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Isabella Tosi

Showing results (1-10 of 24) with videos related to

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Atherosclerosis|November 11, 2006
Genetic defects causing familial hypercholesterolaemia: identification of deletions and duplications in the LDL-receptor gene and summary of all mutations found in patients attending the Hammersmith Hospital Lipid ClinicIsabella Tosi, Paola Toledo-Leiva, Clare Neuwirth, et al.
Human Molecular Genetics|March 18, 2005
Evidence for effect of mutant PCSK9 on apolipoprotein B secretion as the cause of unusually severe dominant hypercholesterolaemiaXi-Ming Sun, Emily R Eden, Isabella Tosi, et al.
Journal of Vascular and Interventional Radiology : JVIR|August 12, 2008
Quantitative 3T MR imaging of the descending thoracic aorta: patients with familial hypercholesterolemia have an increased aortic plaque burden despite long-term lipid-lowering therapyStephan A Schmitz, Declan P O'Regan, Julie Fitzpatrick, et al.
Neuroradiology|July 24, 2007
MRI at 3 Tesla detects no evidence for ischemic brain damage in intensively treated patients with homozygous familial hypercholesterolemiaStephan A Schmitz, Declan P O'Regan, Julie Fitzpatrick, et al.
Frontiers in Immunology|May 20, 2025
Circulating CD8 T cells from patients with mild-to-moderate psoriasis are functionally impairedYiqiao Chen, Chiara Tontini, Isabella Tosi, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 15, 2005
Severe hypercholesterolemia in four British families with the D374Y mutation in the PCSK9 gene: long-term follow-up and treatment responseRossi P Naoumova, Isabella Tosi, Dilip Patel, et al.
The Journal of Investigative Dermatology|April 13, 2012
Regulation of T-plastin expression by promoter hypomethylation in primary cutaneous T-cell lymphomaChristine L Jones, Silvia Ferreira, Robert C T McKenzie, et al.
The Journal of Investigative Dermatology|September 18, 2009
Downregulation of Fas gene expression in Sézary syndrome is associated with promoter hypermethylationChristine L Jones, E Mary Wain, Chung-Ching Chu, et al.
The Journal of Investigative Dermatology|December 20, 2013
Characterization of innate lymphoid cells in human skin and blood demonstrates increase of NKp44+ ILC3 in psoriasisFederica Villanova, Barry Flutter, Isabella Tosi, et al.
Plos One|March 3, 2011
The IL23R R381Q gene variant protects against immune-mediated diseases by impairing IL-23-induced Th17 effector response in humansPaola Di Meglio, Antonella Di Cesare, Ute Laggner, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Atherosclerosis|November 11, 2006
Genetic defects causing familial hypercholesterolaemia: identification of deletions and duplications in the LDL-receptor gene and summary of all mutations found in patients attending the Hammersmith Hospital Lipid ClinicIsabella Tosi, Paola Toledo-Leiva, Clare Neuwirth, et al.
Human Molecular Genetics|March 18, 2005
Evidence for effect of mutant PCSK9 on apolipoprotein B secretion as the cause of unusually severe dominant hypercholesterolaemiaXi-Ming Sun, Emily R Eden, Isabella Tosi, et al.
Journal of Vascular and Interventional Radiology : JVIR|August 12, 2008
Quantitative 3T MR imaging of the descending thoracic aorta: patients with familial hypercholesterolemia have an increased aortic plaque burden despite long-term lipid-lowering therapyStephan A Schmitz, Declan P O'Regan, Julie Fitzpatrick, et al.
Neuroradiology|July 24, 2007
MRI at 3 Tesla detects no evidence for ischemic brain damage in intensively treated patients with homozygous familial hypercholesterolemiaStephan A Schmitz, Declan P O'Regan, Julie Fitzpatrick, et al.
Frontiers in Immunology|May 20, 2025
Circulating CD8 T cells from patients with mild-to-moderate psoriasis are functionally impairedYiqiao Chen, Chiara Tontini, Isabella Tosi, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|October 15, 2005
Severe hypercholesterolemia in four British families with the D374Y mutation in the PCSK9 gene: long-term follow-up and treatment responseRossi P Naoumova, Isabella Tosi, Dilip Patel, et al.
The Journal of Investigative Dermatology|April 13, 2012
Regulation of T-plastin expression by promoter hypomethylation in primary cutaneous T-cell lymphomaChristine L Jones, Silvia Ferreira, Robert C T McKenzie, et al.
The Journal of Investigative Dermatology|September 18, 2009
Downregulation of Fas gene expression in Sézary syndrome is associated with promoter hypermethylationChristine L Jones, E Mary Wain, Chung-Ching Chu, et al.
The Journal of Investigative Dermatology|December 20, 2013
Characterization of innate lymphoid cells in human skin and blood demonstrates increase of NKp44+ ILC3 in psoriasisFederica Villanova, Barry Flutter, Isabella Tosi, et al.
Plos One|March 3, 2011
The IL23R R381Q gene variant protects against immune-mediated diseases by impairing IL-23-induced Th17 effector response in humansPaola Di Meglio, Antonella Di Cesare, Ute Laggner, et al.
Pageof 3