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Lista de obras de Nelson Leung-Sang Tang

3-methyglutaconic aciduria in a Chinese patient with glycogen storage disease Ib.

artículo científico publicado en 2003

5-HT2A T102C receptor polymorphism and neuropsychiatric symptoms in Alzheimer's disease

artículo científico publicado en 2004

A Decade in Review after Idiopathic Scoliosis Was First Called a Complex Trait—A Tribute to the Late Dr. Yves Cotrel for His Support in Studies of Etiology of Scoliosis

artículo científico publicado en 2021

A Relook Into the Association of the Estrogen Receptor α Gene (PvuII, XbaI) and Adolescent Idiopathic Scoliosis

article

A community-based study of insomnia in Hong Kong Chinese children: Prevalence, risk factors and familial aggregation

artículo científico publicado en 2009

A genomic approach to mutation analysis of holocarboxylase synthetase gene in three Chinese patients with late-onset holocarboxylase synthetase deficiency

artículo científico publicado en 2003

A hidden two-locus disease association pattern in genome-wide association studies

artículo científico publicado en 2011

A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groups

artículo científico publicado en 2014

A novel ALDH5A1 mutation in a patient with succinic semialdehyde dehydrogenase deficiency.

artículo científico publicado en 2012

A novel functional assay for simultaneous determination of total fatty acid beta-oxidation flux and acylcarnitine profiling in human skin fibroblasts using (2)H(31)-palmitate by isotope ratio mass spectrometry and electrospray tandem mass spectromet

artículo científico publicado en 2007

A novel mutation (G233D) in the glycogen phosphorylase gene in a patient with hepatic glycogen storage disease and residual enzyme activity

artículo científico publicado en 2003

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

article

A single nucleotide polymorphism in microRNA-146a is associated with the risk for nasopharyngeal carcinoma

artículo científico publicado en 2012

A study on whey protein supplement on physical performance and quality of life among elderly patients with chronic obstructive pulmonary disease

scholarly article by Christopher Lum et al published December 2007 in Australasian Journal on Ageing

ACE2 gene polymorphisms do not affect outcome of severe acute respiratory syndrome

artículo científico publicado en 2004

AGTR1 has undergone natural selection in Euro-Asian populations in relation to ambient temperature that predisposes Chinese populations to essential hypertension

artículo científico publicado en 2016

Abnormal expressions of the subunits of the UDP-N-acetylglucosamine: lysosomal enzyme, N-acetylglucosamine-1-phosphotransferase, result in the formation of cytoplasmic vacuoles resembling those of the I-cells

artículo científico publicado en 2006

Absence of association between angiotensin converting enzyme polymorphism and development of adult respiratory distress syndrome in patients with severe acute respiratory syndrome: a case control study

artículo científico publicado en 2005

Acute Renal Failure and Proximal Tubule Lesions after Trichosanthin Injection in Rats

artículo científico publicado en 1997

An upregulation in the expression of vanilloid transient potential channels 2 enhances hypotonicity-induced cytosolic Ca²⁺ rise in human induced pluripotent stem cell model of Hutchinson-Gillford Progeria.

artículo científico publicado en 2014

Apolipoprotein E epsilon4 allele is associated with vascular dementia.

artículo científico publicado en 2006

Apolipoprotein epsilon-4 allele and the two-year progression of cognitive function in Chinese subjects with late-onset Alzheimer's disease.

artículo científico publicado en 2006

Applicability of BALAD score in prognostication of hepatitis B-related hepatocellular carcinoma.

artículo científico

Application of Urine Magnesium/Creatinine Ratio as an Indicator for Insufficient Magnesium Intake

artículo científico publicado en 2000

Assessment of total energy expenditure in a Chinese population by a physical activity questionnaire: examination of validity

artículo científico publicado en 2001

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

article

Association between HLA-A alleles and Alzheimer's disease in a southern Chinese community.

artículo científico publicado en 2008

Association between TARC C-431T and atopy and asthma in children

artículo científico publicado en 2004

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

artículo científico publicado en 2007

Association between tumor necrosis factor-alpha promoter polymorphism and Alzheimer's disease.

artículo científico publicado en 2004

Association of SRD5A2 variants and serum androstane-3alpha,17beta-diol glucuronide concentration in Chinese elderly men.

artículo científico publicado en 2010

Association of disease-predisposition polymorphisms of the melatonin receptors and sunshine duration in the global human populations

artículo científico publicado en 2009

Association of gene expression and methylation of UQCRC1 to the predisposition of Alzheimer's disease in a Chinese population.

artículo científico publicado en 2016

Association of genetic variations in aromatase gene with serum estrogen and estrogen/testosterone ratio in Chinese elderly men.

artículo científico publicado en 2009

Association of plasma soluble CTLA-4 with lung function and gene polymorphism in Chinese asthmatic children

article

Association of polymorphisms in the Chr18q11.2 locus with tuberculosis in Chinese population

artículo científico publicado en 2013

Association of prostaglandin-endoperoxide synthase 2 (PTGS2) polymorphisms and Alzheimer's disease in Chinese.

artículo científico publicado en 2007

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

article

Association ofearly growth response-1gene polymorphisms with total IgE and atopy in asthmatic children

article

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

article

Asthma and atopy are associated with DEFB1 polymorphisms in Chinese children.

artículo científico publicado en 2006

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

article

Avoiding cardiopulmonary bypass in multivessel CABG reduces cytokine response and myocardial injury

article

BOOST: A fast approach to detecting gene-gene interactions in genome-wide case-control studies

artículo científico publicado en 2010

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

artículo científico publicado en 2007

Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies

artículo científico publicado en 2005

CBS gene mutations found in a Chinese pyridoxine-responsive homocystinuria patient

article

CD14 and toll-like receptors: potential contribution of genetic factors and mechanisms to inflammation and allergy

artículo científico publicado en 2005

CISH and susceptibility to infectious diseases

artículo científico publicado en 2010

CNGA2 contributes to ATP-induced noncapacitative Ca2+ influx in vascular endothelial cells.

artículo científico publicado en 2009

Carnitine level in Chinese epileptic patients taking sodium valproate

artículo científico publicado en 2003

Characterization of early IgA nephropathy

artículo científico publicado en 2000

Chemotherapy-Related Amenorrhea and Menopause in Young Chinese Breast Cancer Patients: Analysis on Incidence, Risk Factors and Serum Hormone Profiles

artículo científico publicado en 2015

Chinese Tea and Telomere Length in Elderly Chinese Men

article

Chinese tea consumption is associated with longer telomere length in elderly Chinese men.

artículo científico publicado en 2009

Choice of study phenotype in osteoporosis genetic research

artículo científico publicado en 2009

Cholesterol 24-hydroxylase (CYP46A1) polymorphisms are associated with faster cognitive deterioration in Chinese older persons: a two-year follow up study

artículo científico publicado en 2009

Classical galactosaemia in Chinese: A case report and review of disease incidence.

artículo científico publicado en 1999

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

artículo científico publicado en 2010

Comparative analysis of protein-coding genes and long non-coding RNAs of prostate cancer between Caucasian and Chinese populations

article

Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy.

artículo científico publicado en 2007

Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposis

artículo científico publicado en 2001

Correlation of telomere length shortening with TP53 somatic mutations, polymorphisms and allelic loss in breast tumors and esophageal cancer

scientific article published on 22 October 2012

Correlations of health-related quality of life with serum inflammatory indicators IL-8 and mIBI in patients with hepatocellular carcinoma

article

Corrigendum: Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis.

artículo científico publicado en 2017

Deciphering global signal features of high-throughput array data from cancers

artículo científico publicado en 2014

Decompression and stable internal fixation of femoral neck fractures in children can affect the outcome

artículo científico publicado en 1999

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

artículo científico publicado en 2007

Detecting two-locus associations allowing for interactions in genome-wide association studies

artículo científico publicado en 2010

Determinants of Cervical Human Papillomavirus Infection: Differences between High‐ and Low‐Oncogenic Risk Types

scientific article published on 05 December 2001

Determination of the risk for familial disease in RET mutation-negative patients with medullary thyroid cancer

scientific article published on 01 August 1998

Diagnoses of newborns and mothers with carnitine uptake defects through newborn screening

artículo científico publicado en 2009

Diagnosing Wilson's disease in a 5-year-old child

artículo científico publicado en 2002

Dietary intake, blood pressure and osteoporosis

artículo científico publicado en 2008

Discovering Genetic Factors for psoriasis through exhaustively searching for significant second order SNP-SNP interactions

artículo científico publicado en 2018

Distribution in allele frequencies of predisposition-to-atopy genotypes in Chinese children

artículo científico publicado en 2002

Dopamine receptor D4 gene -521C/T polymorphism is associated with opioid dependence through cold-pain responses

artículo científico publicado en 2008

Dynamic changes of DNA epigenetic marks in mouse oocytes during natural and accelerated aging.

artículo científico publicado en 2015

Early enhanced expression of interferon-inducible protein-10 (CXCL-10) and other chemokines predicts adverse outcome in severe acute respiratory syndrome

artículo científico

Effect of whole soy and purified isoflavone daidzein on renal function--a 6-month randomized controlled trial in equol-producing postmenopausal women with prehypertension

artículo científico

Energy intake and expenditure profile in chronic peritoneal dialysis patients complicated with circulatory congestion

artículo científico publicado en 2009

Estrogen receptor α polymorphisms and the risk of cognitive decline: A 2-year follow-up study

artículo científico publicado en 2013

European bone mineral density loci are also associated with BMD in East-Asian populations

artículo científico publicado en 2010

Evaluation of an algorithm of tagging SNPs selection by linkage disequilibrium.

artículo científico publicado en 2006

Exome sequencing identifies a rare HSPG2 variant associated with familial idiopathic scoliosis

artículo científico publicado en 2014

Familial aggregation and heritability of insomnia in a community-based study

artículo científico publicado en 2012

Familial aggregation of narcolepsy.

artículo científico publicado en 2011

Fine-scale stratification analysis of Hong Kong Chinese population

article

Frequent hypermethylation of promoter region ofRASSF1A in tumor tissues and voided urine of urinary bladder cancer patients

article

Functional interaction between SNPs and microsatellite in the transcriptional regulation of insulin-like growth factor 1.

artículo científico publicado en 2013

GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

artículo científico publicado en 2019

Gaucher disease among Chinese patients: review on genotype/phenotype correlation from 29 patients and identification of novel and rare alleles

artículo científico publicado en 2006

Gender and telomere length: systematic review and meta-analysis

artículo científico publicado en 2013

Gender difference of serum angiotensin-converting enzyme (ACE) activity in DD genotype of ACE insertion/deletion polymorphism in elderly Chinese

artículo científico publicado en 2013

Gene-gene interactions for asthma and plasma total IgE concentration in Chinese children

article

Genes Regulate Blood Pressure, but "Environments" Cause Hypertension

scientific article published on 09 November 2020

Genetic Association Study of Growth Hormone Receptor and Idiopathic Scoliosis

scientific article published on 01 September 2007

Genetic Variant of PAX1 Gene is Functionally Associated With Adolescent Idiopathic Scoliosis in The Chinese Population.

artículo científico publicado en 2017

Genetic adaptation of the hypoxia-inducible factor pathway to oxygen pressure among eurasian human populations.

artículo científico publicado en 2012

Genetic association between a chemokine gene CXCL-10 (IP-10, interferon gamma inducible protein 10) and susceptibility to tuberculosis

article

Genetic association of complex traits: using idiopathic scoliosis as an example

artículo científico publicado en 2007

Genetic association study between mbl2 and asthma phenotypes in Chinese children

artículo científico publicado en 2006

Genetic epidemiology and heritability of AIS: A study of 415 Chinese female patients

artículo científico publicado en 2012

Genetic imbalances in pT2 breast cancers of southern Chinese women.

artículo científico publicado en 2001

Genetic variant of BNC2 gene is functionally associated with adolescent idiopathic scoliosis in Chinese population

artículo científico publicado en 2017

Genome-wide association and replication studies identified TRHR as an important gene for lean body mass

artículo científico publicado en 2009

Genome-wide association study identifies new susceptibility loci for adolescent idiopathic scoliosis in Chinese girls

artículo científico publicado en 2015

Genome-wide association study identifies novel susceptible loci and highlights Wnt/beta-catenin pathway in the development of adolescent idiopathic scoliosis

artículo científico publicado en 2017

Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

artículo científico publicado en 2012

Genotype spectrum of cervical human papillomavirus infection among sexually transmitted disease clinic patients in Hong Kong

artículo científico publicado en 2002

Glycogen synthase kinase-3beta and tau genes interact in Alzheimer's disease

artículo científico publicado en 2008

Green space, psychological restoration, and telomere length

artículo científico publicado en 2009

Haplotype effect in the IGF1 promoter accounts for the association between microsatellite and serum IGF1 concentration

artículo científico publicado en 2011

Hepatitis C virus genotype distribution among intravenous drug user and the general population in Hong Kong

artículo científico publicado en 2006

High-level expression of early growth response-1 and association of polymorphism with total IgE and atopy in allergic rhinitis adults.

artículo científico publicado en 2009

How the SARS coronavirus causes disease: host or organism?

artículo científico publicado en 2006

Hypermethylation of multiple genes in tumor tissues and voided urine in urinary bladder cancer patients

artículo científico publicado en 2002

Impact of experimental acute hyponatremia on severe traumatic brain injury in rats: influences on injuries, permeability of blood-brain barrier, ultrastructural features, and aquaporin-4 expression

artículo científico publicado en 2002

Inhalant allergens as risk factors for the development and severity of mild-to-moderate asthma in Hong Kong Chinese children.

artículo científico publicado en 2002

Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutations

artículo científico

Insomnia, sleep quality, pain, and somatic symptoms: sex differences and shared genetic components

artículo científico publicado en 2012

Interindividual and interethnic variation in genomewide gene expression: insights into the biological variation of gene expression and clinical implications

artículo científico publicado en 2009

Isolate diffuse thickening of glomerular capillary basement membrane: a renal lesion in prediabetes?

artículo científico publicado en 2004

Isolated persistent elevation of alanine transaminase for early diagnosis of pre-symptomatic Wilson's disease in Chinese children

artículo científico publicado en 2013

Lack of Association Between the Promoter Polymorphisms of MMP-3 and IL-6 Genes and Adolescent Idiopathic Scoliosis

article

Lack of association between polymorphisms from genome-wide association studies and tuberculosis in the Chinese population

artículo científico publicado en 2012

Lack of association between the promoter polymorphism of the MTNR1A gene and adolescent idiopathic scoliosis.

artículo científico publicado en 2008

Lack of association of the interleukin-1beta gene polymorphism with Alzheimer's disease in a Chinese population.

artículo científico publicado en 2003

Low-density lipoprotein receptor-related protein 8 (apolipoprotein E receptor 2) gene polymorphisms in Alzheimer's disease

artículo científico publicado en 2002

MegaSNPHunter: a learning approach to detect disease predisposition SNPs and high level interactions in genome wide association study

artículo científico publicado en 2009

Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis.

artículo científico publicado en 2007

MicroRNAs mediated targeting on the Yin-yang dynamics of DNA methylation in disease and development

artículo científico

Mitochondrial DNA haplogroup Y is associated to Leigh syndrome in Chinese population

artículo científico publicado en 2012

Molecular evolution in the CREB1 signal pathway and a rare haplotype in CREB1 with genetic predisposition to schizophrenia

artículo científico publicado en 2014

Mutational and haplotype analysis of AGL in patients with glycogen storage disease type III

scientific article published on 01 January 2002

Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency

artículo científico publicado en 1999

MxA polymorphisms are associated with risk and age-at-onset in Alzheimer disease and accelerated cognitive decline in Chinese elders

artículo científico publicado en 2012

NEDD9 gene polymorphism influences the risk of Alzheimer disease and cognitive function in Chinese older persons.

artículo científico publicado en 2012

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

artículo científico publicado en 2008

New Evidence Supporting the Role of FBN1 in the Development of Adolescent Idiopathic Scoliosis

scientific article published on 01 February 2019

New Features of Renal Lesion Induced by Stroma Free Hemoglobin

scientific article published on 01 September 2000

No Association Between Physical Activity and Telomere Length in an Elderly Chinese Population 65 Years and Older

article

No mutation in the KCNE3 potassium channel gene in Chinese thyrotoxic hypokalaemic periodic paralysis patients.

artículo científico publicado en 2004

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

article

Novel mutations in ETFDH gene in Chinese patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency

artículo científico publicado en 2009

Novel mutations in PHKA2 gene in glycogen storage disease type IX patients from Hong Kong, China.

artículo científico publicado en 2010

Novel mutations in type 2 Gaucher disease in Chinese and their functional characterization by heterologous expression.

artículo científico publicado en 2005

Older men with higher self-rated socioeconomic status have shorter telomeres

artículo científico publicado en 2009

Outcome of IgA nephropathy in adults graded by chronic histological lesions

article

Overview of common inherited metabolic diseases in a Southern Chinese population of Hong Kong.

artículo científico publicado en 2001

PHF11 is not a major candidate gene for asthma or eczema in Chinese children

article

Pathology of fatal human infection associated with avian influenza A H5N1 virus

artículo científico publicado en 2001

Polar spongioblastoma with cerebrospinal fluid metastases

artículo científico publicado en 1994

Polarized secretion of interleukin (IL)-6 and IL-8 by human airway epithelia 16HBE14o- cells in response to cationic polypeptide challenge

artículo científico publicado en 2010

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

article

Polymorphisms of the estrogen receptor alpha (ESR1) gene and the risk of Alzheimer's disease in a southern Chinese community

artículo científico publicado en 2009

Predictive rule inference for epistatic interaction detection in genome-wide association studies

artículo científico publicado en 2009

Prevalence and genotype distribution of TT virus in various specimen types from thalassaemic patients

artículo científico publicado en 2001

Prevalence of Mutations in the BRCA1 Gene Among Chinese Patients With Breast Cancer

article

Prevalence of breast cancer predisposition gene mutations in Chinese women and guidelines for genetic testing

article

Primary plasmalemmal carnitine transporter defect manifested with dicarboxylic aciduria and impaired fatty acid oxidation

scientific article published on 01 June 1998

Profiles of lipids, blood pressure and weight changes among premenopausal Chinese breast cancer patients after adjuvant chemotherapy

artículo científico publicado en 2017

Promoter polymorphism of matrilin-1 gene predisposes to adolescent idiopathic scoliosis in a Chinese population

artículo científico publicado en 2008

Publisher Correction: GWAS of bone size yields twelve loci that also affect height, BMD, osteoarthritis or fractures

scientific article published on 24 May 2019

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

artículo científico publicado en 2005

Rare variants in FBN1 and FBN2 are associated with severe adolescent idiopathic scoliosis

artículo científico publicado en 2014

Renal outcome in type 2 diabetic patients with or without coexisting nondiabetic nephropathies

artículo científico publicado en 2002

Replication Study for the Association of GWAS-associated Loci With Adolescent Idiopathic Scoliosis Susceptibility and Curve Progression in a Chinese Population

scientific article published on 01 April 2019

Resting Energy Expenditure and Subsequent Mortality Risk in Peritoneal Dialysis Patients

artículo científico publicado en 2004

Role of pharmacogenetics on adjuvant chemotherapy-induced neutropenia in Chinese breast cancer patients

artículo científico publicado en 2012

SCALY RASH

artículo científico publicado en 2010

Seasonal pattern of tuberculosis in Hong Kong

artículo científico publicado en 2005

Sensitization to Common Food Allergens Is a Risk Factor for Asthma in Young Chinese Children in Hong Kong

article

Severe hypokalemic myopathy in Gitelman's syndrome

artículo científico publicado en 1999

Sex-specific effect of Pirin gene on bone mineral density in a cohort of 4000 Chinese

artículo científico publicado en 2009

Shorter telomere length is associated with greater decrease in ankle-brachial index in elderly Chinese women but not men.

artículo científico publicado en 2010

Somatic β-catenin mutation in gastric carcinoma – an infrequent event that is not specific for microsatellite instability

artículo científico publicado en 2001

Status of inflammation in relation to health related quality of life in hepatocellular carcinoma patients

scientific article published on 29 April 2019

Study of genegene interactions for endophenotypic quantitative traits in Chinese asthmatic children

article

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

artículo científico publicado en 2013

Telomere length is associated with decline in grip strength in older persons aged 65 years and over

artículo científico publicado en 2014

Telomere length is not associated with frailty in older Chinese elderly: Cross-sectional and longitudinal analysis

article

Telomeres and frailty

artículo científico publicado en 2008

The ?1Ssubunit of the L-type calcium channel is not a predisposition gene for thyrotoxic periodic paralysis

article

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

artículo científico publicado en 2012

The C-159T polymorphism in the CD14 promoter is associated with serum total IgE concentration in atopic Chinese children.

artículo científico publicado en 2003

The VNTR polymorphism of the DC-SIGNR gene and susceptibility to HIV-1 infection: a meta-analysis

artículo científico publicado en 2012

The association between promoter polymorphism of the interleukin-10 gene and Alzheimer's disease.

artículo científico publicado en 2004

The association of liver function and quality of life of patients with liver cancer

artículo científico publicado en 2019

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

artículo científico publicado en 2009

The first reported HLCS gene mutation causing holocarboxylase synthetase deficiency in a Vietnamese patient

article

The mechanism of transactivation regulation due to polymorphic short tandem repeats (STRs) using IGF1 promoter as a model

artículo científico publicado en 2016

The neck-region polymorphism of DC-SIGNR in peri-centenarian from Han Chinese population

artículo científico publicado en 2009

The origin and evolution of variable number tandem repeat of CLEC4M gene in the global human population

artículo científico publicado en 2012

The predisposition to thyrotoxic periodic paralysis (TPP) is due to a genetic variant in the inward-rectifying potassium channel, KCNJ2.

artículo científico publicado en 2013

The role of the Ala746Thr variant in the ATP13A2 gene among Chinese patients with Parkinson's disease.

artículo científico publicado en 2013

Thromboxane A2 receptor gene polymorphism is associated with the serum concentration of cat-specific immunoglobulin E as well as the development and severity of asthma in Chinese children

artículo científico publicado en 2002

Top theories for the etiopathogenesis of adolescent idiopathic scoliosis.

artículo científico publicado en 2011

Type I Gaucher disease with exophthalmos and pulmonary arteriovenous malformation

artículo científico publicado en 2005

Uniaxial cyclic stretch stimulates TRPV4 to induce realignment of human embryonic stem cell-derived cardiomyocytes.

artículo científico publicado en 2015

Urinary sodium excretion and dietary sources of sodium intake in Chinese postmenopausal women with prehypertension

artículo científico publicado en 2014

VCNet: Vector based gene Co-expression Network construction and its application to RNA-seq data

artículo científico publicado en 2017

Validation of prediction equations for basal metabolic rate in chinese subjects.

artículo científico publicado en 2000

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

artículo científico publicado en 2006

Vitamin B12 deficiency—need for a new guideline

artículo científico publicado en 2001

Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis

artículo científico publicado en 2017

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