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Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with Rubinstein Taybi Syndrome

Stem cell research, 2024-08, Vol.78, p.103456, Article 103456

2024

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Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies

Nature communications, 2024-02, Vol.15 (1), p.1794-1794, Article 1794

2024

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A Dual-Plasmid-Based CRISPR/Cas9-Mediated Strategy Enables Targeted Editing of pH Regulatory Gene pacC in a Clinical Isolate of Trichophyton rubrum

Journal of fungi (Basel), 2022-11, Vol.8 (12), p.1241

2022

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The mitochondrial gene-CMPK2 functions as a rheostat for macrophage homeostasis

Frontiers in immunology, 2022-11, Vol.13, p.935710-935710

2022

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A conserved SNP variation in the pre-miR396c flanking region in Oryza sativa indica landraces correlates with mature miRNA abundance

Scientific reports, 2023-02, Vol.13 (1), p.2195-2195, Article 2195

2023

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The CRISPR/Cas9 System for Targeted Genome Engineering in Free-Living Fungi: Advances and Opportunities for Lichenized Fungi

Frontiers in microbiology, 2019-02, Vol.10, p.62

2019

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Generation and characterization of induced pluripotent stem cell line (IGIBi001-A) from a sickle cell anemia patient with homozygous β-globin mutation

Stem cell research, 2019-08, Vol.39, p.101484-101484, Article 101484

2019

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Genome Editing Revolution in Life Sciences

Resonance, 2021-07, Vol.26 (7), p.971-998

2021

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Ajay Kumar Parida (1963–2022), an eminent plant biotechnologist with a passion for mangrove biology

Physiology and molecular biology of plants, 2023-08, Vol.29 (8), p.1073-1079

2023

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Establishment and characterization of induced pluripotent stem cell line (IGIBi002-A) from a β-thalassemia patient with IVS1-5 mutation by non-integrating reprogramming approach

Stem cell research, 2021-01, Vol.50, p.102124-102124, Article 102124

2021

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Targeting PfProhibitin 2-Hu-Hsp70A1A complex as a unique approach towards malaria vaccine development

iScience, 2024-06, Vol.27 (6), p.109918-109918, Article 109918

2024

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A Simple, Cost-Effective, and Extraction-Free Molecular Diagnostic Test for Sickle Cell Disease Using a Noninvasive Buccal Swab Specimen for a Limited-Resource Setting

Diagnostics (Basel), 2022-07, Vol.12 (7), p.1765

2022

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Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform

Frontiers in molecular biosciences, 2023-12, Vol.10, p.1244244-1244244

2023

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Programmable Site-Specific Nucleases for Targeted Genome Engineering in Higher Eukaryotes: PROGRAMMABLE SITE-SPECIFIC NUCLEASES

Journal of cellular physiology, 2016-11, Vol.231 (11), p.2380-2392

2016

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Pharmacological and molecular approaches for the treatment of β‐hemoglobin disorders

Journal of cellular physiology, 2018-06, Vol.233 (6), p.4563-4577

2018

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CRISPR way to engineer the human genome

Genome biology, 2013-01, Vol.14 (2), p.107-107

2013

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Role of HSP70 chaperone in protein aggregate phenomenon of GNE mutant cells: Therapeutic lead for GNE Myopathy

The international journal of biochemistry & cell biology, 2022-08, Vol.149, p.106258-106258, Article 106258

2022

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Francisella novicida Cas9 interrogates genomic DNA with very high specificity and can be used for mammalian genome editing

Proceedings of the National Academy of Sciences - PNAS, 2019-10, Vol.116 (42), p.20959-20968

2019

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Discovery of potent DNMT1 inhibitors against sickle cell disease using structural-based virtual screening, MM-GBSA and molecular dynamics simulation-based approaches

Journal of biomolecular structure & dynamics, 2024-01, Vol.42 (1), p.261-273

2024

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AAV mediated genome engineering with a bypass coagulation factor alleviates the bleeding phenotype in a murine model of hemophilia B

Thrombosis research, 2024-06, Vol.238, p.151-160

2024

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A Dual-Plasmid-Based CRISPR/Cas9-Mediated Strategy Enables Targeted Editing of pH Regulatory Gene IpacC/I in a Clinical Isolate of ITrichophyton rubrum/I

Journal of fungi (Basel), 2022-11, Vol.8 (12)

2022

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Lipopolymeric Nanocarrier Enables Effective Delivery of CRISPR/Cas9 Expressing Plasmid

Macromolecular rapid communications., 2023-07, Vol.44 (14), p.e2300101-n/a

2023

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Rewriting the blueprint of life by synthetic genomics and genome engineering

Genome Biology, 2015-06, Vol.16 (1), p.125-125, Article 125

2015

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Autosomal dominant retinitis pigmentosa with toxic gain of function: Mechanisms and therapeutics

European Journal of Ophthalmology, 2021-03, Vol.31 (2), p.304-320

2021

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CRISPR Correction of the GBA Mutation in Human-Induced Pluripotent Stem Cells Restores Normal Function to Gaucher Macrophages and Increases Their Susceptibility to Mycobacterium tuberculosis

The Journal of infectious diseases, 2023-09, Vol.228 (6), p.777-782

2023

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Generation of an induced pluripotent stem cell line IGIBi18-A from an Indian patient with Rubinstein Taybi Syndrome

Development of pathophysiologically relevant models of sickle cell disease and β-thalassemia for therapeutic studies

A Dual-Plasmid-Based CRISPR/Cas9-Mediated Strategy Enables Targeted Editing of pH Regulatory Gene pacC in a Clinical Isolate of Trichophyton rubrum

The mitochondrial gene-CMPK2 functions as a rheostat for macrophage homeostasis

A conserved SNP variation in the pre-miR396c flanking region in Oryza sativa indica landraces correlates with mature miRNA abundance

The CRISPR/Cas9 System for Targeted Genome Engineering in Free-Living Fungi: Advances and Opportunities for Lichenized Fungi

Generation and characterization of induced pluripotent stem cell line (IGIBi001-A) from a sickle cell anemia patient with homozygous β-globin mutation

Genome Editing Revolution in Life Sciences

Ajay Kumar Parida (1963–2022), an eminent plant biotechnologist with a passion for mangrove biology

Establishment and characterization of induced pluripotent stem cell line (IGIBi002-A) from a β-thalassemia patient with IVS1-5 mutation by non-integrating reprogramming approach

Targeting PfProhibitin 2-Hu-Hsp70A1A complex as a unique approach towards malaria vaccine development

A Simple, Cost-Effective, and Extraction-Free Molecular Diagnostic Test for Sickle Cell Disease Using a Noninvasive Buccal Swab Specimen for a Limited-Resource Setting

Scalable noninvasive amplicon-based precision sequencing (SNAPseq) for genetic diagnosis and screening of β-thalassemia and sickle cell disease using a next-generation sequencing platform

Programmable Site-Specific Nucleases for Targeted Genome Engineering in Higher Eukaryotes: PROGRAMMABLE SITE-SPECIFIC NUCLEASES

Pharmacological and molecular approaches for the treatment of β‐hemoglobin disorders

CRISPR way to engineer the human genome

Role of HSP70 chaperone in protein aggregate phenomenon of GNE mutant cells: Therapeutic lead for GNE Myopathy

Francisella novicida Cas9 interrogates genomic DNA with very high specificity and can be used for mammalian genome editing

Discovery of potent DNMT1 inhibitors against sickle cell disease using structural-based virtual screening, MM-GBSA and molecular dynamics simulation-based approaches

AAV mediated genome engineering with a bypass coagulation factor alleviates the bleeding phenotype in a murine model of hemophilia B

A Dual-Plasmid-Based CRISPR/Cas9-Mediated Strategy Enables Targeted Editing of pH Regulatory Gene IpacC/I in a Clinical Isolate of ITrichophyton rubrum/I

Lipopolymeric Nanocarrier Enables Effective Delivery of CRISPR/Cas9 Expressing Plasmid

Rewriting the blueprint of life by synthetic genomics and genome engineering

Autosomal dominant retinitis pigmentosa with toxic gain of function: Mechanisms and therapeutics

CRISPR Correction of the GBA Mutation in Human-Induced Pluripotent Stem Cells Restores Normal Function to Gaucher Macrophages and Increases Their Susceptibility to Mycobacterium tuberculosis

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