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Author Details

Zoraida Diaz-Perez
University of Miami Miller School of Medicine
2005
14
11
PMIDPaper TitleJournal TitlePublished Year
36993333Reduction of Spermine Synthase Suppresses Tau Accumulation Through Autophagy Modulation in Tauopathy.bioRxiv2023
35801587Phenylbutyrate modulates polyamine acetylase and ameliorates Snyder-Robinson syndrome in a Drosophila model and patient cells.JCI Insight2022
34919052NMNAT promotes glioma growth through regulating post-translational modifications of P53 to inhibit apoptosis.Elife2021
33322328Exposure to Aerosolized Algal Toxins in South Florida Increases Short- and Long-Term Health Risk in <i>Drosophila</i> Model of Aging.Toxins (Basel)2020
31484760Nmnat restores neuronal integrity by neutralizing mutant Huntingtin aggregate-induced progressive toxicity.Proc Natl Acad Sci U S A2019
29348635Publisher Correction: Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome.Nat Commun2018
28603714Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.Front Med (Lausanne)2017
29097652Spermine synthase deficiency causes lysosomal dysfunction and oxidative stress in models of Snyder-Robinson syndrome.Nat Commun2017
27266628Simultaneous production of amylases and proteases by Bacillus subtilis in brewery wastes.Braz J Microbiol2016
22086914Generation and functional characterization of knock-in mice harboring the cardiac troponin I-R21C mutation associated with hypertrophic cardiomyopathy.J Biol Chem2012
17356007Fast skeletal muscle regulatory light chain is required for fast and slow skeletal muscle development.FASEB J2007
16837010Prolonged Ca2+ and force transients in myosin RLC transgenic mouse fibers expressing malignant and benign FHC mutations.J Mol Biol2006
16076902The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.J Cell Sci2005
16115869F110I and R278C troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibers.J Biol Chem2005
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Collaborators

Rong Grace Zhai
Leonard M. Miller School of Medicine, University of Miami
Co-authored papers 6
Chong Li
University of Miami Miller School of Medicine
Co-authored papers 5
Yi Zhu
University of Miami Miller School of Medicine
Co-authored papers 5
Jennifer M Brazill
Washington University
Co-authored papers 4
Christofer Bello
University of Miami Miller School of Medicine
Co-authored papers 3
William A Gahl
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Cornelius F Boerkoel
University of British Columbia
Co-authored papers 3
May Christine V Malicdan
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Joun Park
University of Miami Miller School of Medicine
Co-authored papers 2
Luigi Boccuto
Co-authored papers 2
Charles E Schwartz
Co-authored papers 2
Joie Davis
National Institutes of Health
Co-authored papers 1
Michele Nehrebecky
National Human Genome Research Institute, National Institutes of Health (NIH)
Co-authored papers 1
Richard Steet
Co-authored papers 1
Jeremy Elson
Co-authored papers 1
Camilo Toro
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
Elise Flynn
Royal Children's Hospital
Co-authored papers 1
Rena Godfrey
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
Thomas C Markello
National Institutes of Health
Co-authored papers 1
David Draper
National Institutes of Health
Co-authored papers 1
Damian Smedley
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 1
Lynne A Wolfe
National Institutes of Health Undiagnosed Diseases Program
Co-authored papers 1
Zaheer Valivullah
Center for Mendelian Genomics, Broad Institute of MIT and Harvard
Co-authored papers 1
William P Bone
University of Pennsylvania - Perelman School of Medicine
Co-authored papers 1
Mariska Davids
University of Pretoria
Co-authored papers 1
Valerie Maduro
NIH and National Human Genome Research Institute
Co-authored papers 1
Roxanne Fischer
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 1
Melissa A Haendel
Co-authored papers 1
Dimitre R Simeonov
University of California San Francisco
Co-authored papers 1
Miao He
Children's Hospital of Philadelphia
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Release 1.2