Andrea A. Guerrero

ORCID: 0000-0002-5324-8232
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About
Contact & Profiles
Research Areas
  • Protein Structure and Dynamics
  • Cardiac Arrhythmias and Treatments
  • Cardiovascular Function and Risk Factors
  • Intracranial Aneurysms: Treatment and Complications
  • Venous Thromboembolism Diagnosis and Management
  • Lymphatic System and Diseases
  • Congenital heart defects research
  • Neuroscience and Neuropharmacology Research
  • Cellular transport and secretion
  • Acute Myocardial Infarction Research
  • Vascular Malformations Diagnosis and Treatment
  • Atrial Fibrillation Management and Outcomes
  • Cardiac Imaging and Diagnostics
  • Intracerebral and Subarachnoid Hemorrhage Research

Brandeis University
2022

Cardiovascular Institute Hospital
2021

University of Pennsylvania
2020

In recent decades, treatments for myocardial infarction (MI), such as stem and progenitor cell therapy, have attracted considerable scientific clinical attention but failed to improve patient outcomes. These efforts indicate that more rigorous mechanistic functional testing of potential MI therapies is required. Recent studies suggested augmenting post-MI lymphatic growth via VEGF-C administration improves cardiac function. However, the mechanisms underlying this proposed therapeutic...

10.1172/jci147070 article EN Journal of Clinical Investigation 2021-08-17

Cerebral cavernous malformations (CCMs) form following loss of the CCM protein complex in brain endothelial cells due to increased MEKK3 signaling and KLF2/4 transcription factor expression, but downstream events that drive lesion formation remain undefined. Recent studies have revealed lesions expand by incorporating neighboring wild-type cells, indicative a cell nonautonomous mechanism. Here we find ADAMTS5 reduced neonatal mouse model. Conversely, gain conferred early genesis absence...

10.1084/jem.20200140 article EN cc-by-nc-sa The Journal of Experimental Medicine 2020-07-10

Homeostatic synaptic plasticity requires widespread remodeling of signaling and scaffolding networks, but the role post-translational modifications in this process has not been systematically studied. Using deep-scale quantitative analysis phosphoproteome mouse neocortical neurons, we found temporally complex changes during scaling up down. We observed 424 bidirectionally modulated phosphosites that were strongly enriched for synapse-associated proteins, including S1539 autism spectrum...

10.7554/elife.74277 article EN cc-by eLife 2022-04-26
Guillaume Roger Grégory Ducrocq Jules Mesnier Neila Sayah Jérémie Abtan and 95 more Roberto Ferrari Ian Ford Kim Fox Jean‐Claude Tardif Michał Tendera Laurent J. Feldman Yedid Elbez Philippe Gabríel Steg Philippe Gabríel Steg Roberto Ferrari Ian Ford Kim Fox Jean‐Claude Tardif Michał Tendera Fernando Sökn Christopher M. Reid Iréne Lang F. Van Den Branden Luis Machado César Nazar Luqman Assen Goudev Paul Dorian Dayi Hu Petr Widimský Christian Hassager Nicolas Danchin Stefan Kääb Panos Vardas Kadhim Sulaiman Wael Al Mahmeed Jassim Al Suwaidi Ibrahim Al Rashdan Fuad Abdulkader Béla Merkely Upendra Kaul Kieran Daly Luigi Tavazzi Roberto Ferrari Yangsoo Jang Andrejs Ērglis Aleksandras Laucevičius Ahmad Nizar Jamaluddin Marco Alcocer Gamba Igor I. Tulevski Janina Stępińska Jońo Morais Cezar Macarie Р. Г. Оганов S. А. Shalnova Muayed Al‐Zaibag Mak Koon Hou Assoc Gabriel Kamensky Zlatko Fras Vojko Kanič D.P. Naidoo José Luis Zamorano Hans Rickli Andres Jaussi Assoc Charn Sriratanasathavorn Paul R. Kalra Mykhailo Lutai Oleksandr Parkhomenko Lan Viet Nguyen Ronald M.A. Henry Andrea A. Guerrero Michael L. Basara Fernando Belcastro J A Bertarini C Cazenave H Dreycopp J. Egido Jeannelyn S. Estrella Diana C. Garofalo Jennifer Giordano H Lagioia Nieves Martínez Lago R La Greca Leonor Varela Lema Néstor López-Cabanillas Hugo A Luquez Chad Miller Elena Prada Paloma Albacete Ródenas R G Schena G Suárez Alejandro Tomatti David Colquhoun A. Conradie Shanice Cox Deanna Cross Robert Fathi B. Fitzgerald Ian Hamilton‐Craig Geoff Holt Sakunthala Jayasinghe

Abstract Background and Aims It has been reported that patients without standard modifiable cardiovascular (CV) risk factors (SMuRFs—diabetes, dyslipidaemia, hypertension, smoking) presenting with first myocardial infarction (MI), especially women, have a higher in-hospital mortality than factors, possibly lower long-term provided they survive the post-infarct period. This study aims to explore outcomes of SMuRF-less stable coronary artery disease (CAD). Methods CLARIFY is an observational...

10.1093/eurheartj/ehae299 article EN European Heart Journal 2024-05-20
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