Showing results (6091-6100 of 7,441) with videos related to
Sort By:
Pageof 745
Nature Genetics|September 6, 2000
Pidd, a new death-domain-containing protein, is induced by p53 and promotes apoptosisY Lin, W Ma, S BenchimolNature Genetics|October 4, 2000
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitusY Horikawa, N Oda, N J Cox, et al.Nature Genetics|October 4, 2000
Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotesK Inoue, K Nakada, A Ogura, et al.Nature Genetics|October 4, 2000
OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28C Alexander, M Votruba, U E Pesch, et al.Nature Genetics|October 4, 2000
Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase geneT O Akama, K Nishida, J Nakayama, et al.Nature Genetics|August 10, 2000
Mesp2 initiates somite segmentation through the Notch signalling pathwayY Takahashi, K Koizumi, A Takagi, et al.Nature Genetics|August 10, 2000
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndromeH van Bokhoven, J Celli, H Kayserili, et al.Nature Genetics|August 10, 2000
Insertion of Inhbb into the Inhba locus rescues the Inhba-null phenotype and reveals new activin functionsC W Brown, D E Houston-Hawkins, T K Woodruff, et al.Nature Genetics|April 7, 1999
A common human skin tumour is caused by activating mutations in beta-cateninE F Chan, U Gat, J M McNiff, et al.Nature Genetics|April 7, 1999
Identification of the gene responsible for gelatinous drop-like corneal dystrophyM Tsujikawa, H Kurahashi, T Tanaka, et al.Pageof 745