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1.03 - Human iPSC Models in Drug Discovery: Opportunities and Challenges

Comprehensive Medicinal Chemistry III, 2017, p.48-73

Third Edition, 2017

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11 - Novel Technologies for Plant Functional Genomics

Current Developments in Biotechnology and Bioengineering, 2017, p.241-257

2017

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A 14-amino acids deletion in BmShadow results to non-moult on the 2nd instar in the bivoltine silkworm, Bombyx mori

Gene, 2021-04, Vol.777, p.145450-145450, Article 145450

2021

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16S ribosomal RNA-depletion PCR and its application in cause analysis of yogurt package shrinkage

Journal of dairy science, 2022-09, Vol.105 (9), p.7288-7297

2022

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19 - Genetics of Trypanosoma cruzi

American Trypanosomiasis Chagas Disease, 2017, p.429-454

Second Edition, 2017

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2.49 - Gene Therapy Approaches for Cochlear Repair

The Senses, 2020, p.962-984

Second Edition, 2020

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25(OH)D3 stimulates the expression of vitamin D target genes in renal tubular cells when Cyp27b1 is abrogated

The Journal of steroid biochemistry and molecular biology, 2020-05, Vol.199, p.105593-105593, Article 105593

2020

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3.53 - Synthetic Biology: An Overview

Comprehensive Biotechnology, 2019, p.659-670

Third Edition, 2019

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3′Nucleotidase/nuclease is required for Leishmania infantum clinical isolate susceptibility to miltefosine

EBioMedicine, 2022-12, Vol.86, p.104378, Article 104378

2022

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3′Nucleotidase/nuclease is required for Leishmania infantum clinical isolate susceptibility to miltefosineResearch in context

EBioMedicine, 2022-12, Vol.86, p.104378

2022

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IL‐34 deficiency impairs FOXP3+ Treg function in a model of autoimmune colitis and decreases immune tolerance homeostasis

Clinical and translational medicine, 2022-08, Vol.12 (8), p.e988-n/a

2022

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3Bs of CRISPR-Cas mediated genome editing in plants: exploring the basics, bioinformatics and biosafety landscape

Physiology and molecular biology of plants, 2023-12, Vol.29 (12), p.1825-1850

2023

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4.32 Gene Editing Tools

Comprehensive Biomaterials II, 2017, p.589-599

Second Edition, 2017

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5S rRNA Promoter for Guide RNA Expression Enabled Highly Efficient CRISPR/Cas9 Genome Editing in Aspergillus niger

ACS synthetic biology, 2019-07, Vol.8 (7), p.1568-1574

2019

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IL-6 Mutation Attenuates Liver Injury Caused by Aeromonas hydrophila Infection by Reducing Oxidative Stress in Zebrafish

International journal of molecular sciences, 2023-12, Vol.24 (24), p.17215

2023

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66 - Translational research in pediatric cardiology

Nadas' Pediatric Cardiology, 2025, p.790-802

Third Edition, 2025

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9- cis -Epoxycarotenoid Dioxygenase 3 Regulates Plant Growth and Enhances Multi-Abiotic Stress Tolerance in Rice

Frontiers in plant science, 2018-03, Vol.9, p.162-162

2018

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A A Review on the Potential of Application of CRISPR/Cas9 Technology in CYP3A4 and CYP2D6 Genes: A Way to Move Forward in Identifying New Drug Targets

ASM science journal, 2022-11, Vol.17, p.1-21

2022

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An AANAT/ASMT transgenic animal model constructed with CRISPR/Cas9 system serving as the mammary gland bioreactor to produce melatonin‐enriched milk in sheep

Journal of pineal research, 2017-08, Vol.63 (1), p.n/a

2017

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AAV-based gene editing of type 1 collagen mutation to treat osteogenesis imperfecta

Molecular therapy. Nucleic acids, 2024-03, Vol.35 (1), p.102111-102111, Article 102111

2024

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AAV-CRISPR/Cas9 Gene Editing Preserves Long-Term Vision in the P23H Rat Model of Autosomal Dominant Retinitis Pigmentosa

Pharmaceutics, 2022-04, Vol.14 (4), p.824

2022

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AAV-CRISPR/Cas9-Mediated Depletion of VEGFR2 Blocks Angiogenesis In Vitro

Investigative ophthalmology & visual science, 2017-12, Vol.58 (14), p.6082-6090

2017

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The AAV-mediated and RNA-guided CRISPR/Cas9 system for gene therapy of DMD and BMD

Brain & development (Tokyo. 1979), 2017-08, Vol.39 (7), p.547-556

2017

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AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo

Investigative ophthalmology & visual science, 2016-06, Vol.57 (7), p.3470-3476

2016

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1.03 - Human iPSC Models in Drug Discovery: Opportunities and Challenges

11 - Novel Technologies for Plant Functional Genomics

A 14-amino acids deletion in BmShadow results to non-moult on the 2nd instar in the bivoltine silkworm, Bombyx mori

16S ribosomal RNA-depletion PCR and its application in cause analysis of yogurt package shrinkage

19 - Genetics of Trypanosoma cruzi

2.49 - Gene Therapy Approaches for Cochlear Repair

226th ENMC International Workshop:: Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20–22 January 2017, Heemskerk, The Netherlands

25(OH)D3 stimulates the expression of vitamin D target genes in renal tubular cells when Cyp27b1 is abrogated

3.53 - Synthetic Biology: An Overview

3′Nucleotidase/nuclease is required for Leishmania infantum clinical isolate susceptibility to miltefosine

3′Nucleotidase/nuclease is required for Leishmania infantum clinical isolate susceptibility to miltefosineResearch in context

IL‐34 deficiency impairs FOXP3+ Treg function in a model of autoimmune colitis and decreases immune tolerance homeostasis

3Bs of CRISPR-Cas mediated genome editing in plants: exploring the basics, bioinformatics and biosafety landscape

4.32 Gene Editing Tools

5S rRNA Promoter for Guide RNA Expression Enabled Highly Efficient CRISPR/Cas9 Genome Editing in Aspergillus niger

IL-6 Mutation Attenuates Liver Injury Caused by Aeromonas hydrophila Infection by Reducing Oxidative Stress in Zebrafish

66 - Translational research in pediatric cardiology

9- cis -Epoxycarotenoid Dioxygenase 3 Regulates Plant Growth and Enhances Multi-Abiotic Stress Tolerance in Rice

A A Review on the Potential of Application of CRISPR/Cas9 Technology in CYP3A4 and CYP2D6 Genes: A Way to Move Forward in Identifying New Drug Targets

An AANAT/ASMT transgenic animal model constructed with CRISPR/Cas9 system serving as the mammary gland bioreactor to produce melatonin‐enriched milk in sheep

AAV-based gene editing of type 1 collagen mutation to treat osteogenesis imperfecta

AAV-CRISPR/Cas9 Gene Editing Preserves Long-Term Vision in the P23H Rat Model of Autosomal Dominant Retinitis Pigmentosa

AAV-CRISPR/Cas9-Mediated Depletion of VEGFR2 Blocks Angiogenesis In Vitro

The AAV-mediated and RNA-guided CRISPR/Cas9 system for gene therapy of DMD and BMD

AAV-Mediated CRISPR/Cas Gene Editing of Retinal Cells In Vivo

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