*Asterisks denote genes found mutated in probands with OD or MS in this study.</p
High magnification views of confocal images of the NE-NB transition A,B. Effect of l’sc RNAi at the ...
<p>A, Effect of rs61743453 on delta HbF in discovery cohort. B, Effect of rs61743453 on MTD HbF in v...
(A, B) Changed levels of gene expression in PfGCN5-ΔBrd and PfPHD1-ΔPHD are negatively correlated wi...
Asterisks denote genes found mutated in probands with OD or MS in this study.</p
(A) Selected example illustrating impact observed on the transcriptome of THP-1 cells following the ...
A. RNA-seq comparison of hypoxia-induced differentially expressed genes from primary fibroblasts fro...
Ollier disease (OD) and Maffucci Syndrome (MS) are rare disorders characterized by multiple enchondr...
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterised by short stature, m...
Minor allele frequency (MAF) for each variant was accessed from the gnomAD version v2.1.1 on October...
Upstream ORFs (uORFs) are mRNA elements defined by a start codon in the 5′ UTR that is out-of-frame ...
*<p>Asterisk indicates that the proportion of the indicated gene type is significantly different fro...
Item does not contain fulltextPheochromocytomas and paragangliomas (PPGLs) are catecholamine-produci...
Gorlin syndrome is a genetic disorder of autosomal dominant inheritance that predisposes the affecte...
<p>Haplotypes of KIF1B gene variants when Cases III+IV groups were compared to case II (active group...
The first two murine models of IDH1(R132H) mutation provide mechanistic insights into transformation...
High magnification views of confocal images of the NE-NB transition A,B. Effect of l’sc RNAi at the ...
<p>A, Effect of rs61743453 on delta HbF in discovery cohort. B, Effect of rs61743453 on MTD HbF in v...
(A, B) Changed levels of gene expression in PfGCN5-ΔBrd and PfPHD1-ΔPHD are negatively correlated wi...
Asterisks denote genes found mutated in probands with OD or MS in this study.</p
(A) Selected example illustrating impact observed on the transcriptome of THP-1 cells following the ...
A. RNA-seq comparison of hypoxia-induced differentially expressed genes from primary fibroblasts fro...
Ollier disease (OD) and Maffucci Syndrome (MS) are rare disorders characterized by multiple enchondr...
Meier-Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterised by short stature, m...
Minor allele frequency (MAF) for each variant was accessed from the gnomAD version v2.1.1 on October...
Upstream ORFs (uORFs) are mRNA elements defined by a start codon in the 5′ UTR that is out-of-frame ...
*<p>Asterisk indicates that the proportion of the indicated gene type is significantly different fro...
Item does not contain fulltextPheochromocytomas and paragangliomas (PPGLs) are catecholamine-produci...
Gorlin syndrome is a genetic disorder of autosomal dominant inheritance that predisposes the affecte...
<p>Haplotypes of KIF1B gene variants when Cases III+IV groups were compared to case II (active group...
The first two murine models of IDH1(R132H) mutation provide mechanistic insights into transformation...
High magnification views of confocal images of the NE-NB transition A,B. Effect of l’sc RNAi at the ...
<p>A, Effect of rs61743453 on delta HbF in discovery cohort. B, Effect of rs61743453 on MTD HbF in v...
(A, B) Changed levels of gene expression in PfGCN5-ΔBrd and PfPHD1-ΔPHD are negatively correlated wi...