Reyna Hernández‐Benítez

Altos Labs

Biochemistry, Genetics and Molecular Biology · Life Sciences

18h-index2.4kcitations33works7.02yr avg
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Research Topics

Aldose Reductase and Taurine(9), Pluripotent Stem Cells Research(7), RNA Research and Splicing(6), Prenatal Substance Exposure Effects(6), CRISPR and Genetic Engineering(5)

Publications33 total

Generation of a set of genetically modified long QT syndrome induced pluripotent stem cell lines carrying knock-in variants rs120074178 (KCNQ1 c.569G > A; p.Arg190Gln) and rs137854600 (SCN5A c.4865G > A; p.Arg1622Gln) and isogenic control lines
Stem Cell Research·2025Open Access
Intervention with metabolites emulating endogenous cell transitions accelerates muscle regeneration in young and aged mice
Cell Reports Medicine·2024· 14 citedOpen Access
Author Correction: Wiskott-Aldrich syndrome protein forms nuclear condensates and regulates alternative splicing
Nature Communications·2022Open Access
Wiskott-Aldrich syndrome protein forms nuclear condensates and regulates alternative splicing
Nature Communications·2022· 19 citedOpen Access
In vivo partial cellular reprogramming enhances liver plasticity and regeneration
Cell Reports·2022· 97 citedOpen Access
Cross-species metabolomic analysis identifies uridine as a potent regeneration promoting factor
Cell Discovery·2022· 122 citedOpen Access
Chimeric Contribution of Human Extended Pluripotent Stem Cells to Monkey Embryos Ex Vivo
Obstetrical & Gynecological Survey·2021
Chimeric contribution of human extended pluripotent stem cells to monkey embryos ex vivo
Cell·2021· 24 citedOpen Access
Chimeric contribution of human extended pluripotent stem cells to monkey embryos ex vivo
Cell·2021· 121 citedOpen Access
First progeria monkey model generated using base editor
Protein & Cell·2020· 4 citedOpen Access
αKLOTHO and sTGFβR2 treatment counteract the osteoarthritic phenotype developed in a rat model
Protein & Cell·2020· 25 citedOpen Access
Precise in vivo genome editing via single homology arm donor mediated intron-targeting gene integration for genetic disease correction
Cell Research·2019· 67 citedOpen Access
Single-dose CRISPR–Cas9 therapy extends lifespan of mice with Hutchinson–Gilford progeria syndrome
Nature Medicine·2019· 153 cited
In vivo reprogramming of wound-resident cells generates skin epithelial tissue
Nature·2018· 140 citedOpen Access
At the Heart of Genome Editing and Cardiovascular Diseases
Circulation Research·2018· 8 citedOpen Access
Wiskott-Aldrich Syndrome Protein Regulates Nuclear Organization, Alternative Splicing and Cell Proliferation
SSRN Electronic Journal·2018Open Access
Integration of CpG-free DNA induces de novo methylation of CpG islands in pluripotent stem cells
Science·2017· 73 citedOpen Access
In vivo genome editing via CRISPR/Cas9 mediated homology-independent targeted integration
Nature·2016· 1.1k citedOpen Access
Taurine Enhances Proliferation and Promotes Neuronal Specification of Murine and Human Neural Stem/Progenitor Cells
Advances in experimental medicine and biology·2015· 16 cited
LA TAURINA EN EL DESARROLLO DE CÉLULAS TRONCALES NEURALES
Gaceta UNAM (2010-2016)·2014
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Frequent Co-authors

Juan Carlos Izpisúa Belmonte(17), Concepción Rodrı́guez Esteban(12), Gerardo Ramos‐Mandujano(12), Herminia Pasantes‐Morales(12), Tomoaki Hishida(10), Estrella Núñez‐Delicado(10), Guang‐Hui Liu(9), Keiichiro Suzuki(8), Jing Qu(7), Pradeep Reddy(7), Maxim N. Shokhirev(7), Jun Wu(6), Mako Yamamoto(6), Fumiyuki Hatanaka(5), Mo Li(5), Emi Aizawa(5), Pierre J. Magistretti(5), Yuta Takahashi(5), Ling Huang(5), Masakazu Kurita(4)