Lista de obras - Dong Han - Dominio Público Uruguay

A TGFβ-Smad4-Fgf6 signaling cascade controls myogenic differentiation and myoblast fusion during tongue development

artículo científico publicado en 2012

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population.

artículo científico publicado en 2012

A novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis

scientific article published on 18 March 2019

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia

artículo científico publicado en 2014

Alk5-mediated transforming growth factor β signaling acts upstream of fibroblast growth factor 10 to regulate the proliferation and maintenance of dental epithelial stem cells.

artículo científico publicado en 2011

Association between EDAR Polymorphisms and Non-Syndromic Tooth Agenesis in the Chinese Han Population.

artículo científico publicado en 2017

Association between rs11001553 of DKK1 and non-syndromic tooth agenesis in the Chinese Han population.

artículo científico publicado en 2014

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated non-syndromic oligodontia

scientific article published on 09 September 2020

Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations

scientific article published on 30 March 2011

DLX3 mutation negatively regulates odontogenic differentiation of human dental pulp cells

artículo científico publicado en 2017

DLX3 negatively regulates osteoclastic differentiation through microRNA-124.

artículo científico publicado en 2016

DLX3 promotes bone marrow mesenchymal stem cell proliferation through H19/miR-675 axis.

artículo científico publicado en 2017

Disruption of the ERK/MAPK pathway in neural crest cells as a potential cause of Pierre Robin sequence.

artículo científico publicado en 2015

Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia

artículo científico publicado en 2018

Down-regulation of Wnt10a affects odontogenesis and proliferation in mesenchymal cells.

artículo científico publicado en 2013

Epithelial Wnt10a Is Essential for Tooth Root Furcation Morphogenesis

artículo científico publicado en 2020

Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis

scientific journal article

Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia

artículo científico publicado en 2017

Functional study of novel PAX9 variants: the paired domain and non-syndromic oligodontia

artículo científico publicado en 2020

Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis

artículo científico publicado en 2018

Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population

artículo científico publicado en 2013

Lrp6 Dynamic Expression in Tooth Development and Mutations in Oligodontia

artículo científico publicado en 2020

Molecular and Cellular Regulatory Mechanisms of Tongue Myogenesis ⬇️

artículo científico publicado el 4 de enero de 2012

Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.

artículo científico publicado en 2015

Mutations in WNT10B Are Identified in Individuals with Oligodontia

artículo científico publicado en 2016

Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.

artículo científico publicado en 2017

Novel MSX1 variants identified in families with nonsyndromic oligodontia

artículo científico publicado en 2021

Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis

artículo científico publicado en 2019

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia

artículo científico publicado en 2013

Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.

artículo científico publicado en 2016

Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia.

artículo científico publicado en 2015

Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders

scientific article published on 02 May 2019

Two novel heterozygous mutations of EVC2 cause a mild phenotype of Ellis-van Creveld syndrome in a Chinese family

artículo científico publicado en 2011

miR-675 promotes odontogenic differentiation of human dental pulp cells by epigenetic regulation of DLX3.

artículo científico publicado en 2018

mmu-miR-1963 negatively regulates the ameloblast differentiation of LS8 cell line by directly targeting Smoc2 3'UTR.

artículo científico publicado en 2017

rs929387 of GLI3 is involved in tooth agenesis in Chinese Han population.

artículo científico publicado en 2013

Lista de obras de Dong Han

A TGFβ-Smad4-Fgf6 signaling cascade controls myogenic differentiation and myoblast fusion during tongue development

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population.

A novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia

Alk5-mediated transforming growth factor β signaling acts upstream of fibroblast growth factor 10 to regulate the proliferation and maintenance of dental epithelial stem cells.

Association between EDAR Polymorphisms and Non-Syndromic Tooth Agenesis in the Chinese Han Population.

Association between rs11001553 of DKK1 and non-syndromic tooth agenesis in the Chinese Han population.

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated non-syndromic oligodontia

Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations

DLX3 mutation negatively regulates odontogenic differentiation of human dental pulp cells

DLX3 negatively regulates osteoclastic differentiation through microRNA-124.

DLX3 promotes bone marrow mesenchymal stem cell proliferation through H19/miR-675 axis.

Disruption of the ERK/MAPK pathway in neural crest cells as a potential cause of Pierre Robin sequence.

Distinct impacts of bi-allelic WNT10A mutations on the permanent and primary dentitions in odonto-onycho-dermal dysplasia

Down-regulation of Wnt10a affects odontogenesis and proliferation in mesenchymal cells.

Epithelial Wnt10a Is Essential for Tooth Root Furcation Morphogenesis

Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis

Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia

Functional study of novel PAX9 variants: the paired domain and non-syndromic oligodontia

Genetic analysis: Wnt and other pathways in nonsyndromic tooth agenesis

Involvement of and interaction between WNT10A and EDA mutations in tooth agenesis cases in the Chinese population

Lrp6 Dynamic Expression in Tooth Development and Mutations in Oligodontia

Molecular and Cellular Regulatory Mechanisms of Tongue Myogenesis ⬇️

Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.

Mutations in WNT10B Are Identified in Individuals with Oligodontia

Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype.

Novel MSX1 variants identified in families with nonsyndromic oligodontia

Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia

Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome.

Simultaneous Occurence of an Autosomal Dominant Inherited MSX1 Mutation and an X-linked Recessive Inherited EDA Mutation in One Chinese Family with Non-syndromic Oligodontia.

Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disorders

Two novel heterozygous mutations of EVC2 cause a mild phenotype of Ellis-van Creveld syndrome in a Chinese family

miR-675 promotes odontogenic differentiation of human dental pulp cells by epigenetic regulation of DLX3.

mmu-miR-1963 negatively regulates the ameloblast differentiation of LS8 cell line by directly targeting Smoc2 3'UTR.

rs929387 of GLI3 is involved in tooth agenesis in Chinese Han population.