Functional interaction between the Werner Syndrome protein and DNA polymerase delta - Wikidata - awgldk - TriplyDB

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

http://www.wikidata.org/entity/Q33899465

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Werner Syndrome Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins Physical and functional interaction of the Werner syndrome protein with poly-ADP ribosyl transferase Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1 Werner syndrome protein interacts functionally with translesion DNA polymerases Identification of delta helicase as the bovine homolog of HUPF1: demonstration of an interaction with the third subunit of DNA polymerase delta.The RecQ DNA helicases in DNA repair Analysis of the unwinding activity of the dimeric RECQ1 helicase in the presence of human replication protein A Roles of Werner syndrome protein in protection of genome integrity Model of human aging: recent findings on Werner's and Hutchinson-Gilford progeria syndromes The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase delta Werner protein recruits DNA polymerase delta to the nucleolus Human premature aging, DNA repair and RecQ helicases exo1-Dependent mutator mutations: model system for studying functional interactions in mismatch repair.Mediation of proliferating cell nuclear antigen (PCNA)-dependent DNA replication through a conserved p21(Cip1)-like PCNA-binding motif present in the third subunit of human DNA polymerase delta Regulation of the Werner helicase through a direct interaction with a subunit of protein kinase A Reconstitution of human DNA polymerase delta using recombinant baculoviruses: the p12 subunit potentiates DNA polymerizing activity of the four-subunit enzyme The processing of Holliday junctions by BLM and WRN helicases is regulated by p53 A novel protein interacts with the Werner's syndrome gene product physically and functionally The Werner syndrome exonuclease facilitates DNA degradation and high fidelity DNA polymerization by human DNA polymerase δ POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome Age-dependent down-regulation of DNA polymerase δ1 in human lymphocytes Evidence for a replication function of FFA-1, the Xenopus orthologue of Werner syndrome protein.RecQ helicases: guardian angels of the DNA replication fork.Selective blockage of the 3'-->5' exonuclease activity of WRN protein by certain oxidative modifications and bulky lesions in DNA.DNA structure and the Werner protein modulate human DNA polymerase delta-dependent replication dynamics within the common fragile site FRA16D.Differential regulation of human RecQ family helicases in cell transformation and cell cycle.Werner's syndrome protein is required for correct recovery after replication arrest and DNA damage induced in S-phase of cell cycle.Acetylation of Werner syndrome protein (WRN): relationships with DNA damage, DNA replication and DNA metabolic activities.Interactions of DNA helicases with damaged DNA: possible biological consequences.Mouse WRN Helicase Domain Is Not Required for Spontaneous Homologous Recombination-Mediated DNA Deletion WRN helicase accelerates the transcription of ribosomal RNA as a component of an RNA polymerase I-associated complex.Characterization of the DNA-unwinding activity of human RECQ1, a helicase specifically stimulated by human replication protein A.The Werner syndrome protein stimulates DNA polymerase beta strand displacement synthesis via its helicase activity.TRF2 recruits the Werner syndrome (WRN) exonuclease for processing of telomeric DNA.Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure.Further characterization of human DNA polymerase delta interacting protein 38.Alternate pathways involving Sgs1/Top3, Mus81/ Mms4, and Srs2 prevent formation of toxic recombination intermediates from single-stranded gaps created by DNA replication.Molecular bases of progeroid syndromes.

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P2860

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

http://www.wikidata.org/entity/Q33899465

description

2000 nî lūn-bûn

@nan

2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2000 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2000年の論文

@ja

2000年論文

@yue

2000年論文

@zh-hant

2000年論文

@zh-hk

2000年論文

@zh-mo

2000年論文

@zh-tw

2000年论文

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name

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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type

label

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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prefLabel

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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Proceedings of the National Academy of Sciences of the United States of America

P1476

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

@en

P2093

A S Kamath-Loeb

http://www.w3.org/2001/XMLSchema#string

E Johansson

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L A Loeb

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P M Burgers

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P2860

Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes

Isolation and identification of the third subunit of mammalian DNA polymerase delta by PCNA-affinity chromatography of mouse FM3A cell extracts

Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

Oligomeric ring structure of the Bloom's syndrome helicase

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

The Werner syndrome protein is a DNA helicase

The Bloom's syndrome gene product is a 3'-5' DNA helicase

The Bloom's syndrome gene product is homologous to RecQ helicases

Cloning and characterization of RECQL, a potential human homologue of the Escherichia coli DNA helicase RecQ

p53-mediated apoptosis is attenuated in Werner syndrome cells

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4603-4608

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9

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2000-04-01T00:00:00Z

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12535835

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18279

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