Induction of enhanced green fluorescent protein expression in response to lesions in the nervous system

2004 ◽  
Vol 474 (1) ◽  
pp. 108-122 ◽  
Author(s):  
Michel Dubois-Dauphin ◽  
Lorenza Eder-Colli ◽  
Philippe Vallet ◽  
Andr� Stutz ◽  
Serge Nef ◽  
...  
Keyword(s):  
Nervous System ◽  
Green Fluorescent Protein ◽  
Protein Expression ◽  
Enhanced Green Fluorescent Protein ◽  
Green Fluorescent Protein Expression ◽  
Fluorescent Protein ◽  
Green Fluorescent

scholarly journals Stem/Progenitor Cell-Specific Enhanced Green Fluorescent Protein Expression Driven by the Endogenous Mcm2 Promoter

Stem Cells ◽  
2006 ◽  
Vol 25 (1) ◽  
pp. 132-138 ◽  
Author(s):  
Alexander Y. Maslov ◽  
Kimberly J. Bailey ◽  
Lawrence M. Mielnicki ◽  
Amy L. Freeland ◽  
Xiaolei Sun ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Protein Expression ◽  
Progenitor Cell ◽  
Enhanced Green Fluorescent Protein ◽  
Green Fluorescent Protein Expression ◽  
Fluorescent Protein ◽  
Green Fluorescent

Oviduct-Specific Enhanced Green Fluorescent Protein Expression in Transgenic Chickens

2011 ◽  
Vol 75 (4) ◽  
pp. 646-649 ◽  
Author(s):  
Sung June BYUN ◽  
Sung Woo KIM ◽  
Kyung-Woon KIM ◽  
Jeom Sun KIM ◽  
In-Sul HWANG ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Protein Expression ◽  
Enhanced Green Fluorescent Protein ◽  
Green Fluorescent Protein Expression ◽  
Fluorescent Protein ◽  
Green Fluorescent ◽  
Transgenic Chickens

scholarly journals Noninvasive optical diagnostics of enhanced green fluorescent protein expression in skeletal muscle for comparison of electroporation and sonoporation efficiencies

2016 ◽  
Vol 21 (4) ◽  
pp. 045003 ◽  
Author(s):  
Mindaugas Tamošiunas ◽  
Roberts Kadikis ◽  
Inga Saknite ◽  
Juozas Baltušnikas ◽  
Audrius Kilikevicius ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Green Fluorescent Protein ◽  
Protein Expression ◽  
Enhanced Green Fluorescent Protein ◽  
Green Fluorescent Protein Expression ◽  
Fluorescent Protein ◽  
Optical Diagnostics ◽  
Green Fluorescent

Transgenic mice with pancellular enhanced green fluorescent protein expression in primitive hematopoietic cells and all blood cell progeny

genesis ◽  
2005 ◽  
Vol 42 (1) ◽  
pp. 17-22 ◽  
Author(s):  
Massimo Dominici ◽  
Merhdad Tadjali ◽  
Steven Kepes ◽  
Esther R. Allay ◽  
Kelli Boyd ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Transgenic Mice ◽  
Blood Cell ◽  
Protein Expression ◽  
Enhanced Green Fluorescent Protein ◽  
Green Fluorescent Protein Expression ◽  
Fluorescent Protein ◽  
Hematopoietic Cells ◽  
Green Fluorescent

scholarly journals A liver enhancer in the fibrinogen gene cluster

Blood ◽  
2011 ◽  
Vol 117 (1) ◽  
pp. 276-282 ◽  
Author(s):  
Alexandre Fort ◽  
Richard J. Fish ◽  
Catia Attanasio ◽  
Roland Dosch ◽  
Axel Visel ◽  
...  
Keyword(s):  
Green Fluorescent Protein ◽  
Protein Expression ◽  
Enhanced Green Fluorescent Protein ◽  
Green Fluorescent Protein Expression ◽  
Fluorescent Protein ◽  
Luciferase Reporter ◽  
Human Fibrinogen ◽  
Gene Assay ◽  
Regulatory Potential ◽  
Green Fluorescent

Abstract The plasma concentration of fibrinogen varies in the healthy human population between 1.5 and 3.5 g/L. Understanding the basis of this variability has clinical importance because elevated fibrinogen levels are associated with increased cardiovascular disease risk. To identify novel regulatory elements involved in the control of fibrinogen expression, we used sequence conservation and in silico–predicted regulatory potential to select 14 conserved noncoding sequences (CNCs) within the conserved block of synteny containing the fibrinogen locus. The regulatory potential of each CNC was tested in vitro using a luciferase reporter gene assay in fibrinogen-expressing hepatoma cell lines (HuH7 and HepG2). 4 potential enhancers were tested for their ability to direct enhanced green fluorescent protein expression in zebrafish embryos. CNC12, a sequence equidistant from the human fibrinogen alpha and beta chain genes, activates strong liver enhanced green fluorescent protein expression in injected embryos and their transgenic progeny. A transgenic assay in embryonic day 14.5 mouse embryos confirmed the ability of CNC12 to activate transcription in the liver. While additional experiments are necessary to prove the role of CNC12 in the regulation of fibrinogen, our study reveals a novel regulatory element in the fibrinogen locus that is active in the liver and may contribute to variable fibrinogen expression in humans.

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