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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 12095 scientific papers returned from the database with the search filters currently being used below.

Haem homeostasis is regulated by the conserved and concerted functions of HRG-1 proteins

Authors:
Rajagopal A, Rao AU, Amigo J, Tian M, Upadhyay SK, Hall C, Uhm S, Mathew MK, Fleming MD, Paw BH, Krause M, Hamza I
Citation:
Nature. 2008 Jun 19;453(7198):1127-31. Epub 2008 Apr 16
Epub:
Not Epub
Abstract:
Haems are metalloporphyrins that serve as prosthetic groups for various biological processes including respiration, gas sensing...
Organism or Cell Type:
zebrafish
Citation Extract:
Rajagopal A, Rao AU, Amigo J, Tian M, Upadhyay SK, Hall C, Uhm S, Mathew MK, Fleming MD, Paw BH, Krause M, Hamza I. Haem homeostasis is regulated by the conserved and concerted functions of HRG-1 proteins. Nature. 2008 Jun 19;453(7198):1127-31. Epub 2008 Apr 16.

Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development

Authors:
Qi HH, Sarkissian M, Hu GQ, Wang Z, Bhattacharjee A, Gordon DB, Gonzales M, Lan F, Ongusaha PP, Huarte M, Yaghi NK, Lim H, Garcia BA, Brizuela L, Zhao K, Roberts TM, Shi Y
Citation:
Nature. 2010 Jul 22;466(7305):503-7. Epub 2010 Jul 11
Epub:
Not Epub
Abstract:
X-linked mental retardation (XLMR) is a complex human disease that causes intellectual disability. Causal mutations have been...
Organism or Cell Type:
zebrafish
Citation Extract:
Qi HH, Sarkissian M, Hu GQ, Wang Z, Bhattacharjee A, Gordon DB, Gonzales M, Lan F, Ongusaha PP, Huarte M, Yaghi NK, Lim H, Garcia BA, Brizuela L, Zhao K, Roberts TM, Shi Y. Histone H4K20/H3K9 demethylase PHF8 regulates zebrafish brain and craniofacial development. Nature. 2010 Jul 22;466(7305):503-7. Epub 2010 Jul 11.

Hitting Bacteria at the Heart of the Central Dogma: Sequence-Specific Inhibition

Authors:
Rasmussen LC, Sperling-Petersen HU, Mortensen KK
Citation:
Microb Cell Fact. 2007 Aug 10;6(1):24 [Epub ahead of print]
Epub:
Not Epub
Abstract:
ABSTRACT: An important objective in developing new drugs is the achievement of high specificity to maximize curing effect and...
Organism or Cell Type:
Bacteria (review)
Citation Extract:
Rasmussen LC, Sperling-Petersen HU, Mortensen KK. Hitting Bacteria at the Heart of the Central Dogma: Sequence-Specific Inhibition. Microb Cell Fact. 2007 Aug 10;6(1):24 [Epub ahead of print] .

Identification and Functional Analysis of the Vision-Specific BBS3 (ARL6) Long Isoform

Authors:
Pretorius PR, Baye LM, Nishimura DY, Searby CC, Bugge K, Yang B, Mullins RF, Stone EM, Sheffield VC, Slusarski DC
Citation:
PLoS Genet. 2010 Mar 19;6(3):e1000884
Epub:
Not Epub
Abstract:
Bardet-Biedl Syndrome (BBS) is a heterogeneous syndromic form of retinal degeneration. We have identified a novel transcript of...
Delivery Method:
Microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Pretorius PR, Baye LM, Nishimura DY, Searby CC, Bugge K, Yang B, Mullins RF, Stone EM, Sheffield VC, Slusarski DC. Identification and Functional Analysis of the Vision-Specific BBS3 (ARL6) Long Isoform. PLoS Genet. 2010 Mar 19;6(3):e1000884.

Identification of zebrafish ARNT1 homologs: TCDD toxicity in the developing zebrafish requires ARNT1

Authors:
Prasch AL, Tanguay RL, Mehta V, Heideman W, Peterson RE
Citation:
2006 Mar;69(3):776-87. Epub 2005 Nov 23.
Epub:
Not Epub
Abstract:
In order to use the zebrafish as a model to study 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) developmental toxicity, it is...
Delivery Method:
Microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Prasch AL, Tanguay RL, Mehta V, Heideman W, Peterson RE. Identification of zebrafish ARNT1 homologs: TCDD toxicity in the developing zebrafish requires ARNT1. 2006 Mar;69(3):776-87. Epub 2005 Nov 23..

Impaired neural development in a zebrafish model for Lowe syndrome

Authors:
Ramirez IB, Pietka G, Jones DR, Divecha N, Alia A, Baraban SC, Hurlstone AF, Lowe M
Citation:
Hum Mol Genet. 2012 Apr 15;21(8):1744-59. Epub 2011 Dec 30.
Epub:
Not Epub
Abstract:
Lowe syndrome, which is characterized by defects in the central nervous system, eyes and kidneys, is caused by mutation of the...
Delivery Method:
Microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Ramirez IB, Pietka G, Jones DR, Divecha N, Alia A, Baraban SC, Hurlstone AF, Lowe M. Impaired neural development in a zebrafish model for Lowe syndrome. Hum Mol Genet. 2012 Apr 15;21(8):1744-59. Epub 2011 Dec 30..

In the Absence of Sonic Hedgehog, p53 Induces Apoptosis and Inhibits Retinal Cell Proliferation, Cell-Cycle Exit and Differentiation in Zebrafish

Authors:
Prykhozhij SV
Citation:
PLoS ONE. 2010;5(10): e13549. doi:10.1371/journal.pone.0013549
Epub:
Not Epub
Abstract:
Background Sonic hedgehog (Shh) signaling regulates cell proliferation during vertebrate development via induction of cell-...
Delivery Method:
Microinjection
Organism or Cell Type:
zebrafish
Citation Extract:
Prykhozhij SV. In the Absence of Sonic Hedgehog, p53 Induces Apoptosis and Inhibits Retinal Cell Proliferation, Cell-Cycle Exit and Differentiation in Zebrafish. PLoS ONE. 2010;5(10): e13549. doi:10.1371/journal.pone.0013549.

Insm1a-mediated gene repression is essential for the formation and differentiation of Müller glia-derived progenitors in the injured retina

Authors:
Ramachandran R, Zhao XF, Goldman D
Citation:
Nat Cell Biol. 2012 Oct;14(10):1013-23. doi: 10.1038/ncb2586. Epub 2012 Sep 23
Epub:
Not Epub
Abstract:
In zebrafish, retinal injury stimulates Müller glia (MG) reprograming, allowing them to generate multipotent progenitors that...
Delivery Method:
in vivo: injection then electroporation
Organism or Cell Type:
zebrafish
Citation Extract:
Ramachandran R, Zhao XF, Goldman D. Insm1a-mediated gene repression is essential for the formation and differentiation of Müller glia-derived progenitors in the injured retina. Nat Cell Biol. 2012 Oct;14(10):1013-23. doi: 10.1038/ncb2586. Epub 2012 Sep 23.

Integration of Canonical and Noncanonical Wnt Signaling Pathways Patterns the Neuroectoderm Along the Anterior–Posterior Axis of Sea Urchin Embryos

Authors:
Range RC, Angerer RC, Angerer LM
Citation:
PLoS Biol. 2013 11(1):e1001467. doi:10.1371/journal.pbio.1001467
Epub:
Not Epub
Abstract:
The initial regulatory state of most cells in many deuterostome embryos, including those of vertebrates and sea urchins,...
Delivery Method:
Microinjection
Organism or Cell Type:
Sea urchin, Strongylocentrotus purpuratus
Citation Extract:
Range RC, Angerer RC, Angerer LM. Integration of Canonical and Noncanonical Wnt Signaling Pathways Patterns the Neuroectoderm Along the Anterior–Posterior Axis of Sea Urchin Embryos. PLoS Biol. 2013 11(1):e1001467. doi:10.1371/journal.pbio.1001467.

KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes

Authors:
Putoux A, Thomas S, Coene KL, Davis EE, Alanay Y, Ogur G, Uz E, Buzas D, Gomes C, Patrier S, Bennett CL, Elkhartoufi N, Frison MH, Rigonnot L, Joyé N, Pruvost S, Utine GE, Boduroglu K, Nitschke P, Fertitta L, Thauvin-Robinet C, Munnich A, Cormier-Daire V, Hennekam R, Colin E, Akarsu NA, Bole-Feysot C, Cagnard N, Schmitt A, Goudin N, Lyonnet S, Encha-Razavi F, Siffroi JP, Winey M, Katsanis N, Gonzales M, Vekemans M, Beales PL, Attié-Bitach T
Citation:
Nat Genet. 2011 Jun;43(6):601-6. Epub 2011 May 8
Epub:
Not Epub
Abstract:
KIF7, the human ortholog of Drosophila Costal2, is a key component of the Hedgehog signaling pathway. Here we report mutations...
Organism or Cell Type:
zebrafish
Citation Extract:
Putoux A, Thomas S, Coene KL, Davis EE, Alanay Y, Ogur G, Uz E, Buzas D, Gomes C, Patrier S, Bennett CL, Elkhartoufi N, Frison MH, Rigonnot L, Joyé N, Pruvost S, Utine GE, Boduroglu K, Nitschke P, Fertitta L, Thauvin-Robinet C, Munnich A, Cormier-Daire V, Hennekam R, Colin E, Akarsu NA, Bole-Feysot C, Cagnard N, Schmitt A, Goudin N, Lyonnet S, Encha-Razavi F, Siffroi JP, Winey M, Katsanis N, Gonzales M, Vekemans M, Beales PL, Attié-Bitach T. KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes. Nat Genet. 2011 Jun;43(6):601-6. Epub 2011 May 8.

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