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ENH split aim 2 into a and b

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Nathan Dwarshuis 2021-07-25 23:11:30 -04:00
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tex/thesis.tex
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@ -478,9 +478,9 @@ cells compared to state-of-the-art beads using \invivo{} mouse models for
In Chapter~\ref{background}, we provide additional background on the current
state of T cell manufacturing and how the work in this dissertation moves the
field forward. In Chapters~\ref{aim1},~\ref{aim2}, and~\ref{aim3} we present the
work pertaining to Aims 1, 2, and 3 respectively. Finally, we present our final
conclusions in Chapter~\ref{conclusions}.
field forward. In Chapters~\ref{aim1},~\ref{aim2a},~\ref{aim2b}, and~\ref{aim3}
we present the work pertaining to Aims 1, 2, and 3 respectively. Finally, we
present our final conclusions in Chapter~\ref{conclusions}.
\chapter{background and significance}\label{background}
\section*{background}
@ -1545,7 +1545,14 @@ immunotherapies are activated and expanded with either soluble mAbs or
bead-immobilized mAbs, our system will likely serve as a drop-in substitution to
provide these benefits.
\chapter{aim 2}\label{aim2}
\chapter{aim 2a}\label{aim2a}
\section{introduction}
\section{methods}
\section{results}
\section{discussion}
\chapter{aim 2b}\label{aim2b}
\section{introduction}
\section{methods}