A novel heterozygous HIF2AM535I mutation reinforces the role of oxygen sensing pathway disturbances in the pathogenesis of familial erythrocytosis

Medicine and Dentistry

• Erythrocytosis 100%
• Hypoxia Inducible Factor 100%
• Adrenomedullin 75%
• Hypoxia 50%
• Gene 50%
• Mammalian Cell 50%
• Oxygen Sensing 50%
• Position 50%
• Pathogenesis 25%
• Age 25%
• Angiogenesis 25%
• Gene Mutation 25%
• Methionine 25%
• Messenger RNA 25%
• Vasculotropin 25%
• Exon 25%
• Isoleucine 25%
• Erythropoiesis 25%
• Erythropoietin Receptor 25%
• Transferrin Receptor 25%
• Family 25%
• Regulatory Mechanism 25%
• Base 25%
• Inpatient 25%

Biochemistry, Genetics and Molecular Biology

• Mutation 100%
• Hypoxia-Inducible Factors 100%
• Nested Gene 50%
• Oxygen Sensing 50%
• Position 50%
• Angiogenesis 25%
• Isoleucine 25%
• Methionine 25%
• Transferrin Receptor 25%
• Erythropoiesis 25%
• Vascular Endothelial Growth Factor 25%
• Erythropoietin Receptor 25%
• Transcription Factor IIA 25%
• N-Myc 25%
• Age 25%
• Regulatory Mechanism 25%
• Messenger RNA 25%

Neuroscience

• Hypoxia-Inducible Factors 100%
• Gene 50%
• Oxygen Sensing 50%
• Angiogenesis 25%
• Erythropoiesis 25%
• Gene Mutation 25%
• Exon 25%
• Isoleucine 25%
• Methionine 25%
• N-Myc 25%
• Erythropoietin Receptor 25%
• Transferrin Receptor 25%
• Transcription Factor IIA 25%