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American Journal of Human Genetics
|
July 1, 1990
Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I
Y Shiloh, G Litvak, Y Ziv, et al.
Genes & Development
|
December 16, 1998
Defective potassium currents in ataxia telangiectasia fibroblasts
N Rhodes, T D'Souza, C D Foster, et al.
Science (New York, N.Y.)
|
September 11, 1998
Enhanced phosphorylation of p53 by ATM in response to DNA damage
S Banin, L Moyal, S Shieh, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 26, 1998
ATM binds to beta-adaptin in cytoplasmic vesicles
D S Lim, D G Kirsch, C E Canman, et al.
Human Molecular Genetics
|
July 1, 1993
Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23
C M McConville, P J Byrd, H J Ambrose, et al.
Rejuvenation Research
|
September 23, 2008
Age-dependent spatial memory loss can be partially restored by immune activation
N Ron-Harel, Y Segev, G M Lewitus, et al.
Human Mutation
|
February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel
S Gilad, R Khosravi, R Harnik, et al.
Somatic Cell and Molecular Genetics
|
March 1, 1995
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cells
Y Ziv, A Bar-Shira, T J Jorgensen, et al.
The Journal of Biological Chemistry
|
May 10, 2000
Utilization of oriented peptide libraries to identify substrate motifs selected by ATM
T O'Neill, A J Dwyer, Y Ziv, 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 syndrome
Y Ziv, M Frydman, E Lange, et al.
Page
of 12
Search research articles
Search
Showing results (91-100 of 112) with videos related to
Sort By:
Page
of 12
American Journal of Human Genetics
|
July 1, 1990
Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.I
Y Shiloh, G Litvak, Y Ziv, et al.
Genes & Development
|
December 16, 1998
Defective potassium currents in ataxia telangiectasia fibroblasts
N Rhodes, T D'Souza, C D Foster, et al.
Science (New York, N.Y.)
|
September 11, 1998
Enhanced phosphorylation of p53 by ATM in response to DNA damage
S Banin, L Moyal, S Shieh, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 26, 1998
ATM binds to beta-adaptin in cytoplasmic vesicles
D S Lim, D G Kirsch, C E Canman, et al.
Human Molecular Genetics
|
July 1, 1993
Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23
C M McConville, P J Byrd, H J Ambrose, et al.
Rejuvenation Research
|
September 23, 2008
Age-dependent spatial memory loss can be partially restored by immune activation
N Ron-Harel, Y Segev, G M Lewitus, et al.
Human Mutation
|
February 5, 1998
Identification of ATM mutations using extended RT-PCR and restriction endonuclease fingerprinting, and elucidation of the repertoire of A-T mutations in Israel
S Gilad, R Khosravi, R Harnik, et al.
Somatic Cell and Molecular Genetics
|
March 1, 1995
Human cDNA clones that modify radiomimetic sensitivity of ataxia-telangiectasia (group A) cells
Y Ziv, A Bar-Shira, T J Jorgensen, et al.
The Journal of Biological Chemistry
|
May 10, 2000
Utilization of oriented peptide libraries to identify substrate motifs selected by ATM
T O'Neill, A J Dwyer, Y Ziv, 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 syndrome
Y Ziv, M Frydman, E Lange, et al.
Page
of 12