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FIGF wt Allele

Known as: VEGF-D, VEGFD, c-Fos Induced Growth Factor (Vascular Endothelial Growth Factor D) wt Allele 
Human FIGF wild-type allele is located in the vicinity of Xp22.31 and is approximately 39 kb in length. This allele, which encodes vascular… 
National Institutes of Health

Related topics

Related topics

10 relations
Angiogenic ProcessCell Proliferation Regulatory ProcessChemotaxisFIGF gene

Papers overview

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2017
2017
Tuberous sclerosis is an inherited tumour syndrome caused by mutations in TSC1 or TSC2 that lead to aberrant activation of mTOR and development of tumours in multiple organs
Tuberous sclerosis is an inherited tumour syndrome caused by mutations in TSC1 or TSC2 that lead to aberrant activation of mTOR… 
Review
2016
Review
2016
PAGOD syndrome and vascular anomalies: is a defect embryonic angiogenesis? A case report and review.
PAGOD Syndrome is an acronym for lung and pulmonary arteries hypoplasia, agonadism, omphalocele / diaphragmatic defect and… 
2016
2016
Combination of everolimus with sorafenib for solid renal tumours in Tsc2 mice is superior to everolimus alone Authors and affiliations:
Tuberous sclerosis is an inherited tumour syndrome caused by mutations in TSC1 or TSC2 that lead to aberrant activation of mTOR… 
2015
2015
Μελέτη λεμφαγγειογενετικών παραγόντων και δεικτών στο καρκίνωμα του τραχήλου της μήτρας
Lymph node metastasis is an important prognostic factor in human cervical carcinoma. However, results regarding correlation of… 
2012
2012
Therapeutic Discovery SAR 131675 , a Potent and Selective VEGFR-3 – TK Inhibitor with Antilymphangiogenic , Antitumoral , and Antimetastatic Activities
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine kinase activity and VEGFR-3…