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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.
Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation
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Citation:
Brain. 2018;[Epub ahead of print] doi:10.1093/brain/awy020 Epub:
Yes Abstract:
Vein of Galen aneurysmal malformation is a congenital anomaly of the cerebral vasculature representing 30% of all paediatric... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Vivanti A, Ozanne A, Grondin C, Saliou G, Quevarec L, Maurey H, Aubourg P, Benachi A, Gut M, Gut I, Martinovic J, Sénat MV, Tawk M, Melki J. Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation. Brain. 2018;[Epub ahead of print] doi:10.1093/brain/awy020. |
Sema3a plays a role in the pathogenesis of CHARGE syndrome
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Citation:
Hum Mol Genet. 2018;[Epub] doi:10.1093/hmg/ddy045 Epub:
Yes Abstract:
CHARGE syndrome is an autosomal dominant malformation disorder caused by heterozygous loss of function mutations in the... Organism or Cell Type:
Xenopus Citation Extract: Ufartes R, Schwenty-Lara J, Freese L, Neuhofer C, Möller J, Wehner P, van Ravenswaaij-Arts CMA, Wong MTY Schanze I, Tzschach A, Bartsch O, Borchers A, Pauli S. Sema3a plays a role in the pathogenesis of CHARGE syndrome. Hum Mol Genet. 2018;[Epub] doi:10.1093/hmg/ddy045. |
Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility
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Citation:
Am J Hum Genet. 2018;[Epub ahead of print] doi:doi.org/10.1016/j.ajhg.2018.01.009 Epub:
Yes Abstract:
Despite the rapid discovery of genes for rare genetic disorders, we continue to encounter individuals presenting with syndromic... Organism or Cell Type:
zebrafish Citation Extract: Maudinas R, Mazodier K, Rimet Y, Rivière J-B, Roquelaure B, Sigaudy S, Stephenne X, Thauvin-Robinet C, Thevenon J, Sarles J, Levy N, Badens C, Goulet O, Hugot J-P, Katsanis N, Faivre L, Fabre A. Loss-of-Function Mutations in UNC45A Cause a Syndrome Associating Cholestasis, Diarrhea, Impaired Hearing, and Bone Fragility. Am J Hum Genet. 2018;[Epub ahead of print] doi:doi.org/10.1016/j.ajhg.2018.01.009. |
An Attractive Reelin Gradient Establishes Synaptic Lamination in the Vertebrate Visual System
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Citation:
Neuron. 2018;[Epub ahead of print] doi:10.1016/j.neuron.2018.01.030 Epub:
Yes Abstract:
A conserved organizational and functional principle of neural networks is the segregation of axon-dendritic synaptic... Organism or Cell Type:
zebrafish Citation Extract: Di Donato V, De Santis F, Albadri S, Auer TO, Duroure K, Charpentier M, Concordet J-P, Gebhardt C, Del Bene F. An Attractive Reelin Gradient Establishes Synaptic Lamination in the Vertebrate Visual System. Neuron. 2018;[Epub ahead of print] doi:10.1016/j.neuron.2018.01.030. |
Effects of long-term treatment with eteplirsen on cardiac function
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Citation:
Neuromusc Disord. 2017;27(suppl 2):S114 doi:10.1016/j.nmd.2017.06.083 Epub:
Not Epub Delivery Method:
i.v. infusion Organism or Cell Type:
human Citation Extract: Cripe L, Colan S. Eliopoulos H, Moody S, Mendell J. Effects of long-term treatment with eteplirsen on cardiac function. Neuromusc Disord. 2017;27(suppl 2):S114 doi:10.1016/j.nmd.2017.06.083. |
NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease
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Citation:
Acta Neuropath. 2018;[Epub ahead of print] doi:10.1007/s00401-018-1817-z Epub:
Not Epub Abstract:
A novel multi-organ disease that is fatal in early childhood was identified in three patients from two non-consanguineous... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Uusimaa J, Kaarteenaho R, Paakkola T, Tuominen H, Karjalainen MK, Nadaf J,Varilo T, Uusi-Mäkelä M, Suo-Palosaari M, Pietilä I, Hiltunen AE, Ruddock L, Alanen H, Biterova E, Miinalainen I, Salminen A, Soininen R, Manninen A, Sormunen R, Kaakinen M, Vuolteenaho R, Herva R, Vieira P, Teija Dunder T, Kokkonen H, Moilanen JS, Rantala H, Nogee LM, Majewski J, Rämet M, Hallman M, Hinttala R. NHLRC2 variants identified in patients with fibrosis, neurodegeneration, and cerebral angiomatosis (FINCA): characterisation of a novel cerebropulmonary disease. Acta Neuropath. 2018;[Epub ahead of print] doi:10.1007/s00401-018-1817-z. |
Heg1 and Ccm1/2 proteins control endocardial mechanosensitivity during zebrafish valvulogenesis
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Citation:
Elife. 2018 Feb 1;7. pii: e28939. doi: 10.7554/eLife.28939 Epub:
Not Epub Abstract:
Endothelial cells respond to different levels of fluid shear stress through adaptations of their mechanosensitivity. Currently... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Donat S, Lourenço M, Paolini A, Otten C, Renz M, Abdelilah-Seyfried S. Heg1 and Ccm1/2 proteins control endocardial mechanosensitivity during zebrafish valvulogenesis. Elife. 2018 Feb 1;7. pii: e28939. doi: 10.7554/eLife.28939. |
Growth Differentiation Factor 6 Promotes Vascular Stability by Restraining Vascular Endothelial Growth Factor Signaling
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Citation:
Arterioscler Thromb Vasc Biol. 2018 Feb;38(2):353-362. doi: 10.1161/ATVBAHA.117.309571. Epub 2017 Dec 28 Epub:
Not Epub Abstract:
OBJECTIVE: The assembly of a functional vascular system requires a coordinated and dynamic transition from activation to... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Krispin S, Stratman AN, Melick CH, Stan RV, Malinverno M, Gleklen J, Castranova D, Dejana E, Weinstein BM. Growth Differentiation Factor 6 Promotes Vascular Stability by Restraining Vascular Endothelial Growth Factor Signaling. Arterioscler Thromb Vasc Biol. 2018 Feb;38(2):353-362. doi: 10.1161/ATVBAHA.117.309571. Epub 2017 Dec 28. |
Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein
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Citation:
PLoS Genet. 2018;14(2):e1007212. doi:10.1371/journal.pgen.1007212 Epub:
Not Epub Abstract:
The lack of a mutant phenotype in homozygous mutant individuals’ due to compensatory gene expression triggered upstream of... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Sztal TE, McKaige EA, Williams C, Ruparelia AA, Bryson-Richardson RJ. Genetic compensation triggered by actin mutation prevents the muscle damage caused by loss of actin protein. PLoS Genet. 2018;14(2):e1007212. doi:10.1371/journal.pgen.1007212. |
Functional roles of ornithine decarboxylase and arginine decarboxylase during the peri-implantation period of pregnancy in sheep
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Citation:
J Anim Sci Biotechnol. 2018 Jan 24;9:10. doi: 10.1186/s40104-017-0225-x. eCollection 2018 Epub:
Not Epub Abstract:
Background: Polyamines stimulate DNA transcription and mRNA translation for protein synthesis in trophectoderm cells, as well... Delivery Method:
Endo-Porter Organism or Cell Type:
Ovis aries (sheep) Citation Extract: Lenis YY, Johnson GA, Wang X, Tang WW, Dunlap KA, Satterfield MC, Wu G, Hansen TR, Bazer FW. Functional roles of ornithine decarboxylase and arginine decarboxylase during the peri-implantation period of pregnancy in sheep. J Anim Sci Biotechnol. 2018 Jan 24;9:10. doi: 10.1186/s40104-017-0225-x. eCollection 2018. |