Literature DB >> 8782494

Immortalization of four new Fanconi anemia fibroblast cell lines by an improved procedure.

P M Jakobs1, P Sahaayaruban, H Saito, C Reifsteck, S Olson, H Joenje, R E Moses, M Grompe.   

Abstract

Fanconi anemia (FA) is an autosomal recessive disease characterized by birth defects, progressive bone marrow failure and increased risk for leukemia. FA cells display chromosome breakage and increased cell killing in response to DNA crosslinking agents. At least 5 genes have been defined by cell complementation studies, but only one of these, FAC has been cloned to date. Efforts to map and isolate new FA genes by functional complementation have been hampered by the lack of immortalized FA fibroblast cell lines. Here we report the use of a novel immortalization strategy to create 4 new immortalized FA fibroblast lines, including one from the rare complementation group D.

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Year:  1996        PMID: 8782494     DOI: 10.1007/bf02369905

Source DB:  PubMed          Journal:  Somat Cell Mol Genet        ISSN: 0740-7750


  12 in total

Review 1.  The Fanconi anemia ID2 complex: dueling saxes at the crossroads.

Authors:  Rebecca A Boisvert; Niall G Howlett
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

2.  Functional complementation by electroporation of human BACs into mammalian fibroblast cells.

Authors:  J A Hejna; P L Johnstone; S L Kohler; D A Bruun; C A Reifsteck; S B Olson; R E Moses
Journal:  Nucleic Acids Res       Date:  1998-02-15       Impact factor: 16.971

3.  Human Fanconi anemia monoubiquitination pathway promotes homologous DNA repair.

Authors:  Koji Nakanishi; Yun-Gui Yang; Andrew J Pierce; Toshiyasu Taniguchi; Martin Digweed; Alan D D'Andrea; Zhao-Qi Wang; Maria Jasin
Journal:  Proc Natl Acad Sci U S A       Date:  2005-01-13       Impact factor: 11.205

4.  A distinct replication fork protection pathway connects Fanconi anemia tumor suppressors to RAD51-BRCA1/2.

Authors:  Katharina Schlacher; Hong Wu; Maria Jasin
Journal:  Cancer Cell       Date:  2012-07-10       Impact factor: 31.743

5.  Localization of the Fanconi anemia complementation group D gene to a 200-kb region on chromosome 3p25.3.

Authors:  J A Hejna; C D Timmers; C Reifsteck; D A Bruun; L W Lucas; P M Jakobs; S Toth-Fejel; N Unsworth; S L Clemens; D K Garcia; S L Naylor; M J Thayer; S B Olson; M Grompe; R E Moses
Journal:  Am J Hum Genet       Date:  2000-04-12       Impact factor: 11.025

6.  Acquisition of Relative Interstrand Crosslinker Resistance and PARP Inhibitor Sensitivity in Fanconi Anemia Head and Neck Cancers.

Authors:  Anne J Lombardi; Elizabeth E Hoskins; Grant D Foglesong; Kathryn A Wikenheiser-Brokamp; Lisa Wiesmüller; Helmut Hanenberg; Paul R Andreassen; Allison J Jacobs; Susan B Olson; Winifred W Keeble; Laura E Hays; Susanne I Wells
Journal:  Clin Cancer Res       Date:  2015-01-21       Impact factor: 12.531

7.  FANCD2-deficient human fibroblasts are hypersensitive to ionising radiation at oxygen concentrations of 0% and 3% but not under normoxic conditions.

Authors:  Verena M Kuhnert; Lisa A Kachnic; Li Li; Martin Purschke; Liliana Gheorghiu; Richard Lee; Kathryn D Held; Henning Willers
Journal:  Int J Radiat Biol       Date:  2009-06       Impact factor: 2.694

8.  FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2.

Authors:  Maria Castella; Celine Jacquemont; Elizabeth L Thompson; Jung Eun Yeo; Ronald S Cheung; Jen-Wei Huang; Alexandra Sobeck; Eric A Hendrickson; Toshiyasu Taniguchi
Journal:  PLoS Genet       Date:  2015-10-02       Impact factor: 5.917

9.  Identification of the FANCI protein, a monoubiquitinated FANCD2 paralog required for DNA repair.

Authors:  Agata Smogorzewska; Shuhei Matsuoka; Patrizia Vinciguerra; E Robert McDonald; Kristen E Hurov; Ji Luo; Bryan A Ballif; Steven P Gygi; Kay Hofmann; Alan D D'Andrea; Stephen J Elledge
Journal:  Cell       Date:  2007-04-05       Impact factor: 41.582

10.  Biomarkers and mechanisms of FANCD2 function.

Authors:  Henning Willers; Lisa A Kachnic; Chen-Mei Luo; Li Li; Martin Purschke; Kerstin Borgmann; Kathryn D Held; Simon N Powell
Journal:  J Biomed Biotechnol       Date:  2008
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