Centering, Global Focus, and Right Dislocation (2007)
this paper, we demonstrate that centering can also aid in explaining a particular syntactic structure, right dislocation (henceforth, RD). RD
Defective potassium currents in ataxia telangiectasia fibroblasts (1998)
Rhodes, Nelson, D'Souza, Theresa, Foster, Christine D., Ziv, Yael, Kirsch, David G., Shiloh, Yosef, ...
Savitsky, Kinneret, Sfez, Sharon, Tagle, Danilo A., Ziv, Yael, Sartiel, Adam, Collins, Francis S., ...
Ataxia-telangiectasia (A-T) is an autosomal recessive disorder involving cerebellar degeneration, immunodeficiency, radiation sensitivity, and cancer predisposition. A-T heterozygotes are moderately...
M.McConville, Carmel, J.Byrd, Philip, J.Ambrose, Helen, Stankovic, Tanja, Ziv, Yael, Bar-Shira, Anat, ...
The high resolution mapping of the ataxia telangiectasia (A-T) locus on chromosome 11q22–23 requires the generation of new polymorphic markers specifically within the segment of 11q22–23 to which...
Vita.
Brown, Kevin D., Ziv, Yael, Sadanandan, Sunanda N., Chessa, Luciana, Collins, Francis S., Shiloh, Yosef, ...
The product of the ataxia-telangiectasia gene (ATM) was identified by using an antiserum developed to a peptide corresponding to the deduced amino acid sequence. The ATM protein is a single,...
ATM binds to β-adaptin in cytoplasmic vesicles
Lim, Dae-Sik, Kirsch, David G., Canman, Christine E., Ahn, Jin-Hyun, Ziv, Yael, Newman, Lori S., ...
Inherited mutations in the ATM gene lead to a complex clinical phenotype characterized by neuronal degeneration, oculocutaneous telangiectasias, immune dysfunction, and cancer predisposition. Using...
Defective potassium currents in ataxia telangiectasia fibroblasts
Rhodes, Nelson, D’Souza, Theresa, Foster, Christine D., Ziv, Yael, Kirsch, David G., Shiloh, Yosef, ...
Similarities exist between the progressive cerebellar ataxia in ataxia telangiectasia (AT) patients and a number of neurodegenerative diseases in both mouse and man involving specific mutations in...
Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.1
Shiloh, Yosef, Litvak, Gilad, Ziv, Yael, Lehner, Thomas, Sandkuyl, Lodewijk, Hildesheimer, Minka, ...
X-linked albinism-deafness syndrome (ADFN) was described in one Israeli Jewish family and is characterized by congenital nerve deafness and piebaldness. The ADFN mutation probably affects the...
Brown, Kevin D., Ziv, Yael, Sadanandan, Sunanda N., Chessa, Luciana, Collins, Francis S., Shiloh, Yosef, ...
The product of the ataxia-telangiectasia gene (ATM) was identified by using an antiserum developed to a peptide corresponding to the deduced amino acid sequence. The ATM protein is a single,...
ATM binds to β-adaptin in cytoplasmic vesicles
Lim, Dae-Sik, Kirsch, David G., Canman, Christine E., Ahn, Jin-Hyun, Ziv, Yael, Newman, Lori S., ...
Inherited mutations in the ATM gene lead to a complex clinical phenotype characterized by neuronal degeneration, oculocutaneous telangiectasias, immune dysfunction, and cancer predisposition. Using...
Defective potassium currents in ataxia telangiectasia fibroblasts
Rhodes, Nelson, D’Souza, Theresa, Foster, Christine D., Ziv, Yael, Kirsch, David G., Shiloh, Yosef, ...
Similarities exist between the progressive cerebellar ataxia in ataxia telangiectasia (AT) patients and a number of neurodegenerative diseases in both mouse and man involving specific mutations in...
Genetic mapping of X-linked albinism-deafness syndrome (ADFN) to Xq26.3-q27.1
Shiloh, Yosef, Litvak, Gilad, Ziv, Yael, Lehner, Thomas, Sandkuyl, Lodewijk, Hildesheimer, Minka, ...
X-linked albinism-deafness syndrome (ADFN) was described in one Israeli Jewish family and is characterized by congenital nerve deafness and piebaldness. The ADFN mutation probably affects the...
Lange, Ethan, Borresen, Anna-Lise, Chen, Xiaoguang, Chessa, Luciana, Chiplunkar, Sujata, Concannon, Patrick, ...
We describe a 20-point linkage analysis map of chromosome 11q22-23 that is based on genotyping 249 families (59 CEPH and 190 A-T). Monte Carlo linkage analyses of 176 ataxia-telangiectasia (A-T)...