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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.
Aminolevulinate synthase 2 mediates erythrocyte differentiation by regulating larval globin expression during Xenopus primary hematopoiesis
Citation:
Biochem Biophys Res Commun. 2014 Dec 4. pii: S0006-291X(14)02151-2. doi: 10.1016/j.bbrc.2014.11.110. [Epub ahead of print] Epub:
Yes Abstract:
Hemoglobin synthesis by erythrocytes continues throughout a vertebrate's lifetime. The mechanism of mammalian heme... Delivery Method:
microinjection Organism or Cell Type:
Xenopus laevis Citation Extract: Ogawa-Otomo A, Kurisaki A, Ito Y. Aminolevulinate synthase 2 mediates erythrocyte differentiation by regulating larval globin expression during Xenopus primary hematopoiesis. Biochem Biophys Res Commun. 2014 Dec 4. pii: S0006-291X(14)02151-2. doi: 10.1016/j.bbrc.2014.11.110. [Epub ahead of print]. |
Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes
Citation:
J Med Genet. 2014 Dec 5. pii: jmedgenet-2014-102856. doi: 10.1136/jmedgenet-2014-102856. [Epub ahead of print] Epub:
Yes Abstract:
BACKGROUND: Oliver-McFarlane syndrome is characterised by trichomegaly, congenital hypopituitarism and retinal degeneration... Organism or Cell Type:
zebrafish Citation Extract: Hufnagel RB, Arno G, Hein ND, Hersheson J, Prasad M, Anderson Y, Krueger LA, Gregory LC, Stoetzel C, Jaworek TJ, Hull S, Li A, Plagnol V, Willen CM, Morgan TM, Prows CA, Hegde RS, Riazuddin S, Grabowski GA, Richardson RJ, Dieterich K, Huang T, Revesz T, Martinez-Barbera JP, Sisk RA, Jefferies C, Houlden H, Dattani MT, Fink JK, Dollfus H, Moore AT, Ahmed ZM. Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. J Med Genet. 2014 Dec 5. pii: jmedgenet-2014-102856. doi: 10.1136/jmedgenet-2014-102856. [Epub ahead of print]. |
In vivo loss of function study reveals the short stature homeobox-containing (shox) gene plays indispensable roles in early embryonic growth and bone formation in zebrafish
Citation:
Dev Dyn. 2014 Dec 8. doi: 10.1002/dvdy.24239. [Epub ahead of print] Epub:
Yes Abstract:
Background: Congenital loss of the SHOX gene is considered to be a genetic cause of short stature phenotype in Turner syndrome... Organism or Cell Type:
zebrafish Citation Extract: Sawada R, Kamei H, Hakuno F, Takahashi SI, Shimizu T. In vivo loss of function study reveals the short stature homeobox-containing (shox) gene plays indispensable roles in early embryonic growth and bone formation in zebrafish. Dev Dyn. 2014 Dec 8. doi: 10.1002/dvdy.24239. [Epub ahead of print]. |
Zebrafish Rab5 proteins and a role for Rab5ab in nodal signalling
Citation:
Dev Biol. 2014 Dec 3. pii: S0012-1606(14)00584-3. doi: 10.1016/j.ydbio.2014.11.007. [Epub ahead of print] Epub:
Not Epub Abstract:
The RAB5 gene family is the best characterised of all human RAB families and is essential for in vitro homotypic fusion of... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Kenyon EJ, Campos I, Bull JC, Williams PH, Stemple DL, Clark MD. Zebrafish Rab5 proteins and a role for Rab5ab in nodal signalling. Dev Biol. 2014 Dec 3. pii: S0012-1606(14)00584-3. doi: 10.1016/j.ydbio.2014.11.007. [Epub ahead of print]. |
CTNND2-a candidate gene for reading problems and mild intellectual disability
Citation:
J Med Genet. 2014 Dec 3. pii: jmedgenet-2014-102757. doi: 10.1136/jmedgenet-2014-102757. [Epub ahead of print] Epub:
Yes Abstract:
BACKGROUND: Cytogenetically visible chromosomal translocations are highly informative as they can pinpoint strong effect genes... Organism or Cell Type:
zebrafish Citation Extract: Hofmeister W, Nilsson D, Topa A, Anderlid BM, Darki F, Matsson H, Tapia Páez I, Klingberg T, Samuelsson L, Wirta V, Vezzi F, Kere J, Nordenskjöld M, Syk Lundberg E, Lindstrand A. CTNND2-a candidate gene for reading problems and mild intellectual disability. J Med Genet. 2014 Dec 3. pii: jmedgenet-2014-102757. doi: 10.1136/jmedgenet-2014-102757. [Epub ahead of print]. |
The amniote primitive streak is defined by epithelial cell intercalation before gastrulation
Citation:
Nature. 2007 Oct 25;449(7165):1049-52. Epub 2007 Oct 10. Epub:
Not Epub Abstract:
During gastrulation, a single epithelial cell layer, the ectoderm, generates two others: the mesoderm and the endoderm. In... Delivery Method:
electroporation Organism or Cell Type:
chick Citation Extract: Voiculescu O, Bertocchini F, Wolpert L, Keller RE, Stern CD. The amniote primitive streak is defined by epithelial cell intercalation before gastrulation. Nature. 2007 Oct 25;449(7165):1049-52. Epub 2007 Oct 10.. |
RGM Regulates BMP-Mediated Secondary Axis Formation in the Sea Anemone Nematostella vectensis
Citation:
Cell Rep. 2014;[Epub ahead of print] doi:10.1016/j.celrep.2014.11.009 Epub:
Yes Abstract:
Patterning of the metazoan dorsoventral axis is mediated by a complex interplay of BMP signaling regulators. Repulsive guidance... Delivery Method:
microinjection Organism or Cell Type:
Nematostella vectensis (cnidarian) Citation Extract: Leclère L, Rentzsch F. RGM Regulates BMP-Mediated Secondary Axis Formation in the Sea Anemone Nematostella vectensis. Cell Rep. 2014;[Epub ahead of print] doi:10.1016/j.celrep.2014.11.009. |
Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency
Citation:
Haemophilia. 2014 Dec 3. doi: 10.1111/hae.12554. [Epub ahead of print] Epub:
Yes Abstract:
Coagulation factor V (FV) deficiency is a rare autosomal recessive bleeding disorder. We investigated a patient with severe FV... Citation Extract: Nuzzo F, Bulato C, Nielsen BI, Lee K, Wielders SJ, Simioni P, Key NS, Castoldi E. Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency. Haemophilia. 2014 Dec 3. doi: 10.1111/hae.12554. [Epub ahead of print]. |
Both the folate cycle and betaine-homocysteine methyltransferase contribute methyl groups for DNA methylation in mouse blastocysts
Citation:
FASEB J. 2014 Dec 2. pii: fj.14-261131. [Epub ahead of print] Epub:
Yes Abstract:
The embryonic pattern of global DNA methylation is first established in the inner cell mass (ICM) of the mouse blastocyst. The... Delivery Method:
Lipofectin Organism or Cell Type:
Eight-cell stage mouse embryos Citation Extract: Zhang B, Denomme MM, White CR, Leung KY, Lee MB, Greene ND, Mann MR, Trasler JM, Baltz JM. Both the folate cycle and betaine-homocysteine methyltransferase contribute methyl groups for DNA methylation in mouse blastocysts. FASEB J. 2014 Dec 2. pii: fj.14-261131. [Epub ahead of print]. |
DNA methyltransferase 3B regulates duration of neural crest production via repression of Sox10
Citation:
Proc Natl Acad Sci U S A. 2014 Dec 1. pii: 201318408. [Epub ahead of print] Epub:
Yes Abstract:
Neural crest stem cells arise within the central nervous system but then undergo an epithelial-to-mesenchymal transition to... Delivery Method:
electroporation Organism or Cell Type:
Gallus gallus (chick) Citation Extract: Hu N, Strobl-Mazzulla PH, Simoes-Costa M, Sánchez-Vásquez E, Bronner ME. DNA methyltransferase 3B regulates duration of neural crest production via repression of Sox10. Proc Natl Acad Sci U S A. 2014 Dec 1. pii: 201318408. [Epub ahead of print]. |