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Make protein macro species-specific
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‎thesis.cls‎

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@@ -486,10 +486,11 @@
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\newcommand*\gene@hsa[1]{\textsc{\MakeTextLowercase{\textit{#1}}}}
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\newcommand*\gene@mmu[1]{\textit{#1}}
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\newcommand*\gene[2]{\csuse{gene@#1}{#2}}
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\newcommand*\protein[1]{\textrm{\textsc{\MakeTextLowercase{#1}}}}
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\newcommand*\protein@hsa[1]{\textrm{\textsc{\MakeTextLowercase{#1}}}}
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\newcommand*\protein@mmu[1]{\textrm{\textsc{\MakeTextLowercase{#1}}}}
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\newcommand*\protein[2]{\csuse{protein@#1}{#2}}
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% Formatting of biological sequences
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‎trna-development.tex‎

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@@ -101,14 +101,14 @@ \section{Protein-coding gene expression changes dynamically during mouse
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illustrated by looking at individual gene expression counts, plotted against
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their genomic location (\cref{fig:mrna-expression-change}). For example, in the
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liver we can confirm the functional relevance of apolipoprotein B
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(\protein{APOB}) as the primary carrier of lipoproteins, which becomes
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(\protein{mmu}{APOB}) as the primary carrier of lipoproteins, which becomes
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increasingly relevant as the organ shifts to metabolism \citep{Knott:1986}.
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Similarly, \mrna gene expression changes highlight the role of α-fetoproteine
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(\protein{AFP}) as the fetal version of serum albumin (\cref{fig:apob-afp})
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(\protein{mmu}{AFP}) as the fetal version of serum albumin (\cref{fig:apob-afp})
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\citep{Chen:1997}. In the brain, shifts can be seen in the activity of the
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neural \tf \protein{FOXP2}, the expression of which continuously decreases, and
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in calmodulin (\protein{CALM1}), where transcription increases after birth
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\citep{Tsui:2013,Huang:2011}.
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neural \tf \protein{mmu}{FOXP2}, the expression of which continuously decreases,
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and in calmodulin (\protein{mmu}{CALM1}), where transcription increases after
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birth \citep{Tsui:2013,Huang:2011}.
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\textfloat{mrna-expression-change}{spill}{%
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\centering

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