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Nature Genetics|December 18, 2001
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21Rachel V Baxter, Kamel Ben Othmane, Julie M Rochelle, et al.Nature Genetics|June 29, 2002
Crossover clustering and rapid decay of linkage disequilibrium in the Xp/Yp pseudoautosomal gene SHOXCelia A May, Angela C Shone, Luba Kalaydjieva, et al.Nature Genetics|June 29, 2002
Deletion in Catna2, encoding alpha N-catenin, causes cerebellar and hippocampal lamination defects and impaired startle modulationChankyu Park, William Falls, Jacqueline H Finger, et al.Nature Genetics|June 18, 2002
Radixin deficiency causes conjugated hyperbilirubinemia with loss of Mrp2 from bile canalicular membranesShojiro Kikuchi, Masaki Hata, Kanehisa Fukumoto, et al.Nature Genetics|June 18, 2002
Mitochondrial transcription factors B1 and B2 activate transcription of human mtDNAMaria Falkenberg, Martina Gaspari, Anja Rantanen, et al.Nature Genetics|June 18, 2002
Mutations in SUFU predispose to medulloblastomaMichael D Taylor, Ling Liu, Corey Raffel, et al.Nature Genetics|May 22, 2002
Amplification of PPM1D in human tumors abrogates p53 tumor-suppressor activityDmitry V Bulavin, Oleg N Demidov, Shin'ichi Saito, et al.Nature Genetics|July 23, 2002
PP1 binds Sara and negatively regulates Dpp signaling in Drosophila melanogasterDaimark Bennett, Luke AlpheyNature Genetics|July 2, 2002
Uncontrolled C3 activation causes membranoproliferative glomerulonephritis in mice deficient in complement factor HMatthew C Pickering, H Terence Cook, Joanna Warren, et al.Nature Genetics|September 10, 2002
Evidence for two apoptotic pathways in light-induced retinal degenerationWenshan Hao, Andreas Wenzel, Martin S Obin, et al.Pageof 744