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R Aledo

Showing results (11-20 of 19) with videos related to

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Human Molecular Genetics|December 15, 2000
Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulationsE Serra, T Rosenbaum, U Winner, et al.
Atherosclerosis|October 29, 2010
Selective role of sterol regulatory element binding protein isoforms in aggregated LDL-induced vascular low density lipoprotein receptor-related protein-1 expressionP Costales, R Aledo, S Vérnia, et al.
Neuroscience Letters|July 17, 1998
Apolipoprotein E epsilon 4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothersM Ezquerra, F Ballesta, R Queralt, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiencyR Aledo, C Mir, R N Dalton, et al.
Human Genetics|August 2, 2001
Genetic basis of mitochondrial HMG-CoA synthase deficiencyR Aledo, J Zschocke, J Pié, et al.
Human Molecular Genetics|April 1, 1995
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinityS Demczuk, R Aledo, J Zucman, et al.
Atherosclerosis|January 15, 2013
Lipopolysaccharide downregulates CD91/low-density lipoprotein receptor-related protein 1 expression through SREBP-1 overexpression in human macrophagesP Costales, J Castellano, E Revuelta-López, et al.
Human Genetics|July 1, 1987
Isoacentric and isocentric chromosomes originating after deletions of human chromosomesB Dutrillaux, W Al Achkar, R Aledo, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
A single-residue mutation, G203E, causes 3-hydroxy-3-methylglutaric aciduria by occluding the substrate channel in the 3D structural model of HMG-CoA lyaseC Mir, E Lopez-Viñas, R Aledo, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Human Molecular Genetics|December 15, 2000
Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulationsE Serra, T Rosenbaum, U Winner, et al.
Atherosclerosis|October 29, 2010
Selective role of sterol regulatory element binding protein isoforms in aggregated LDL-induced vascular low density lipoprotein receptor-related protein-1 expressionP Costales, R Aledo, S Vérnia, et al.
Neuroscience Letters|July 17, 1998
Apolipoprotein E epsilon 4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothersM Ezquerra, F Ballesta, R Queralt, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiencyR Aledo, C Mir, R N Dalton, et al.
Human Genetics|August 2, 2001
Genetic basis of mitochondrial HMG-CoA synthase deficiencyR Aledo, J Zschocke, J Pié, et al.
Human Molecular Genetics|April 1, 1995
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinityS Demczuk, R Aledo, J Zucman, et al.
Atherosclerosis|January 15, 2013
Lipopolysaccharide downregulates CD91/low-density lipoprotein receptor-related protein 1 expression through SREBP-1 overexpression in human macrophagesP Costales, J Castellano, E Revuelta-López, et al.
Human Genetics|July 1, 1987
Isoacentric and isocentric chromosomes originating after deletions of human chromosomesB Dutrillaux, W Al Achkar, R Aledo, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
A single-residue mutation, G203E, causes 3-hydroxy-3-methylglutaric aciduria by occluding the substrate channel in the 3D structural model of HMG-CoA lyaseC Mir, E Lopez-Viñas, R Aledo, et al.
Pageof 2