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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 12156 scientific papers returned from the database with the search filters currently being used below.
There are 12156 scientific papers returned from the database with the search filters currently being used below.
Zebrafish Model for Non-Syndromic X-linked Sensorineural Deafness, DFNX1
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Citation:
Anat Rec (Hoboken). 2019 Mar 15. doi: 10.1002/ar.24115. [Epub ahead of print] Epub:
Yes Abstract:
Hereditary deafness is often a neurosensory disorder and affects the quality of life of humans. Only three X-linked genes (POU... Organism or Cell Type:
zebrafish Citation Extract: DeSmidt AA, Zou B, Grati M, Yan D, Mittal R, Yao Q, Richmond MT, Denyer S, Liu XZ, Lu Z. Zebrafish Model for Non-Syndromic X-linked Sensorineural Deafness, DFNX1. Anat Rec (Hoboken). 2019 Mar 15. doi: 10.1002/ar.24115. [Epub ahead of print]. |
cMet signaling functions during zebrafish hindbrain development
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Citation:
Dev Biol. 2008;329(2):541. doi:10.1016/j.ydbio.2008.05.270 Epub:
Not Epub Abstract:
During development, cMet signaling regulates a range of cellular processes, including growth, survival and migration (... Organism or Cell Type:
zebrafish Citation Extract: Elsen GE, Choi LY, Prince VE, Ho RK. cMet signaling functions during zebrafish hindbrain development. Dev Biol. 2008;329(2):541. doi:10.1016/j.ydbio.2008.05.270. |
Generation of anisotropic strain dysregulates wild-type cell division at the interface between host and oncogenic tissue
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Citation:
Curr Biol. 2021 Aug 9;31(15):3409-3418.e6. doi: 10.1016/j.cub.2021.05.023. Epub 2021 Jun 9. PMID: 34111402; PMCID: PMC8360906 Epub:
Not Epub Abstract:
Epithelial tissues are highly sensitive to anisotropies in mechanical force, with cells altering fundamental behaviors, such as... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Moruzzi M, Nestor-Bergmann A, Goddard GK, Tarannum N, Brennan K, Woolner S. Generation of anisotropic strain dysregulates wild-type cell division at the interface between host and oncogenic tissue. Curr Biol. 2021 Aug 9;31(15):3409-3418.e6. doi: 10.1016/j.cub.2021.05.023. Epub 2021 Jun 9. PMID: 34111402; PMCID: PMC8360906. |
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]. |