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Nature Genetics|March 31, 2000
NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndromeN Boute, O Gribouval, S Roselli, et al.Nature Genetics|March 31, 2000
Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cellsH Niwa, J Miyazaki, A G SmithNature Genetics|February 15, 2001
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositsH Puccio, D Simon, M Cossée, et al.Nature Genetics|February 15, 2001
Linkage disequilibrium of a type 1 diabetes susceptibility locus with a regulatory IL12B alleleG Morahan, D Huang, S I Ymer, et al.Nature Genetics|May 13, 1999
Action of BTN1, the yeast orthologue of the gene mutated in Batten diseaseD A Pearce, T Ferea, S A Nosel, et al.Nature Genetics|May 13, 1999
Inactivating mutations and overexpression of BCL10, a caspase recruitment domain-containing gene, in MALT lymphoma with t(1;14)(p22;q32)Q Zhang, R Siebert, M Yan, et al.Nature Genetics|May 13, 1999
Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cellsB Coffee, F Zhang, S T Warren, et al.Nature Genetics|May 13, 1999
Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusionsS Engelender, Z Kaminsky, X Guo, et al.Nature Genetics|March 31, 2000
Abnormal adaptations to stress and impaired cardiovascular function in mice lacking corticotropin-releasing hormone receptor-2S C Coste, R A Kesterson, K A Heldwein, et al.Nature Genetics|March 31, 2000
Stereocilia defects in the sensory hair cells of the inner ear in mice deficient in integrin alpha8beta1A Littlewood Evans, U MüllerPageof 743