(Q24305550)

identical protein binding

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author name string

Baomin Li

1

0 references

Sonia Navarro

2

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Noriyuki Kasahara

3

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Lucio Comai

Journal of Biological Chemistry

4

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language of work or name

English

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publication date

2 April 2004

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published in

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volume

279

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issue

14

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page(s)

13659-67

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cites work

A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The premature ageing syndromes: insights into the ageing process

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Mutator phenotype of Werner syndrome is characterized by extensive deletions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

RecQ family helicases: roles in cancer and aging

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The proofreading domain of Escherichia coli DNA polymerase I and other DNA and/or RNA exonuclease domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Werner helicase is localized to transcriptionally active nucleoli of cycling cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The premature ageing syndrome protein, WRN, is a 3'-->5' exonuclease

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Werner syndrome protein. I. DNA helicase and dna exonuclease reside on the same polypeptide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence and stimulation by replication protein A

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Werner syndrome helicase contains a 5'-->3' exonuclease activity that digests DNA and RNA strands in DNA/DNA and RNA/DNA duplexes dependent on unwinding

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

WRN helicase expression in Werner syndrome cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

p53 Modulates the exonuclease activity of Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Functional and physical interaction between WRN helicase and human replication protein A

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Physical and functional interaction between p53 and the Werner's syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

p53-mediated apoptosis is attenuated in Werner syndrome cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

WRN interacts physically and functionally with the recombination mediator protein RAD52

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Functional interaction between Ku and the werner syndrome protein in DNA end processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

DNA double strand break repair in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

DNA repair protein Ku80 suppresses chromosomal aberrations and malignant transformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Growth retardation and leaky SCID phenotype of Ku70-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The nonhomologous end-joining pathway of DNA repair is required for genomic stability and the suppression of translocations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Deletion of Ku86 causes early onset of senescence in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

PARP-1: a regulator of genomic stability linked with mammalian longevity

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Poly(ADP-ribose) polymerase: a molecular nick-sensor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The Werner syndrome protein is a DNA helicase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

A high-titer lentiviral production system mediates efficient transduction of differentiated cells including beating cardiac myocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Poly(ADP-ribose) polymerase and Ku autoantigen form a complex and synergistically bind to matrix attachment sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Stimulation of the DNA-dependent protein kinase by poly(ADP-ribose) polymerase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Binding of adenosine diphosphoribosyltransferase to the termini and internal regions of linear DNAs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Physical and functional interaction of the Werner syndrome protein with poly‐ADP ribosyl transferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Genetic cooperation between the Werner syndrome protein and poly(ADP-ribose) polymerase-1 in preventing chromatid breaks, complex chromosomal rearrangements, and cancer in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Coenzymatic activity of randomly broken or intact double-stranded DNAs in auto and histone H1 trans-poly(ADP-ribosylation), catalyzed by poly(ADP-ribose) polymerase (PARP I).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Poly(ADP-ribosylation) of histones in intact human keratinocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

ADP-ribosylation of ADPR-transferase and topoisomerase I in intact mouse epidermal cells JB6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

ADP-ribosylation of p53 tumor suppressor protein: mutant but not wild-type p53 is modified

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Poly(ADP-ribose) binds to specific domains of p53 and alters its DNA binding functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Histone shuttling by poly ADP-ribosylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

The therapeutic potential of poly(ADP-ribose) polymerase inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Poly(ADP-ribose) polymerase is a mediator of necrotic cell death by ATP depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Cleavage of automodified poly(ADP-ribose) polymerase during apoptosis. Evidence for involvement of caspase-7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Mediation of poly(ADP-ribose) polymerase-1-dependent cell death by apoptosis-inducing factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Poly(ADP-ribose) polymerase activity in mononuclear leukocytes of 13 mammalian species correlates with species-specific life span

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Impaired nuclear localization of defective DNA helicases in Werner's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Pathways defective in the human premature aging disease Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Spontaneous and induced chromosomal instability in Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Variations in ADP-ribosylation of nuclear scaffold proteins during the HeLa cell cycle

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M311606200