Sox18 encodes a member of the Sry-related high mobility group box (SOX) family of developmental transcription factors. Examination of Sox18 expression during embryogenesis has shown that Sox18 is expressed transiently in endothelial cells of developing blood vessels, and mutations in Sox18 have been found to underlie the mouse vascular and hair follicle mutant ragged. In this study we have examined the expression of Sox18 in angiogenesis during wound healing. Full-thickness skin wounds were created in mice, and subsequent expression of vascular endothelial growth factor (VEGF), the VEGF receptor Flk-1, alpha1 (iv) collagen (Col4a1), and Sox18 were studied using in situ hybridization. As has been previously reported, VEGF was expressed predo...
Endothelial to mesenchymal transition (EndMT) is a leading cause of fibrosis and disease, however it...
Mutations in the transcription factor SOX18 are responsible for specific cardiovascular defects in h...
Analysis of classical mouse mutations has been useful in the identification and study of many genes....
SOX18 is a transcription factor that is transiently expressed in nascent endothelial cells during em...
The main focus of our laboratory is clarifying the roles of DNA binding proteins belonging to the HM...
The lymphatic system plays a key role in tissue fluid regulation and tumour metastasis, and lymphati...
VCAM-1 (vascular cell adhesion molecule-1) and Sox18 are involved in vascular development. VCAM-1 is...
Angiogenesis, the process of generating new blood vessels, is essential to embryonic development, or...
Recently, we demonstrated that mutations in the Sry-related HMG box gene Sox18 underlie vascular and...
Sex-determining region Y box 18 (Sox18/SOX18) gene is an important regulator of vascular development...
Mutations in SOX18 cause the human Hypotrichosis-Lymphedema-Telangiectasia (HLT) syndrome. Their mur...
Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects...
Background. The growth of solid tumors depends on establishing blood supply; thus, inhibiting tumor ...
Mutations in SOX18 cause the human hypotrichosis-lymphedema-telangiectasia (HILT) syndrome. Their mu...
Endothelial to mesenchymal transition (EndMT) is a leading cause of fibrosis and disease, however it...
Endothelial to mesenchymal transition (EndMT) is a leading cause of fibrosis and disease, however it...
Mutations in the transcription factor SOX18 are responsible for specific cardiovascular defects in h...
Analysis of classical mouse mutations has been useful in the identification and study of many genes....
SOX18 is a transcription factor that is transiently expressed in nascent endothelial cells during em...
The main focus of our laboratory is clarifying the roles of DNA binding proteins belonging to the HM...
The lymphatic system plays a key role in tissue fluid regulation and tumour metastasis, and lymphati...
VCAM-1 (vascular cell adhesion molecule-1) and Sox18 are involved in vascular development. VCAM-1 is...
Angiogenesis, the process of generating new blood vessels, is essential to embryonic development, or...
Recently, we demonstrated that mutations in the Sry-related HMG box gene Sox18 underlie vascular and...
Sex-determining region Y box 18 (Sox18/SOX18) gene is an important regulator of vascular development...
Mutations in SOX18 cause the human Hypotrichosis-Lymphedema-Telangiectasia (HLT) syndrome. Their mur...
Mutations in the transcription factor gene SOX18 cause vascular, lymphatic and hair follicle defects...
Background. The growth of solid tumors depends on establishing blood supply; thus, inhibiting tumor ...
Mutations in SOX18 cause the human hypotrichosis-lymphedema-telangiectasia (HILT) syndrome. Their mu...
Endothelial to mesenchymal transition (EndMT) is a leading cause of fibrosis and disease, however it...
Endothelial to mesenchymal transition (EndMT) is a leading cause of fibrosis and disease, however it...
Mutations in the transcription factor SOX18 are responsible for specific cardiovascular defects in h...
Analysis of classical mouse mutations has been useful in the identification and study of many genes....