Common variation in GPC5 is associated with acquired nephrotic syndrome
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PodocytesOpportunities and Challenges of Genotyping Patients With Nephrotic Syndrome in the Genomic EraPathophysiology of heparan sulphate: many diseases, few drugsCell biology and pathology of podocytesCrystal Structure of N -Glycosylated Human Glypican-1 Core ProteinCalcium regulates podocyte actin dynamics.Insights into the key roles of proteoglycans in breast cancer biology and translational medicineGenome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of FallotOverview of BioBank Japan follow-up data in 32 diseases.Glypican-5 Increases Susceptibility to Nephrotic Damage in Diabetic Kidney.Defining nephrotic syndrome from an integrative genomics perspective.Fine-mapping additive and dominant SNP effects using group-LASSO and fractional resample model averaging.Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancers.HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic SyndromeGLCCI1 single nucleotide polymorphisms in pediatric nephrotic syndrome.Analysis of cascading failure in gene networksAn introduction to proteoglycans and their localizationFishing for biliary atresia susceptibility genes.Single Nucleotide Polymorphisms in Pediatric Idiopathic Nephrotic Syndrome.The Genetics of Nephrotic Syndrome.Actualizing the Benefits of Genomic Discovery in Pediatric Nephrology.Genes, Exomes, Genomes, Copy Number: What is Their Future in Pediatric Renal Disease.Physiopathology of idiopathic nephrotic syndrome: lessons from glucocorticoids and epigenetic perspectives.Balancing calcium signals through TRPC5 and TRPC6 in podocytes.New developments in steroid-resistant nephrotic syndrome.Animal models of nephrotic syndrome.Signal transduction in podocytes--spotlight on receptor tyrosine kinases.Human genetics of nephrotic syndrome and the quest for precision medicine.Lessons from Genome-Wide Search for Disease-Related Genes with Special Reference to HLA-Disease Associations.A targeted functional RNA interference screen uncovers glypican 5 as an entry factor for hepatitis B and D viruses.Association between CCDC132, FDX1 and TNFSF13 gene polymorphisms and the risk of IgA nephropathy.An inducible mouse model of podocin-mutation-related nephrotic syndrome.GPC5 rs2352028 polymorphism and risk of lung cancer in Han Chinese.Genetic testing in steroid-resistant nephrotic syndrome: why, who, when and how?Lessons from CKD-Related Genetic Association Studies-Moving Forward.A Drosophila model system to assess the function of human monogenic podocyte mutations that cause nephrotic syndrome.Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies
P2860
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P2860
Common variation in GPC5 is associated with acquired nephrotic syndrome
description
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
articolo scientifico
@it
artículu científicu espublizáu en 2011
@ast
im Mai 2011 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2011/05/01)
@nl
наукова стаття, опублікована в травні 2011
@uk
مقالة علمية (نشرت في مايو 2011)
@ar
name
Common variation in GPC5 is associated with acquired nephrotic syndrome
@ast
Common variation in GPC5 is associated with acquired nephrotic syndrome
@en
type
label
Common variation in GPC5 is associated with acquired nephrotic syndrome
@ast
Common variation in GPC5 is associated with acquired nephrotic syndrome
@en
prefLabel
Common variation in GPC5 is associated with acquired nephrotic syndrome
@ast
Common variation in GPC5 is associated with acquired nephrotic syndrome
@en
P2093
P2860
P3181
P356
P1433
P1476
Common variation in GPC5 is associated with acquired nephrotic syndrome
@en
P2093
Akihiko Mabuchi
Atsushi Takahashi
Hodaka Suzuki
Katsushi Tokunaga
Koji Okamoto
Michiaki Kubo
Nao Nishida
Shiro Maeda
Tetsuo Katoh
P2860
P2888
P304
P3181
P356
10.1038/NG.792
P407
P50
P577
2011-03-27T00:00:00Z