Investigador(a)

Teresa Escalante Muñoz

  • Correo electrónico: TERESA.ESCALANTE@ucr.ac.cr
  • Categoría Regimen Académico: CATEDRATICO
  • Grado Académico: DRA.
  • Unidad Base: INSTITUTO CLODOMIRO PICADO

Proyectos

Mostrando 0 proyectos

Núm. de proyecto Descripción Unidad de Investigación

Distinciones

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BECAS

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Publicaciones

Mostrando 33 publicaciones

TÍTULO TIPO FECHA PROYECTO
Unresolved issues in the understanding of the pathogenesis of local tissue damage induced by snake venoms
  • artículo original
2018

No disponible

Metaloproteinasas dependientes de Zinc: Protagonistas centrales en la Fisiopatología de Envenenamientos por Serpientes de la familia Viperidae
  • capítulo de libro
2016

No disponible

Muscle Tissue Damage Induced by the Venom of Bothrops asper: Identification of Early and Late Pathological Events through Proteomic Analysis
  • artículo original
2016

No disponible

Hemorrhage Caused by Snake Venom Metalloproteinases: A Journey of Discovery and Understanding
  • artículo original
2016

No disponible

Novel catalytically-inactive PII metalloproteinases from a viperid snake venom with substitutions in the canonical zinc-binding motif
  • artículo original
2016
Novel insights into capillary vessel basement membrane damage by snake venom hemorrhagic metalloproteinases: A biochemical and immunohistochemical study
  • artículo original
2016

No disponible

Tissue Localization and Extracellular Matrix Degradation by PI, PII and PIII Snake Venom Metalloproteinases: Clues on the Mechanisms of Venom-Induced Hemorrhage
  • artículo original
2015

No disponible

The lethality test used for estimating the potency of antivenoms against Bothrops asper snake venom: Pathophysiological mechanisms, prophylactic analgesia, and a surrogate in vitro assay
  • artículo original
2015
Understanding structural and functional aspects of PII snake venom metalloproteinases: Characterization of BlatH1, a hemorrhagic dimeric enzyme from the venom of Bothriechis lateralis
  • artículo original
2014

No disponible

Effect of the metalloproteinase inhibitor batimastat in the systemic toxicity induced by Bothrops asper snake venom: understanding the role of metalloproteinases in envenomation
  • artículo original
2014
Homogenates of skeletal muscle injected with snake venom inhibit myogenic differentiation in cell culture
  • artículo original
2013

No disponible

Proteomic analysis of Bothrops pirajai snake venom and characterization of BpirMP, a new P-I metalloproteinase
  • artículo original
2013

No disponible

Efficacy of IgG and F(ab′)2 Antivenoms to Neutralize Snake Venom-induced Local Tissue Damage as Assessed by the Proteomic Analysis of Wound Exudate
  • artículo original
2012
Proteomics of Wound Exudate in Snake Venom-Induced Pathology: Search for Biomarkers To Assess Tissue Damage and Therapeutic Success
  • artículo original
2011

No disponible

Key events in microvascular damage induced by snake venom hemorrhagic metalloproteinases
  • artículo original
2011
Role of collagens and perlecan in microvascular stability: exploring the mechanism of capillary vessel damage by snake venom metalloproteinases
  • artículo original
2011

No disponible

High resolution analysis of snake venom metalloproteinase (SVMP) peptide bond cleavage specificity using proteome based peptide libraries and mass spectrometry
  • artículo original
2011

No disponible

Tissue pathology induced by snake venoms: How to understand a complex pattern of alterations from a systems biology perspective?
  • artículo original
2010

No disponible

Wound exudate as a proteomic window to reveal different mechanisms of tissue damage by snake venom toxins
  • artículo original
2009

No disponible

Experimental pathology of local tissue damage induced by Bothrops asper snake venom
  • artículo original
2009

No disponible

Experimental pathophysiology of systemic alterations induced by Bothrops asper snake venom
  • artículo original
2009

No disponible

Skin Pathology Induced by Snake Venom Metalloproteinase: Acute Damage, Revascularization, and Re-epithelization in a Mouse Ear Model
  • artículo original
2008

No disponible

Blood flow is required for rapid endothelial cell damage induced by a snake venom hemorrhagic metalloproteinase
  • artículo original
2006

No disponible

Role of the snake venom toxin jararhagin in proinflammatory pathogenesis: In vitro and in vivo gene expression analysis of the effects of the toxin
  • artículo original
2005

No disponible

Thrombocytopenia and platelet hypoaggregation induced by Bothrops asper snake venom. Toxins involved and their contribution to metalloproteinase-induced pulmonary hemorrhage.
  • artículo original
2005

No disponible

Hemorrhage induced by snake venom metalloproteinases: biochemical and biophysical mechanisms involved in microvessel damage
  • artículo original
2005

No disponible

Bothrops asper metalloproteinase BaP1 is inhibited by alpha(2)-macroglobulin and mouse serum and does not induce systemic hemorrhage or coagulopathy
  • artículo original
2004

No disponible

Pulmonary hemorrhage induced by jararhagin, a metalloproteinase from Bothrops jararaca snake venom
  • artículo original
2003
Increments in cytokines and matrix metalloproteinases in skeletal muscle after injection of tissue-damaging toxins from the venom of the snake Bothrops asper
  • artículo original
2002

No disponible

The venom of Bothrops asper from Guatemala: toxic activities and neutralization by antivenoms
  • artículo original
2001
Characterization of aspercetin, a platelet aggregating component from the venom of the snake Bothrops asper which induces thrombocytopenia and potentiates metalloproteinase-induced hemorrhage
  • artículo original
2001
Effectiveness of batimastat, a synthetic inhibitor of matrix metalloproteinases, in neutralizing local tissue damage induced by BaP1, a hemorrhagic metalloproteinase from the venom of the snake Bothrops asper
  • artículo original
2000
Inhibition of local hemorrhage and dermonecrosis induced by Bothrops asper snake venom: effectiveness of early in situ administration of the peptidomimetic metalloproteinase inhibitor batimastat and the chelating agent CaNa2EDTA
  • artículo original
2000