194 related articles for article (PubMed ID: 1581963)
1. Mutations in the DNA ligase I gene of an individual with immunodeficiencies and cellular hypersensitivity to DNA-damaging agents.
Barnes DE; Tomkinson AE; Lehmann AR; Webster AD; Lindahl T
Cell; 1992 May; 69(3):495-503. PubMed ID: 1581963
[TBL] [Abstract][Full Text] [Related]
2. Aberrant DNA repair and DNA replication due to an inherited enzymatic defect in human DNA ligase I.
Prigent C; Satoh MS; Daly G; Barnes DE; Lindahl T
Mol Cell Biol; 1994 Jan; 14(1):310-7. PubMed ID: 8264597
[TBL] [Abstract][Full Text] [Related]
3. Phenotypic correction of a human cell line (46BR) with aberrant DNA ligase I activity.
Somia NV; Jessop JK; Melton DW
Mutat Res; 1993 Jun; 294(1):51-8. PubMed ID: 7683758
[TBL] [Abstract][Full Text] [Related]
4. Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndrome.
Lehmann AR; Willis AE; Broughton BC; James MR; Steingrimsdottir H; Harcourt SA; Arlett CF; Lindahl T
Cancer Res; 1988 Nov; 48(22):6343-7. PubMed ID: 3180052
[TBL] [Abstract][Full Text] [Related]
5. Normal V(D)J coding junction formation in DNA ligase I deficiency syndromes.
Petrini JH; Donovan JW; Dimare C; Weaver DT
J Immunol; 1994 Jan; 152(1):176-83. PubMed ID: 8254190
[TBL] [Abstract][Full Text] [Related]
6. Interaction between PCNA and DNA ligase I is critical for joining of Okazaki fragments and long-patch base-excision repair.
Levin DS; McKenna AE; Motycka TA; Matsumoto Y; Tomkinson AE
Curr Biol; 2000 Jul 27-Aug 10; 10(15):919-22. PubMed ID: 10959839
[TBL] [Abstract][Full Text] [Related]
7. Cells from an immunodeficient patient (46BR) with a defect in DNA ligation are hypomutable but hypersensitive to the induction of sister chromatid exchanges.
Henderson LM; Arlett CF; Harcourt SA; Lehmann AR; Broughton BC
Proc Natl Acad Sci U S A; 1985 Apr; 82(7):2044-8. PubMed ID: 3856882
[TBL] [Abstract][Full Text] [Related]
8. Structure and function of mammalian DNA ligases.
Tomkinson AE; Mackey ZB
Mutat Res; 1998 Feb; 407(1):1-9. PubMed ID: 9539976
[TBL] [Abstract][Full Text] [Related]
9. DNA ligase IV mutations identified in patients exhibiting developmental delay and immunodeficiency.
O'Driscoll M; Cerosaletti KM; Girard PM; Dai Y; Stumm M; Kysela B; Hirsch B; Gennery A; Palmer SE; Seidel J; Gatti RA; Varon R; Oettinger MA; Neitzel H; Jeggo PA; Concannon P
Mol Cell; 2001 Dec; 8(6):1175-85. PubMed ID: 11779494
[TBL] [Abstract][Full Text] [Related]
10. Specific function of DNA ligase I in simian virus 40 DNA replication by human cell-free extracts is mediated by the amino-terminal non-catalytic domain.
Mackenney VJ; Barnes DE; Lindahl T
J Biol Chem; 1997 Apr; 272(17):11550-6. PubMed ID: 9111070
[TBL] [Abstract][Full Text] [Related]
11. Structural alterations of DNA ligase I in Bloom syndrome.
Willis AE; Weksberg R; Tomlinson S; Lindahl T
Proc Natl Acad Sci U S A; 1987 Nov; 84(22):8016-20. PubMed ID: 3479778
[TBL] [Abstract][Full Text] [Related]
12. A newly identified DNA ligase of Saccharomyces cerevisiae involved in RAD52-independent repair of DNA double-strand breaks.
Schär P; Herrmann G; Daly G; Lindahl T
Genes Dev; 1997 Aug; 11(15):1912-24. PubMed ID: 9271115
[TBL] [Abstract][Full Text] [Related]
13. Mammalian DNA ligase III: molecular cloning, chromosomal localization, and expression in spermatocytes undergoing meiotic recombination.
Chen J; Tomkinson AE; Ramos W; Mackey ZB; Danehower S; Walter CA; Schultz RA; Besterman JM; Husain I
Mol Cell Biol; 1995 Oct; 15(10):5412-22. PubMed ID: 7565692
[TBL] [Abstract][Full Text] [Related]
14. The DNA Ligase IV Syndrome R278H Mutation Impairs B Lymphopoiesis via Error-Prone Nonhomologous End-Joining.
Park J; Welner RS; Chan MY; Troppito L; Staber PB; Tenen DG; Yan CT
J Immunol; 2016 Jan; 196(1):244-55. PubMed ID: 26608917
[TBL] [Abstract][Full Text] [Related]
15. A wild-type DNA ligase I gene is expressed in Bloom's syndrome cells.
Petrini JH; Huwiler KG; Weaver DT
Proc Natl Acad Sci U S A; 1991 Sep; 88(17):7615-9. PubMed ID: 1881902
[TBL] [Abstract][Full Text] [Related]
16. Growth retardation and immunodeficiency in a patient with mutations in the DNA ligase I gene.
Webster AD; Barnes DE; Arlett CF; Lehmann AR; Lindahl T
Lancet; 1992 Jun; 339(8808):1508-9. PubMed ID: 1351188
[TBL] [Abstract][Full Text] [Related]
17. A biochemical defect in the repair of alkylated DNA in cells from an immunodeficient patient (46BR).
Teo IA; Broughton BC; Day RS; James MR; Karran P; Mayne LV; Lehmann AR
Carcinogenesis; 1983; 4(5):559-64. PubMed ID: 6850987
[TBL] [Abstract][Full Text] [Related]
18. Novel compound heterozygous DNA ligase IV mutations in an adolescent with a slowly-progressing radiosensitive-severe combined immunodeficiency.
Tamura S; Higuchi K; Tamaki M; Inoue C; Awazawa R; Mitsuki N; Nakazawa Y; Mishima H; Takahashi K; Kondo O; Imai K; Morio T; Ohara O; Ogi T; Furukawa F; Inoue M; Yoshiura K; Kanazawa N
Clin Immunol; 2015 Oct; 160(2):255-60. PubMed ID: 26172957
[TBL] [Abstract][Full Text] [Related]
19. Identification of Saccharomyces cerevisiae DNA ligase IV: involvement in DNA double-strand break repair.
Teo SH; Jackson SP
EMBO J; 1997 Aug; 16(15):4788-95. PubMed ID: 9303323
[TBL] [Abstract][Full Text] [Related]
20. Unchanged PCNA and DNMT1 dynamics during replication in DNA ligase I-deficient cells but abnormal chromatin levels of non-replicative histone H1.
Bhandari SK; Wiest N; Sallmyr A; Du R; Ferry L; Defossez PA; Tomkinson AE
Sci Rep; 2023 Mar; 13(1):4363. PubMed ID: 36928068
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
