𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Generation of a mouse for conditional excision of progesterone receptor

✍ Scribed by Minako K. Hashimoto-Partyka; John P. Lydon; M. Luisa Iruela-Arispe


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
500 KB
Volume
44
Category
Article
ISSN
1526-954X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Generation of a conditional allele of th
✍ AndrΓ© Schneider; YouFei Guan; Yahua Zhang; Mark A. Magnuson; Cathy Pettepher; Ch πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 379 KB

## Abstract Genetic disruption of the mouse EP~4~ receptor results in perinatal lethality associated with persistent patent ductus areteriosus (PDA). To circumvent this, an EP~4~ allele amenable to conditional deletion using the Cre/loxP system was generated. The targeting construct was comprised o

Generation of a conditional null allele
✍ Jian Q. Feng; Greg Scott; Dayong Guo; Baichun Jiang; Marie Harris; Toni Ward; Ma πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 296 KB πŸ‘ 1 views
Generation of a floxed allele of Smad5 f
✍ Lieve Umans; Liesbeth Vermeire; Annick Francis; Hua Chang; Danny Huylebroeck; An πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 348 KB

## Abstract Summary: Smad5 is a member of the Smad family of intracellular mediators of BMP signals and in endothelial cells of TGF‐β signals. We and others previously showed that loss of Smad5 in the mouse results in embryonic lethality (between E9.5–E11.5) due to multiple embryonic and extraembry

Generation of mice with a conditional al
✍ Wen-Tao Peng; Chi-Jiunn Pan; Eric J. Lee; Heiner Westphal; Janice Y. Chou πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 474 KB πŸ‘ 1 views

## Abstract Glucose‐6‐phosphatase‐α (G6Pase‐α or G6PC) catalyzes the hydrolysis of glucose‐6‐phosphate to glucose and is a key enzyme in interprandial glucose homeostasis. Mutations in the human __G6PC__ gene, expressed primarily in the liver, kidney, and intestine, cause glycogen storage disease T