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Genes & Development|May 2, 2001
ATM-dependent phosphorylation of Mdm2 on serine 395: role in p53 activation by DNA damageR Maya, M Balass, S T Kim, et al.The Journal of Biological Chemistry|May 10, 2000
Utilization of oriented peptide libraries to identify substrate motifs selected by ATMT O'Neill, A J Dwyer, Y Ziv, et al.Human Genetics|September 1, 1997
The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samplesF Calì, I Dianzani, L R Desviat, et al.Human Genetics|March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndromeY Ziv, M Frydman, E Lange, et al.Genomics|July 1, 1994
Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23L Vanagaite, K Savitsky, G Rotman, et al.Human Molecular Genetics|December 1, 1996
Ataxia-telangiectasia: founder effect among north African JewsS Gilad, A Bar-Shira, R Harnik, et al.Nature|May 29, 1997
Interaction between ATM protein and c-Abl in response to DNA damageT Shafman, K K Khanna, P Kedar, et al.Human Genetics|April 1, 1995
A high-density microsatellite map of the ataxia-telangiectasia locusL Vanagaite, M R James, G Rotman, et al.Human Mutation|October 29, 1998
Ataxia-telangiectasia in the Japanese population: identification of R1917X, W2491R, R2909G, IVS33+2T-->A, and 7883del5, the latter two being relatively common mutationsT Fukao, X Q Song, T Yoshida, et al.Cancer Research|June 5, 2001
Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotypeK Spring, S Cross, C Li, et al.Pageof 13