R. Aledo

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Aliases
R Aledo, R. Aledo, Rosa Aledo
Publication record
41 papers · 1,056 citations · H-index 16

PAPERS

MicroRNA-145 Regulates the Differentiation of Adipose Stem Cells Toward Microvascular Endothelial Cells and Promotes Angiogenesis.
201961 citationsauthor #3
LRP 1 Gene Polymorphisms Are Associated With Premature Risk of Cardiovascular Disease in Patients With Familial Hypercholesterolemia
20171 citationsauthor #1
Abbreviations CVD : cardiovascular disease FH : familial hypercholesterolemia GWAS : genome-wide association studies HDL : high-density lipoproteins LDL : low-density lipoproteins
20170 citationsauthor #1
PAR2-SMAD3 in microvascular endothelial cells is indispensable for vascular stability via tissue factor signaling.
201624 citationsauthor #4
Macrophages of genetically characterized familial hypercholesterolaemia patients show up‐regulation of LDL‐receptor‐related proteins
201616 citationsauthor #5
High Levels of Antifibrinolytic Proteins Are Found in Plasma of Older Octogenarians With Cardiovascular Disease and Cognitive Decline.
201512 citationsauthor #4
rs11613352 polymorphism (TT genotype) associates with a decrease of triglycerides and an increase of HDL in familial hypercholesterolemia patients.
20152 citationsauthor #1
Monocyte-secreted Wnt5a interacts with FZD5 in microvascular endothelial cells and induces angiogenesis through tissue factor signaling.
201443 citationsauthor #4
C0230: Monocytes Through Wnt Signaling Trigger Tissue Factor Expression in Microvascular Endothelial Cells During Tube Formation
20140 citationsauthor #4
550ETS1/SMAD3 cooperation regulates TF-induced microvascular endothelial cell angiotube formation
20140 citationsauthor #3
induces angiogenesis through tissue factor signaling
20142 citationsauthor #4
549Monocytes activate the non-canonical Wnt5a pathway in microvascular endothelial cells and induce tissue factor expression and tube formation
20140 citationsauthor #3
ESPAÑOLA DE CARDIOLOGÍA SAFEHEART STUDY AND CARDIOVASCULAR DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA Study Design and Recruitment
20140 citationsauthor #1
Molecular and functional characterization of LRP1 promoter polymorphism c.1-25 C>G (rs138854007).
20145 citationsauthor #1
Ets-1 transcription is required in tissue factor driven microvessel formation and stabilization
20120 citationsauthor #3
LRP1 gene polymorphisms are associated with premature risk of cardiovascular disease in patients with familial hypercholesterolemia.
201213 citationsauthor #1
Ets-1 transcription is required in tissue factor driven microvessel formation and stabilization
201232 citationsauthor #3
Low-density lipoprotein receptor-related protein 1 mediates hypoxia-induced very low density lipoprotein-cholesteryl ester uptake and accumulation in cardiomyocytes.
201283 citationsauthor #4
Tissue Factor Regulates Microvessel Formation and Stabilization by Induction of Chemokine (C-C motif) Ligand 2 Expression
201158 citationsauthor #3
Hypoxia Stimulates Low-Density Lipoprotein Receptor–Related Protein-1 Expression Through Hypoxia-Inducible Factor-1&agr; in Human Vascular Smooth Muscle Cells
201164 citationsauthor #2
P362 HYPOXIA UP-REGULATES FIBULIN-5 IN ENDOTHELIAL CELLS THROUGH A HIF-1 DEPENDENT MECHANISM
20100 citationsauthor #3
Fibulin-5 Is Up-regulated by Hypoxia in Endothelial Cells through a Hypoxia-inducible Factor-1 (HIF-1α)-dependent Mechanism*
201070 citationsauthor #6
Saturday, 17 July 2010
20100 citationsauthor #36
PO5-130 ANALYSIS OF LRP1 PROMOTER POLYMORPHISMS IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA (HFH)
20070 citationsauthor #1
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiency
200642 citationsauthor #1
Structural (βα)8 TIM Barrel Model of 3-Hydroxy-3-methylglutaryl-Coenzyme A Lyase*
200316 citationsauthor #7
CDP-choline prevents glutamate-mediated cell death in cerebellar granule neurons
200350 citationsauthor #3
Structural (betaalpha)8 TIM barrel model of 3-hydroxy-3-methylglutaryl-coenzyme A lyase.
20033 citationsauthor #7
The diagnosis of mitochondrial HMG-CoA synthase deficiency.
200234 citationsauthor #5
Genetic basis of mitochondrial HMG-CoA synthase deficiency
200147 citationsauthor #1
Schwann cells harbor the somatic NF1 mutation in neurofibromas: evidence of two different Schwann cell subpopulations.
2000251 citationsauthor #4
Apolipoprotein E ϵ4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers
199810 citationsauthor #4
High Variability of CYP21 Gene Rearrangements in Spanish Patients with Classic Form of Congenital Adrenal Hyperplasia
199820 citationsauthor #2
Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.
19989 citationsauthor #2
Chromosome localization and characterization of a family of long interspersed repetitive DNA elements from the genus Zea
199510 citationsauthor #1
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.
199569 citationsauthor #2
Increase of sister chromatid exchanges in excision repair deficient xeroderma pigmentosum
19891 citationsauthor #1
Contribution a l'etude cytogenetique du xeroderma pigmentosum
19890 citationsauthor #1
Spontaneous chromosomal anomalies in lymphocytes from xeroderma pigmentosum. A study of ten patients.
19884 citationsauthor #1
Isoacentric and isocentric chromosomes originating after deletions of human chromosomes
19874 citationsauthor #3
Abstracts_1 7..11
year unknown0 citationsauthor #6

TIMELINE

1987 4 citations

1988 4 citations

1989 1 citations

1995 79 citations

1998 39 citations

2000 251 citations

2001 47 citations

2002 34 citations

2003 69 citations

2006 42 citations

2007 0 citations

2010 70 citations

2011 122 citations

2012 128 citations

2014 50 citations

2015 14 citations

2016 40 citations

2017 1 citations

2019 61 citations

Unknown 0 citations

R. Aledo

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