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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 12420 scientific papers returned from the database with the search filters currently being used below.

Paternal genome rescues mouse preimplantation embryo development in the absence of maternally-recruited EZH2 activity

Authors:
Wang H, Paulson EE, Ma L, Ross PJ, Schultz RM
Citation:
Epigenetics. 2019 Jan 19. doi: 10.1080/15592294.2019.1570771. [Epub ahead of print]
Epub:
Yes
Abstract:
Enhancer of zeste homolog 2 (EZH2), a component of the PRC2 complex, trimethylates H3K27, a transcriptionally repressive...
Organism or Cell Type:
mouse eggs & diploidized parthenotes
Citation Extract:
Wang H, Paulson EE, Ma L, Ross PJ, Schultz RM. Paternal genome rescues mouse preimplantation embryo development in the absence of maternally-recruited EZH2 activity. Epigenetics. 2019 Jan 19. doi: 10.1080/15592294.2019.1570771. [Epub ahead of print].

A dual function of FGF signaling in Xenopus left-right axis formation

Authors:
Schneider I, Kreis J, Schweickert A, Blum M, Vick P
Citation:
Development. 2019 May 10;146(9):dev173575. doi: 10.1242/dev.173575. PMID: 31036544
Epub:
Not Epub
Abstract:
Organ left-right (LR) asymmetry is a conserved vertebrate feature, which is regulated by left-sided activation of Nodal...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Schneider I, Kreis J, Schweickert A, Blum M, Vick P . A dual function of FGF signaling in Xenopus left-right axis formation. Development. 2019 May 10;146(9):dev173575. doi: 10.1242/dev.173575. PMID: 31036544.

De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism

Authors:
Zawerton A, Yao B, Yeager JP, Pippucci T, Haseeb A, Smith JD, Wischmann L, Kühl SJ, Dean JCS, Pilz DT, Holder SE, Deciphering Developmental Disorders Study, University of Washington Center for Mendelian Genomics, McNeill A, Graziano C, Lefebvre V
Citation:
Am J Hum Genet. 2019;[Epub ahead of print] doi:10.1016/j.ajhg.2018.12.014
Epub:
Yes
Abstract:
SOX4, together with SOX11 and SOX12, forms group C of SRY-related (SOX) transcription factors. They play key roles, often in...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus
Citation Extract:
Zawerton A, Yao B, Yeager JP, Pippucci T, Haseeb A, Smith JD, Wischmann L, Kühl SJ, Dean JCS, Pilz DT, Holder SE, Deciphering Developmental Disorders Study, University of Washington Center for Mendelian Genomics, McNeill A, Graziano C, Lefebvre V. De Novo SOX4 Variants Cause a Neurodevelopmental Disease Associated with Mild Dysmorphism. Am J Hum Genet. 2019;[Epub ahead of print] doi:10.1016/j.ajhg.2018.12.014.

TETs Regulate Proepicardial Cell Migration through Extracellular Matrix Organization during Zebrafish Cardiogenesis

Authors:
Lan Y, Pan H, Li C, Banks KM, Sam J, Ding B, Elemento O, Goll MG, Evans T
Citation:
Cell Rep. 2019;26:720-32. doi:10.1016/j.celrep.2018.12.076
Epub:
Not Epub
Abstract:
Ten-eleven translocation (Tet) enzymes (Tet1/2/3) mediate 5-methylcytosine (5mC) hydroxylation, which can facilitate DNA...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Lan Y, Pan H, Li C, Banks KM, Sam J, Ding B, Elemento O, Goll MG, Evans T. TETs Regulate Proepicardial Cell Migration through Extracellular Matrix Organization during Zebrafish Cardiogenesis. Cell Rep. 2019;26:720-32. doi:10.1016/j.celrep.2018.12.076.

Peri-arterial specification of vascular mural cells from naïve mesenchyme requires Notch signaling

Authors:
Ando K, Wang W, Peng D, Ayano Chiba, Lagendijk A, Barske L, Crump JG, Stainier DYR, Lendahl U, Koltowska K, Hogan BM, Fukuhara S, Mochizuki N, Betsholtz C
Citation:
Development. 2019;[Epub ahead of print] doi:10.1242/dev.165589
Epub:
Yes
Abstract:
Mural cells (MCs) are essential for blood vessel stability and function; however, the mechanisms regulating MC development...
Organism or Cell Type:
zebrafish
Citation Extract:
Ando K, Wang W, Peng D, Ayano Chiba, Lagendijk A, Barske L, Crump JG, Stainier DYR, Lendahl U, Koltowska K, Hogan BM, Fukuhara S, Mochizuki N, Betsholtz C. Peri-arterial specification of vascular mural cells from naïve mesenchyme requires Notch signaling. Development. 2019;[Epub ahead of print] doi:10.1242/dev.165589.

Drug-free macromolecular therapeutics induce apoptosis in cells isolated from patients with B cell malignancies with enhanced apoptosis induction by pretreatment with gemcitabine

Authors:
Wang J, Li L, Yang J, Clair PM, Glenn MJ, Stephens DM, Christopher Radford D, Kosak KM, Deininger MW, Shami PJ, Kopeček J
Citation:
Nanomedicine. 2019 Jan 9. pii: S1549-9634(19)30004-8. doi: 10.1016/j.nano.2018.12.011. [Epub ahead of print]
Epub:
Yes
Abstract:
Drug-free macromolecular therapeutics (DFMT) is a new paradigm for the treatment of B cell malignancies. Apoptosis is initiated...
Organism or Cell Type:
cell culture: primary cultures from B-cell malignancies
Citation Extract:
Wang J, Li L, Yang J, Clair PM, Glenn MJ, Stephens DM, Christopher Radford D, Kosak KM, Deininger MW, Shami PJ, Kopeček J. Drug-free macromolecular therapeutics induce apoptosis in cells isolated from patients with B cell malignancies with enhanced apoptosis induction by pretreatment with gemcitabine. Nanomedicine. 2019 Jan 9. pii: S1549-9634(19)30004-8. doi: 10.1016/j.nano.2018.12.011. [Epub ahead of print].

A Heterologous Model of Thrombospondin Type 1 Domain-Containing 7A-Associated Membranous Nephropathy

Authors:
Tomas NM, Meyer-Schwesinger C, von Spiegel H, Kotb AM, Zahner G, Hoxha E, Helmchen U, Endlich N, Koch-Nolte F, Stahl RAK
Citation:
J Am Soc Nephrol. 2017 Nov;28(11):3262-3277. doi: 10.1681/ASN.2017010030. Epub 2017 Aug 16
Epub:
Not Epub
Abstract:
Thrombospondin type 1 domain-containing 7A (THSD7A) is a target for autoimmunity in patients with membranous nephropathy (MN)....
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Tomas NM, Meyer-Schwesinger C, von Spiegel H, Kotb AM, Zahner G, Hoxha E, Helmchen U, Endlich N, Koch-Nolte F, Stahl RAK. A Heterologous Model of Thrombospondin Type 1 Domain-Containing 7A-Associated Membranous Nephropathy. J Am Soc Nephrol. 2017 Nov;28(11):3262-3277. doi: 10.1681/ASN.2017010030. Epub 2017 Aug 16.

Focal adhesions are essential to drive zebrafish heart valve morphogenesis

Authors:
Gunawan F, Gentile A, Fukuda R, Tsedeke AT, Jiménez-Amilburu V, Ramadass R, Iida A, Sehara-Fujisawa A, Stainier DYR
Citation:
J Cell Biol. 2019 Jan 11. pii: jcb.201807175. doi: 10.1083/jcb.201807175. [Epub ahead of print]
Epub:
Yes
Abstract:
Elucidating the morphogenetic events that shape vertebrate heart valves, complex structures that prevent retrograde blood flow...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Gunawan F, Gentile A, Fukuda R, Tsedeke AT, Jiménez-Amilburu V, Ramadass R, Iida A, Sehara-Fujisawa A, Stainier DYR. Focal adhesions are essential to drive zebrafish heart valve morphogenesis. J Cell Biol. 2019 Jan 11. pii: jcb.201807175. doi: 10.1083/jcb.201807175. [Epub ahead of print].

Xenopus slc7a5 is essential for notochord function and eye development

Authors:
Katada T, Sakurai H
Citation:
Mech Dev. 2019 Jan 6. pii: S0925-4773(18)30135-7. doi: 10.1016/j.mod.2019.01.001. [Epub ahead of print]
Epub:
Yes
Abstract:
slc7a5 (also known as LAT1), largely accepted as an amino acid transporter, has been shown to play important roles in cancer...
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Katada T, Sakurai H. Xenopus slc7a5 is essential for notochord function and eye development. Mech Dev. 2019 Jan 6. pii: S0925-4773(18)30135-7. doi: 10.1016/j.mod.2019.01.001. [Epub ahead of print].

Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome

Authors:
Helm BM, Willer JR, Sadeghpour A, Golzio C, Crouch E, Vergano SS, Katsanis N, Davis EE
Citation:
Hum Genomics. 2017 Jul 19;11(1):16. doi: 10.1186/s40246-017-0111-9
Epub:
Not Epub
Abstract:
BACKGROUND: The ciliopathies represent an umbrella group of >50 clinical entities that share both clinical features and...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Helm BM, Willer JR, Sadeghpour A, Golzio C, Crouch E, Vergano SS, Katsanis N, Davis EE. Partial uniparental isodisomy of chromosome 16 unmasks a deleterious biallelic mutation in IFT140 that causes Mainzer-Saldino syndrome. Hum Genomics. 2017 Jul 19;11(1):16. doi: 10.1186/s40246-017-0111-9.

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