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The complexity of the translation ability of circRNAs

Biochimica et biophysica acta, 2016-10, Vol.1859 (10), p.1245-1251

2016

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Engineering of the current nucleoside-modified mRNA-LNP vaccines against SARS-CoV-2

Biomedicine & pharmacotherapy, 2021-10, Vol.142, p.111953-111953, Article 111953

2021

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CRISPR/Cas13-Based Approaches for Ultrasensitive and Specific Detection of microRNAs

Cells (Basel, Switzerland), 2021-07, Vol.10 (7), p.1655

2021

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Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant

Molecular genetics & genomic medicine, 2023-09, Vol.11 (9), p.e2234-n/a

2023

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Implementation of high‐resolution melting analysis of the porcupine (PORCN) gene for molecular diagnosis of focal dermal hypoplasia: Identification of a novel mutation

The journal of gene medicine, 2020-05, Vol.22 (5), p.e3165-n/a

2020

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A single miRNA and miRNA sponge expression system for efficient modulation of miR‐223 availability in mammalian cells

The journal of gene medicine, 2019-08, Vol.21 (8), p.e3100-n/a

2019

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Identification of human miR‐1839‐5p by small RNA‐seq, a miRNA enriched in neoplastic tissues

The journal of gene medicine, 2019-10, Vol.21 (10), p.e3117-n/a

2019

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CRISPR-Cas13 Precision Transcriptome Engineering in Cancer

Cancer research (Chicago, Ill.), 2018-08, Vol.78 (15), p.4107-4113

2018

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Diet and Maternal Obesity Are Associated with Increased Oxidative Stress in Newborns: A Cross-Sectional Study

Nutrients, 2022-02, Vol.14 (4), p.746

2022

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The impact of mechanical forces in heart morphogenesis

Circulation. Cardiovascular genetics, 2012-02, Vol.5 (1), p.132-142

2012

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Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

Congenital heart disease, 2012-03, Vol.7 (2), p.151-159

2012

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Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis

Genes, 2021-04, Vol.12 (4), p.531

2021

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VHL mutation as a cause of three generations familial pheochromocytoma

Egyptian Journal of Medical Human Genetics, 2024-06, Vol.25 (1), p.69, Article 69

2024

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Dietary and Antioxidant Vitamins Limit the DNA Damage Mediated by Oxidative Stress in the Mother-Newborn Binomial

Life (Basel, Switzerland), 2022-07, Vol.12 (7), p.1012

2022

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International heterogeneity in coronavirus disease 2019 pediatric mortality rates

Boletin medico del Hospital Infantil de Mexico, 2021-01, Vol.78 (1), p.24-28

2021

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Maternal Obesity as a Risk Factor for the Development of Total Anomalous Pulmonary Venous Connection in Their Offspring

Archives of medical research, 2018-02, Vol.49 (2), p.109-113

2018

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Does the linear Sry transcript function as a ceRNA for miR-138? The sense of antisense [version 2; peer review: 2 approved]

F1000 research, 2014-11, Vol.3

2014

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The TATA-box motif and its impact on transcriptional gene regulation by miRNAs

Biomolecular concepts, 2015-04, Vol.6 (2), p.157-161

2015

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Association between maternal diet, smoking, and the placenta MTHFR 677C/T genotype and global placental DNA methylation

Placenta (Eastbourne), 2024-02, Vol.146, p.17-24

2024

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Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

Nature genetics, 2013-07, Vol.45 (7), p.822-824

2013

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α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

Human molecular genetics, 2010-10, Vol.19 (20), p.4007-4016

2010

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Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

PloS one, 2009-03, Vol.4 (3), p.e4978-e4978

2009

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Reversal of multidrug resistance of leukemia cells is not necessarily induced by direct miR-138/MDR1 promoter interaction

Leukemia research, 2017-06, Vol.57, p.55-56

2017

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The complexity of the translation ability of circRNAs

Engineering of the current nucleoside-modified mRNA-LNP vaccines against SARS-CoV-2

CRISPR/Cas13-Based Approaches for Ultrasensitive and Specific Detection of microRNAs

Opitz GBBB syndrome with total anomalous pulmonary venous connection: A new MID1 gene variant

Implementation of high‐resolution melting analysis of the porcupine (PORCN) gene for molecular diagnosis of focal dermal hypoplasia: Identification of a novel mutation

A single miRNA and miRNA sponge expression system for efficient modulation of miR‐223 availability in mammalian cells

Identification of human miR‐1839‐5p by small RNA‐seq, a miRNA enriched in neoplastic tissues

CRISPR-Cas13 Precision Transcriptome Engineering in Cancer

Diet and Maternal Obesity Are Associated with Increased Oxidative Stress in Newborns: A Cross-Sectional Study

The impact of mechanical forces in heart morphogenesis

Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

Genotyping of the Major SARS-CoV-2 Clade by Short-Amplicon High-Resolution Melting (SA-HRM) Analysis

VHL mutation as a cause of three generations familial pheochromocytoma

Dietary and Antioxidant Vitamins Limit the DNA Damage Mediated by Oxidative Stress in the Mother-Newborn Binomial

International heterogeneity in coronavirus disease 2019 pediatric mortality rates

Maternal Obesity as a Risk Factor for the Development of Total Anomalous Pulmonary Venous Connection in Their Offspring

Does the linear Sry transcript function as a ceRNA for miR-138? The sense of antisense [version 2; peer review: 2 approved]

The TATA-box motif and its impact on transcriptional gene regulation by miRNAs

Association between maternal diet, smoking, and the placenta MTHFR 677C/T genotype and global placental DNA methylation

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16

α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects

Genetic variation in VEGF does not contribute significantly to the risk of congenital cardiovascular malformation

Reversal of multidrug resistance of leukemia cells is not necessarily induced by direct miR-138/MDR1 promoter interaction

Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

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