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SHOX2 is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Additionally we are shipping Short Stature Homeobox 2 Antibodies (36) and Short Stature Homeobox 2 Proteins (7) and many more products for this protein.
We have identified that SHOX2 expression or methylation are potent independent prognostic indicators for predicting LGG patient survival, and have potential to identify an important subset of LGG patients with IDHwt status with significantly better overall survival.
Whole-genome microarray mRNA-expression profiles of myofibroblasts and skin fibroblasts revealed four additional genes that are significantly differentially expressed in these two cell types: NKX2-3 and LRRC17 (show LRRC17 ELISA Kits) in myofibroblasts and SHOX2 and TBX5 (show TBX5 ELISA Kits) in skin fibroblasts
these results suggest a genetic contribution of SHOX2 in early-onset atrial fibrillation
SHOX2 overexpression favors differentiation of embryonic stem cells into cardiac pacemaker cells, improving biological pacing ability.
SHOX2 DNA methylation (show HELLS ELISA Kits) identified 66% of the patients with cancer subsequent to a cytological equivocal diagnosis. SHOX2 complements the cytological diagnosis and the methylation marker panel.
miR (show MLXIP ELISA Kits)-375/SHOX2 functional relationship regulates breast tumorigenesis by controlling the process of EMT (show ITK ELISA Kits).
SHOX2, like SHOX, regulates NPPB directly whilst activates ACAN via its cooperation with the SOX trio.
prognostic value of SHOX2 and SEPT9 (show SEPT9 ELISA Kits) DNA methylation (show HELLS ELISA Kits) in benign, paramalignant and malignant pleural effusions
Elevated SHOX2 expression is associated with tumor recurrence of hepatocellular carcinoma.
The combination of EBUS-TBNA and SHOX2 methylation level strongly improves the assessment of the nodal status by identifying additional malignant lesions and confirming benign nodes and therefore avoiding invasive follow-up procedures.
Results demonstrate that elimination of Shox2 in the brain results in disruptions in the development of the facial (VII (show TH ELISA Kits)) nerves and the facial motor nucleus
the Shox2-Nkx2-5 (show NKX2-5 ELISA Kits) antagonistic mechanism primes the pacemaker cell fate in the pulmonary vein myocardium and sinoatrial node
Shox2 expression restricted to the proximal limb along with Hoxd9 (show HOXD9 ELISA Kits) and Hoxa11 (show HOXA11 ELISA Kits) expression, juxtaposing the distal expression of Hoxa13 (show HOXA13 ELISA Kits) and Hoxd13 (show HOXD13 ELISA Kits).
study suggested that a certain concentration of FA causes the bone marrow toxicity by regulating the expression of Prx3 (show PRDX3 ELISA Kits)
Data indicate the importance of short stature homeobox 2 (Shox2) in the cerebellum.
Shox2 regulates dorsal mesenchymal protrusion fate and development by controlling BMP signaling through the Smad (show SMAD1 ELISA Kits)-dependent pathway to drive tissue growth and to induce Hcn4 (show HCN3 ELISA Kits) expression
phosphorylation essential for repression of Nkx2.5 (show NKX2-5 ELISA Kits) expression during sinoatrial node development and differentiation
These data extend our understanding of the role and regulation of Tbx4 (show TBX4 ELISA Kits) and Shox2 in limb development and limb associated diseases.
Although human SHOX (show SHOX ELISA Kits) can exert similar functions to mouse Shox2 in regulating early temporomandibular joint development, it apparently has a distinct function in the regulation of those molecules that are involved in tissue homeostasis.
Shox2 regulates progression through chondrogenesis at two distinct stages--the onset of early differentiation and the transition to maturation and hypertrophy.
Shox2 deficiency interferes with pacemaking function in zebrafish embryos. Shox2 has a critical function in the recruitment of sinus venosus myocardium comprising the sinoatrial nodal region.
This gene is a member of the homeobox family of genes that encode proteins containing a 60-amino acid residue motif that represents a DNA binding domain. Homeobox genes have been characterized extensively as transcriptional regulators involved in pattern formation in both invertebrate and vertebrate species. Several human genetic disorders are caused by aberrations in human homeobox genes. This locus represents a pseudoautosomal homeobox gene that is thought to be responsible for idiopathic short stature, and it is implicated in the short stature phenotype of Turner syndrome patients. This gene is considered to be a candidate gene for Cornelia de Lange syndrome. Alternative splicing results in multiple transcript variants.
short stature homeobox 2
, SHOX homologous gene on chromosome 3
, homeobox protein Og12X
, paired-related homeobox protein SHOT
, short stature homeobox protein 2
, paired family homeodomain protein Prx3