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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 12390 scientific papers returned from the database with the search filters currently being used below.

Serum and Glucocorticoid-Regulated Kinase 1 Regulates Neutrophil Clearance during Inflammation Resolution

Authors:
Burgon J, Robertson AL, Sadiku P, Wang X, Hooper-Greenhill E, Prince LR, Walker P, Hoggett EE, Ward JR, Farrow SN, Zuercher WJ, Jeffrey P, Savage CO, Ingham PW, Hurlstone AF, Whyte MKB, Renshaw SA
Citation:
J Immunol. 2014;[Epub ahead of print] doi:10.4049/jimmunol.1300087
Epub:
Yes
Abstract:
The inflammatory response is integral to maintaining health by functioning to resist microbial infection and repair tissue...
Organism or Cell Type:
zebrafish
Citation Extract:
Burgon J, Robertson AL, Sadiku P, Wang X, Hooper-Greenhill E, Prince LR, Walker P, Hoggett EE, Ward JR, Farrow SN, Zuercher WJ, Jeffrey P, Savage CO, Ingham PW, Hurlstone AF, Whyte MKB, Renshaw SA. Serum and Glucocorticoid-Regulated Kinase 1 Regulates Neutrophil Clearance during Inflammation Resolution. J Immunol. 2014;[Epub ahead of print] doi:10.4049/jimmunol.1300087.

40LoVe and Samba Are Involved in Xenopus Neural Development and Functionally Distinct from hnRNP AB

Authors:
Andreou M, Yan CYI, Skourides PA
Citation:
PLoS ONE. 2014;9(1):e85026. doi:10.1371/journal.pone.0085026
Epub:
Not Epub
Abstract:
Heterogeneous nuclear ribonucleoproteins (hnRNPs) comprise a large group of modular RNA-binding proteins classified according...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Andreou M, Yan CYI, Skourides PA. 40LoVe and Samba Are Involved in Xenopus Neural Development and Functionally Distinct from hnRNP AB. PLoS ONE. 2014;9(1):e85026. doi:10.1371/journal.pone.0085026.

Elavl1a regulates zebrafish erythropoiesis via post-transcriptional control of gata1

Authors:
Li X, Lu YC, Dai K, Torregroza I, Hla T, Evans T
Citation:
Blood. 2014 Feb 27;123(9):1384-92. doi: 10.1182/blood-2013-09-526962. Epub 2014 Jan 14
Epub:
Not Epub
Abstract:
The RNA-binding protein Elavl1 (also know as HuR) regulates gene expression at the post-transcriptional level. Early embryonic...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Li X, Lu YC, Dai K, Torregroza I, Hla T, Evans T. Elavl1a regulates zebrafish erythropoiesis via post-transcriptional control of gata1. Blood. 2014 Feb 27;123(9):1384-92. doi: 10.1182/blood-2013-09-526962. Epub 2014 Jan 14.

Retinoic Acid Receptor Subtype-Specific Transcriptotypes in the Early Zebrafish Embryo

Authors:
Samarut E, Gaudin C, Hughes S, Gillet B, de Bernard S, Jouve PE, Buffat L, Allot A, Lecompte O, Berekelya L, Rochette-Egly C, Laudet V
Citation:
Mol Endocrinol. 2014 Jan 9:me20131358. [Epub ahead of print]
Epub:
Yes
Abstract:
Retinoic acid (RA) controls many aspects of embryonic development by binding to specific receptors (retinoic acid receptors [...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Samarut E, Gaudin C, Hughes S, Gillet B, de Bernard S, Jouve PE, Buffat L, Allot A, Lecompte O, Berekelya L, Rochette-Egly C, Laudet V. Retinoic Acid Receptor Subtype-Specific Transcriptotypes in the Early Zebrafish Embryo. Mol Endocrinol. 2014 Jan 9:me20131358. [Epub ahead of print].

Coordinated genomic control of ciliogenesis and cell movement by RFX2

Authors:
Chung M-I, Kwon T, Tu F, Brooks ER, Gupta R, Meyer M, Baker JC, Marcotte EM, Wallingford JB
Citation:
eLife. 2014; 3: e01439. Published online 2014 January 14. doi: 10.7554/eLife.01439
Epub:
Not Epub
Abstract:
The mechanisms linking systems-level programs of gene expression to discrete cell biological processes in vivo remain poorly...
Delivery Method:
microinjection
Organism or Cell Type:
Xenopus laevis
Citation Extract:
Chung M-I, Kwon T, Tu F, Brooks ER, Gupta R, Meyer M, Baker JC, Marcotte EM, Wallingford JB. Coordinated genomic control of ciliogenesis and cell movement by RFX2. eLife. 2014; 3: e01439. Published online 2014 January 14. doi: 10.7554/eLife.01439.

Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome

Authors:
Garaffo G, Provero P, Molineris I, Pinciroli P, Peano C, Battaglia C, Tomaiuolo D, Etzion T, Gothilf Y, Santoro M, Merlo GR
Citation:
Front Endocrinol (Lausanne). 2013;4:203. doi:10.3389/fendo.2013.00203
Epub:
Not Epub
Abstract:
During embryonic development, immature neurons in the olfactory epithelium (OE) extend axons through the nasal mesenchyme, to...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Garaffo G, Provero P, Molineris I, Pinciroli P, Peano C, Battaglia C, Tomaiuolo D, Etzion T, Gothilf Y, Santoro M, Merlo GR. Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome. Front Endocrinol (Lausanne). 2013;4:203. doi:10.3389/fendo.2013.00203.

PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa

Authors:
Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C
Citation:
Hum Mol Genet. 2014 Jan 12. [Epub ahead of print]
Epub:
Yes
Abstract:
Retinitis pigmentosa (RP), a disease characterized by progressive loss of photoreceptors, exhibits significant genetic...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Chen X, Liu Y, Sheng X, Tam PO, Zhao K, Chen X, Rong W, Liu Y, Liu X, Pan X, Chen LJ, Zhao Q, Vollrath D, Pang CP, Zhao C. PRPF4 Mutations Cause Autosomal Dominant Retinitis Pigmentosa. Hum Mol Genet. 2014 Jan 12. [Epub ahead of print].

Zebrafish Stem/Progenitor Factor msi2b Exhibits Two Phases of Activity Mediated by Different Splice Variants

Authors:
Hochgreb-Hägele T, Koo DE, Das NM, Bronner ME
Citation:
Stem Cells. 2014 Feb;32(2):558-71. doi: 10.1002/stem.1583
Epub:
Not Epub
Abstract:
The Musashi (Msi) family of RNA-binding proteins is important in stem and differentiating cells in many species. Here, we...
Organism or Cell Type:
zebrafish
Citation Extract:
Hochgreb-Hägele T, Koo DE, Das NM, Bronner ME. Zebrafish Stem/Progenitor Factor msi2b Exhibits Two Phases of Activity Mediated by Different Splice Variants. Stem Cells. 2014 Feb;32(2):558-71. doi: 10.1002/stem.1583.

Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish

Authors:
Yadav GV, Chakraborty A, Uechi T, Kenmochi N
Citation:
Int J Biochem Cell Biol. 2014 Jan 10. pii: S1357-2725(14)00015-6. doi: 10.1016/j.biocel.2014.01.006. [Epub ahead of print]
Epub:
Yes
Abstract:
Diamond-Blackfan anemia is an inherited genetic disease caused by mutations in ribosomal protein genes. The disease is...
Organism or Cell Type:
zebrafish
Citation Extract:
Yadav GV, Chakraborty A, Uechi T, Kenmochi N. Ribosomal protein deficiency causes Tp53-independent erythropoiesis failure in zebrafish. Int J Biochem Cell Biol. 2014 Jan 10. pii: S1357-2725(14)00015-6. doi: 10.1016/j.biocel.2014.01.006. [Epub ahead of print].

Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy

Authors:
Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S
Citation:
Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13
Epub:
Not Epub
Abstract:
Deletion 1p36 syndrome is recognized as the most common terminal deletion syndrome. Here, we describe the loss of a gene within...
Delivery Method:
microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13.

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