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Molecular Biology

D-Index
44
Citations
7932
World Ranking
2923
National Ranking
1395

Overview

Vince A. Chiodo is affiliated with the University of Florida in the United States and has contributed to research primarily within the fields of Medicine, Biochemistry, Genetics, and Molecular Biology. Their work spans various subfields including Molecular Biology, Ophthalmology, Cellular and Molecular Neuroscience, Geriatrics and Gerontology, and Pharmacology.

Their research focuses significantly on retinal development and disorders, glaucoma and retinal disorders, photoreceptor and optogenetics research, connexins and lens biology, retinal diseases and treatments, sirtuins and resveratrol in medicine, and healthcare and venom research.

Recent published papers by Vince A. Chiodo include:

  • Prdm1 overexpression causes a photoreceptor fate-shift in nascent, but not mature, bipolar cells, 2020, Developmental Biology
  • Neuroprotective Gene Therapy by Overexpression of the Transcription Factor MAX in Rat Models of Glaucomatous Neurodegeneration, 2022, Investigative Ophthalmology & Visual Science
  • Intravitreal Administration of AAV2-SIRT1 Reverses Diabetic Retinopathy in a Mouse Model of Type 2 Diabetes, 2023, Translational Vision Science & Technology
  • Transgene expression of Stanniocalcin-1 provides sustained intraocular pressure reduction by increasing outflow facility, 2022, PLoS ONE
  • AAV2-Mediated Expression of HspB1 in RGCs Prevents Somal Damage and Axonal Transport Deficits in a Mouse Model of Ocular Hypertension, 2022, Translational Vision Science & Technology

Coauthors who frequently collaborate with Vince A. Chiodo include:

  • William W. Hauswirth
  • W. Clay Smith
  • Noah Goodson
  • Ko U. Park
  • Jason S. Silver

Their work is often published in these venues:

  • Translational Vision Science & Technology
  • Developmental Biology
  • Investigative Ophthalmology & Visual Science
  • PLoS ONE

Best Publications

  • DICER1 deficit induces Alu RNA toxicity in age-related macular degeneration

    Hiroki Kaneko;Sami Dridi;Valeria Tarallo;Bradley D. Gelfand

  • Production and purification of serotype 1, 2, and 5 recombinant adeno-associated viral vectors.

    Sergei Zolotukhin;Mark Potter;Irene Zolotukhin;Yoshihisa Sakai

  • DICER1 Loss and Alu RNA Induce Age-Related Macular Degeneration via the NLRP3 Inflammasome and MyD88

    Valeria Tarallo;Yoshio Hirano;Bradley D. Gelfand;Sami Dridi

  • High-efficiency Transduction of the Mouse Retina by Tyrosine-mutant AAV Serotype Vectors

    Hilda Petrs-Silva;Astra Dinculescu;Qiuhong Li;Seok-Hong Min

  • Gene therapy rescues cone function in congenital achromatopsia

    András M. Komáromy;John J. Alexander;John J. Alexander;Jessica S. Rowlan;Monique M. Garcia;Monique M. Garcia

  • Gene therapy rescues photoreceptor blindness in dogs and paves the way for treating human X-linked retinitis pigmentosa

    William A. Beltran;Artur V. Cideciyan;Alfred S. Lewin;Simone Iwabe

  • Novel Properties of Tyrosine-mutant AAV2 Vectors in the Mouse Retina

    Hilda Petrs-Silva;Astra Dinculescu;Qiuhong Li;Wen-Tao Deng

  • Gene therapy restores vision-dependent behavior as well as retinal structure and function in a mouse model of RPE65 Leber congenital amaurosis.

    Ji-jing Pang;Bo Chang;Ashok Kumar;Steven Nusinowitz

  • Intraocular route of AAV2 vector administration defines humoral immune response and therapeutic potential.

    Qiuhong Li;Rehae Miller;Ping-Yang Han;Jijing Pang

  • IL-10 Suppresses Chemokines, Inflammation, and Fibrosis in a Model of Chronic Renal Disease

    Wei Mu;Xiaosen Ouyang;Anupam Agarwal;Li Zhang

  • Gene delivery to mitochondria by targeting modified adenoassociated virus suppresses Leber’s hereditary optic neuropathy in a mouse model

    Hong Yu;Rajeshwari D. Koilkonda;Tsung Han Chou;Vittorio Porciatti

  • Retinal gene therapy with a large MYO7A cDNA using adeno-associated virus

    Vanda S. Lopes;Shannon E. Boye;Carrie M. Louie;Sanford Boye

  • AAV-mediated cone rescue in a naturally occurring mouse model of CNGA3-achromatopsia.

    Ji-jing Pang;Ji-jing Pang;Wen-Tao Deng;Xufeng Dai;Xufeng Dai;Bo Lei

  • Identification, genetic analysis and DNA sequence of a 7.8‐kb virulence region of the Salmonella typhimurium virulence plasmid

    Paul A. Gulig;Allison L. Caldwell;Vince A. Chiodo

  • The human rhodopsin kinase promoter in an AAV5 vector confers rod- and cone-specific expression in the primate retina.

    Shannon E. Boye;John J. Alexander;Sanford L. Boye;Clark D. Witherspoon

  • Dual Adeno-Associated Virus Vectors Result in Efficient In Vitro and In Vivo Expression of an Oversized Gene, MYO7A

    Frank M. Dyka;Sanford L. Boye;Vince A. Chiodo;William W. Hauswirth

  • Comparative analysis of in vivo and in vitro AAV vector transduction in the neonatal mouse retina: Effects of serotype and site of administration

    Ji-jing Pang;Amanda Lauramore;Wen-tao Deng;Qiuhong Li

  • Production of pseudotyped recombinant aav virions

    Richard O. Snyder;Sergei Zolotukhin;Yoshihisa Sakai;Barry J. Byrne

  • Safety and Effects of the Vector for the Leber Hereditary Optic Neuropathy Gene Therapy Clinical Trial

    Rajeshwari D. Koilkonda;Hong Yu;Tsung Han Chou;William J. Feuer

  • ERK1/2 activation is a therapeutic target in age-related macular degeneration

    Sami Dridi;Yoshio Hirano;Valeria Tarallo;Younghee Kim

Frequent Co-Authors

William W. Hauswirth
William W. Hauswirth University of Florida
Sanford L. Boye
Sanford L. Boye University of Florida
Alfred S. Lewin
Alfred S. Lewin University of Florida
Gustavo D. Aguirre
Gustavo D. Aguirre University of Pennsylvania
Andrea Amalfitano
Andrea Amalfitano Michigan State University
Bo Chang
Bo Chang University of California, Los Angeles
Wolfgang Baehr
Wolfgang Baehr University of Utah
Guangping Gao
Guangping Gao University of Massachusetts Chan Medical School
Monica L. Vetter
Monica L. Vetter University of Utah
Samuel G. Jacobson
Samuel G. Jacobson University of Pennsylvania

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