About: Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome

Facets (new session)
Description
Metadata
Settings
- owl:sameAs
- Inference Rule:

About: Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome Goto Sponge NotDistinct Permalink

An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

scientific journal article

Attributes	Values
rdf:type	Item
description	article scientifique publié en 2005 (fr) artículu científicu espublizáu en 2005 (ast) vědecký článek publikovaný v roce 2005 (cs) 2005 թվականի մարտին հրատարակված գիտական հոդված (hy) 2005 թուականի Մարտին հրատարակուած գիտական յօդուած (hyw) наукова стаття, опублікована в березні 2005 (uk) wetenschappelijk artikel (gepubliceerd op 2005/03/15) (nl) vedecký článok (publikovaný 2005/03/15) (sk) مقالة علمية (نشرت في 15-3-2005) (ar) im März 2005 veröffentlichter wissenschaftlicher Artikel (de) scientific journal article (en)
publication date	wds:Q28505974-8D2E1C53-B396-45AD-8477-F0B67D1A3608
publication date	2005-03-15 00:00:00Z (xsd:dateTime)
author name string	wds:Q28505974-111A4841-9EBD-45FA-9600-66900584B2F4 wds:Q28505974-42E03411-5984-4E3E-A9F0-60DFD6339FC5 wds:Q28505974-502A7586-8970-4EC1-84BE-A295FDF2278C wds:Q28505974-62AF2392-AAC9-4B99-BB31-BCF0122376A2 wds:Q28505974-CF9CE512-8836-4B4E-B5AD-E25E52F8F1D1
OpenCitations bibliographic resource ID	wds:Q28505974-12233CD6-B062-4389-BC65-7AE1E600AE20
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/1803210
author name string	Guangbin Luo Ellen Barnes Hannes Vogel Craig A. Hodges Terry J. Hassold
OpenCitations bibliographic resource ID	1803210
rdfs:label	Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (en) Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (nl) Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (ast)
skos:prefLabel	Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (en) Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (nl) Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (ast)
name	Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (en) Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (nl) Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (ast)
author	wds:Q28505974-8B3FF62A-CBAC-41DC-BDDA-6B01A9768E8F
author	Michael B. Mann
title	wds:Q28505974-19E8F777-6063-44D8-8BF7-D25DEB4E3C29
title	Defective sister-chromatid cohesion, aneuploidy and cancer predisposition in a mouse model of type II Rothmund-Thomson syndrome (en)
page(s)	wds:Q28505974-9AF81F5A-3CA3-48A2-9530-263F6510D5BE
page(s)	813–825
instance of	wds:Q28505974-F6CDA3A0-391B-48F6-B433-B23C8B033ADE
instance of	scholarly article
main subject	wds:Q28505974-2BB5D063-2CCF-478D-B420-93404A87890E wds:Q28505974-D5667740-B9E5-43CC-B4E3-F2C022E83C8F
main subject	Rothmund-Thomson syndrome RecQ protein-like 4
PubMed ID	wds:Q28505974-B2654DDE-7485-4E96-A668-8FE0C9ECB4AF
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/15703196
PubMed ID	15703196
published in	wds:Q28505974-57EB2E6C-E905-4462-B8CE-2649C94B3C3D
published in	Human Molecular Genetics
issue	wds:Q28505974-34AFB938-AC53-47AE-9C22-8527B0D9D103
volume	wds:Q28505974-E8F1574C-E1D9-4A19-ADA8-39A390761DCE
issue	6
volume	14
DOI	wds:Q28505974-EDE34EF0-C1D1-45E4-B895-A83FDE8F9555
DOI	http://dx.doi.org/10.1093/HMG/DDI075
DOI	10.1093/HMG/DDI075
ResearchGate publication ID	wds:Q28505974-9070A418-A491-46EC-85D6-49A1C3F23FB7
ResearchGate publication ID	8030102
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q28505974
is cites work of	The DNA helicase recql4 is required for normal osteoblast expansion and osteosarcoma formation Osteosarcoma: Molecular Pathogenesis and iPSC Modeling RECQL4 Regulates p53 Function In Vivo During Skeletogenesis. MCM10 mediates RECQ4 association with MCM2-7 helicase complex during DNA replication RECQ DNA helicases and osteosarcoma. The etiopathogenesis of cleft lip and cleft palate: usefulness and caveats of mouse models Dual DNA unwinding activities of the Rothmund-Thomson syndrome protein, RECQ4 The mutation spectrum in RECQL4 diseases Transcriptional dysregulation in NIPBL and cohesin mutant human cells RecQ helicases in DNA double strand break repair and telomere maintenance Rising from the RecQ-age: the role of human RecQ helicases in genome maintenance Recql5 plays an important role in DNA replication and cell survival after camptothecin treatment Mitotic defects lead to pervasive aneuploidy and accompany loss of RB1 activity in mouse LmnaDhe dermal fibroblasts Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers Osteosarcomagenesis: modeling cancer initiation in the mouse Roles of RECQ helicases in recombination based DNA repair, genomic stability and aging Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability The role of vertebrate models in understanding craniosynostosis RECQL5/Recql5 helicase regulates homologous recombination and suppresses tumor formation via disruption of Rad51 presynaptic filaments RecQ helicases: multifunctional genome caretakers Human RecQ helicases in DNA repair, recombination, and replication. Molecular functions and cellular roles of the ChlR1 (DDX11) helicase defective in the rare cohesinopathy Warsaw breakage syndrome The Rothmund-Thomson gene product RECQL4 localizes to the nucleolus in response to oxidative stress Loss of miR-10a activates lpo and collaborates with activated Wnt signaling in inducing intestinal neoplasia in female mice Identification of RecQL1 as a Holliday junction processing enzyme in human cell lines Rothmund-Thomson syndrome Identification of Mom7, a novel modifier of Apc(Min/+) on mouse chromosome 18. APC and its modifiers in colon cancer. Replication stress and cancer Borrowing nuclear DNA helicases to protect mitochondrial DNA. RECQL4 in genomic instability and aging Senescence induced by RECQL4 dysfunction contributes to Rothmund-Thomson syndrome features in mice Activation of p38 MAP kinase and stress signalling in fibroblasts from the progeroid Rothmund-Thomson syndrome The RecQ DNA helicases in DNA repair Unzipped and loaded: the role of DNA helicases and RFC clamp-loading complexes in sister chromatid cohesion RECQL4, the protein mutated in Rothmund-Thomson syndrome, functions in telomere maintenance Sister chromatid cohesion control and aneuploidy.

Faceted Search & Find service v1.16.117 as of May 05 2024

Alternative Linked Data Documents: ODE Content Formats:

RDF

ODATA

Microdata

About

OpenLink Virtuoso version 07.20.3239 as of May 5 2024, on Linux (x86_64-centos_6-linux-gnu), Single-Server Edition (378 GB total memory, 172 GB memory in use)
Data on this page belongs to its respective rights holders.
Virtuoso Faceted Browser Copyright © 2009-2024 OpenLink Software