Q. Mo

发表

Rapid, simultaneous genotyping of 10 Southeast Asian glucose-6-phosphate dehydrogenase deficiency-causing mutations and a silent polymorphism by multiplex primer extension/denaturing HPLC assay.

C. Liao, P. Pearson, R. Cai, 2005, Clinical chemistry.

Reliable Detection of Paternal SNPs within Deletion Breakpoints for Non-Invasive Prenatal Exclusion of Homozygous α0-Thalassemia in Maternal Plasma

Wanjun Zhou, Tizhen Yan, Xiang-min Xu, 2011, PloS one.

The prevalence and spectrum of alpha and beta thalassaemia in Guangdong Province: implications for the future health burden and population screening.

Y. Li, G. Luo, C. Liao, 2004, Journal of clinical pathology.

Rapid, accurate genotyping of the common −α4.2 thalassaemia deletion based on the use of denaturing HPLC

X. Xu, Q. Mo, H. Ou-yang, 2004, Journal of Clinical Pathology.

Rapid, accurate genotyping of alcohol dehydrogenase-1B and aldehyde dehydrogenase-2 based on the use of denaturing HPLC

Liang Li, Xiang-min Xu, Q. Mo, 2005, Clinical chemistry and laboratory medicine.

Evaluation of clinical application of gap-PCR as a routine method for alpha-thalassemia carrier detection.

Xiang-min Xu, Q. Mo, Yu-Qiu Zhou, 2002, Di 1 jun yi da xue xue bao = Academic journal of the first medical college of PLA.

The prevalence and spectrum of α and β thalassaemia in Guangdong Province: implications for the future health burden and population screening

G. Luo, C. Liao, M. Zhong, 2004, Journal of Clinical Pathology.

[Prevalence survey and molecular characterization of alpha and beta thalassemia in Liuzhou city of Guangxi].

R. Cai, H. Ouyang, Q. Mo, 2002, Zhonghua liu xing bing xue za zhi = Zhonghua liuxingbingxue zazhi.

Molecular characterization and PCR detection of a deletional HPFH: Application to rapid prenatal diagnosis for compound heterozygotes of this defect with β‐thalassemia in a Chinese family

Xiang-min Xu, Q. Mo, Yong-zhong Zhao, 2000, American journal of hematology.

A rare beta-thalassaemia mutation (C-T) at position -90 of the beta-globin gene discovered in a Chinese family.

Xiangmin Xu, Q. Mo, S. Jia, 2003, Haematologica.

Carrier screening for α‐ and β‐thalassemia in pregnancy: the results of an 11‐year prospective program in Guangzhou Maternal and Neonatal hospital

Xiang-min Xu, C. Liao, Jian Li, 2005 .

Direct fluorescence detection of point mutations in human genomic DNA using microbead-based ligase chain reaction.

Kemin Wang, Xiaohai Yang, Yongjun Tan, 2010, Talanta.

Carrier screening for alpha- and beta-thalassemia in pregnancy: the results of an 11-year prospective program in Guangzhou Maternal and Neonatal hospital.

Xiang-min Xu, C. Liao, Jian Li, 2005, Prenatal diagnosis.

Optimization and head-to-head comparison of MISSR-PCR, ERIC-PCR, RAPD and 16S rRNA evolutionary clock for the genotyping of Vibrio cholerae isolated in China

J. Lin, Q. Wang, H. Wang, 2015, Indian journal of medical microbiology.

Comparative detection of rotavirus RNA by conventional RT-PCR, TaqMan RT-PCR and real-time nucleic acid sequence-based amplification.

Qi Wang, H. Tan, Q. Mo, 2015, Journal of virological methods.

Rapid and simultaneous detection of three major diarrhea-causing viruses by multiplex real-time nucleic acid sequence-based amplification

Qi Wang, H. Tan, Q. Mo, 2015, Archives of Virology.

HIV Vaccine Research: The Challenge and the Way Forward

Q. Mo, Hai-Bo Wang, Ze Yang, 2015, Journal of immunology research.

α0 Thalassaemia as a result of a novel 11.1 kb deletion eliminating both of the duplicated α globin genes

C. Liao, J. Li, L. Li, 2004, Journal of Clinical Pathology.

A novel mutation of −73(A→T) in the CCAAT box of the β-globin gene identified in a patient with the mild β-thalassemia intermedia

Xiang-min Xu, Qiang Li, Q. Mo, 2007, Annals of Hematology.

A novel mutation of -73(A-->T) in the CCAAT box of the beta-globin gene identified in a patient with the mild beta-thalassemia intermedia.

Xiang-min Xu, Qiang Li, Q. Mo, 2007, Annals of hematology.

A novel frameshift mutation (+G) at codons 15/16 in a β0 thalassaemia gene results in a significant reduction of β globin mRNA values

Y.-L. He, Q. Mo, C-F Li, 2005, Journal of Clinical Pathology.

A novel frameshift mutation ( + G) at codons 15/16 in a b 0 thalassaemia gene results in a significant reduction of b globin mRNA values

Q. Mo, C-F Li, X-R Li, 2005 .

A novel frameshift mutation (+G) at codons 15/16 in a b thalassaemia gene results in a significant reduction of b globin mRNA values

Q. Mo, C-F Li, X-R Li, 2005 .

A novel frameshift mutation (+G) at codons 15/16 in a b thalassaemia gene results in a significant reduction of b globin mRNA values

Q. Mo, C-F Li, X-R Li, 2005 .

A novel frameshift mutation (+G) at codons 15/16 in a beta0 thalassaemia gene results in a significant reduction of beta globin mRNA values.

Y.-L. He, Q. Mo, C-F Li, 2005, Journal of clinical pathology.

High HIV-1 prevalence and viral diversity among entry-exit populations at frontier ports of China, 2012-2016: A cross-sectional molecular epidemiology study.

H. Tan, Hong Zhu, Q. Mo, 2018, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[A rare thalassemia intermedia case caused by co-existence of Hb H disease (--(SEA)/-alpha(4.2)) and beta-thalassemia major (beta (CD17A)>T/beta (IVS2-654C)>T): implications for prenatal diagnosis].

Qiang Li, Q. Mo, Li-yan Li, 2008, Nan fang yi ke da xue xue bao = Journal of Southern Medical University.

Probe-free and sensitive detection of diarrhea-causing pathogens using RT-PCR combined high resolution melting analysis.

Qi Wang, Q. Mo, Z. Feng, 2016, Biologicals : journal of the International Association of Biological Standardization.

Development and Evaluation of an iiPCR Assay for Salmonella and Shigella Detection on a Field-Deployable PCR System

Q. Mo, Hai-Bo Wang, Ji-Hong Lin, 2020, The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale.

Rapid and simultaneous detection of three major diarrhea-causing viruses by multiplex real-time nucleic acid sequence-based amplification

Qi Wang, H. Tan, Q. Mo, 2015, Archives of Virology.

Complete nucleotide sequence analysis of the norovirus GII.17: A newly emerging and dominant variant in China, 2015.

Qi Wang, Q. Mo, Hai-Bo Wang, 2016, Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases.

[HAND system-based four multiplex RT-PCR for simultaneous detection of four diarrhea viruses].

Hong Sun, Dejian Zhao, Qi Wang, 2013, Nan fang yi ke da xue xue bao = Journal of Southern Medical University.

Rapid simultaneous screening of seven clinically important enteric pathogens using a magnetic bead based DNA microarray

Lei Shi, Hong Sun, W. Lu, 2011 .

Alpha0 thalassaemia as a result of a novel 11.1 kb deletion eliminating both of the duplicated alpha globin genes.

C. Liao, J. Li, L. Li, 2004, Journal of clinical pathology.

Rapid, accurate genotyping of β‐thalassaemia mutations using a novel multiplex primer extension/denaturing high‐performance liquid chromatography assay

Xiang-min Xu, Grant Wu, Jim J. Zhu, 2003, British journal of haematology.

[Rapid detection of three common deletional alpha thalassemias in Chinese by single-tube multiplex PCR].

Xiangmin Xu, Q. Mo, Liyan Li, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Fidelity genotyping of point mutation by enhanced melting point difference using DNA ligase.

Kemin Wang, W. Tan, Xiaohai Yang, 2007, Talanta.

The establishment and clinical evaluation of a novel, rapid, no-wash one-step immunoassay for the detection of dengue virus non-structural protein 1.

Q. Mo, Hai-Bo Wang, Ze Yang, 2019, Journal of virological methods.

Reliable and high-throughput mutation screening for beta-thalassemia by a single-base extension/fluorescence polarization assay.

Xiang-min Xu, Q. Mo, Li-yan Li, 2004, Genetic testing.