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Thiyagaraj Mayuranathan

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European Journal of Haematology|January 30, 2014
Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian populationThiyagaraj Mayuranathan, Janakiram Rayabaram, Reena Das, et al.
Blood Advances|February 28, 2025
BCL11A-deficient human erythropoiesis is impaired in vitro and after xenotransplantation into miceYoonjeong Jang, Ruopeng Feng, Lance E Palmer, et al.
JCI Insight|November 22, 2022
An RPS19-edited model for Diamond-Blackfan anemia reveals TP53-dependent impairment of hematopoietic stem cell activitySenthil Velan Bhoopalan, Jonathan S Yen, Thiyagaraj Mayuranathan, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Multiplex Base Editing to Protect from CD33-Directed Therapy: Implications for Immune and Gene TherapyFlorence Borot, Olivier Humbert, Gregory A Newby, et al.
Nature|October 12, 2022
Activation of γ-globin expression by hypoxia-inducible factor 1αRuopeng Feng, Thiyagaraj Mayuranathan, Peng Huang, et al.
Nature Communications|July 27, 2025
Removal of promoter CpG methylation by epigenome editing reverses HBG silencingHenry W Bell, Ruopeng Feng, Manan Shah, et al.
Nature Genetics|May 26, 2022
Dual function NFI factors control fetal hemoglobin silencing in adult erythroid cellsKunhua Qin, Peng Huang, Ruopeng Feng, et al.
Molecular Cell|December 10, 2020
ZNF410 Uniquely Activates the NuRD Component CHD4 to Silence Fetal Hemoglobin ExpressionXianjiang Lan, Ren Ren, Ruopeng Feng, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2024
Preclinical development of lentiviral vector gene therapy for Diamond-Blackfan anemia syndromeSenthil Velan Bhoopalan, Thiyagaraj Mayuranathan, Nana Liu, et al.
Nature Communications|May 27, 2025
Multiplex base editing to protect from CD33 directed drugs for immune and gene therapyFlorence Borot, Olivier Humbert, Jeffrey T Ehmsen, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
European Journal of Haematology|January 30, 2014
Identification of rare and novel deletions that cause (δβ)0-thalassaemia and hereditary persistence of foetal haemoglobin in Indian populationThiyagaraj Mayuranathan, Janakiram Rayabaram, Reena Das, et al.
Blood Advances|February 28, 2025
BCL11A-deficient human erythropoiesis is impaired in vitro and after xenotransplantation into miceYoonjeong Jang, Ruopeng Feng, Lance E Palmer, et al.
JCI Insight|November 22, 2022
An RPS19-edited model for Diamond-Blackfan anemia reveals TP53-dependent impairment of hematopoietic stem cell activitySenthil Velan Bhoopalan, Jonathan S Yen, Thiyagaraj Mayuranathan, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Multiplex Base Editing to Protect from CD33-Directed Therapy: Implications for Immune and Gene TherapyFlorence Borot, Olivier Humbert, Gregory A Newby, et al.
Nature|October 12, 2022
Activation of γ-globin expression by hypoxia-inducible factor 1αRuopeng Feng, Thiyagaraj Mayuranathan, Peng Huang, et al.
Nature Communications|July 27, 2025
Removal of promoter CpG methylation by epigenome editing reverses HBG silencingHenry W Bell, Ruopeng Feng, Manan Shah, et al.
Nature Genetics|May 26, 2022
Dual function NFI factors control fetal hemoglobin silencing in adult erythroid cellsKunhua Qin, Peng Huang, Ruopeng Feng, et al.
Molecular Cell|December 10, 2020
ZNF410 Uniquely Activates the NuRD Component CHD4 to Silence Fetal Hemoglobin ExpressionXianjiang Lan, Ren Ren, Ruopeng Feng, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 14, 2024
Preclinical development of lentiviral vector gene therapy for Diamond-Blackfan anemia syndromeSenthil Velan Bhoopalan, Thiyagaraj Mayuranathan, Nana Liu, et al.
Nature Communications|May 27, 2025
Multiplex base editing to protect from CD33 directed drugs for immune and gene therapyFlorence Borot, Olivier Humbert, Jeffrey T Ehmsen, et al.
Pageof 2