Exact(1)
Wild type C57BL6 mice were used for Spry expression pattern profile analysis.
Similar(59)
LMG194 host cells (Invitrogen) were used for protein expression.
Two plasmids were used for transient expression.
Primers used for CChIP and expression analysis.
GAPDH was used for normalization of expression.
Primers used for enzyme expressions.
U6 was used for normalization of miR-124 expression.
Regular expression used for controlling account creation.
Rpl19 expression was used for internal normalization.
To gain more insight into the vascular defects associate with Spry expression, additional studies using endothelial cell specific Cre-mediated gain- and loss-of-function of Spry1 alone or in combination with other Spry family members will be necessary to address this issue.
SPRY expression is induced by MAPK signaling upon growth factor stimulation, such as FGF2 [ 18].
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