Prevent smiley.

diff --git a/biblio/30154186.mdwn b/biblio/30154186.mdwn
index ecbc8a1e677e448cf8c958c5b1dde1a62e0f1368..fe84ccf97de8caed6ca8272ea3be7dd65ab70c0b 100644 (file)
--- a/biblio/30154186.mdwn
+++ b/biblio/30154186.mdwn
@@ -7,4 +7,4 @@ Chen Y, Zhang Y, Wang Y, Zhang L, Brinkman EK, Adam SA, Goldman R, van Steensel
 
 Mapping 3D genome organization relative to nuclear compartments using TSA-Seq as a cytological ruler 
 
-[[!pmid 30154186 desc="Tyramide free radicals can label DNA directly.  In TSA-Seq (Tyramide Signal Amplification-Sequencing), HRP is targeted on proteins of interest, biotinylated TSA labels neighboring DNA, and biotin-DNA complexes are purified and sequenced.  Distances between chromosome domains and nuclear speckles is reproducible across experiments. Between peripheral lamina (marked by lamin A and B) and nuclear speckles (marked by SON), an increasing gradient of transcriptional activity is clearly visible."]]
+[[!pmid 30154186 desc="Tyramide free radicals can label DNA directly.  In TSA-Seq (Tyramide Signal Amplification-Sequencing), HRP is targeted on proteins of interest, biotinylated TSA labels neighboring DNA, and biotin-DNA complexes are purified and sequenced.  Distances between chromosome domains and nuclear speckles is reproducible across experiments. Between peripheral lamina, marked by lamin A and B, and nuclear speckles (marked by SON), an increasing gradient of transcriptional activity is clearly visible."]]