Deficiency of the Fanconi anemia E2 ubiqitin conjugase UBE2T only partially abrogates Alu-mediated recombination in a new model of homology dependent recombination-Reference-Cited by-同舟云学术

Deficiency of the Fanconi anemia E2 ubiqitin conjugase UBE2T only partially abrogates Alu-mediated recombination in a new model of homology dependent recombination

Published:2019-02-01 Issue:7 Volume:47 Page:3503-3520
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:

Author:

Lewis Todd W¹,Barthelemy Joanna R¹,Virts Elizabeth L²,Kennedy Felicia M²,Gadgil Rujuta Y¹,Wiek Constanze³,Linka Rene M³,Zhang Feng⁴,Andreassen Paul R⁴⁵,Hanenberg Helmut³⁶,Leffak Michael¹

Affiliation:

1. Department of Biochemistry and Molecular Biology, Boonshoft School of Medicine, Wright State University, Dayton, OH, USA

2. Department of Pediatrics and Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN 46202, USA

3. Department of Otorhinolaryngology and Head/Neck Surgery, Heinrich Heine University, 40225 Duüsseldorf, Germany

4. Division of Experimental Hematology & Cancer Biology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA

5. Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA

6. Department of Pediatrics III, University Children's Hospital Essen, University of Duisburg-Essen, 45122 Essen, Germany

Funder

National Institutes of Health

Department of Defense

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/47/7/3503/28467778/gkz026.pdf

Reference129 articles.

1. Initial sequencing and analysis of the human genome;Lander;Nature,2001

2. Chromosomal translocation mechanisms at intronic alu elements in mammalian cells;Elliott;Mol. Cell,2005

3. Alu repeats and human disease;Deininger;Mol. Genet. Metab.,1999

4. Alu repeats and human genomic diversity;Batzer;Nat. Rev. Genet.,2002

5. Identification of Alu-mediated deletions in the Fanconi anemia gene FAA;Levran;Hum. Mutat.,1998

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