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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.
Lymphocytic Choriomeningitis Virus Infection in FVB Mouse Produces Hemorrhagic Disease
Citation:
PLoS Pathog. 2012;8(12):e1003073. doi:10.1371/journal.ppat.1003073 Epub:
Not Epub Abstract:
The viral family Arenaviridae includes a number of viruses that can cause hemorrhagic fever in humans. Arenavirus infection... Delivery Method:
peptide-coupled Organism or Cell Type:
mice Citation Extract: Schnell FJ, Sundholm S, Crumley S, Iversen PL, Mourich DV. Lymphocytic Choriomeningitis Virus Infection in FVB Mouse Produces Hemorrhagic Disease. PLoS Pathog. 2012;8(12):e1003073. doi:10.1371/journal.ppat.1003073. |
Matrix Gla Protein Reinforces Angiogenic Resolution
Citation:
Microvasc Res. 2012;[Epub ahead of print] doi:10.1016/j.mvr.2012.10.005 Epub:
Not Epub Abstract:
Matrix Gla Protein (MGP) is an ECM molecule commonly associated with dysfunctions of large blood vessels such as... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Sharma B, Albig AR. Matrix Gla Protein Reinforces Angiogenic Resolution. Microvasc Res. 2012;[Epub ahead of print] doi:10.1016/j.mvr.2012.10.005. |
Metazoan Scc4 Homologs Link Sister Chromatid Cohesion to Cell and Axon Migration Guidance
Citation:
PLoS Biol. 2006 Jul 4;4(8):e242 [Epub ahead of print] Epub:
Not Epub Abstract:
Saccharomyces cerevisiae Scc2 binds Scc4 to form an essential complex that loads cohesin onto chromosomes. The prevalence of... Delivery Method:
Microinjection Organism or Cell Type:
Xenopus tropicalis Citation Extract: Seitan VC, Banks P, Laval S, Majid NA, Dorsett D, Rana A, Smith J, Bateman A, Krpic S, Hostert A, Rollins RA, Erdjument-Bromage H, Tempst P, Benard CY, Hekimi S, Newbury SF, Strachan T. Metazoan Scc4 Homologs Link Sister Chromatid Cohesion to Cell and Axon Migration Guidance. PLoS Biol. 2006 Jul 4;4(8):e242 [Epub ahead of print]. |
Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts
Citation:
Nature. 2012;[Epub ahead of print] doi:10.1038/nature11536 Epub:
Not Epub Abstract:
Defects in the availability of haem substrates or the catalytic activity of the terminal enzyme in haem biosynthesis,... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Shah DI, Takahashi-Makise N, Cooney JD, Li L, Schultz IJ, Pierce EL, Narla A, Seguin A, Hattangadi SM, Medlock AE, Langer NB, Dailey TA, Hurst SN, Faccenda D, Wiwczar JM, Heggers SK, Vogin G, Chen W, Chen C, Campagna DR, Brugnara C, Zhou Y, Ebert BL, Danial NN, Fleming MD, Ward DM, Campanella M, Dailey HA, Kaplan J,Paw BH. Mitochondrial Atpif1 regulates haem synthesis in developing erythroblasts. Nature. 2012;[Epub ahead of print] doi:10.1038/nature11536. |
Mitoferrin is essential for erythroid iron assimilation
Citation:
Nature. 2006 Mar 2;440(7080):96-100 Epub:
Not Epub Abstract:
Iron has a fundamental role in many metabolic processes, including electron transport, deoxyribonucleotide synthesis, oxygen... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Shaw GC, Cope JJ, Li L, Corson K, Hersey C, Ackermann GE, Gwynn B, Lambert AJ, Wingert RA, Traver D, Trede NS, Barut BA, Zhou Y, Minet E, Donovan A, Brownlie A, Balzan R, Weiss MJ, Peters LL, Kaplan J, Zon LI, Paw BH. Mitoferrin is essential for erythroid iron assimilation. Nature. 2006 Mar 2;440(7080):96-100. |
Molecular analysis and functions of p53R2 in zebrafish
Citation:
Gene. 2010 Dec 28. [Epub ahead of print] Epub:
Not Epub Abstract:
The p53R2 is a newly identified small subunit of ribonucleotide reductase and plays a pivotal role in the supply of dNTPs for... Organism or Cell Type:
zebrafish Citation Extract: Shang H, Li Q, Feng G, Cui Z. Molecular analysis and functions of p53R2 in zebrafish. Gene. 2010 Dec 28. [Epub ahead of print]. |
Morpholino-induced knockdown of zebrafish engrailed genes eng2 and eng3 reveals redundant and unique functions in midbrain-hindbrain boundary development.
Citation:
Genesis. 2001 Jul;30(3):129-33 Epub:
Not Epub Abstract:
No abstract available. Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Scholpp S, Brand M. Morpholino-induced knockdown of zebrafish engrailed genes eng2 and eng3 reveals redundant and unique functions in midbrain-hindbrain boundary development.. Genesis. 2001 Jul;30(3):129-33. |
Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome
Citation:
Am J Hum Genet. 2008 May;82(5):1178-84. Epub:
Not Epub Abstract:
Several dysmorphic syndromes affect the development of both the eye and the ear, but only a few are restricted to the eye and... Organism or Cell Type:
zebrafish Citation Extract: Schorderet DF, Nichini O, Boisset G, Polok B, Tiab L, Mayeur H, Raji B, de la Houssaye G, Abitbol MM, Munier FL. Mutation in the Human Homeobox Gene NKX5-3 Causes an Oculo-Auricular Syndrome. Am J Hum Genet. 2008 May;82(5):1178-84.. |
Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.
Citation:
Nat Genet. 2005 Apr;37(4):418-22. Epub 2005 Feb 27. Epub:
Not Epub Abstract:
We identified a human mutation that causes dilated cardiomyopathy and heart failure preceded by sensorineural hearing loss (... Delivery Method:
Microinjection Organism or Cell Type:
zebrafish Citation Extract: Schonberger J, Wang L, Shin JT, Kim SD, Depreux FF, Zhu H, Zon L, Pizard A, Kim JB, Macrae CA, Mungall AJ, Seidman JG, Seidman CE. Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.. Nat Genet. 2005 Apr;37(4):418-22. Epub 2005 Feb 27.. |
Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II
Citation:
Nat Genet. 2009 Jun 28. [Epub ahead of print] Epub:
Not Epub Abstract:
Congenital dyserythropoietic anemias (CDAs) are phenotypically and genotypically heterogeneous diseases. CDA type II (CDAII) is... Organism or Cell Type:
zebrafish Citation Extract: Schwarz K, Iolascon A, Verissimo F, Trede NS, Horsley W, Chen W, Paw BH, Hopfner KP, Holzmann K, Russo R, Esposito MR, Spano D, De Falco L, Heinrich K, Joggerst B, Rojewski MT, Perrotta S, Denecke J, Pannicke U, Delaunay J, Pepperkok R, Heimpel H. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II. Nat Genet. 2009 Jun 28. [Epub ahead of print]. |