Showing results (2391-2400 of 7,438) with videos related to
Sort By:
Pageof 744
Nature Genetics|March 31, 2000
Human LINE retrotransposons generate processed pseudogenesC Esnault, J Maestre, T HeidmannNature Genetics|March 31, 2000
Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossificationA O Wilkie, Z Tang, N Elanko, et al.Nature Genetics|March 31, 2000
The direction of microsatellite mutations is dependent upon allele lengthX Xu, M Peng, Z FangNature Genetics|March 31, 2000
Mice deficient for corticotropin-releasing hormone receptor-2 display anxiety-like behaviour and are hypersensitive to stressT L Bale, A Contarino, G W Smith, et al.Nature Genetics|March 31, 2000
Deletion of crhr2 reveals an anxiolytic role for corticotropin-releasing hormone receptor-2T Kishimoto, J Radulovic, M Radulovic, et al.Nature Genetics|March 31, 2000
The SH2 tyrosine phosphatase shp2 is required for mammalian limb developmentT M Saxton, B G Ciruna, D Holmyard, et al.Nature Genetics|October 3, 1999
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2R E Amir, I B Van den Veyver, M Wan, et al.Nature Genetics|October 3, 1999
Disruption of the mouse necdin gene results in early post-natal lethalityM Gérard, L Hernandez, R Wevrick, et al.Nature Genetics|October 3, 1999
Repression of the gene encoding the TGF-beta type II receptor is a major target of the EWS-FLI1 oncoproteinK B Hahm, K Cho, C Lee, et al.Pageof 744