Yosef Shiloh

Publication List Details

Period

1982 - 2008

Number

80

Co-Authors

Article Genome-Wide In Silico Identification of Transcriptional Regulators Controlling the Cell Cycle in (2008)

Human Cells, Ran Elkon, Chaim Linhart, Roded Sharan, Ron Shamir, Yosef Shiloh

Dissection of regulatory networks that control gene transcription is one of the greatest challenges of functional genomics. Using human genomic sequences, models for binding sites of known...

SPIKE – a database, visualization and analysis tool of cellular signaling pathways (2008)

Elkon, Ran, Vesterman, Rita, Amit, Nira, Ulitsky, Igor, Zohar, Idan, Weisz, Mali, ...

Abstract Background Biological signaling pathways that govern cellular physiology form an intricate web of tightly regulated interlocking processes. Data on these regulatory networks are accumulating...

The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression (2008)

Shema, Efrat, Tirosh, Itay, Aylon, Yael, Huang, Jing, Ye, Chaoyang, Moskovits, Neta, ...

Histone monoubiquitylation is implicated in critical regulatory processes. We explored the roles of histone H2B ubiquitylation in human cells by reducing the expression of hBRE1/RNF20, the major...

BIOINFORMATICS APPLICATIONS NOTE PIVOT: Protein Interactions VisualizatiOn Tool (2007)

Nir Orlev, Ron Shamir, Yosef Shiloh

Summary: PIVOT is a visualization tool for proteinprotein interactions. It allows the user to create personal datasets of interactions by combining information from private and public data sources....

Functional genomic delineation of TLR-induced transcriptional networks (2007)

Elkon, Ran, Linhart, Chaim, Halperin, Yonit, Shiloh, Yosef, Shamir, Ron

Abstract Background The innate immune system is the first line of defense mechanisms protecting the host from invading pathogens such as bacteria and viruses. The innate immunity responses are...

Inhibition of transforming growth factor-ß1 signaling attenuates ataxia telangiectasia mutated activity in response to genotoxic stress (2006)

Jobling, Michael F, Kirshner, Julia, Pajares, Maria Jose, Ravani, Shraddha A., Glick, Adam B., Lavin, Martin J., ...

Ionizing radiation causes DNA damage that elicits a cellular program of damage control coordinated by the kinase activity of ataxia telangiectasia mutated protein (ATM). Transforming growth factor...

Inhibition of transforming growth factor-ß1 signaling attenuates ataxia telangiectasia mutated activity in response to genotoxic stress (2006)

Jobling, Michael F, Kirshner, Julia, Pajares, Maria Jose, Ravani, Shraddha A., Glick, Adam B., Lavin, Martin J., ...

Ionizing radiation causes DNA damage that elicits a cellular program of damage control coordinated by the kinase activity of ataxia telangiectasia mutated protein (ATM). Transforming growth factor...

Inhibition of transforming growth factor-ß1 signaling attenuates ataxia telangiectasia mutated activity in response to genotoxic stress (2006)

Jobling, Michael F, Kirshner, Julia, Pajares, Maria Jose, Ravani, Shraddha A., Glick, Adam B., Lavin, Martin J., ...

Ionizing radiation causes DNA damage that elicits a cellular program of damage control coordinated by the kinase activity of ataxia telangiectasia mutated protein (ATM). Transforming growth factor...

Inhibition of transforming growth factor-ß1 signaling attenuates ataxia telangiectasia mutated activity in response to genotoxic stress (2006)

Jobling, Michael F, Kirshner, Julia, Pajares, Maria Jose, Ravani, Shraddha A., Glick, Adam B., Lavin, Martin J., ...

Ionizing radiation causes DNA damage that elicits a cellular program of damage control coordinated by the kinase activity of ataxia telangiectasia mutated protein (ATM). Transforming growth factor...

EXPANDER– an integrative program suite for microarray data analysis (2005)

Shamir, Ron, Maron-Katz, Adi, Tanay, Amos, Linhart, Chaim, Steinfeld, Israel, Sharan, Roded, ...

Abstract Background Gene expression microarrays are a prominent experimental tool in functional genomics which has opened the opportunity for gaining global, systems-level understanding of...

Dissection of a DNA-damage-induced transcriptional network using a combination of microarrays, RNA interference and computational promoter analysis (2005)

Elkon, Ran, Rashi-Elkeles, Sharon, Lerenthal, Yaniv, Linhart, Chaim, Tenne, Tamar, Amariglio, Ninette, ...

Abstract Background Gene-expression microarrays and RNA interferences (RNAi) are among the most prominent techniques in functional genomics. The combination of the two holds promise for systematic,...

Article type Software (2005)

Bmc Bioinformatics, Amos Tanay, Chaim Linhart, Roded Sharan, Ron Shamir, Adi Maron-katz, ...

This Provisional PDF corresponds to the article as it appeared upon acceptance. The fully-formatted PDF version will become available shortly after the date of publication, from the URL listed below....

Impaired genomic stability and increased oxidative stress exacerbate different features of Ataxia-telangiectasia (2005)

Ziv, Shelly, Brenner, Ori, Amariglio, Ninette, Smorodinsky, Nechama I., Galron, Ronit, Carrion, Danaise V., ...

Ataxia–telangiectasia (A-T) is a multisystem, cancer-predisposing genetic disorder caused by deficiency of the ATM protein. To dissect the A-T phenotype, we augmented specific features of the human...

Impaired genomic stability and increased oxidative stress exacerbate different features of A-T (2005)

Ziv, Shelly, Brenner, Ori, Amariglio, Ninette, Smorodinsky, Nechama I., Galron, Ronit, Carrion, Danaise V, ...

Ataxia-telangiectasia (A-T) is a multisystem, cancer-predisposing genetic disorder caused by deficiency of the ATM protein. In order to dissect the A-T phenotype, we augmented specific features of...

associated (2004)

Ran Elkon, Karen I. Zeller, Chaim Linhart, Chi V. Dang, Ron Shamir, Yosef Shiloh

silico identification of transcriptional regulators

PIVOT: protein interactions visualization tool (2004)

Orlev, Nir, Shamir, Ron, Shiloh, Yosef

Summary: PIVOT is a visualization tool for protein-protein interactions. It allows the user to create personal datasets of interactions by combining information from private and public data sources....

PIVOT: Protein Interacions VisualizatiOn Tool (2004)

Orlev, Nir, Shamir, Ron, Shiloh, Yosef

Summary: Protein Interaction VisualizatiOn Tool (PIVOT) is a visualization tool for protein–protein interactions. It allows the user to create personal data sets of interactions by combining...

In silico identification of transcriptional regulators associated with c-Myc (2004)

Elkon, Ran, Zeller, Karen I., Linhart, Chaim, Dang, Chi V., Shamir, Ron, Shiloh, Yosef

The development of powerful experimental strategies for functional genomics and accompanying computational tools has brought major advances in the delineation of transcriptional networks in organisms...

PIVOT: protein interactions visualization tool (2004)

Orlev, Nir, Shamir, Ron, Shiloh, Yosef

Summary: PIVOT is a visualization tool for protein-protein interactions. It allows the user to create personal datasets of interactions by combining information from private and public data sources....

Genome-Wide In Silico Identification of Transcriptional Regulators Controlling the Cell Cycle in Human Cells (2003)

Elkon, Ran, Linhart, Chaim, Sharan, Roded, Shamir, Ron, Shiloh, Yosef

Dissection of regulatory networks that control gene transcription is one of the greatest challenges of functional genomics. Using human genomic sequences, models for binding sites of known...

Atm Knock-in Mice Harboring an In-frame Deletion Corresponding to the Human ATM 7636del9 Common Mutation Exhibit a Variant Phenotype (2001)

Kevin Spring, Simone Cross, Chung Li, Dianne Watters, Liat Ben-Senior, Paul Waring, ...

This was the first description of a "knock-in" Atm mutant mouse. While it had overlap with Atm "knockout" mice in its phenotype it had a distinct tumorigenic phenotype and has proved a very useful...

Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotype (2001)

Spring, Kevin, Cross, Simone, Li, Chung, Watters, Dianne Josephine, Ben-Senior, Liat, Waring, Paul, ...

ATM, the gene mutated in the human immunodeficiency disorder ataxia-telangiectasia (A-T), plays a central role in recognizing ionizing radiation damage in DNA and in controlling several cell cycle...

Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotype (2001)

Spring, Kevin, Cross, Simone, Li, Chung, Watters, Dianne Josephine, Ben-Senior, Liat, Waring, Paul, ...

ATM, the gene mutated in the human immunodeficiency disorder ataxia-telangiectasia (A-T), plays a central role in recognizing ionizing radiation damage in DNA and in controlling several cell cycle...

Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotype (2001)

Spring, Kevin, Cross, Simone, Li, Chung, Watters, Dianne Josephine, Ben-Senior, Liat, Waring, Paul, ...

ATM, the gene mutated in the human immunodeficiency disorder ataxia-telangiectasia (A-T), plays a central role in recognizing ionizing radiation damage in DNA and in controlling several cell cycle...

Atm knock-in mice harboring an in-frame deletion corresponding to the human ATM 7636del9 common mutation exhibit a variant phenotype (2001)

Spring, Kevin, Cross, Simone, Li, Chung, Watters, Dianne Josephine, Ben-Senior, Liat, Waring, Paul, ...

ATM, the gene mutated in the human immunodeficiency disorder ataxia-telangiectasia (A-T), plays a central role in recognizing ionizing radiation damage in DNA and in controlling several cell cycle...

The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species (1995)

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...

Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23 (1993)

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...

Induction and repair of DNA damage in normal and ataxiatelangiectasia skin fibroblasts treated with neocarzinostatin (1983)

Shiloh, Yosef, Becker, Yechiel

Cells from patients with the hereditary multisystem disorder ataxia-telangiectasia (A-T) are hypersensitive to the cytotoxic action of DNA-breaking agents, such as X-rays, bleomycin and...

Abnormal response of ataxia-telangiectasia cells to agents that break the deoxyribose moiety of DNA via a targeted free radical mechanism (1983)

Shiloh, Yosef, Tabor, Eynat, Becker, Yachiel

A defect in DNA repair coupled to anomalous DNA synthesis after induction of certain radiogenic DNA damage is suspected to underlie the radiosensitivity of cells from patients with...

The response of ataxia-telangiectasia homozygous and heterozygous skin fibroblasts to neocarzinostatin (1982)

Shiloh, Yosef, Tabor, Eynat, Becker, Yechiel

Skin fibroblast strains from patients with ataxia-telangiectasia (A-T) were recently reported to be hypersensitive to the antitumor antibiotic neocarzinostatin (NCS). In this study, the distinct...

The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damage

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...

Selective loss of dopaminergic nigro-striatal neurons in brains of Atm-deficient mice

Eilam, Raya, Peter, Yakov, Elson, Ari, Rotman, Galit, Shiloh, Yosef, Groner, Yoram, ...

Ataxia-telangiectasia (AT) is a human disease caused by mutations in the ATM gene. The neural phenotype of AT includes progressive cerebellar neurodegeneration, which results in ataxia and eventual...

Rapid ATM-dependent phosphorylation of MDM2 precedes p53 accumulation in response to DNA damage

Khosravi, Rami, Maya, Ruth, Gottlieb, Tanya, Oren, Moshe, Shiloh, Yosef, Shkedy, Dganit

The p53 tumor-suppressor protein, a key regulator of cellular responses to genotoxic stress, is stabilized and activated after DNA damage. This process is associated with posttranslational...

Ataxia telangiectasia-mutated phosphorylates Chk2 in vivo and in vitro

Matsuoka, Shuhei, Rotman, Galit, Ogawa, Akira, Shiloh, Yosef, Tamai, Katsuyuki, Elledge, Stephen J.

The protein kinase Chk2, the mammalian homolog of the budding yeast Rad53 and fission yeast Cds1 checkpoint kinases, is phosphorylated and activated in response to DNA damage by ionizing radiation...

Jun NH2-Terminal Kinase Phosphorylation of p53 on Thr-81 Is Important for p53 Stabilization and Transcriptional Activities in Response to Stress

Buschmann, Thomas, Potapova, Olga, Bar-Shira, Anat, Ivanov, Vladimir N., Fuchs, Serge Y., Henderson, Scott, ...

The p53 tumor suppressor protein plays a key role in the regulation of stress-mediated growth arrest and apoptosis. Stress-induced phosphorylation of p53 tightly regulates its stability and...

Elevated Cu/Zn-SOD exacerbates radiation sensitivity and hematopoietic abnormalities of Atm-deficient mice

Peter, Yakov, Rotman, Galit, Lotem, Joseph, Elson, Ari, Shiloh, Yosef, Groner, Yoram

Patients with the genetic disorder ataxia-telangiectasia (A-T) display a pleiotropic phenotype that includes neurodegeneration, immunodeficiency, cancer predisposition and hypersensitivity to...

Requirement of the MRN complex for ATM activation by DNA damage

Uziel, Tamar, Lerenthal, Yaniv, Moyal, Lilach, Andegeko, Yair, Mittelman, Leonid, Shiloh, Yosef

The ATM protein kinase is a primary activator of the cellular response to DNA double-strand breaks (DSBs). In response to DSBs, ATM is activated and phosphorylates key players in various branches of...

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...

Genome-Wide In Silico Identification of Transcriptional Regulators Controlling the Cell Cycle in Human Cells

Elkon, Ran, Linhart, Chaim, Sharan, Roded, Shamir, Ron, Shiloh, Yosef

Dissection of regulatory networks that control gene transcription is one of the greatest challenges of functional genomics. Using human genomic sequences, models for binding sites of known...

In silico identification of transcriptional regulators associated with c-Myc

Elkon, Ran, Zeller, Karen I., Linhart, Chaim, Dang, Chi V., Shamir, Ron, Shiloh, Yosef

The development of powerful experimental strategies for functional genomics and accompanying computational tools has brought major advances in the delineation of transcriptional networks in organisms...

Phosphorylation of Hdmx mediates its Hdm2- and ATM-dependent degradation in response to DNA damage

Pereg, Yaron, Shkedy, Dganit, De Graaf, Petra, Meulmeester, Erik, Edelson-Averbukh, Marina, Salek, Mogjiborahman, ...

Maintenance of genomic stability depends on the DNA damage response, an extensive signaling network that is activated by DNA lesions such as double-strand breaks (DSBs). The primary activator of the...

Dissection of a DNA-damage-induced transcriptional network using a combination of microarrays, RNA interference and computational promoter analysis

Elkon, Ran, Rashi-Elkeles, Sharon, Lerenthal, Yaniv, Linhart, Chaim, Tenne, Tamar, Amariglio, Ninette, ...

Microarray and RNAi technologies were applied to dissect a transcriptional network induced by DNA damage in human cells, revealing that two pivotal stress-induced transcription factors (NFκB and...

Ionizing radiation induces ataxia telangiectasia mutated kinase (ATM)-mediated phosphorylation of LKB1/STK11 at Thr-366.

Sapkota, Gopal P, Deak, Maria, Kieloch, Agnieszka, Morrice, Nick, Goodarzi, Aaron A, Smythe, Carl, ...

The serine/threonine protein kinase LKB1 functions as a tumour suppressor, and mutations in this enzyme lead to the inherited Peutz-Jeghers cancer syndrome. We previously found that LKB1 was...

DNA Damage-Induced Phosphorylation of MdmX at Serine 367 Activates p53 by Targeting MdmX for Mdm2-Dependent Degradation†

Okamoto, Koji, Kashima, Kenji, Pereg, Yaron, Ishida, Michiko, Yamazaki, Satomi, Nota, Ayumi, ...

Understanding how p53 activity is regulated is crucial in elucidating mechanisms of cellular defense against cancer. Genetic data indicate that Mdmx as well as Mdm2 plays a major role in maintaining...

ATM-dependent phosphorylation of Mdm2 on serine 395: role in p53 activation by DNA damage

Maya, Ruth, Balass, Moshe, Kim, Seong-Tae, Shkedy, Dganit, Leal, Juan-Fernando Martinez, Shifman, Ohad, ...

The p53 tumor suppressor protein, a key regulator of cellular responses to genotoxic stress, is stabilized and activated after DNA damage. The rapid activation of p53 by ionizing radiation and...

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...

The ataxia-telangiectasia gene product, a constitutively expressed nuclear protein that is not up-regulated following genome damage

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...

Selective loss of dopaminergic nigro-striatal neurons in brains of Atm-deficient mice

Eilam, Raya, Peter, Yakov, Elson, Ari, Rotman, Galit, Shiloh, Yosef, Groner, Yoram, ...

Ataxia-telangiectasia (AT) is a human disease caused by mutations in the ATM gene. The neural phenotype of AT includes progressive cerebellar neurodegeneration, which results in ataxia and eventual...

Rapid ATM-dependent phosphorylation of MDM2 precedes p53 accumulation in response to DNA damage

Khosravi, Rami, Maya, Ruth, Gottlieb, Tanya, Oren, Moshe, Shiloh, Yosef, Shkedy, Dganit

The p53 tumor-suppressor protein, a key regulator of cellular responses to genotoxic stress, is stabilized and activated after DNA damage. This process is associated with posttranslational...

Ataxia telangiectasia-mutated phosphorylates Chk2 in vivo and in vitro

Matsuoka, Shuhei, Rotman, Galit, Ogawa, Akira, Shiloh, Yosef, Tamai, Katsuyuki, Elledge, Stephen J.

The protein kinase Chk2, the mammalian homolog of the budding yeast Rad53 and fission yeast Cds1 checkpoint kinases, is phosphorylated and activated in response to DNA damage by ionizing radiation...

Jun NH2-Terminal Kinase Phosphorylation of p53 on Thr-81 Is Important for p53 Stabilization and Transcriptional Activities in Response to Stress

Buschmann, Thomas, Potapova, Olga, Bar-Shira, Anat, Ivanov, Vladimir N., Fuchs, Serge Y., Henderson, Scott, ...

The p53 tumor suppressor protein plays a key role in the regulation of stress-mediated growth arrest and apoptosis. Stress-induced phosphorylation of p53 tightly regulates its stability and...

Elevated Cu/Zn-SOD exacerbates radiation sensitivity and hematopoietic abnormalities of Atm-deficient mice

Peter, Yakov, Rotman, Galit, Lotem, Joseph, Elson, Ari, Shiloh, Yosef, Groner, Yoram

Patients with the genetic disorder ataxia-telangiectasia (A-T) display a pleiotropic phenotype that includes neurodegeneration, immunodeficiency, cancer predisposition and hypersensitivity to...

Requirement of the MRN complex for ATM activation by DNA damage

Uziel, Tamar, Lerenthal, Yaniv, Moyal, Lilach, Andegeko, Yair, Mittelman, Leonid, Shiloh, Yosef

The ATM protein kinase is a primary activator of the cellular response to DNA double-strand breaks (DSBs). In response to DSBs, ATM is activated and phosphorylates key players in various branches of...

ATM-dependent phosphorylation of Mdm2 on serine 395: role in p53 activation by DNA damage

Maya, Ruth, Balass, Moshe, Kim, Seong-Tae, Shkedy, Dganit, Leal, Juan-Fernando Martinez, Shifman, Ohad, ...

The p53 tumor suppressor protein, a key regulator of cellular responses to genotoxic stress, is stabilized and activated after DNA damage. The rapid activation of p53 by ionizing radiation and...

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...

Genome-Wide In Silico Identification of Transcriptional Regulators Controlling the Cell Cycle in Human Cells

Elkon, Ran, Linhart, Chaim, Sharan, Roded, Shamir, Ron, Shiloh, Yosef

Dissection of regulatory networks that control gene transcription is one of the greatest challenges of functional genomics. Using human genomic sequences, models for binding sites of known...

In silico identification of transcriptional regulators associated with c-Myc

Elkon, Ran, Zeller, Karen I., Linhart, Chaim, Dang, Chi V., Shamir, Ron, Shiloh, Yosef

The development of powerful experimental strategies for functional genomics and accompanying computational tools has brought major advances in the delineation of transcriptional networks in organisms...

Phosphorylation of Hdmx mediates its Hdm2- and ATM-dependent degradation in response to DNA damage

Pereg, Yaron, Shkedy, Dganit, De Graaf, Petra, Meulmeester, Erik, Edelson-Averbukh, Marina, Salek, Mogjiborahman, ...

Maintenance of genomic stability depends on the DNA damage response, an extensive signaling network that is activated by DNA lesions such as double-strand breaks (DSBs). The primary activator of the...

Dissection of a DNA-damage-induced transcriptional network using a combination of microarrays, RNA interference and computational promoter analysis

Elkon, Ran, Rashi-Elkeles, Sharon, Lerenthal, Yaniv, Linhart, Chaim, Tenne, Tamar, Amariglio, Ninette, ...

Microarray and RNAi technologies were applied to dissect a transcriptional network induced by DNA damage in human cells, revealing that two pivotal stress-induced transcription factors (NFκB and...

Ionizing radiation induces ataxia telangiectasia mutated kinase (ATM)-mediated phosphorylation of LKB1/STK11 at Thr-366.

Sapkota, Gopal P, Deak, Maria, Kieloch, Agnieszka, Morrice, Nick, Goodarzi, Aaron A, Smythe, Carl, ...

The serine/threonine protein kinase LKB1 functions as a tumour suppressor, and mutations in this enzyme lead to the inherited Peutz-Jeghers cancer syndrome. We previously found that LKB1 was...

DNA Damage-Induced Phosphorylation of MdmX at Serine 367 Activates p53 by Targeting MdmX for Mdm2-Dependent Degradation†

Okamoto, Koji, Kashima, Kenji, Pereg, Yaron, Ishida, Michiko, Yamazaki, Satomi, Nota, Ayumi, ...

Understanding how p53 activity is regulated is crucial in elucidating mechanisms of cellular defense against cancer. Genetic data indicate that Mdmx as well as Mdm2 plays a major role in maintaining...

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...

Differential Roles of ATM- and Chk2-Mediated Phosphorylations of Hdmx in Response to DNA Damage†

Pereg, Yaron, Lam, Suzanne, Teunisse, Amina, Biton, Sharon, Meulmeester, Erik, Mittelman, Leonid, ...

The p53 tumor suppressor plays a major role in maintaining genomic stability. Its activation and stabilization in response to double strand breaks (DSBs) in DNA are regulated primarily by the ATM...

Localization of an Ataxia-Telangiectasia Gene to an −500-kb Interval on Chromosome 11q23.1: Linkage Analysis of 176 Families by an International Consortium

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)...

Condensin I recruitment and uneven chromatin condensation precede mitotic cell death in response to DNA damage

Blank, Michael, Lerenthal, Yaniv, Mittelman, Leonid, Shiloh, Yosef

Mitotic cell death (MCD) is a prominent but poorly defined form of death that stems from aberrant mitosis. One of the early steps in MCD is premature mitosis and uneven chromatin condensation (UCC)....

WRN Is Required for ATM Activation and the S-Phase Checkpoint in Response to Interstrand Cross-Link–Induced DNA Double-Strand Breaks

Cheng, Wen-Hsing, Muftic, Diana, Muftuoglu, Meltem, Dawut, Lale, Morris, Christa, Helleday, Thomas, ...

Werner syndrome (WS) is a human genetic disorder characterized by extensive clinical features of premature aging. Ataxia-telengiectasia (A-T) is a multisystem human genomic instability syndrome that...

The histone H2B-specific ubiquitin ligase RNF20/hBRE1 acts as a putative tumor suppressor through selective regulation of gene expression

Shema, Efrat, Tirosh, Itay, Aylon, Yael, Huang, Jing, Ye, Chaoyang, Moskovits, Neta, ...

Histone monoubiquitylation is implicated in critical regulatory processes. We explored the roles of histone H2B ubiquitylation in human cells by reducing the expression of hBRE1/RNF20, the major...