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BRE is an antiapoptotic protein in vivo and overexpressed in human hepatocellular carcinoma

Oncogene, 2008-02, Vol.27 (9), p.1208-1217

2008

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Study of gene-gene interactions for endophenotypic quantitative traits in Chinese asthmatic children

Allergy (Copenhagen), 2008-08, Vol.63 (8), p.1031-1039

2008

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effect of telomere length, a marker of biological aging, on bone mineral density in elderly population

Osteoporosis international, 2010, Vol.21 (1), p.89-97

2010

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ALU polymorphism of angiotensin I converting enzyme (ACE) and atherosclerosis, incident chronic diseases and mortality in an elderly Chinese population

The Journal of nutrition, health & aging, 2012-03, Vol.16 (3), p.262-268

2012

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Asthma and atopy are associated with chromosome 17q21 markers in Chinese children

Allergy, 2009-04, Vol.64 (4), p.621-628

2009

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Narcolepsy in Southern Chinese patients: clinical characteristics, HLA typing and seasonality of birth

Journal of neurology, neurosurgery and psychiatry, 2008-11, Vol.79 (11), p.1262-1267

2008

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Telomeres and frailty

Mechanisms of ageing and development, 2008-11, Vol.129 (11), p.642-648

2008

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Antibiotic-resistant Propionibacterium acnes among acne patients in a regional skin centre in Hong Kong

Journal of the European Academy of Dermatology and Venereology, 2013-01, Vol.27 (1), p.31-36

2013

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Deficiency of the carnitine transporter (OCTN2) with partial N‐acetylglutamate synthase (NAGS) deficiency

Journal of inherited metabolic disease, 2007-10, Vol.30 (5), p.816-816

2007

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Single-cell RNA sequencing identifies molecular targets associated with poor in vitro maturation performance of oocytes collected from ovarian stimulation

Human reproduction (Oxford), 2021-06, Vol.36 (7), p.1907-1921

2021

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Mutations of OCTN2, an Organic Cation/Carnitine Transporter, Lead to Deficient Cellular Carnitine Uptake in Primary Carnitine Deficiency

Human molecular genetics, 1999-04, Vol.8 (4), p.655-660

1999

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Nitric oxide synthase polymorphisms and asthma phenotypes in Chinese children

Clinical and experimental allergy, 2005-10, Vol.35 (10), p.1288-1294

2005

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Polymorphisms in the C-type lectin genes cluster in chromosome 19 and predisposition to severe acute respiratory syndrome coronavirus (SARS-CoV) infection

Journal of medical genetics, 2008-11, Vol.45 (11), p.752-758

2008

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Association analysis of GABA receptor subunit genes on 5q33 with heroin dependence in a Chinese male population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2007-06, Vol.144B (4), p.439-443

2007

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Association between candidate genes and lung function growth in Chinese asthmatic children

Clinical and experimental allergy, 2007-10, Vol.37 (10), p.1480-1486

2007

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A polymorphism in the coding region of interleukin-13 gene is associated with atopy but not asthma in Chinese children

Clinical and experimental allergy, 2001-10, Vol.31 (10), p.1515-1521

2001

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Association study between adolescent idiopathic scoliosis and the DPP9 gene which is located in the candidate region identified by linkage analysis

Postgraduate medical journal, 2008-09, Vol.84 (995), p.498-501

2008

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Topical 5-fluorouracil has no additional benefit in treating common warts with cryotherapy: a single-centre, double-blind, randomized, placebo-controlled trial

Clinical and experimental dermatology, 2006-05, Vol.31 (3), p.394-397

2006

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Association of prostaglandin-endoperoxide synthase 2 gene polymorphisms with asthma and atopy in Chinese children

Allergy, 2007-07, Vol.62 (7), p.802-809

2007

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Immunogenetic studies in SARS: developing a clinical prognostic profile for severe diseases

Hong Kong medical journal = Xianggang yi xue za zhi, 2009-12, Vol.15 Suppl 8, p.8-10

Tang, N L S

2009

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Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure

The European respiratory journal, 2006-08, Vol.28 (2), p.447-450

2006

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RANTES G-401A polymorphism is associated with allergen sensitization and FEV1 in Chinese children

Respiratory medicine, 2005-02, Vol.99 (2), p.216-219

2005

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Total daily energy expenditure in wasted chronic obstructive pulmonary disease patients

European journal of clinical nutrition, 2002-04, Vol.56 (4), p.282-287

2002

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Telomere length and cognitive function in southern Chinese community-dwelling male elders

Age and ageing, 2013-07, Vol.42 (4), p.450-455

2013

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Novel missense mutations in the first Chinese patient with very-long-chain acyl-CoA dehydrogenase deficiency

Clinica chimica acta, 2007, Vol.375 (1), p.173-174

2007

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BRE is an antiapoptotic protein in vivo and overexpressed in human hepatocellular carcinoma

Study of gene-gene interactions for endophenotypic quantitative traits in Chinese asthmatic children

effect of telomere length, a marker of biological aging, on bone mineral density in elderly population

ALU polymorphism of angiotensin I converting enzyme (ACE) and atherosclerosis, incident chronic diseases and mortality in an elderly Chinese population

Asthma and atopy are associated with chromosome 17q21 markers in Chinese children

Narcolepsy in Southern Chinese patients: clinical characteristics, HLA typing and seasonality of birth

Telomeres and frailty

Antibiotic-resistant Propionibacterium acnes among acne patients in a regional skin centre in Hong Kong

Deficiency of the carnitine transporter (OCTN2) with partial N‐acetylglutamate synthase (NAGS) deficiency

Single-cell RNA sequencing identifies molecular targets associated with poor in vitro maturation performance of oocytes collected from ovarian stimulation

Mutations of OCTN2, an Organic Cation/Carnitine Transporter, Lead to Deficient Cellular Carnitine Uptake in Primary Carnitine Deficiency

Nitric oxide synthase polymorphisms and asthma phenotypes in Chinese children

Polymorphisms in the C-type lectin genes cluster in chromosome 19 and predisposition to severe acute respiratory syndrome coronavirus (SARS-CoV) infection

Association analysis of GABA receptor subunit genes on 5q33 with heroin dependence in a Chinese male population

Association between candidate genes and lung function growth in Chinese asthmatic children

A polymorphism in the coding region of interleukin-13 gene is associated with atopy but not asthma in Chinese children

Association study between adolescent idiopathic scoliosis and the DPP9 gene which is located in the candidate region identified by linkage analysis

Topical 5-fluorouracil has no additional benefit in treating common warts with cryotherapy: a single-centre, double-blind, randomized, placebo-controlled trial

Association of prostaglandin-endoperoxide synthase 2 gene polymorphisms with asthma and atopy in Chinese children

Immunogenetic studies in SARS: developing a clinical prognostic profile for severe diseases

Very long-chain acyl-CoA dehydrogenase deficiency presenting as acute hypercapnic respiratory failure

RANTES G-401A polymorphism is associated with allergen sensitization and FEV1 in Chinese children

Total daily energy expenditure in wasted chronic obstructive pulmonary disease patients

Telomere length and cognitive function in southern Chinese community-dwelling male elders

Novel missense mutations in the first Chinese patient with very-long-chain acyl-CoA dehydrogenase deficiency

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