V. Campuzano

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Aliases
V Campuzano, V. Campuzano, Victoria Campuzano
Publication record
41 papers · 6,851 citations · H-index 21

PAPERS

Hyperuricaemia Does Not Interfere with Aortopathy in a Murine Model of Marfan Syndrome
20230 citationsauthor #6
The Combined Treatment of Curcumin with Verapamil Ameliorates the Cardiovascular Pathology in a Williams–Beuren Syndrome Mouse Model
20234 citationsauthor #6
Dysfunctional Mitochondria in the Cardiac Fibers of a Williams–Beuren Syndrome Mouse Model
20230 citationsauthor #6
Early Neurobehavioral Characterization of the CD Mouse Model of Williams–Beuren Syndrome
20233 citationsauthor #6
Curcumin combined with verapamil improve cardiovascular phenotype of a Williams-Beuren Syndrome mice model reducing oxidative stress
20220 citationsauthor #6
Application of the adverse outcome pathway to identify molecular changes in prenatal brain programming induced by IUGR: Discoveries after EGCG exposure.
20224 citationsauthor #8
Anti-TGFβ (Transforming Growth Factor β) Therapy With Betaglycan-Derived P144 Peptide Gene Delivery Prevents the Formation of Aortic Aneurysm in a Mouse Model of Marfan Syndrome
202115 citationsauthor #5
Cannabinoid signaling modulation through JZL184 restores key phenotypes of a mouse model for Williams–Beuren syndrome
202118 citationsauthor #14
Verapamil/Curcumin treatment attenuates the behavioral alterations observed in Williams Syndrome mice by regulation of MAPK pathway and Microglia overexpression
20210 citationsauthor #4
ALLOPURINOL BLOCKS AORTIC ANEURYSM IN A MOUSE MODEL OF MARFAN SYNDROME VIA REDUCING AORTIC OXIDATIVE STRESS
202122 citationsauthor #9
Co-Treatment With Verapamil and Curcumin Attenuates the Behavioral Alterations Observed in Williams–Beuren Syndrome Mice by Regulation of MAPK Pathway and Microglia Overexpression
20219 citationsauthor #5
Reactive Oxygen Species and Oxidative Stress in the Pathogenesis and Progression of Genetic Diseases of the Connective Tissue
202028 citationsauthor #3
Chlorzoxazone, A BKCa Channel Agonist, Rescues The Pathological Phenotypes Of Williams-Beuren Syndrome In A Preclinical Model
20204 citationsauthor #7
Stenosis coexists with compromised α1-adrenergic contractions in the ascending aorta of a mouse model of Williams-Beuren syndrome
202013 citationsauthor #8
Altered Neocortical Dynamics in a Mouse Model of Williams–Beuren Syndrome
201914 citationsauthor #6
Epigallocatechin-3-gallate improves cardiac hypertrophy and short-term memory deficits in a Williams-Beuren syndrome mouse model
201827 citationsauthor #8
Synaptic plasticity and spatial working memory are impaired in the CD mouse model of Williams-Beuren syndrome
201623 citationsauthor #7
Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren Syndrome.
201540 citationsauthor #4
Metabolic abnormalities in Williams–Beuren syndrome
201532 citationsauthor #6
Heterozygous deletion of the Williams-Beuren syndrome critical interval in mice recapitulates most features of the human disorder.
201470 citationsauthor #13
TFII-I regulates target genes in the PI-3K and TGF-β signaling pathways through a novel DNA binding motif.
201321 citationsauthor #4
Reduction of NADPH-Oxidase Activity Ameliorates the Cardiovascular Phenotype in a Mouse Model of Williams-Beuren Syndrome
201230 citationsauthor #1
Essential role of the N-terminal region of TFII-I in viability and behavior
201043 citationsauthor #15
Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion.
200877 citationsauthor #6
Síndrome de Williams: aspectos clínicos y bases moleculares
200612 citationsauthor #4
Protein farnesyltransferase in embryogenesis, adult homeostasis, and tumor development.
2005105 citationsauthor #7
Tumor induction by an endogenous K-ras oncogene is highly dependent on cellular context.
2003587 citationsauthor #7
Frataxin point mutations in two patients with Friedreich's ataxia and unusual clinical features
200059 citationsauthor #6
Maturation of wild-type and mutated frataxin by the mitochondrial processing peptidase.
1998125 citationsauthor #2
Frataxin is reduced in Friedreich ataxia patients and is associated with mitochondrial membranes.
1997741 citationsauthor #1
Studies of human, mouse and yeast homologues indicate a mitochondrial function for frataxin
1997472 citationsauthor #2
Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations.
1997340 citationsauthor #3
The frataxin story
19970 citationsauthor #1
Friedreich's Ataxia: Autosomal Recessive Disease Caused by an Intronic GAA Triplet Repeat Expansion
19962,727 citationsauthor #1
Clinical and genetic abnormalities in patients with Friedreich's ataxia.
19961,056 citationsauthor #4
TheFriedreich AtaxiaCritical RegionSpansa I50-kbInterval on Chromosome9q13
19950 citationsauthor #6
Genetic characterization of two phototropism mutants of Phycomyces with defects in the genes madl and madJ
199511 citationsauthor #1
Isolation, characterization and transformation, by autonomous replication, ofMucor circinelloides OMPdecase-deficient mutants
199538 citationsauthor #2
Isolation, characterization and mapping of pyrimidine auxotrophs of Phycomyces blakesleeanus
19939 citationsauthor #1
Cloning and sequence analysis of the Mucor circinelloides pyrG gene encoding orotidine-5'-monophosphate decarboxylase: use of pyrG for homologous transformation.
199267 citationsauthor #4
A new gene (madI) involved in the phototropic response of Phycomyces
19906 citationsauthor #1

TIMELINE

1990 6 citations

1992 67 citations

1993 9 citations

1995 49 citations

1996 3,783 citations

1997 1,553 citations

1998 125 citations

2000 59 citations

2003 587 citations

2005 105 citations

2006 12 citations

2008 77 citations

2010 43 citations

2012 30 citations

2013 21 citations

2014 70 citations

2015 72 citations

2016 23 citations

2018 27 citations

2019 14 citations

2020 45 citations

2021 64 citations

2022 4 citations

2023 7 citations

V. Campuzano

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