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Alan Lehmann is a molecular geneticist whose research has helped to show how cells are able to repair damaged DNA, and how these repair processes can go wrong in patients with certain genetic disorders. His work has furthered our understanding of the links between DNA repair and cancer.
He identified a faulty gene that is responsible for the skin condition xeroderma pigmentosum (XP), which causes extreme sensitivity to sunlight and a strong predisposition to skin cancer. He subsequently showed how mutations in the same gene can cause two other conditions that are clinically very different from XP.
Alan has developed diagnostic tests for XP and his laboratory runs a worldwide diagnostic service for XP, as well as Cockayne Syndrome and Trichothiodystrophy — other conditions resulting from mutations in the same or related genes. His XP diagnostic service is an integral part of the national XP multidisciplinary clinic. He is a Fellow of both the Academy of Medical Sciences and the Society of Biology.
研究兴趣
论文共 231 篇作者统计合作学者相似作者
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Paola Giunti,Hector Garcia-Moreno, Douglas Langbehn,Adesoji Abiona,Isabel Garrood,Zofia Fleszar, Marta Manes,Ana Morley, Emma Craythorne, Shehla Mohammed, Tanya Henshaw, Sally Turner,
Journal of the Neurological Sciences (2023): 121146
Hector Garcia-Moreno, Douglas R. Langbehn, Adesoji Abiona, Isabel Garrood,Zofia Fleszar, Marta Antonia Manes, Ana M. Susana Morley, Emma Craythorne,Shehla Mohammed, Tanya Henshaw,Sally Turner,Harsha Naik,
BRAINno. 12 (2023): 5044-5059
medRxiv (Cold Spring Harbor Laboratory) (2023)
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Andrey A. Yurchenko,Fatemeh Rajabi,Tirzah Braz-Petta,Hiva Fassihi,Alan Lehmann,Chikako Nishigori, Jinxin Wang,Ismael Padioleau,Konstantin Gunbin,Leonardo Panunzi,Fanny Morice-Picard, Pierre Laplante,
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biorxiv(2022)
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