Published in Biochem Biophys Res Commun on May 02, 2003
Mapping human genetic diversity in Asia. Science (2009) 7.40
Selection and evaluation of tagging SNPs in the neuronal-sodium-channel gene SCN1A: implications for linkage-disequilibrium gene mapping. Am J Hum Genet (2003) 4.58
High incidence of allelic loss at 16q12.2 region spanning RBL2/p130 gene in retinoblastoma. Cancer Biol Ther (2009) 1.47
Anti-inflammatory effects of mitogen-activated protein kinase kinase inhibitor U0126 in an asthma mouse model. J Immunol (2004) 1.46
The contributions of oxytocin and vasopressin pathway genes to human behavior. Horm Behav (2011) 1.40
Spinal muscular atrophy: from gene discovery to clinical trials. Ann Hum Genet (2013) 1.15
Inhaled p38alpha mitogen-activated protein kinase antisense oligonucleotide attenuates asthma in mice. Am J Respir Crit Care Med (2004) 1.11
Dynamics of co-transcriptional pre-mRNA folding influences the induction of dystrophin exon skipping by antisense oligonucleotides. PLoS One (2008) 1.09
Reduced transcriptional activity in individuals with IL-18 gene variants detected from functional but not association study. Biochem Biophys Res Commun (2005) 1.04
Energy homeostasis and cachexia in chronic kidney disease. Pediatr Nephrol (2006) 0.93
Mechanisms of disease: Cytokine and adipokine signaling in uremic cachexia. Nat Clin Pract Nephrol (2006) 0.90
Cachexia in chronic kidney disease: role of inflammation and neuropeptide signaling. Curr Opin Nephrol Hypertens (2007) 0.90
Galpha(16/z) chimeras efficiently link a wide range of G protein-coupled receptors to calcium mobilization. J Biomol Screen (2003) 0.90
Orexigenic and anorexigenic mechanisms in the control of nutrition in chronic kidney disease. Pediatr Nephrol (2005) 0.90
Interleukin-13 genetic polymorphisms in Singapore Chinese children correlate with long-term outcome of minimal-change disease. Nephrol Dial Transplant (2005) 0.88
U-shaped relation between plasma oxytocin levels and behavior in the trust game. PLoS One (2012) 0.88
Dopaminergic polymorphisms associated with time-on-task declines and fatigue in the Psychomotor Vigilance Test. PLoS One (2012) 0.87
A prospective study in the rational design of efficient antisense oligonucleotides for exon skipping in the DMD gene. Hum Gene Ther (2012) 0.86
CD14 promoter polymorphisms have no functional significance and are not associated with atopic phenotypes. Pharmacogenet Genomics (2006) 0.85
Adipokines and gut hormones in end-stage renal disease. Perit Dial Int (2007) 0.84
Hepatitis B surface antigen carrier status and its correlation to gestational hypertension. Aust N Z J Obstet Gynaecol (2003) 0.84
Identification and characterisation of human dysferlin transcript variants: implications for dysferlin mutational screening and isoforms. Hum Genet (2009) 0.84
Inhibitors of tyrosine kinase signaling cascade attenuated antigen challenge of guinea-pig airways in vitro. Am J Respir Crit Care Med (2000) 0.83
A randomised comparison of side effects and patient inconvenience of two vaginal progesterone formulations used for luteal support in in vitro fertilisation cycles. Eur J Obstet Gynecol Reprod Biol (2003) 0.83
Paramyotonia congenita: from clinical diagnosis to in silico protein modeling analysis. Pediatr Int (2012) 0.81
Automated DNA mutation detection using universal conditions direct sequencing: application to ten muscular dystrophy genes. BMC Genet (2009) 0.81
Inhibitors of the tyrosine kinase signaling cascade attenuated thrombin-induced guinea pig airway smooth muscle cell proliferation. Biochem Biophys Res Commun (2002) 0.81
Identification and characterization of a novel human dysferlin transcript: dysferlin_v1. Hum Genet (2006) 0.80
Ghrelin in chronic kidney disease: too much or too little? Perit Dial Int (2006) 0.80
Influence of extracellular matrix proteins and substratum topography on corneal epithelial cell alignment and migration. Tissue Eng Part A (2013) 0.80
Absence of the toll-like receptor 4 gene polymorphisms Asp299Gly and Thr399Ile in Singaporean Chinese. Ther Clin Risk Manag (2005) 0.79
Dimeric gold nanoparticle assembly for detection and discrimination of single nucleotide mutation in Duchenne muscular dystrophy. Biosens Bioelectron (2010) 0.79
Therapeutic strategy for cachexia in chronic kidney disease. Curr Opin Nephrol Hypertens (2007) 0.78
Identification of a stretch of six divergent amino acids on the alpha5 helix of Galpha16 as a major determinant of the promiscuity and efficiency of receptor coupling. Biochem J (2004) 0.78
Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions. Expert Rev Mol Diagn (2005) 0.77
Replacement of the alpha5 helix of Galpha16 with Galphas-specific sequences enhances promiscuity of Galpha16 toward Gs-coupled receptors. Cell Signal (2004) 0.77
Intramural pregnancy. J Am Assoc Gynecol Laparosc (2004) 0.75
Diagnostic strategy for the detection of dystrophin gene mutations in asian patients and carriers using immortalized cell lines. J Child Neurol (2006) 0.75
Oral mini-implants to facilitate orthodontic movement of teeth. Dent Today (2007) 0.75
Efficient mining of haplotype patterns for linkage disequilibrium mapping. J Bioinform Comput Biol (2010) 0.75