日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Corrigendum: Expression of constitutive fusion of ubiquitin to PCNA restores the level of immunoglobulin A/T mutations during somatic hypermutation in the Ramos cell line

更正：在Ramos细胞系中，泛素与PCNA的组成型融合表达可恢复体细胞高频突变期间免疫球蛋白A/T突变的水平。

期刊:Frontiers in Immunology
影响因子:5.9
doi:10.3389/fimmu.2024.1419493
Lerner, Leticia K; Bonte, Dorine; Le Guillou, Morwenna; Mohammad, Mahwish Mian; Kasraian, Zeinab; Sarasin, Alain; Despras, Emmanuelle; Aoufouchi, Said
PCNA
免疫/内分泌
细胞生物学
发表日期：2024
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Epigenomic signature of accelerated ageing in progeroid Cockayne syndrome

早衰样科凯恩综合征的表观基因组加速衰老特征

期刊:Aging Cell
影响因子:7.1
doi:10.1111/acel.13959
Crochemore, Clément; Chica, Claudia; Garagnani, Paolo; Lattanzi, Giovanna; Horvath, Steve; Sarasin, Alain; Franceschi, Claudio; Bacalini, Maria Giulia; Ricchetti, Miria
衰老
表观遗传
发表日期：2023
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The French Cohort of DNA Repair-Deficient Xeroderma Pigmentosum Patients: Risk of Hematological Malignancies

法国DNA修复缺陷型着色性干皮病患者队列：血液系统恶性肿瘤风险

期刊:Cancers
影响因子:4.4
doi:10.3390/cancers15102706
Sarasin, Alain
肿瘤
肿瘤免疫
发表日期：2023
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Increased risk of internal tumors in DNA repair-deficient xeroderma pigmentosum patients: analysis of four international cohorts

DNA修复缺陷型着色性干皮病患者发生内脏肿瘤的风险增加：四项国际队列研究分析

期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-022-02203-1
Nikolaev, Sergey; Yurchenko, Andrey A; Sarasin, Alain
肿瘤
肿瘤免疫
发表日期：2022
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XPC and POLH/XPV Genes Mutated in a Genetic Cluster of Xeroderma Pigmentosum Patients in Northeast Brazil

巴西东北部着色性干皮病患者遗传群中XPC和POLH/XPV基因发生突变

期刊:Frontiers in Genetics
影响因子:2.8
doi:10.3389/fgene.2021.784963
Castro, Ligia Pereira; Batista-Vieira, Danilo; de Souza, Tiago Antonio; Timoteo, Ana Rafaela de Souza; Coutinho, Jessica Dayanna Landivar; Pinheiro de Almeida, Isabel Cristina; Henriques, Sheila Ramos de Miranda; de Azevedo, Fabio Medeiros; Rosa, Reginaldo Cruz Alves; Kannouche, Patricia L; Sarasin, Alain; Menck, Carlos Frederico Martins; Petta, Tirzah Braz
POLH
XPC
发表日期：2021
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XPC deficiency increases risk of hematologic malignancies through mutator phenotype and characteristic mutational signature

XPC缺陷通过突变表型和特征性突变特征增加血液系统恶性肿瘤的风险。

期刊:Nature Communications
影响因子:15.7
doi:10.1038/s41467-020-19633-9
Yurchenko, Andrey A; Padioleau, Ismael; Matkarimov, Bakhyt T; Soulier, Jean; Sarasin, Alain; Nikolaev, Sergey
肿瘤
XPC
肿瘤免疫
发表日期：2020
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Bi-allelic TARS Mutations Are Associated with Brittle Hair Phenotype

双等位基因TARS突变与脆发表型相关

期刊:American Journal of Human Genetics
影响因子:8.1
doi:10.1016/j.ajhg.2019.06.017
Theil, Arjan F; Botta, Elena; Raams, Anja; Smith, Desiree E C; Mendes, Marisa I; Caligiuri, Giuseppina; Giachetti, Sarah; Bione, Silvia; Carriero, Roberta; Liberi, Giordano; Zardoni, Luca; Swagemakers, Sigrid M A; Salomons, Gajja S; Sarasin, Alain; Lehmann, Alan; van der Spek, Peter J; Ogi, Tomoo; Hoeijmakers, Jan H J; Vermeulen, Wim; Orioli, Donata
发表日期：2019
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How history and geography may explain the distribution in the Comorian archipelago of a novel mutation in DNA repair-deficient xeroderma pigmentosum patients

历史和地理因素如何解释科摩罗群岛中一种新型DNA修复缺陷型着色性干皮病患者的突变分布

期刊:Genetics and Molecular Biology
影响因子:1.3
doi:10.1590/1678-4685-GMB-2019-0046
Sarasin, Alain; Munier, Patrick; Cartault, François
发表日期：2019
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Targeted gene therapy of xeroderma pigmentosum cells using meganuclease and TALEN™.

利用巨核酸酶和TALEN™对着色性干皮病细胞进行靶向基因治疗

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0078678
Dupuy Aurélie, Valton Julien, Leduc Sophie, Armier Jacques, Galetto Roman, Gouble Agnès, Lebuhotel Céline, Stary Anne, Pâques Frédéric, Duchateau Philippe, Sarasin Alain, Daboussi Fayza
细胞生物学
发表日期：2013
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UVSSA and USP7: new players regulating transcription-coupled nucleotide excision repair in human cells

UVSSA 和 USP7：调控人类细胞中转录偶联核苷酸切除修复的新成员

期刊:Genome Medicine
影响因子:11.2
doi:10.1186/gm343
Sarasin, Alain
信号转导
细胞生物学
SP7
发表日期：2012
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