tweak multimarkdown citations slightly

[don.git] / resume / research_statement.mdwn

diff --git a/resume/research_statement.mdwn b/resume/research_statement.mdwn
index 92026d220a7a2a23cea7f118b8824d2151c2395f..70283a36fa30367b785085ae36eae4334e8b2fe4 100644 (file)
--- a/resume/research_statement.mdwn
+++ b/resume/research_statement.mdwn
@@ -51,18 +51,18 @@ I developed novel bioinformatic methods which increase
 
 likelihood of identifying reproducible genetic associations using
 prior knowledge from publicly available databases and expert
 
 likelihood of identifying reproducible genetic associations using
 prior knowledge from publicly available databases and expert

-information [#Armstrong2008:function2gene]. Using these methods, I
-was able to identify genes previously unassociated with SLE in a
+information [#Armstrong2008:function2gene]. Using these methods, I was
+able to identify genes previously unassociated with SLE in a

 trio-based study [#Jacob2007:ar_lupus]. These genes were then
 replicated in a larger case-control study which was funded by the NIH
 trio-based study [#Jacob2007:ar_lupus]. These genes were then
 replicated in a larger case-control study which was funded by the NIH

-on the basis of the original findings
-[#Jacob2009:sle_irak1],[#Armstrong2009:sle_gi]. Among other findings,
-this larger study identified a missense allele in NCF2 (H389Q,
-rs17849502) which was associated with SLE. Collaborative work
-indicated that H389Q altered the binding energy of NCF2 with VAV1
-using docking simulations, and in vitro experiments confirmed that
-H389Q altered NADPH oxidase function [#Jacob2012:sle_ncf2], thus
-identifying it as a causative SLE mutation.
+on the basis of the original findings [#Jacob2009:sle_irak1] ,
+[#Armstrong2009:sle_gi]. Among other findings, this larger study
+identified a missense allele in NCF2 (H389Q, rs17849502) which was
+associated with SLE. Collaborative work indicated that H389Q altered
+the binding energy of NCF2 with VAV1 using docking simulations, and in
+vitro experiments confirmed that H389Q altered NADPH oxidase function
+[#Jacob2012:sle_ncf2], thus identifying it as a causative SLE
+mutation.

 
 ## Cancer Stem Cells in Glioblastoma
 
 
 ## Cancer Stem Cells in Glioblastoma