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Lingchuan Hu, Ph.D. - Publications

Affiliations: 
2012 Molecular Medicine The University of Texas Health Science Center at San Antonio, San Antonio, TX, United States 
Area:
Genetics, Molecular Biology, Biochemistry
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Kim TM, Son MY, Dodds S, Hu L, Luo G, Hasty P. RECQL5 and BLM exhibit divergent functions in cells defective for the Fanconi anemia pathway. Nucleic Acids Research. 43: 893-903. PMID 25520194 DOI: 10.1093/Nar/Gku1334  0.714
2014 Kim TM, Son MY, Dodds S, Hu L, Hasty P. Deletion of BRCA2 exon 27 causes defects in response to both stalled and collapsed replication forks. Mutation Research. 766: 66-72. PMID 25847274 DOI: 10.1016/J.Mrfmmm.2014.06.003  0.717
2014 Kim TM, Son MY, Dodds S, Hu L, Hasty P. Deletion of BRCA2 exon 27 causes defects in response to both stalled and collapsed replication forks. Mutation Research. 766: 66-72. PMID 25773776 DOI: 10.1016/j.mrfmmm.2014.06.003  0.686
2013 Hu L, Kim TM, Son MY, Kim SA, Holland CL, Tateishi S, Kim DH, Yew PR, Montagna C, Dumitrache LC, Hasty P. Two replication fork maintenance pathways fuse inverted repeats to rearrange chromosomes. Nature. 501: 569-72. PMID 24013173 DOI: 10.1038/Nature12500  0.639
2012 Kim TM, Ko JH, Hu L, Kim SA, Bishop AJ, Vijg J, Montagna C, Hasty P. RAD51 mutants cause replication defects and chromosomal instability. Molecular and Cellular Biology. 32: 3663-80. PMID 22778135 DOI: 10.1128/Mcb.00406-12  0.718
2011 Dumitrache LC, Hu L, Son MY, Li H, Wesevich A, Scully R, Stark J, Hasty P. Trex2 enables spontaneous sister chromatid exchanges without facilitating DNA double-strand break repair. Genetics. 188: 787-97. PMID 21546543 DOI: 10.1534/Genetics.111.129833  0.656
2011 Kim TM, Ko JH, Choi YJ, Hu L, Hasty P. The phenotype of FancB-mutant mouse embryonic stem cells. Mutation Research. 712: 20-7. PMID 21458466 DOI: 10.1016/J.Mrfmmm.2011.03.010  0.669
2009 Dumitrache LC, Hu L, Hasty P. TREX2 exonuclease defective cells exhibit double-strand breaks and chromosomal fragments but not Robertsonian translocations. Mutation Research. 662: 84-7. PMID 19094998 DOI: 10.1016/J.Mrfmmm.2008.11.012  0.637
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