Characterization of the two inducible Cre recombinase-based mouse models NG2- CreERTM and PDGFRb-P2A-CreERT2 for pericyte labeling in the retina

Author(s):  
Daniela Mayr ◽  
Julia Preishuber-Pflügl ◽  
Andreas Koller ◽  
Susanne M. Brunner ◽  
Christian Runge ◽  
...  
Keyword(s):  
The Prostate ◽  
2021 ◽  
Author(s):  
Amber E. Groot ◽  
Kayla V. Myers ◽  
Timothy E. G. Krueger ◽  
Ashley L. Kiemen ◽  
Natalia H. Nagy ◽  
...  

2014 ◽  
Vol 3 (6) ◽  
pp. 1147-1158 ◽  
Author(s):  
Katherine C. Krueger ◽  
Maria José Costa ◽  
Hongqing Du ◽  
Brian J. Feldman

Pancreas ◽  
2015 ◽  
Vol 44 (6) ◽  
pp. 882-887 ◽  
Author(s):  
Shiping Xu ◽  
Chintan Chheda ◽  
Yassine Ouhaddi ◽  
Hajar Benhaddou ◽  
Mouloud Bourhim ◽  
...  

2008 ◽  
Vol 95 (3) ◽  
pp. 152-162 ◽  
Author(s):  
Iwan Jones ◽  
Xingxuan He ◽  
Fourogh Katouzian ◽  
Peter I. Darroch ◽  
Edward H. Schuchman

Author(s):  
Miyuki Hirabayashi ◽  
James K. Chambers ◽  
Takuya E. Kishimoto ◽  
Nguyen V. Son ◽  
Yuichi Ishikawa ◽  
...  

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Xin Wang ◽  
António Pinto-Duarte ◽  
M. Margarita Behrens ◽  
Xianjin Zhou ◽  
Terrence J. Sejnowski

2010 ◽  
Vol 42 (2) ◽  
pp. 310-316 ◽  
Author(s):  
Stephanie L. Pierce ◽  
William Kutschke ◽  
Rafael Cabeza ◽  
Sarah K. England

Transgenic and knockout mouse models have proven useful in the study of genes necessary for parturition—including genes that affect the timing and/or progression of labor contractions. However, taking full advantage of these models will require a detailed characterization of the contractile patterns in the mouse uterus. Currently the best methodology for this has been measurement of isometric tension in isolated muscle strips in vitro. However, this methodology does not provide a real-time measure of changes in uterine pressure over the course of pregnancy. Recent advances have opened the possibility of using radiotelemetric devices to more accurately and comprehensively study intrauterine pressure in vivo. We tested the effectiveness of this technology in the mouse, in both wild-type (WT) mice and a mouse model of defective parturition (SK3 channel-overexpressing mice), after surgical implant of telemetry transmitters into the uterine horn. Continuous recordings from day 18 of pregnancy through delivery revealed that WT mice typically deliver during the 12-h dark cycle after 19.5 days postcoitum. In these mice, intrauterine pressure gradually increases during this cycle, to threefold greater than that measured during the 12-h cycle before delivery. SK3-overexpressing mice, by contrast, exhibited lower intrauterine pressure over the same period. These results are consistent with the outcome of previous in vitro studies, and they indicate that telemetry is an accurate method for measuring uterine contraction, and hence parturition, in mice. The use of this technology will lead to important novel insights into changes in intrauterine pressure during the course of pregnancy.


2017 ◽  
Vol 11 (1) ◽  
pp. 44-58 ◽  
Author(s):  
Susan E. Maloney ◽  
Krystal C. Chandler ◽  
Corina Anastasaki ◽  
Michael A. Rieger ◽  
David H. Gutmann ◽  
...  

2020 ◽  
Author(s):  
Tobias M. Franks ◽  
Sharie J. Haugabook ◽  
Elizabeth A. Ottinger ◽  
Meghan S. Vermillion ◽  
Kevin M. Pawlik ◽  
...  

AbstractMouse models of sickle cell disease (SCD) that faithfully switch from fetal to adult hemoglobin (Hb) have been important research tools that accelerated advancement towards treatments and cures for SCD. Red blood cells (RBCs) in these animals sickled in vivo, occluded small vessels in many organs and resulted in severe anemia like in human patients. SCD mouse models have been valuable in advancing clinical translation of some therapeutics and providing a better understanding of the pathophysiology of SCD. However, mouse models vary greatly from humans in their anatomy and physiology and therefore have limited application for certain translational efforts to transition from the bench to bedside. These differences create the need for a higher order animal model to continue the advancement of efforts in not only understanding relevant underlying pathophysiology, but also the translational aspects necessary for the development of better therapeutics to treat or cure SCD. Here we describe the development of a humanized porcine sickle cell model that like the SCD mice, expresses human ɑ-, β− and γ-globin genes under the control of the respective endogenous porcine locus control regions (LCR). We also describe our initial characterization of the SCD pigs and plans to make this model available to the broader research community.


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