Lista de obras - Wanqing Liu - Dominio Público Uruguay

A Novel Fully Automated Molecular Diagnostic System (AMDS) for Colorectal Cancer Mutation Detection ⬇️

artículo científico publicado el 9 de mayo de 2013

A genome-wide integrative study of microRNAs in human liver

artículo científico publicado en 2013

A novel insertion mutation in spastin gene is the cause of spastic paraplegia in a Chinese family

scientific article published on 01 June 2003

A novel locus for parietal foramina maps to chromosome 4q21-q23.

artículo científico publicado en 2003

A pharmacogenetic study of aldehyde oxidase I in patients treated with XK469.

artículo científico publicado en 2014

A pharmacogenetic study of vorinostat glucuronidation

artículo científico publicado en 2010

Allele Loss and Down-Regulation of Heparanase Gene Are Associated with the Progression and Poor Prognosis of Hepatocellular Carcinoma ⬇️

artículo científico publicado el 31 de agosto de 2012

Association of APOE gene with schizophrenia in Chinese: a possible risk factor in times of malnutrition

artículo científico publicado en 2003

Congenital absence of permanent teeth in a six-generation Chinese kindred

article

Determination and analysis of single nucleotide polymorphisms and haplotype structure of the human carboxylesterase 2 gene

artículo científico publicado en 2004

Epigenetic regulation of BMP2 by 1,25-dihydroxyvitamin D3 through DNA methylation and histone modification

artículo científico publicado en 2013

Functional EGFR Germline Polymorphisms May Confer Risk for EGFR Somatic Mutations in Non–Small Cell Lung Cancer, with a Predominant Effect on Exon 19 Microdeletions ⬇️

artículo científico publicado el 3 de febrero de 2011

Functional characterization of ABCC2 promoter polymorphisms and allele-specific expression.

artículo científico publicado en 2012

Genetic Polymorphism, Telomere Biology and Non-Small Lung Cancer Risk

artículo científico

Genome-wide search for loss of heterozygosity in Chinese patients with sporadic colorectal cancer

artículo científico publicado en 2003

Haplotypes of variants in the UDP-glucuronosyltransferase1A9 and 1A1 genes.

artículo científico publicado en 2005

Hepatocyte nuclear factor-1 alpha is associated with UGT1A1, UGT1A9 and UGT2B7 mRNA expression in human liver

artículo científico publicado en 2007

Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue

artículo científico publicado en 2011

Impact of the Interaction between 3'-UTR SNPs and microRNA on the Expression of Human Xenobiotic Metabolism Enzyme and Transporter Genes.

artículo científico publicado en 2012

Interactions between MDM2 and TP53 Genetic Alterations, and Their Impact on Response to MDM2 Inhibitors and Other Chemotherapeutic Drugs in Cancer Cells.

artículo científico publicado en 2009

Personalized targeted therapy for lung cancer

artículo científico publicado en 2012

Relationship between differential hepatic microRNA expression and decreased hepatic cytochrome P450 3A activity in cirrhosis

artículo científico publicado en 2013

SNPs affecting serum metabolomic traits may regulate gene transcription and lipid accumulation in the liver

artículo científico publicado en 2012

Searching for tissue-specific expression pattern-linked nucleotides of UGT1A isoforms

artículo científico publicado en 2007

Single nucleotide polymorphism discovery and functional assessment of variation in the UDP-glucuronosyltransferase 2B7 gene

artículo científico publicado en 2008

Synthesis and biological evaluation of novel folic acid receptor-targeted, β-cyclodextrin-based drug complexes for cancer treatment

artículo científico publicado en 2013

Tentative novel mechanism of the bystander effect in glioma gene therapy with HSV-TK/GCV system

artículo científico publicado en 1999

The Werner's syndrome 4330T>C (Cys1367Arg) gene variant does not affect the in vitro cytotoxicity of topoisomerase inhibitors and platinum compounds

artículo científico publicado en 2008

Lista de obras de Wanqing Liu

A Novel Fully Automated Molecular Diagnostic System (AMDS) for Colorectal Cancer Mutation Detection ⬇️

A genome-wide integrative study of microRNAs in human liver

A novel insertion mutation in spastin gene is the cause of spastic paraplegia in a Chinese family

A novel locus for parietal foramina maps to chromosome 4q21-q23.

A pharmacogenetic study of aldehyde oxidase I in patients treated with XK469.

A pharmacogenetic study of vorinostat glucuronidation

Allele Loss and Down-Regulation of Heparanase Gene Are Associated with the Progression and Poor Prognosis of Hepatocellular Carcinoma ⬇️

Association of APOE gene with schizophrenia in Chinese: a possible risk factor in times of malnutrition

Congenital absence of permanent teeth in a six-generation Chinese kindred

Determination and analysis of single nucleotide polymorphisms and haplotype structure of the human carboxylesterase 2 gene

Epigenetic regulation of BMP2 by 1,25-dihydroxyvitamin D3 through DNA methylation and histone modification

Functional EGFR Germline Polymorphisms May Confer Risk for EGFR Somatic Mutations in Non–Small Cell Lung Cancer, with a Predominant Effect on Exon 19 Microdeletions ⬇️

Functional characterization of ABCC2 promoter polymorphisms and allele-specific expression.

Genetic Polymorphism, Telomere Biology and Non-Small Lung Cancer Risk

Genome-wide search for loss of heterozygosity in Chinese patients with sporadic colorectal cancer

Haplotypes of variants in the UDP-glucuronosyltransferase1A9 and 1A1 genes.

Hepatocyte nuclear factor-1 alpha is associated with UGT1A1, UGT1A9 and UGT2B7 mRNA expression in human liver

Identification, replication, and functional fine-mapping of expression quantitative trait loci in primary human liver tissue

Impact of the Interaction between 3'-UTR SNPs and microRNA on the Expression of Human Xenobiotic Metabolism Enzyme and Transporter Genes.

Interactions between MDM2 and TP53 Genetic Alterations, and Their Impact on Response to MDM2 Inhibitors and Other Chemotherapeutic Drugs in Cancer Cells.

Personalized targeted therapy for lung cancer

Relationship between differential hepatic microRNA expression and decreased hepatic cytochrome P450 3A activity in cirrhosis

SNPs affecting serum metabolomic traits may regulate gene transcription and lipid accumulation in the liver

Searching for tissue-specific expression pattern-linked nucleotides of UGT1A isoforms

Single nucleotide polymorphism discovery and functional assessment of variation in the UDP-glucuronosyltransferase 2B7 gene

Synthesis and biological evaluation of novel folic acid receptor-targeted, β-cyclodextrin-based drug complexes for cancer treatment

Tentative novel mechanism of the bystander effect in glioma gene therapy with HSV-TK/GCV system

The Werner's syndrome 4330T>C (Cys1367Arg) gene variant does not affect the in vitro cytotoxicity of topoisomerase inhibitors and platinum compounds