DNA microarrays: a powerful genomic tool for biomedical and clinical research

V Trevino, F Falciani, HA Barrera-Saldaña - Molecular medicine, 2007 - Springer
Among the many benefits of the Human Genome Project are new and powerful tools such as
the genome-wide hybridization devices referred to as microarrays. Initially designed to …

Network pharmacology studies on the bioactive compounds and action mechanisms of natural products for the treatment of diabetes mellitus: a review

W Li, G Yuan, Y Pan, C Wang, H Chen - Frontiers in Pharmacology, 2017 - frontiersin.org
Diabetes mellitus (DM) is a kind of chronic and metabolic disease, which can cause a
number of diseases and severe complications. Network pharmacology approach is …

Human protein reference database—2009 update

TS Keshava Prasad, R Goel, K Kandasamy… - Nucleic acids …, 2009 - academic.oup.com
Abstract Human Protein Reference Database (HPRD—http://www. hprd. org/), initially
described in 2003, is a database of curated proteomic information pertaining to human …

[HTML][HTML] Human protein reference database—2009 update

TSK Prasad, R Goel, K Kandasamy… - Nucleic acids …, 2009 - ncbi.nlm.nih.gov
Abstract Human Protein Reference Database (HPRD—http://www. hprd. org/), initially
described in 2003, is a database of curated proteomic information pertaining to human …

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

JA Todd, NM Walker, JD Cooper, DJ Smyth… - Nature …, 2007 - nature.com
Abstract The Wellcome Trust Case Control Consortium (WTCCC) primary genome-wide
association (GWA) scan on seven diseases, including the multifactorial autoimmune disease …

IthaGenes: an interactive database for haemoglobin variations and epidemiology

P Kountouris, CW Lederer, P Fanis, X Feleki, J Old… - PloS one, 2014 - journals.plos.org
Inherited haemoglobinopathies are the most common monogenic diseases, with millions of
carriers and patients worldwide. At present, we know several hundred disease-causing …

Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases

HC So, AHS Gui, SS Cherny, PC Sham - Genetic epidemiology, 2011 - Wiley Online Library
Recently, an increasing number of susceptibility variants have been identified for complex
diseases. At the same time, the concern of “missing heritability” has also emerged. There is …

Human Protein Reference Database and Human Proteinpedia as discovery tools for systems biology

TSK Prasad, K Kandasamy, A Pandey - Reverse Chemical Genetics …, 2009 - Springer
Although high-throughput technologies used in biology have resulted in the accumulation of
vast amounts of data in the literature, it is becoming difficult for individual investigators to …

PTPN2, a candidate gene for type 1 diabetes, modulates interferon-γ–induced pancreatic β-cell apoptosis

F Moore, ML Colli, M Cnop, MI Esteve, AK Cardozo… - Diabetes, 2009 - Am Diabetes Assoc
OBJECTIVE The pathogenesis of type 1 diabetes has a strong genetic component. Genome-
wide association scans recently identified novel susceptibility genes including the …

Confirmation of HLA class II independent type 1 diabetes associations in the major histocompatibility complex including HLA‐B and HLA‐A

JMM Howson, NM Walker, D Clayton… - Diabetes, Obesity …, 2009 - Wiley Online Library
Aim: Until recently, human leucocyte antigen (HLA) class II‐independent associations with
type 1 diabetes (T1D) in the Major Histocompatibility Complex (MHC) region were not …