Rare mutations associating with serum creatinine and chronic kidney disease

A novel RING finger E3 ligase RNF186 regulate ER stress-mediated apoptosis through interaction with BNip1

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Evolving importance of kidney disease: from subspecialty to global health burden

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The ABCs of membrane transporters in health and disease (SLC series): Introduction

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Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits

(2013) Unnur Styrkarsdottir et al.   NATURE

The Ubiquitin Code

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Twelve Transmembrane Helices Form the Functional Core of Mammalian MATE1 (Multidrug and Toxin Extruder 1) Protein

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The mitochondrial transporter family SLC25: Identification, properties and physiopathology

(2012) Ferdinando Palmieri   MOLECULAR ASPECTS OF MEDICINE

Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations

(2012) Yukinori Okada et al.   NATURE GENETICS

What is the evidence for heterozygote advantage selection?

(2012) Philip W. Hedrick   TRENDS IN ECOLOGY & EVOLUTION

Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function

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NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy

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Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

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Potent and Specific Inhibition of mMate1-Mediated Efflux of Type I Organic Cations in the Liver and Kidney by Pyrimethamine

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The definition, classification, and prognosis of chronic kidney disease: a KDIGO Controversies Conference report

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New loci associated with kidney function and chronic kidney disease

(2010) Anna Köttgen et al.   NATURE GENETICS

Genetic loci influencing kidney function and chronic kidney disease

(2010) John C Chambers et al.   NATURE GENETICS

Association of Variants at UMOD with Chronic Kidney Disease and Kidney Stones—Role of Age and Comorbid Diseases

(2010) Daniel F. Gudbjartsson et al.   PLoS Genetics

RING Finger E3 Ubiquitin Ligases: Structure and Drug Discovery

(2009) Christos Chasapis et al.   CURRENT PHARMACEUTICAL DESIGN

The role of the neutral amino acid transporter B0AT1 (SLC6A19) in Hartnup disorder and protein nutrition

(2009) Stefan Bröer   IUBMB LIFE

Targeted Disruption of the Multidrug and Toxin Extrusion 1 (Mate1) Gene in Mice Reduces Renal Secretion of Metformin

(2009) M. Tsuda et al.   MOLECULAR PHARMACOLOGY

Multiple loci associated with indices of renal function and chronic kidney disease

(2009) Anna Köttgen et al.   NATURE GENETICS

Genetic variants in multidrug and toxic compound extrusion-1, hMATE1, alter transport function

(2009) Ying Chen et al.   PHARMACOGENOMICS JOURNAL

Tissue-Specific Amino Acid Transporter Partners ACE2 and Collectrin Differentially Interact With Hartnup Mutations

(2008) Simone M.R. Camargo et al.   GASTROENTEROLOGY

The Single Subunit Transmembrane E3 Ligase Gene Related to Anergy in Lymphocytes (GRAIL) Captures and Then Ubiquitinates Transmembrane Proteins across the Cell Membrane

(2008) Neil Lineberry et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Role of the E3 ubiquitin ligase gene related to anergy in lymphocytes in glucose and lipid metabolism in the liver

(2008) Sachie Nakamichi et al.   JOURNAL OF MOLECULAR ENDOCRINOLOGY

Detection of sharing by descent, long-range phasing and haplotype imputation

(2008) Augustine Kong et al.   NATURE GENETICS