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Name Card
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Dr Song, You-qiang 宋又强

Title:
Principal Lecturer

Principal Investigator
StatusProject CodeProject TitleAmountFunding Year
 
17117715Study of the pathogenic mechanisms of Hnrnpa1 in congenital heart defects (CHD)7741902015
 
HKU 777212MIdentification of a genetic variant for heart defects (CHD) on chromosome 15 in mice8500002012
 
HKU 7496/04MMapping and cloning a new gene on chromosome 8q24 for amyotrophic lateral sclerosis in a large Chinese family9399682004
 
HKU 775208MDetecting genes and functional analysis of a novel gene (Cer1) significantly associated with bone mineral density (BMD) in mice.10441862008
 
11101032In silico identification of genetic variations that affect resistance to influenza A virus infection9568002011
 
HKU 7509/03MGenetic linkage analysis of early onset degenerative disc disease in Southern Chinese7860002003
 
HKU 7688/05MMapping a genetic modifier for heart defects in Type IIA procollagen deficient mutant mice16356062005
 
08070652Fine mapping candidate loci for nasopharyngeal carcinoma (NPC) in southern Chinese specifically linked to EBV aetiopathogenesis7508122008
 
CityU 141307HA Randomized Controlled Trial of the Therapeutic Effects of Tai Chi and Mahjong on Older Persons With Cognitive Impairment183002007
 
81271226Investigation on Pax6 regulation of neuronal apoptosis in Alzheimer’s disease8792002012
 
01121726Study of Population Specific Linkage Disequilibrium (LD) Patterns of Human Major Histocompatibility Complex (MHC) Region for Cancers, Infectious and Autoimmunity Diseases in Southern Chinese9568002013
 
17114519Genetic study of adolescent idiopathic scoliosis in Chinese and functional analysis of a disease variant8929152019
 
MRP/056/21Inhibition of Pax6 Signaling Linking Between Amyloid β Plaques And Neurofibrillary Tangles In Alzheimer’s Disease Using Repurposed Drugs29908322021
 
C8105-20GProtecting older people from loneliness during the coronavirus (Covid-19) and other novel infectious disease pandemic8929602020
 
08191496Functional interrogation of non-coding regulatory regions identified from Hirschsprung disease patients14241402020
Co-Investigator
StatusProject CodeProject TitleAmountFunding Year
 
17108315Neurochemical basis of the change in attention control and memory encoding in normal aging4172212015
 
13120842Identification of innate immune defect predisposing to severe influenza in a Chinese population4948922013
 
T11-706/18-NPotentiating Host Immunity for HIV-1 Functional Cure311330002018
 
ITS/065/03To construct a haplotype map (HapMap) of 2% of the human genome100000002003
 
02132216Genetic risks for chronic periodontitis: A genome-wide association study9999802014
 
AoE/M-04/04Developmental genomics and skeletal research809740002003
 
T12-708/12-NFunctional Analyses of How Genomic Variation Affects Personal Risk for Degenerative Skeletal Disorders637500002012
 
HKU 7636/05MRole of kinesin-mediated intracellular transportation in Alzheimer's Disease13609572005
 
2203100624A machine learning platform for drug repositioning against future infectious diseases1500002022
 
ITS/133/18Advanced Platform for High-throughput Discovery of Three-way Combination Therapies13999062018
 
InP/373/18Advanced Platform for High-throughput Discovery of Three-way Combination Therapies3584562018
 
HKU 775307MRole of chromosomal 6q23 region in the modulation of HbF production14186162007
 
17126319Deciphering protective factors for intervertebral disc degeneration for mechanistic insights and intervention potentials10292332019
 
06171406Identifying the genetic factors underlying congenital scoliosis in Hong Kong14997522018
 
HKU 7119/05EComputationally Haplotyping Pedigree Data3592242005
 
HKU 7685/06MGenetic and developmental defects of a mouse mutant <I>Mcc</I> with microphthalmia, cataract and closed eyelid12295002006
 
InP/436/19Advanced Platform for High-throughput Discovery of Three-way Combination Therapies1313012019
 
C7031-15GTargeted Genomics and Functional Studies of Novel Cancer Predisposing Genes for Esophageal Squamous Cell Carcinoma75703042015
 
N/ATo construct a haplotype map (HapMap) of 2% of the human genome250000002003
 
InP/054/19Advanced Platform for High-throughput Discovery of Three-way Combination Therapies3392852018
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