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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

257 related items for PubMed ID: 34718701

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  • 3. FAN1 controls mismatch repair complex assembly via MLH1 retention to stabilize CAG repeat expansion in Huntington's disease.
    Goold R, Hamilton J, Menneteau T, Flower M, Bunting EL, Aldous SG, Porro A, Vicente JR, Allen ND, Wilkinson H, Bates GP, Sartori AA, Thalassinos K, Balmus G, Tabrizi SJ.
    Cell Rep; 2021 Aug 31; 36(9):109649. PubMed ID: 34469738
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  • 6. FANCD2-Associated Nuclease 1 Partially Compensates for the Lack of Exonuclease 1 in Mismatch Repair.
    Kratz K, Artola-Borán M, Kobayashi-Era S, Koh G, Oliveira G, Kobayashi S, Oliveira A, Zou X, Richter J, Tsuda M, Sasanuma H, Takeda S, Loizou JI, Sartori AA, Nik-Zainal S, Jiricny J.
    Mol Cell Biol; 2021 Aug 24; 41(9):e0030321. PubMed ID: 34228493
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  • 13. FAN1 acts with FANCI-FANCD2 to promote DNA interstrand cross-link repair.
    Liu T, Ghosal G, Yuan J, Chen J, Huang J.
    Science; 2010 Aug 06; 329(5992):693-6. PubMed ID: 20671156
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  • 14. Exome sequencing of individuals with Huntington's disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset.
    McAllister B, Donaldson J, Binda CS, Powell S, Chughtai U, Edwards G, Stone J, Lobanov S, Elliston L, Schuhmacher LN, Rees E, Menzies G, Ciosi M, Maxwell A, Chao MJ, Hong EP, Lucente D, Wheeler V, Lee JM, MacDonald ME, Long JD, Aylward EH, Landwehrmeyer GB, Rosser AE, REGISTRY Investigators of the European Huntington’s disease network, Paulsen JS, PREDICT-HD Investigators of the Huntington Study Group, Williams NM, Gusella JF, Monckton DG, Allen ND, Holmans P, Jones L, Massey TH.
    Nat Neurosci; 2022 Apr 06; 25(4):446-457. PubMed ID: 35379994
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  • 16. Ubiquitinated Fancd2 recruits Fan1 to stalled replication forks to prevent genome instability.
    Lachaud C, Moreno A, Marchesi F, Toth R, Blow JJ, Rouse J.
    Science; 2016 Feb 19; 351(6275):846-9. PubMed ID: 26797144
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  • 18. FAN1 nuclease helps to delay Huntington disease.
    Wood H.
    Nat Rev Neurol; 2022 Jun 19; 18(6):317. PubMed ID: 35534552
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  • 20. Fan1 deficiency results in DNA interstrand cross-link repair defects, enhanced tissue karyomegaly, and organ dysfunction.
    Thongthip S, Bellani M, Gregg SQ, Sridhar S, Conti BA, Chen Y, Seidman MM, Smogorzewska A.
    Genes Dev; 2016 Mar 15; 30(6):645-59. PubMed ID: 26980189
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