Stroke is the main cause of mortality and morbidity in developed countries. A relevant percentage of strokes is due to several cerebrovascular pathologies with genetic background. While the study of these diseases in animal models is proving inefficient, with the development of the cellular reprogramming technology in 2006, a new approach appeared to overcome the existing barriers found in these models. Thanks to the cellular reprogramming technology, the current thesis supposes the first time that an in vitro cellular model with the patient's own cells is achieved for the study of one of these cerebrovascular pathologies, CADASIL, focusing on the abnormal behavior of the mutated protein NOTCH3
Many central nervous system (CNS) diseases including stroke, spinal cord injury (SCI), and brain tum...
Cerebrovascular disorders pose a global health concern. Advances in basic and clinical research, inc...
Neurodegeneració; MutacióNeurodegeneración; MutaciónNeurodegeneration; MutationThe human iPSC cell l...
Ischemic stroke is the main cause of disability and an immense burden both on the resources of famil...
Stroke is the main cause of disability in Europe and second cause of death. Cell therapy have appear...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)...
Mesenchymal stem cells (MSCs) are a promising clinical therapy for ischemic stroke. However, critica...
Ischemic Stroke is a multifaceted occurrence, caused by the blockage of blood flow/oxygen into the b...
Grande parte do conhecimento atual dos fenótipos celulares relacionados a doenças neurológicas foi o...
[Abstract] Here, we report the establishment of the human iPS cell line N1-FiPS4F#7 generated from ...
L'accident vasculaire cérébral (AVC) représente la première cause de handicap acquis de l'adulte. A ...
© 2013 Dr. Ana AntonicOver 500 therapeutic agents have shown protection against ischaemic injury in ...
CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)...
Tese de Doutoramento em Ciências da Saúde, no ramo de Medicina, apresentada à Faculdade de Medicina ...
Many central nervous system (CNS) diseases including stroke, spinal cord injury (SCI), and brain tum...
Cerebrovascular disorders pose a global health concern. Advances in basic and clinical research, inc...
Neurodegeneració; MutacióNeurodegeneración; MutaciónNeurodegeneration; MutationThe human iPSC cell l...
Ischemic stroke is the main cause of disability and an immense burden both on the resources of famil...
Stroke is the main cause of disability in Europe and second cause of death. Cell therapy have appear...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)...
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)...
Mesenchymal stem cells (MSCs) are a promising clinical therapy for ischemic stroke. However, critica...
Ischemic Stroke is a multifaceted occurrence, caused by the blockage of blood flow/oxygen into the b...
Grande parte do conhecimento atual dos fenótipos celulares relacionados a doenças neurológicas foi o...
[Abstract] Here, we report the establishment of the human iPS cell line N1-FiPS4F#7 generated from ...
L'accident vasculaire cérébral (AVC) représente la première cause de handicap acquis de l'adulte. A ...
© 2013 Dr. Ana AntonicOver 500 therapeutic agents have shown protection against ischaemic injury in ...
CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy)...
Tese de Doutoramento em Ciências da Saúde, no ramo de Medicina, apresentada à Faculdade de Medicina ...
Many central nervous system (CNS) diseases including stroke, spinal cord injury (SCI), and brain tum...
Cerebrovascular disorders pose a global health concern. Advances in basic and clinical research, inc...
Neurodegeneració; MutacióNeurodegeneración; MutaciónNeurodegeneration; MutationThe human iPSC cell l...