PHILIP HASTINGS to Humans
This is a "connection" page, showing publications PHILIP HASTINGS has written about Humans.
Connection Strength
0.122
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Oxygen and RNA in stress-induced mutation. Curr Genet. 2018 Aug; 64(4):769-776.
Score: 0.016
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Stress-induced mutation via DNA breaks in Escherichia coli: a molecular mechanism with implications for evolution and medicine. Bioessays. 2012 Oct; 34(10):885-92.
Score: 0.011
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Genomic rearrangement in three dimensions. Nat Biotechnol. 2011 Dec 08; 29(12):1096-8.
Score: 0.010
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Mechanisms of change in gene copy number. Nat Rev Genet. 2009 Aug; 10(8):551-64.
Score: 0.009
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A microhomology-mediated break-induced replication model for the origin of human copy number variation. PLoS Genet. 2009 Jan; 5(1):e1000327.
Score: 0.009
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Adaptive amplification. Crit Rev Biochem Mol Biol. 2007 Jul-Aug; 42(4):271-83.
Score: 0.008
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Endogenous DNA damage at sites of terminated transcripts. Nature. 2025 Apr; 640(8057):240-248.
Score: 0.007
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Microbiology and evolution. Modulating mutation rates in the wild. Science. 2003 May 30; 300(5624):1382-3.
Score: 0.006
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The multiple de novo copy number variant (MdnCNV) phenomenon presents with peri-zygotic DNA mutational signatures and multilocus pathogenic variation. Genome Med. 2022 10 27; 14(1):122.
Score: 0.006
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Two mechanisms of chromosome fragility at replication-termination sites in bacteria. Sci Adv. 2021 06; 7(25).
Score: 0.005
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Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2. Cell. 2019 03 07; 176(6):1310-1324.e10.
Score: 0.004
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Bacteria-to-Human Protein Networks Reveal Origins of Endogenous DNA Damage. Cell. 2019 01 10; 176(1-2):127-143.e24.
Score: 0.004
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Holliday junction trap shows how cells use recombination and a junction-guardian role of RecQ helicase. Sci Adv. 2016 Nov; 2(11):e1601605.
Score: 0.004
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Absence of heterozygosity due to template switching during replicative rearrangements. Am J Hum Genet. 2015 Apr 02; 96(4):555-64.
Score: 0.003
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Engineered proteins detect spontaneous DNA breakage in human and bacterial cells. Elife. 2013 Oct 29; 2:e01222.
Score: 0.003
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Replicative mechanisms for CNV formation are error prone. Nat Genet. 2013 Nov; 45(11):1319-26.
Score: 0.003
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Mechanisms for recurrent and complex human genomic rearrangements. Curr Opin Genet Dev. 2012 Jun; 22(3):211-20.
Score: 0.003
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Frequency of nonallelic homologous recombination is correlated with length of homology: evidence that ectopic synapsis precedes ectopic crossing-over. Am J Hum Genet. 2011 Oct 07; 89(4):580-8.
Score: 0.003
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Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome. Nat Genet. 2011 Oct 02; 43(11):1074-81.
Score: 0.003
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Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell. 2011 Sep 16; 146(6):889-903.
Score: 0.003
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Mutation as a stress response and the regulation of evolvability. Crit Rev Biochem Mol Biol. 2007 Sep-Oct; 42(5):399-435.
Score: 0.002
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Defective mitochondrial peroxiredoxin-3 results in sensitivity to oxidative stress in Fanconi anemia. J Cell Biol. 2006 Oct 23; 175(2):225-35.
Score: 0.002
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Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients. Am J Hum Genet. 1998 May; 62(5):1023-33.
Score: 0.001