The HSA21 encoded Single-minded 2 (SIM2) transcription factor has key neurological func-tions and is a good candidate to be involved in the cognitive impairment of Down syndrome. We aimed to explore the functional capacity of SIM2 by mapping its DNA binding sites in mouse embryonic stem cells. ChIP-sequencing revealed 1229 high-confidence SIM2-bind-ing sites. Analysis of the SIM2 target genes confirmed the importance of SIM2 in develop-mental and neuronal processes and indicated that SIM2 may be a master transcription regulator. Indeed, SIM2 DNA binding sites share sequence specificity and overlapping do-mains of occupancy with master transcription factors such as SOX2, OCT4 (Pou5f1), NANOG or KLF4. The association between SIM2 and these pi...
As part of our effort to clone genes of human chromosome 21 that may contribute to Down syndrome, we...
As part of our effort to clone genes of human chromosome 21 that may contribute to Down syndrome, we...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...
The HSA21 encoded Single-minded 2 (SIM2) transcription factor has key neurological functions and is ...
The HSA21 encoded Single-minded 2 (SIM2) transcription factor has key neurological functions and is ...
This project aimed to investigate how the murine Simgle minded (mSIM) proteins interact with other a...
The binding sequence for any transcription factor can be found millions of times within a ge-nome, y...
The Drosophila single-minded (sim) transcription factor, is a master regulator of fruitfly neurogene...
. These authors contributed equally to this work. The pluripotency of embryonic stem cells (ESCs) is...
Genes implicated in neurodevelopmental disorders (NDDs) important in cognition and behavior may have...
Spatiotemporal regulation of gene expression in multicellular organisms is mediated by cell-type spe...
In our article, we asked whether Sox2, a transcription factor important in brain development and dis...
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only know...
To date, mutations in ~75 different genes have been associated with mental retardation (MR), but the...
The SOX2 transcription factor is critical for neural stem cell (NSC) maintenance and brain developme...
As part of our effort to clone genes of human chromosome 21 that may contribute to Down syndrome, we...
As part of our effort to clone genes of human chromosome 21 that may contribute to Down syndrome, we...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...
The HSA21 encoded Single-minded 2 (SIM2) transcription factor has key neurological functions and is ...
The HSA21 encoded Single-minded 2 (SIM2) transcription factor has key neurological functions and is ...
This project aimed to investigate how the murine Simgle minded (mSIM) proteins interact with other a...
The binding sequence for any transcription factor can be found millions of times within a ge-nome, y...
The Drosophila single-minded (sim) transcription factor, is a master regulator of fruitfly neurogene...
. These authors contributed equally to this work. The pluripotency of embryonic stem cells (ESCs) is...
Genes implicated in neurodevelopmental disorders (NDDs) important in cognition and behavior may have...
Spatiotemporal regulation of gene expression in multicellular organisms is mediated by cell-type spe...
In our article, we asked whether Sox2, a transcription factor important in brain development and dis...
Mutations in FOXP2, a member of the forkhead family of transcription factor genes, are the only know...
To date, mutations in ~75 different genes have been associated with mental retardation (MR), but the...
The SOX2 transcription factor is critical for neural stem cell (NSC) maintenance and brain developme...
As part of our effort to clone genes of human chromosome 21 that may contribute to Down syndrome, we...
As part of our effort to clone genes of human chromosome 21 that may contribute to Down syndrome, we...
Down syndrome (DS), trisomy for chromosome 21, is the most common genetic cause of intellectual disa...