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The Caldecott lab is focussed on identifying new human DNA repair genes and unraveling the link between defects in DNA strand break repair and human genetic disease. This work has uncovered new genetic causes of neurodegeneration, such as mutations in the human DNA repair genes PNKP, TDP2, and XRCC1, and has enabled the lab to assist clinicians worldwide in the molecular and genetic diagnosis of DNA damage-associated hereditary diseases.
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论文共 170 篇作者统计合作学者相似作者
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MOLECULAR CELLno. 1 (2024): 70-79
TRENDS IN BIOCHEMICAL SCIENCESno. 1 (2024): 68-78
Alice Meroni, Sophie E. Wells, Carmen Fonseca,Arnab Ray Chaudhuri,Keith W. Caldecott,Alessandro Vindigni
JOURNAL OF CELL BIOLOGYno. 4 (2024)
Almudena Serrano-Benitez,Sophie E. Wells, Lylah Drummond-Clarke,Lilian C. Russo,John Christopher Thomas, Giovanna A. Leal,Mark Farrow, James Michael Edgerton,Shankar Balasubramanian,Ming Yang,Christian Frezza,Amit Gautam,
EMBO JOURNALno. 18 (2023): e113190-e113190
Lenka Oplustil O'Connor,Stuart L. Rulten, Aaron N. Cranston,Rajesh Odedra, Henry Brown,Janneke E. Jaspers,Louise Jones,Charlotte Knights,Bastiaan Evers, Attilla Ting, Robert H. Bradbury,Marina Pajic,
crossref(2023)
Molecular genetics & genomic medicineno. 1 (2023): e2295-e2295
medRxiv (Cold Spring Harbor Laboratory) (2023)
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Molecular cellno. 20 (2023): 3669-3678.e7
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