmueller J, Kyrieleis H, Meiner V, McNeill H, Bharti K, Lyonnet S, Wollnik B, Henrion-Caude A, Berraho A, Hildebrandt F, Bezzina CR, Brooks BP, Sefiani A. Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly. Nat Comm. 2019;10:1180. doi:10.1038/s41467-019-08547-w. |
Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer
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Citation:
Vision Res. 2019 Mar;156:66-72. doi: 10.1016/j.visres.2019.01.008. Epub 2019 Feb 2 Epub:
Not Epub Abstract:
Mutation of FOXC1 causes Axenfeld-Rieger Syndrome (ARS) with early onset or congenital glaucoma. We assessed retinal ganglion... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Umali J, Hawkey-Noble A, French CR. Loss of foxc1 in zebrafish reduces optic nerve size and cell number in the retinal ganglion cell layer. Vision Res. 2019 Mar;156:66-72. doi: 10.1016/j.visres.2019.01.008. Epub 2019 Feb 2. |
Proteasomal inhibition attenuates craniofacial malformations in a zebrafish model of Treacher Collins Syndrome
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Citation:
Biochem Pharmacol. 2019 Mar 5. pii: S0006-2952(19)30091-7. doi: 10.1016/j.bcp.2019.03.005. [Epub ahead of print] Epub:
Yes Abstract:
Treacher Collins Syndrome (TCS) is a congenital disease characterized by defects in the craniofacial skeleton and absence of... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Rosas MG, Lorenzatti A, de Peralta MSP, Calcatera NB, Coux G. Proteasomal inhibition attenuates craniofacial malformations in a zebrafish model of Treacher Collins Syndrome. Biochem Pharmacol. 2019 Mar 5. pii: S0006-2952(19)30091-7. doi: 10.1016/j.bcp.2019.03.005. [Epub ahead of print]. |