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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 12378 scientific papers returned from the database with the search filters currently being used below.
There are 12378 scientific papers returned from the database with the search filters currently being used below.
LIM Domain Only 2 Regulates Endothelial Proliferation, Angiogenesis, and Tissue Regeneration
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Citation:
J Am Heart Assoc. 2016 Oct 6;5(10). pii: e004117 Epub:
Not Epub Abstract:
BACKGROUND: LIM domain only 2 (LMO2, human gene) is a key transcription factor that regulates hematopoiesis and vascular... Delivery Method:
Vivo-Morpholino Organism or Cell Type:
zebrafish Citation Extract: Meng S, Matrone G, Lv J, Chen K, Wong WT, Cooke JP. LIM Domain Only 2 Regulates Endothelial Proliferation, Angiogenesis, and Tissue Regeneration. J Am Heart Assoc. 2016 Oct 6;5(10). pii: e004117. |
MicroRNA-126a Directs Lymphangiogenesis Through Interacting With Chemokine and Flt4 Signaling in Zebrafish
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Citation:
Arterioscler Thromb Vasc Biol. 2016 Oct 27. pii: ATVBAHA.116.308120. [Epub ahead of print] Epub:
Yes Abstract:
OBJECTIVE: MicroRNA-126 (miR-126) is an endothelium-enriched miRNA and functions in vascular integrity and angiogenesis. The... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Chen J, Zhu RF, Li FF, Liang YL, Wang C, Qin YW, Huang S, Zhao XX, Jing Q. MicroRNA-126a Directs Lymphangiogenesis Through Interacting With Chemokine and Flt4 Signaling in Zebrafish. Arterioscler Thromb Vasc Biol. 2016 Oct 27. pii: ATVBAHA.116.308120. [Epub ahead of print]. |
Zebrafish embryos as in vivo test tubes to unravel cell-specific mechanisms of neurogenesis during neurodevelopment and in diseases
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Citation:
Neurogenesis (Austin). 2016 Oct 7;3(1):e1232678 Epub:
Not Epub Abstract:
Zebrafish has become a model of choice for developmental studies in particular for studying neural development and related... Organism or Cell Type:
zebrafish Citation Extract: Samarut É. Zebrafish embryos as in vivo test tubes to unravel cell-specific mechanisms of neurogenesis during neurodevelopment and in diseases. Neurogenesis (Austin). 2016 Oct 7;3(1):e1232678. |
Caspase-2 cleavage of tau reversibly impairs memory
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Citation:
Nat Med. 2016 Oct 10. doi: 10.1038/nm.4199 Epub:
Not Epub Abstract:
In Alzheimer's disease (AD) and other tauopathies, the tau protein forms fibrils, which are believed to be neurotoxic.... Delivery Method:
icv infusion Organism or Cell Type:
mice Citation Extract: Zhao X, Kotilinek LA, Smith B, Hlynialuk C, Zahs K, Ramsden M, Cleary J, Ashe KH. Caspase-2 cleavage of tau reversibly impairs memory. Nat Med. 2016 Oct 10. doi: 10.1038/nm.4199. |
Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes
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Citation:
Cell Death Dis. 2016 Oct 6;7(10):e2397. doi: 10.1038/cddis.2016.299 Epub:
Not Epub Abstract:
Treacher Collins Syndrome (TCS) is a rare congenital disease (1:50 000 live births) characterized by craniofacial defects,... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: de Peralta MS, Mouguelar VS, Sdrigotti MA, Ishiy FA, Fanganiello RD, Passos-Bueno MR, Coux G, Calcaterra NB. Cnbp ameliorates Treacher Collins Syndrome craniofacial anomalies through a pathway that involves redox-responsive genes. Cell Death Dis. 2016 Oct 6;7(10):e2397. doi: 10.1038/cddis.2016.299. |
Spatiotemporal expression and transcriptional regulation of heme oxygenase and biliverdin reductase genes in zebrafish (Danio rerio) suggest novel roles during early developmental periods of heightened oxidative stress
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Citation:
Comp Biochem Physiol C Toxicol Pharmacol. 2016 Oct 17. pii: S1532-0456(16)30132-6. doi: 10.1016/j.cbpc.2016.10.006 Epub:
Yes Abstract:
Heme oxygenase 1 (HMOX1) degrades heme into biliverdin, which is subsequently converted to bilirubin by biliverdin reductase (... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Holowiecki A, O'Shields B, Jenny MJ. Spatiotemporal expression and transcriptional regulation of heme oxygenase and biliverdin reductase genes in zebrafish (Danio rerio) suggest novel roles during early developmental periods of heightened oxidative stress. Comp Biochem Physiol C Toxicol Pharmacol. 2016 Oct 17. pii: S1532-0456(16)30132-6. doi: 10.1016/j.cbpc.2016.10.006. |
The zebrafish homologs of SET/I2PP2A oncoprotein: expression patterns and insights into their physiological roles during development
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Citation:
Biochem J. 2016 Oct 17. pii: BCJ20160523 [epub ahead of print]. doi:10.1042/BCJ20160523 Epub:
Yes Abstract:
The oncoprotein SET/I2PP2A participates in various cellular mechanisms such as transcription, cell cycle regulation and cell... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Serifi I, Tzima E, Soupsana K, Karetsou Z, Beis D, Papamarcaki T. The zebrafish homologs of SET/I2PP2A oncoprotein: expression patterns and insights into their physiological roles during development. Biochem J. 2016 Oct 17. pii: BCJ20160523 [epub ahead of print]. doi:10.1042/BCJ20160523. |
Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish
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Citation:
J Pediatr Gastroenterol Nutr. 2016 Nov;63(5):524-530. doi:10.1097/MPG.0000000000001375 Epub:
Not Epub Abstract:
OBJECTIVES: Biliary atresia (BA) is a progressive fibroinflammatory cholangiopathy affecting the bile ducts of neonates.... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Tang V, Cofer ZC, Cui S, Sapp V, Loomes KM, Matthews RP. Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish. J Pediatr Gastroenterol Nutr. 2016 Nov;63(5):524-530. doi:10.1097/MPG.0000000000001375. |
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I
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Citation:
Hum Mutat. 2016 Sep 29. doi: 10.1002/humu.23130 Epub:
Yes Abstract:
Dentin dysplasia type I (DDI) is an autosomal-dominant genetic disorder resulting from dentin defects. The molecular basis of... Delivery Method:
microinjection Organism or Cell Type:
zebrafish Citation Extract: Xiong F, Ji Z, Liu Y, Zhang Y, Hu L, Yang Q, Qiu Q, Zhao L, Chen D, Tian Z, Shang X, Zhang L, Wei X, Liu C, Yu Q, Zhang M, Cheng J, Xiong J, Li D, Wu X, Yuan H, Zhang W, Xu X. Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type I. Hum Mutat. 2016 Sep 29. doi: 10.1002/humu.23130. |
HIF1α-induced PDGFRβ signaling promotes developmental HSC production via IL-6 activation
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Citation:
Exp Hematol. 2016 Oct 14. pii: S0301-472X(16)30657-9. [Epub ahead of print] doi: 10.1016/j.exphem.2016.10.002 Epub:
Yes Abstract:
Hematopoietic stem cells (HSCs) have the ability to both self-renew and differentiate into all the mature blood cell lineages... Citation Extract: Lim SE, Esain V, Kwan W, Theodore LN, Cortes M, Frost IM, Liu SY, North TE. HIF1α-induced PDGFRβ signaling promotes developmental HSC production via IL-6 activation. Exp Hematol. 2016 Oct 14. pii: S0301-472X(16)30657-9. [Epub ahead of print] doi: 10.1016/j.exphem.2016.10.002. |