Lista de obras - Nan Wu - Dominio Público Uruguay

A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis

artículo científico publicado en 2018

A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia

artículo científico publicado en 2020

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

artículo científico publicado en 2019

Cover Image, Volume 118, Number 10, October 2017.

artículo científico publicado en 2017

Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

artículo científico publicado en 2020

Downregulation of stathmin 1 in human gallbladder carcinoma inhibits tumor growth in vitro and in vivo

artículo científico publicado en 2016

Endovascular aneurysm repair in emergent ruptured abdominal aortic aneurysm with a 'real' hostile neck and severely tortuous iliac artery of an elderly patient

artículo científico publicado en 2014

Evaluation of a novel poly(amidoamine) with pendant aminobutyl group on the cellular properties of transfected bone marrow mesenchymal stem cells

artículo científico publicado en 2017

Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese family

scientific article published on 10 August 2019

Full-thickness excision using transanal endoscopic microsurgery for treatment of rectal neuroendocrine tumors

artículo científico publicado en 2015

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

scientific article published on 27 November 2019

Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population ⬇️

artículo científico publicado en 2018

Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis

artículo científico publicado en 2018

Identification of novel FBN1 variations implicated in congenital scoliosis

scientific article published on 11 December 2019

Identification of two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants.

artículo científico publicado en 2018

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice

artículo científico publicado en 2019

Mechanical sensing protein PIEZO1 regulates bone homeostasis via osteoblast-osteoclast crosstalk

artículo científico publicado en 2020

Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia

artículo científico publicado en 2017

Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosis

scientific article published on 20 August 2020

Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis

artículo científico publicado en 2014

Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)

artículo científico publicado en 2018

Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants

scientific article published on 14 October 2020

Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-catenin

scientific article published on 18 March 2020

Possible single-nucleotide polymorphism loci associated with systemic sclerosis susceptibility: a genetic association study in a Chinese Han population

artículo científico publicado en 2014

Progress and Application of CRISPR/Cas Technology in Biological and Biomedical Investigation

artículo científico publicado en 2017

Progress and perspective of TBX6 gene in congenital vertebral malformations

artículo científico publicado en 2016

Prolonged Hoarseness Caused by Arytenoid Dislocation After Anterior Cervical Corpectomy and Fusion

artículo científico publicado en 2015

Recurrence-Associated Long Non-coding RNA Signature for Determining the Risk of Recurrence in Patients with Colon Cancer

artículo científico publicado en 2018

TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease

artículo científico publicado en 2019

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

artículo científico publicado en 2015

The Regulatory Roles of MicroRNAs in Bone Remodeling and Perspectives as Biomarkers in Osteoporosis

artículo científico publicado en 2016

The Role of Semaphorin 3A in Bone Remodeling.

artículo científico publicado en 2017

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

artículo científico publicado en 2018

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

artículo científico publicado en 2018

Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD)

artículo científico publicado en 2018

Whole-spine Computed Tomography Findings in SAPHO Syndrome

artículo científico publicado en 2017

ceRNA in cancer: possible functions and clinical implications.

artículo científico

Lista de obras de Nan Wu

A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis

A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Cover Image, Volume 118, Number 10, October 2017.

Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS)

Downregulation of stathmin 1 in human gallbladder carcinoma inhibits tumor growth in vitro and in vivo

Endovascular aneurysm repair in emergent ruptured abdominal aortic aneurysm with a 'real' hostile neck and severely tortuous iliac artery of an elderly patient

Evaluation of a novel poly(amidoamine) with pendant aminobutyl group on the cellular properties of transfected bone marrow mesenchymal stem cells

Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese family

Full-thickness excision using transanal endoscopic microsurgery for treatment of rectal neuroendocrine tumors

Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1

Genetic polymorphisms of GPR126 are functionally associated with PUMC classifications of adolescent idiopathic scoliosis in a Northern Han population ⬇️

Identification of likely pathogenic and known variants in TSPEAR, LAMB3, BCOR, and WNT10A in four Turkish families with tooth agenesis

Identification of novel FBN1 variations implicated in congenital scoliosis

Identification of two novel null variants in CLN8 by targeted next-generation sequencing: first report of a Chinese patient with neuronal ceroid lipofuscinosis due to CLN8 variants.

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice

Mechanical sensing protein PIEZO1 regulates bone homeostasis via osteoblast-osteoclast crosstalk

Molecular therapeutic strategies for FGFR3 gene-related skeletal dysplasia

Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosis

Novel NTRK1 Frameshift Mutation in Congenital Insensitivity to Pain With Anhidrosis

Perturbations of BMP/TGF-β and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM)

Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants

Piezo1/2 mediate mechanotransduction essential for bone formation through concerted activation of NFAT-YAP1-ß-catenin

Possible single-nucleotide polymorphism loci associated with systemic sclerosis susceptibility: a genetic association study in a Chinese Han population

Progress and Application of CRISPR/Cas Technology in Biological and Biomedical Investigation

Progress and perspective of TBX6 gene in congenital vertebral malformations

Prolonged Hoarseness Caused by Arytenoid Dislocation After Anterior Cervical Corpectomy and Fusion

Recurrence-Associated Long Non-coding RNA Signature for Determining the Risk of Recurrence in Patients with Colon Cancer

TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease

TBX6 null variants and a common hypomorphic allele in congenital scoliosis

The Regulatory Roles of MicroRNAs in Bone Remodeling and Perspectives as Biomarkers in Osteoporosis

The Role of Semaphorin 3A in Bone Remodeling.

The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

Whole-exome sequencing reveals known and novel variants in a cohort of intracranial vertebral–basilar artery dissection (IVAD)

Whole-spine Computed Tomography Findings in SAPHO Syndrome

ceRNA in cancer: possible functions and clinical implications.