Lista de obras - Binbin Wang - Dominio Público Uruguay

A novel mutation of Hyaluronan synthase 2 gene in Chinese children with ventricular septal defect

artículo científico publicado en 2014

A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens

scientific article published on 10 November 2019

A study of TNF-alpha-238 and -308 polymorphisms with different outcomes of persistent hepatitis B virus infection in China ⬇️

artículo científico publicado el 1 de diciembre de 2010

Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD

scientific article published on 19 September 2020

Association between -238 but not -308 polymorphism of Tumor necrosis factor alpha (TNF-alpha)v and unexplained recurrent spontaneous abortion (URSA) in Chinese population ⬇️

artículo científico publicado el 28 de septiembre de 2010

Association between thrombophilia gene polymorphisms and preeclampsia: a meta-analysis

artículo científico publicado en 2014

Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese.

artículo científico publicado en 2015

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

artículo científico publicado en 2016

CYP46A1 functional promoter haplotypes decipher genetic susceptibility to Alzheimer's disease

artículo científico publicado en 2010

Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin-neurophysin II gene

artículo científico publicado en 2012

Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees

scientific article published on 18 November 2018

FABP4: a novel candidate gene for polycystic ovary syndrome

artículo científico publicado en 2009

Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease

artículo científico publicado en 2008

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females

artículo científico publicado en 2016

Genetic association of polymorphism rs1333049 with gout ⬇️

artículo científico publicado el 9 de mayo de 2011

Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study.

artículo científico publicado en 2011

HOXA10, EMX2 and TENM1 expression in the mid-secretory endometrium of infertile women with a Müllerian duct anomaly

artículo científico publicado en 2016

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

artículo científico publicado en 2017

Identified OAS3 gene variants associated with coexistence of HBsAg and anti-HBs in chronic HBV infection.

artículo científico publicado en 2018

Indicators of Male Gout Patients' Comorbidities with the Theory on Traditional Chinese Medicine

article

MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations

artículo científico publicado en 2014

Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese ⬇️

artículo científico publicado el 25 de agosto de 2011

New Gene Variants Associated with the Risk of Chronic HBV Infection

artículo científico publicado en 2020

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients

artículo científico publicado en 2010

Novel mutation in SP2 in a Chinese pedigree with Neural tube defects

artículo científico publicado en 2018

Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans

artículo científico publicado en 2014

On the Origin of Tibetans and Their Genetic Basis in Adapting High-Altitude Environments ⬇️

artículo científico publicado el 28 de febrero de 2011

Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population

artículo científico publicado en 2017

Polymorphisms in the Presumptive Promoter Region of the SLC2A9 Gene Are Associated with Gout in a Chinese Male Population ⬇️

artículo científico publicado el 29 de febrero de 2012

Research progress on molecular genetics of male homosexuality

artículo científico publicado en 2016

Serum Metabolic Profiling Analysis of Gout Patients Treated with Traditional Chinese Medicine Tongfengtai Granules Based on Gas Chromatography-Mass Spectrometry

artículo científico publicado en 2020

Short read mapping for exome sequencing

artículo científico publicado en 2013

The Arg233Lys AQP0 mutation disturbs aquaporin0-calmodulin interaction causing polymorphic congenital cataract

artículo científico publicado en 2012

The DNA methylation profile of PLA2G4C gene promoter in schizophrenia

artículo científico publicado en 2012

Two novel HAND1 mutations in Chinese patients with ventricular septal defect

artículo científico publicado en 2011

Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population

artículo científico publicado en 2013

Lista de obras de Binbin Wang

A novel mutation of Hyaluronan synthase 2 gene in Chinese children with ventricular septal defect

A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens

A study of TNF-alpha-238 and -308 polymorphisms with different outcomes of persistent hepatitis B virus infection in China ⬇️

Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD

Association between -238 but not -308 polymorphism of Tumor necrosis factor alpha (TNF-alpha)v and unexplained recurrent spontaneous abortion (URSA) in Chinese population ⬇️

Association between thrombophilia gene polymorphisms and preeclampsia: a meta-analysis

Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese.

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

CYP46A1 functional promoter haplotypes decipher genetic susceptibility to Alzheimer's disease

Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin-neurophysin II gene

Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees

FABP4: a novel candidate gene for polycystic ovary syndrome

Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females

Genetic association of polymorphism rs1333049 with gout ⬇️

Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study.

HOXA10, EMX2 and TENM1 expression in the mid-secretory endometrium of infertile women with a Müllerian duct anomaly

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

Identified OAS3 gene variants associated with coexistence of HBsAg and anti-HBs in chronic HBV infection.

Indicators of Male Gout Patients' Comorbidities with the Theory on Traditional Chinese Medicine

MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations

Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese ⬇️

New Gene Variants Associated with the Risk of Chronic HBV Infection

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients

Novel mutation in SP2 in a Chinese pedigree with Neural tube defects

Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans

On the Origin of Tibetans and Their Genetic Basis in Adapting High-Altitude Environments ⬇️

Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population

Polymorphisms in the Presumptive Promoter Region of the SLC2A9 Gene Are Associated with Gout in a Chinese Male Population ⬇️

Research progress on molecular genetics of male homosexuality

Serum Metabolic Profiling Analysis of Gout Patients Treated with Traditional Chinese Medicine Tongfengtai Granules Based on Gas Chromatography-Mass Spectrometry

Short read mapping for exome sequencing

The Arg233Lys AQP0 mutation disturbs aquaporin0-calmodulin interaction causing polymorphic congenital cataract

The DNA methylation profile of PLA2G4C gene promoter in schizophrenia

Two novel HAND1 mutations in Chinese patients with ventricular septal defect

Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population