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SATB2 gene

Known as: FLJ21474, KIAA1034, SATB Homeobox 2 Gene 
This gene plays roles in apoptosis and development.
National Institutes of Health

Related topics

Related topics

5 relations
ApoptosisBiologic DevelopmentDNA Binding Protein SATB2Transcriptional Regulation

Broader (1)

Genes

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2016
Review
2016
SATB2‐associated syndrome: Mechanisms, phenotype, and practical recommendations
The SATB2‐associated syndrome is a recently described syndrome characterized by developmental delay/intellectual disability with… 
Highly Cited
2014
Highly Cited
2014
The role of SATB2 as a diagnostic marker for tumors of colorectal origin: Results of a pathology-based clinical prospective study.
OBJECTIVES Immunohistochemistry is an important extension to clinical information and morphology, and prevails as an invaluable… 
Highly Cited
2011
Highly Cited
2011
SATB2 in Combination With Cytokeratin 20 Identifies Over 95% of all Colorectal Carcinomas
The special AT-rich sequence-binding protein 2 (SATB2), a nuclear matrix-associated transcription factor and epigenetic regulator… 
Highly Cited
2011
Highly Cited
2011
Osteoblast-specific Transcription Factor Osterix (Osx) Is an Upstream Regulator of Satb2 during Bone Formation*
Osterix (Osx) is an osteoblast-specific transcription factor essential for osteoblast differentiation and bone formation. Osx… 
Highly Cited
2010
Highly Cited
2010
The role of miR-31 and its target gene SATB2 in cancer-associated fibroblasts
It is well established that there is a dynamic relationship between the expanding tumor and the host surrounding tissue. Cancer… 
Highly Cited
2009
Highly Cited
2009
SATB1 defines the developmental context for gene silencing by Xist in lymphoma and embryonic cells.
Highly Cited
2008
Highly Cited
2008
SATB2 interacts with chromatin‐remodeling molecules in differentiating cortical neurons
During our search for developmental regulators of neuronal differentiation, we identified special AT‐rich sequence‐binding… 
Highly Cited
2007
Highly Cited
2007
Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects
Studies of human chromosomal aberrations and knockout (KO) mice have suggested SATB2 as a candidate gene for a human malformation… 
Highly Cited
2005
Highly Cited
2005
Novel transcription factor Satb2 interacts with matrix attachment region DNA elements in a tissue‐specific manner and demonstrates cell‐type‐dependent expression in the developing mouse CNS
Satb1 is a first cell‐type‐specific transcription factor of a novel type that functions as a regulator of the transcription of… 
Highly Cited
2003
Highly Cited
2003
SUMO modification of a novel MAR-binding protein, SATB2, modulates immunoglobulin mu gene expression.
Nuclear matrix attachment regions (MARs) are regulatory DNA sequences that are important for higher-order chromatin organization… 
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