Hong Luo

Guangzhou Blood Center — China

Medicine · Health Sciences

20h-index1.3kcitations52works0.02yr avg
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Research Topics

Blood groups and transfusion(16), Hemoglobinopathies and Related Disorders(10), Erythrocyte Function and Pathophysiology(8), Developmental Biology and Gene Regulation(6), Prenatal Screening and Diagnostics(6)

Publications52 total

A novel <i>FUT1*c.889C&gt;T</i> allele associated with the <scp>para‐Bombay AB</scp> phenotype and computational evaluation of the mutation effect
Transfusion·2023· 2 cited
C‐MET–dependent signal transduction mediates retinoblastoma growth by regulating PKM2 nuclear translocation
Cell Biochemistry and Function·2019· 12 cited
Broad Promotes Neuroepithelial Stem Cell Differentiation in the <i>Drosophila</i> Optic Lobe
Genetics·2019· 10 citedOpen Access
Table of contents
2019Open Access
[Correlation between special A/O genotype and the O phenotype].
PubMed·2019
A variant RhAG protein encoded by the <i>RHAG*572A</i> allele causes serological weak D expression while maintaining normal RhCE phenotypes
Transfusion·2018· 10 citedOpen Access
[Identification of a novel ABO B(A)07 allele].
PubMed·2017· 1 cited
[Phenotype Types and Genetic Mutation Mechanism of Rhesus D Variant Individuals].
PubMed·2017
<i>RHD</i> genotype and zygosity analysis in the Chinese Southern Han D+, D− and D variant donors using the multiplex ligation‐dependent probe amplification assay
Vox Sanguinis·2017· 27 citedOpen Access
The genetic basis of asymptomatic codon 8 frame‐shift (<i><scp>HBB</scp></i>:c25_26del<scp>AA</scp>) β<sup>0</sup>‐thalassaemia homozygotes
British Journal of Haematology·2016· 4 citedOpen Access
A Candidate Trans-Acting Modulator of Fetal Hemoglobin Gene Expression in the Arab-Indian Haplotype of Sickle Cell Anemia
Blood·2015
Therapeutic fetal-globin inducers reduce transcriptional repression in hemoglobinopathy erythroid progenitors through distinct mechanisms
Blood Cells Molecules and Diseases·2015· 20 citedOpen Access
Application of multiple ligation-dependent probe amplification in allele detection of 2 cases with rare Rh partial D individuals
Guoji shuxue ji xueyexue zazhi·2015
Characterization of a Transcript Found within the HBS1L-MYB Intergenic Region
Blood·2014
Assessment of HbF QTLs Affecting Disease Severity and Genetic Analysis in Patients Homozygous for Codon 8 (–AA) β0-Thalassemia Mutation
Blood·2014
In utero gene therapy rescues microcephaly caused by Pqbp1-hypofunction in neural stem progenitor cells
Molecular Psychiatry·2014· 42 citedOpen Access
Trehalase Regulates Neuroepithelial Stem Cell Maintenance and Differentiation in the Drosophila Optic Lobe
PLoS ONE·2014· 14 citedOpen Access
[The relevance of leukotriene D4 synthase gene A(-444)C polymorphism to clinical responsiveness of leukotriene receptor antagonist in patients with allergic rhinitis].
PubMed·2014
Recombination analysis of autosomal short tandem repeats in <scp>C</scp>hinese <scp>H</scp>an families
Electrophoresis·2013· 9 cited
Evidence for Tissue-Specific JAK/STAT Target Genes in<i>Drosophila</i>Optic Lobe Development
Genetics·2013· 35 citedOpen Access
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Frequent Co-authors

David H.K. Chui(13), Guangping Luo(10), Ling Wei(9), Yanli Ji(8), Hirofumi Suemori(7), Ryuzo Torii(7), Norio Nakatsuji(7), Tatsutoshi Nakahata(7), Chunyan Mo(7), Katsutsugu Umeda(6), Runqing Zhang(6), Charles R. Dearolf(5), Masabumi Shibuya(5), Gen Shinoda(5), Yang Zhao(5), Toshio Heike(4), Jizhi Wen(4), Martin H. Steinberg(4), Masato Arai(4), Feng Ma(4)