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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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CRISPR-Cas13 Precision Transcriptome Engineering in Cancer

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

2018

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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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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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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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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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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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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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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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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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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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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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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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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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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

CRISPR-Cas13 Precision Transcriptome Engineering in Cancer

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

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

The impact of mechanical forces in heart morphogenesis

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

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

International heterogeneity in coronavirus disease 2019 pediatric mortality rates

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

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

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

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

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

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

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

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