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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 12353 scientific papers returned from the database with the search filters currently being used below.
There are 12353 scientific papers returned from the database with the search filters currently being used below.
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]. |
Modelling Duchenne muscular dystrophy in MYOD1-converted urine-derived cells treated with 3-deazaneplanocin A hydrochloride
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Citation:
Sci Rep. 2019;9(1):3807. doi:10.1038/s41598-019-40421-z Epub:
Not Epub Abstract:
Duchenne muscular dystrophy (DMD) is a severe muscle disorder characterised by mutations in the DMD gene. Recently, we have... Delivery Method:
Endo-Porter Organism or Cell Type:
human MYOD1-urine-derived cells and MYOD1-converted fibroblasts Citation Extract: Takizawa H, Hara Y, Mizobe Y, Ohno T, Suzuki S, Inoue K, Takeshita E, Shimizu-Motohashi Y, Ishiyama A, Hoshino M, Komaki H, Takeda S, Aoki Y. Modelling Duchenne muscular dystrophy in MYOD1-converted urine-derived cells treated with 3-deazaneplanocin A hydrochloride. Sci Rep. 2019;9(1):3807. doi:10.1038/s41598-019-40421-z. |
bif1, a new BMP signaling inhibitor, regulates embryonic hematopoiesis in the zebrafish
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Citation:
Development. 2019;dev.164103. doi:10.1242/dev.164103 Epub:
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Hematopoiesis maintains the entire blood system and dysregulation of this process can lead to malignancies (leukemia),... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Ghersi JJ, Mahony CB, Bertrand JY. bif1, a new BMP signaling inhibitor, regulates embryonic hematopoiesis in the zebrafish. Development. 2019;dev.164103. doi:10.1242/dev.164103. |
Etv6 activates vegfa expression through positive and negative transcriptional regulatory networks in Xenopus embryos
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Citation:
Nat Commun. 2019 Mar 6;10(1):1083. doi: 10.1038/s41467-019-09050-y Epub:
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VEGFA signaling controls physiological and pathological angiogenesis and hematopoiesis. Although many context-dependent... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Li L, Rispoli R, Patient R, Ciau-Uitz A, Porcher C. Etv6 activates vegfa expression through positive and negative transcriptional regulatory networks in Xenopus embryos. Nat Commun. 2019 Mar 6;10(1):1083. doi: 10.1038/s41467-019-09050-y. |
L1cam-mediated developmental processes of the nervous system are differentially regulated by proteolytic processing
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Citation:
Sci Rep. 2019 Mar 6;9(1):3716. doi: 10.1038/s41598-019-39884-x Epub:
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Normal brain development depends on tight temporal and spatial regulation of connections between cells. Mutations in L1cam, a... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Linneberg C, Toft CLF, Kjaer-Sorensen K, Laursen LS. L1cam-mediated developmental processes of the nervous system are differentially regulated by proteolytic processing. Sci Rep. 2019 Mar 6;9(1):3716. doi: 10.1038/s41598-019-39884-x. |
Vegfa/vegfr2 signaling is necessary for zebrafish islet vessel development, but is dispensable for beta-cell and alpha-cell formation
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Citation:
Sci Rep. 2019 Mar 5;9(1):3594. doi: 10.1038/s41598-019-40136-1 Epub:
Not Epub Abstract:
The mechanisms underlying zebrafish pancreatic islet vascularization have not been well characterized. We sought to determine... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Toselli CM, Wilkinson BM, Paterson J, Kieffer TJ. Vegfa/vegfr2 signaling is necessary for zebrafish islet vessel development, but is dispensable for beta-cell and alpha-cell formation. Sci Rep. 2019 Mar 5;9(1):3594. doi: 10.1038/s41598-019-40136-1. |