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Nature Genetics|September 6, 2000
Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcriptionT Shimohata, T Nakajima, M Yamada, et al.Nature Genetics|September 6, 2000
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C geneM Bitner-Glindzicz, K J Lindley, P Rutland, et al.Nature Genetics|September 6, 2000
Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndromeN Katsanis, P L Beales, M O Woods, et al.Nature Genetics|September 6, 2000
The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesD Altshuler, J N Hirschhorn, M Klannemark, et al.Nature Genetics|September 6, 2000
Heterozygous germline mutations in BMPR2, encoding a TGF-beta receptor, cause familial primary pulmonary hypertension, K B Lane, R D Machado, et al.Nature Genetics|September 6, 2000
Telomere dysfunction impairs DNA repair and enhances sensitivity to ionizing radiationK K Wong, S Chang, S R Weiler, et al.Nature Genetics|September 6, 2000
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutationsS E Hong, Y Y Shugart, D T Huang, et al.Nature Genetics|September 6, 2000
Telomerase-deficient mice with short telomeres are resistant to skin tumorigenesisE González-Suárez, E Samper, J M Flores, et al.Nature Genetics|August 31, 2001
PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patientsL F Barcellos, S Caillier, L Dragone, et al.Nature Genetics|August 31, 2001
Comparable system-level organization of Archaea and EukaryotesJ Podani, Z N Oltvai, H Jeong, et al.Pageof 743