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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.
Tracking periocular mesenchyme derived anterior segment development using single cell transcriptomic analysis
Citation:
Invest Ophthalmol Vis Sci. 2020;61:3175 Epub:
Not Epub Abstract:
Purpose: The anterior segment (AS) of the eye, as well as further anterior structures, are formed by a subgroup of neural crest... Organism or Cell Type:
zebrafish Citation Extract: Voecking O, Smith J, Famulski J. Tracking periocular mesenchyme derived anterior segment development using single cell transcriptomic analysis. Invest Ophthalmol Vis Sci. 2020;61:3175. |
Optimizing oligotherapeutics for visual loss in Usher syndrome mice
Citation:
Invest Ophthalmol Vis Sci. 2020;Vol.61:2445 Epub:
Not Epub Abstract:
Purpose : Usher syndrome (Usher) is a syndromic form of inherited retinal dystrophy (IRD) characterized by hearing impairment... Delivery Method:
intravitreal injection Organism or Cell Type:
mice Citation Extract: Lentz JJ, Hathaway M, Robillard KN, Ponnath A, Fisher M, Rigo F, Alapure BV. Optimizing oligotherapeutics for visual loss in Usher syndrome mice. Invest Ophthalmol Vis Sci. 2020;Vol.61:2445. |
Cardiac function modulates endocardial cell dynamics to shape the cardiac outflow tract
Citation:
Development. 2020;147:dev185900 doi:10.1242/dev.185900 Epub:
Not Epub Abstract:
Physical forces are important participants in the cellular dynamics that shape developing organs. During heart formation, for... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Sidhwani P, Leerberg DM, Boezio GLM, Capasso TL, Yang H, Chi NC, Roman BL, Stainier DYR, Yelon D. Cardiac function modulates endocardial cell dynamics to shape the cardiac outflow tract. Development. 2020;147:dev185900 doi:10.1242/dev.185900 . |
Duped by a duplication: Heterozygous duplication in PRPF31 causes Retinitis pigmentosa in elusive gene family
Citation:
Invest Ophthalmol Vis Sci. 2020;61(7):4468 Epub:
Not Epub Abstract:
Inherited retinal degenerations (IRD) are an important cause of blindness affecting 1/4000 people worldwide. Presently, over... Organism or Cell Type:
zebrafish Citation Extract: Scott H, Larson A, Chao KR, DiTroia SP, Butcher R, Place E, Pierce EA, Bujakowska K. Duped by a duplication: Heterozygous duplication in PRPF31 causes Retinitis pigmentosa in elusive gene family. Invest Ophthalmol Vis Sci. 2020;61(7):4468. |
Pax6 organizes the anterior eye segment by guiding two distinct neural crest waves
Citation:
PLoS Genet. 2020;16(6):e1008774. doi:10.1371/journal.pgen.1008774 Epub:
Not Epub Abstract:
Cranial neural crest (NC) contributes to the developing vertebrate eye. By multidimensional, quantitative imaging, we traced... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Takamiya M, Stegmaier J, Kobitski AY, Schott B, Weger BD, Margariti D, Delgado ARC, Gourain V, Scherr T, Yang L, Sorge S, Otte JC, Hartmann V, van Wezel J, Stotzka R, Reinhard T, Schlunck G, Dickmeis T, Rastegar S, Mikut R, Nienhaus GU, Strähle U. Pax6 organizes the anterior eye segment by guiding two distinct neural crest waves. PLoS Genet. 2020;16(6):e1008774. doi:10.1371/journal.pgen.1008774. |
Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency
Citation:
Leukemia. 2020;[Epub]. https://doi.org/10.1038/s41375-020-0899-5 Epub:
Yes Abstract:
Deficiency of the transcription factor GATA2 is a highly penetrant genetic disorder predisposing to myelodysplastic syndromes (... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Kozyra EJ, Pastor VB, Lefkopoulos S. Sahoo SS, Busch H, Voss RK, Erlacher M, Lebrecht D, Szvetnik EA, Hirabayashi S, Pasaulienė R, Pedace L, Tartaglia M, Klemann C, Metzger P, Boerries M, Catala A, Hasle H, de Haas V, Kállay K, Masetti R, De Moerloose B, Dworzak M, Schmugge M, Smith O, Starý J, Mejstrikova E, Ussowicz M, Morris E, Singh P, Collin M, Derecka M, Gudrun Göhring G, Flotho C, Strahm B, Locatelli F, Niemeyer CM, Trompouki E, Wlodarski MW, European Working Group of MDS in Childhood (EWOG-MDS). Synonymous GATA2 mutations result in selective loss of mutated RNA and are common in patients with GATA2 deficiency. Leukemia. 2020;[Epub]. https://doi.org/10.1038/s41375-020-0899-5. |
Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis
Citation:
Proc Nat Acad Sci USA. 2020;[Epub ahead of print] doi:10.1073/pnas.2002328117 Epub:
Yes Abstract:
RNA modifications play a fundamental role in cellular function. Pseudouridylation, the most abundant RNA modification, is... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Balogh E, Chandler JC, Varga M, Tahoun M, Menyhárd DK, Schay G, Goncalves T, Hamar R, Légrádi R, Szekeres A, Gribouval O, Kleta R, Stanescu H, Bockenhauer D, Kerti A, Williams H, Kinsler V, Di W-L, Curtis D, Kolatsi-Joannou M, Hammid H, Szőcs A, Perczel K, Maka E, Toldi G, Sava F, Arrondel C, Kardos M, Fintha A, Hossain A, D’Arco F, Kaliakatsos M, Koeglmeier J, Mifsud W, Moosajee M, Faro A, Jávorszky E, Rudas G, Saied MH, Marzouk S, Kelen K, Götze J, Reusz G, Tulassay T, Dragon F, Mollet G, Motameny S, Thiele H, Dorval G, Nürnberg P, Perczel A, Szabó AJ, Long DA, Tomita K, Antignac C, Waters AM, Tory K. Pseudouridylation defect due to DKC1 and NOP10 mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitis. Proc Nat Acad Sci USA. 2020;[Epub ahead of print] doi:10.1073/pnas.2002328117. |
Pre-mRNA Splicing Modulation by Antisense Oligonucleotides
Citation:
Methods Mol Biol. 2018;1828:415-437. doi:10.1007/978-1-4939-8651-4_26 Epub:
Not Epub Abstract:
Pre-mRNA splicing, a dynamic process of intron removal and exon joining, is governed by a combinatorial control exerted by... Delivery Method:
electroporation Organism or Cell Type:
cell culture: SMA-patient-derived primary fibroblasts GM03813 Citation Extract: Singh NN, Luo D, Singh RN. Pre-mRNA Splicing Modulation by Antisense Oligonucleotides. Methods Mol Biol. 2018;1828:415-437. doi:10.1007/978-1-4939-8651-4_26. |
DNA-based fluorescent probes of NOS2 activity in live brains
Citation:
PNAS USA. 2020;[Epub ahead of print] doi:10.1073/pnas.2003034117 Epub:
Yes Abstract:
When a pathogen is engulfed by an immune cell, it is trapped in a transient organelle called the phagosome. The host cell... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Veetil AT, Zou J, Henderson KW, Jani MS, Shaik SM, Sisodia SS, Hale ME, Krishnan Y. DNA-based fluorescent probes of NOS2 activity in live brains. PNAS USA. 2020;[Epub ahead of print] doi:10.1073/pnas.2003034117. |
ADP receptor P2y12 prevents excessive primitive hematopoiesis in zebrafish by inhibiting Gata1
Citation:
Acta Pharmacol Sin. 2020;[Epub] doi:10.1038/s41401-020-0431-5 Epub:
Not Epub Abstract:
In the past two decades, purinergic signaling has emerged as a key regulator of hematopoiesis in physiological and pathological... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Li F, Liang Y, Han X, Guan Y-n, Chen J, Wu P, Zhao X-x, Jing Q
. ADP receptor P2y12 prevents excessive primitive hematopoiesis in zebrafish by inhibiting Gata1. Acta Pharmacol Sin. 2020;[Epub] doi:10.1038/s41401-020-0431-5. |