Lista de obras -

A novel combination of biallelic ALPL mutations associated with adult hypophosphatasia: A phenotype-genotype association and computational analysis study

scientific article published on 08 May 2019

A novel de novo heterozygous ALPL nonsense mutation associated with adult hypophosphatasia

artículo científico publicado en 2020

A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome

article

Comparative proteomic analysis of dental cementum from deciduous and permanent teeth

artículo científico publicado en 2020

Computational analysis for GNAQ mutations: New insights on the molecular etiology of Sturge-Weber syndrome.

artículo científico publicado en 2017

Correction of hypophosphatasia-associated mineralization deficiencies in vitro by phosphate/pyrophosphate modulation in periodontal ligament cells.

artículo científico publicado en 2011

EDA mutation by exome sequencing in non-syndromic X-linked oligodontia.

artículo científico publicado en 2017

Exposure of periodontal ligament progenitor cells to lipopolysaccharide from Escherichia coli changes osteoblast differentiation pattern

artículo científico publicado en 2015

Expression of Smad4 and Smad7 in human thyroid follicular carcinoma cell lines.

artículo científico publicado en 2003

G-quadruplex formation enhances splicing efficiency of PAX9 intron 1.

artículo científico publicado en 2014

Galectin-3 messenger ribonucleic acid and protein are expressed in benign thyroid tumors

scientific article published on 01 October 2002

Hypophosphatasia-associated deficiencies in mineralization and gene expression in cultured dental pulp cells obtained from human teeth.

artículo científico publicado en 2012

Leucine-Rich Amelogenin Peptide (LRAP) Uptake by Cementoblast Requires Flotillin-1 Mediated Endocytosis

artículo científico publicado en 2016

Mice with targeted disruption of the Dio2 gene have cold-induced overexpression of the uncoupling protein 1 gene but fail to increase brown adipose tissue lipogenesis and adaptive thermogenesis.

artículo científico publicado en 2004

Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.

artículo científico publicado en 2013

Novel LRAP-binding partner revealing the plasminogen activation system as a regulator of cementoblast differentiation and mineral nodule formation in vitro

artículo científico publicado en 2019

Periodontitis in Chédiak-Higashi Syndrome: An Altered Immunoinflammatory Response.

artículo científico publicado en 2017

Polymorphism on codon 98 of the galectin-3 gene is not associated to benign and malignant thyroid tumors

artículo científico publicado en 2006

Secretome Profiling of Periodontal Ligament from Deciduous and Permanent Teeth Reveals a Distinct Expression Pattern of Laminin Chains

artículo científico publicado en 2016

Variable expressivity and novel PTEN mutations in Cowden syndrome

artículo científico publicado en 2018

Lista de obras de

A novel combination of biallelic ALPL mutations associated with adult hypophosphatasia: A phenotype-genotype association and computational analysis study

A novel de novo heterozygous ALPL nonsense mutation associated with adult hypophosphatasia

A novel heterozygous mutation in FGFR2 gene causing Pfeiffer syndrome

Comparative proteomic analysis of dental cementum from deciduous and permanent teeth

Computational analysis for GNAQ mutations: New insights on the molecular etiology of Sturge-Weber syndrome.

Correction of hypophosphatasia-associated mineralization deficiencies in vitro by phosphate/pyrophosphate modulation in periodontal ligament cells.

EDA mutation by exome sequencing in non-syndromic X-linked oligodontia.

Exposure of periodontal ligament progenitor cells to lipopolysaccharide from Escherichia coli changes osteoblast differentiation pattern

Expression of Smad4 and Smad7 in human thyroid follicular carcinoma cell lines.

G-quadruplex formation enhances splicing efficiency of PAX9 intron 1.

Galectin-3 messenger ribonucleic acid and protein are expressed in benign thyroid tumors

Hypophosphatasia-associated deficiencies in mineralization and gene expression in cultured dental pulp cells obtained from human teeth.

Leucine-Rich Amelogenin Peptide (LRAP) Uptake by Cementoblast Requires Flotillin-1 Mediated Endocytosis

Mice with targeted disruption of the Dio2 gene have cold-induced overexpression of the uncoupling protein 1 gene but fail to increase brown adipose tissue lipogenesis and adaptive thermogenesis.

Novel ALPL genetic alteration associated with an odontohypophosphatasia phenotype.

Novel LRAP-binding partner revealing the plasminogen activation system as a regulator of cementoblast differentiation and mineral nodule formation in vitro

Periodontitis in Chédiak-Higashi Syndrome: An Altered Immunoinflammatory Response.

Polymorphism on codon 98 of the galectin-3 gene is not associated to benign and malignant thyroid tumors

Secretome Profiling of Periodontal Ligament from Deciduous and Permanent Teeth Reveals a Distinct Expression Pattern of Laminin Chains

Variable expressivity and novel PTEN mutations in Cowden syndrome