Steven C. Pruitt
Affiliations: | State University of New York, Buffalo, Buffalo, NY, United States |
Area:
Biochemistry, Molecular Biology, General BiophysicsGoogle:
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Publications
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| Yin M, Baslan T, Walker RL, et al. (2019) A unique mutator phenotype reveals complementary oncogenic lesions leading to acute leukemia. Jci Insight |
| Tubbs A, Sridharan S, van Wietmarschen N, et al. (2018) Dual Roles of Poly(dA:dT) Tracts in Replication Initiation and Fork Collapse. Cell |
| Yin M, Baslan T, Freeland A, et al. (2018) Mice with a Unique Mutator Phenotype Allow Detection of Lymphoid Leukemia Tumor Suppressor Genes Blood. 132: 1332-1332 |
| Salim D, Bradford WD, Freeland A, et al. (2017) DNA replication stress restricts ribosomal DNA copy number. Plos Genetics. 13: e1007006 |
| Pruitt SC, Qin M, Wang J, et al. (2017) A Signature of Genomic Instability Resulting from Deficient Replication Licensing. Plos Genetics. 13: e1006547 |
| Kunnev D, Freeland A, Qin M, et al. (2015) Effect of minichromosome maintenance protein 2 deficiency on the locations of DNA replication origins. Genome Research. 25: 558-69 |
| Morrison CD, Liu P, Woloszynska-Read A, et al. (2014) Whole-genome sequencing identifies genomic heterogeneity at a nucleotide and chromosomal level in bladder cancer. Proceedings of the National Academy of Sciences of the United States of America. 111: E672-81 |
| Pruitt SC, Freeland A, Rusiniak ME, et al. (2013) Cdkn1b overexpression in adult mice alters the balance between genome and tissue ageing. Nature Communications. 4: 2626 |
| Rusiniak ME, Kunnev D, Freeland A, et al. (2012) Mcm2 deficiency results in short deletions allowing high resolution identification of genes contributing to lymphoblastic lymphoma Oncogene. 31: 4034-4044 |
| Pruitt SC, Freeland A, Kudla A. (2010) Cell cycle heterogeneity in the small intestinal crypt and maintenance of genome integrity. Stem Cells (Dayton, Ohio). 28: 1250-9 |