Lista de obras -

<i>KDM5A</i> mutations identified in autism spectrum disorder using forward genetics

artículo científico publicado en 2020

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

scientific article published in 2021

Assessment of anti-nociceptive effect of allopurinol in a neuropathic pain model

scientific article published on 30 April 2019

Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function

scientific article published on 25 December 2018

Correction to: Metoclopramide role in preventing ileus after cesarean, a clinical trial.

artículo científico publicado en 2017

Correlation Between Meis1 and Msi1 in Esophageal Squamous Cell Carcinoma.

artículo científico publicado en 2016

Crosstalk between SHH and stemness state signaling pathways in esophageal squamous cell carcinoma

artículo científico publicado en 2016

Effects of glucosamine against morphine-induced antinociceptive tolerance and dependence in mice

artículo científico publicado en 2019

Environmental determinants of polycyclic aromatic hydrocarbons exposure at home, at kindergartens and during a commute

artículo científico publicado en 2018

Expanding the clinical phenotype of IARS2-related mitochondrial disease

artículo científico publicado en 2018

Exposure to air pollution during pregnancy and newborn liver function

scientific article published on 30 March 2019

Expression of Pluripotency Markers, SOX2 and OCT4, in Pterygium Development

artículo científico publicado en 2018

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

scientific article published on 24 October 2019

In Silico and In Vitro Evaluation of Cytotoxic Activities of Farnesiferol C and Microlobin on MCF-7, HeLa and KYSE Cell Lines.

artículo científico publicado en 2016

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)

artículo científico publicado en 2018

MEIS1 knockdown may promote differentiation of esophageal squamous carcinoma cell line KYSE-30

scientific article published on 14 May 2019

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss

article

Metoclopramide role in preventing ileus after cesarean, a clinical trial.

artículo científico publicado en 2015

Mortality and morbidity due to exposure to ambient particulate matter

artículo científico publicado en 2018

Negative Regulatory Role of TWIST1 on SNAIL Gene Expression

artículo científico publicado en 2016

Neuroprotective effects of clavulanic acid following permanent bilateral common carotid artery occlusion in rats

scientific article published on 03 September 2019

Novel Loss-of-Function Variants in CDC14A are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients

scientific article published on 02 January 2020

Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child

artículo científico publicado en 2018

Predicting the Correlation of EZH2 and Cancer Stem Cell Markers in Esophageal Squamous Cell Carcinoma.

artículo científico publicado en 2017

Predicting the molecular role of MEIS1 in esophageal squamous cell carcinoma.

artículo científico publicado en 2015

Protective effects of atorvastatin against morphine-induced tolerance and dependence in mice.

artículo científico publicado en 2017

SOX1 is correlated to stemness state regulator SALL4 through progression and invasiveness of esophageal squamous cell carcinoma.

artículo científico publicado en 2016

Signaling roadmap to epithelial-mesenchymal transition in pterygium, TWIST1 centralized

artículo científico publicado en 2019

Stemness state regulators SALL4 and SOX2 are involved in progression and invasiveness of esophageal squamous cell carcinoma

artículo científico publicado en 2014

TWIST1 upregulates the MAGEA4 oncogene.

artículo científico publicado en 2016

The Many Faces of DFNB9: Relating <i>OTOF</i> Variants to Hearing Impairment

scientific article published on 26 November 2020

The role of serotonin and its receptors on the anticonvulsant effect of curcumin in pentylenetetrazol-induced seizures

scientific article published on 19 September 2018

Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome

artículo científico publicado en 2024

Lista de obras de

<i>KDM5A</i> mutations identified in autism spectrum disorder using forward genetics

A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

Assessment of anti-nociceptive effect of allopurinol in a neuropathic pain model

Biallelic loss of function variants in PPP1R21 cause a neurodevelopmental syndrome with impaired endocytic function

Correction to: Metoclopramide role in preventing ileus after cesarean, a clinical trial.

Correlation Between Meis1 and Msi1 in Esophageal Squamous Cell Carcinoma.

Crosstalk between SHH and stemness state signaling pathways in esophageal squamous cell carcinoma

Effects of glucosamine against morphine-induced antinociceptive tolerance and dependence in mice

Environmental determinants of polycyclic aromatic hydrocarbons exposure at home, at kindergartens and during a commute

Expanding the clinical phenotype of IARS2-related mitochondrial disease

Exposure to air pollution during pregnancy and newborn liver function

Expression of Pluripotency Markers, SOX2 and OCT4, in Pterygium Development

Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder

In Silico and In Vitro Evaluation of Cytotoxic Activities of Farnesiferol C and Microlobin on MCF-7, HeLa and KYSE Cell Lines.

MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive cerebellar, ocular, craniofacial and genital features (COFG syndrome)

MEIS1 knockdown may promote differentiation of esophageal squamous carcinoma cell line KYSE-30

MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss

Metoclopramide role in preventing ileus after cesarean, a clinical trial.

Mortality and morbidity due to exposure to ambient particulate matter

Negative Regulatory Role of TWIST1 on SNAIL Gene Expression

Neuroprotective effects of clavulanic acid following permanent bilateral common carotid artery occlusion in rats

Novel Loss-of-Function Variants in CDC14A are Associated with Recessive Sensorineural Hearing Loss in Iranian and Pakistani Patients

Parental Whole-Exome Sequencing Enables Sialidosis Type II Diagnosis due to an Missense Mutation as an Underlying Cause of Nephrotic Syndrome in the Child

Predicting the Correlation of EZH2 and Cancer Stem Cell Markers in Esophageal Squamous Cell Carcinoma.

Predicting the molecular role of MEIS1 in esophageal squamous cell carcinoma.

Protective effects of atorvastatin against morphine-induced tolerance and dependence in mice.

SOX1 is correlated to stemness state regulator SALL4 through progression and invasiveness of esophageal squamous cell carcinoma.

Signaling roadmap to epithelial-mesenchymal transition in pterygium, TWIST1 centralized

Stemness state regulators SALL4 and SOX2 are involved in progression and invasiveness of esophageal squamous cell carcinoma

TWIST1 upregulates the MAGEA4 oncogene.

The Many Faces of DFNB9: Relating <i>OTOF</i> Variants to Hearing Impairment

The role of serotonin and its receptors on the anticonvulsant effect of curcumin in pentylenetetrazol-induced seizures

Zebrafish as a model to investigate a biallelic gain-of-function variant in MSGN1, associated with a novel skeletal dysplasia syndrome